Article
instance of
subclass of
description
Disease Ontology ID
MeSH tree code
Commons category
image
1,4-phenylenediamine allergic contact dermatitis
class of disease
allergic contact dermatitis
allergic contact dermatitis that has allergic trigger 1,4-phenylenediamine
DOID:0040058
1-chloro-2,4-dinitrobenzene allergic contact dermatitis
class of disease
allergic contact dermatitis
allergic contact dermatitis that has allergic trigger 1-chloro-2,4-dinitrobenzene
DOID:0040069
17q11 microdeletion syndrome
class of disease
chromosomal deletion syndrome
partial deletion of the long arm of chromosome 17
Human disease
DOID:0060403
2,4-dinitrophenyl allergic contact dermatitis
class of disease
allergic contact dermatitis
allergic contact dermatitis that has allergic trigger 2,4-dinitrophenyl group
DOID:0040079
2-hydroxyglutaric aciduria
class of disease
amino acid metabolic disorder
neurometabolic disease
cerebral organic aciduria
rare genetic epilepsy
amino acid or protein metabolism disease with epilepsy
amino acid metabolic disorder that is an autosomal recessive neurometabolic disorder characterized by the significant elevation of urinary levels of hydroxyglutaric acid causing progressive brain damage
DOID:0050573
2q37 deletion syndrome
class of disease
chromosome abnormality
intellectual disability
chromosome 2q deletion
chromosomal deletion syndrome
human disease
DOID:0111704
3-methylcrotonyl-CoA carboxylase 1 deficiency
class of disease
3-methylcrotonyl-CoA carboxylase deficiency
3-methylcrotonyl-CoA carboxylase deficiency that has material basis in homozygous or compound heterozygous mutation in the gene encoding the alpha subunit of 3-methylcrotonyl-CoA carboxylase on chromosome 3q27
DOID:0080579
3-methylcrotonyl-CoA carboxylase 2 deficiency
class of disease
3-methylcrotonyl-CoA carboxylase deficiency
human disease
DOID:0080580
3-methylglutaconic aciduria 7A
class of disease
human disease
DOID:0081133
3-methylglutaconic aciduria type 1
class of disease
3-methylglutaconic aciduria
genetic disease
autosomal recessive disease
3-methylglutaconic aciduria that has material basis in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22
DOID:0110002
3-methylglutaconic aciduria type 4
class of disease
3-methylglutaconic aciduria
3-methylglutaconic aciduria that is characterized by mild or intermittent urinary excretion of 3-methylglutaconic acid
DOID:0110006
3-methylglutaconic aciduria type IX
class of disease
3-methylglutaconic aciduria
genetic disease
autosomal recessive disease
3-methylglutaconic aciduria that has material basis in homozygous mutation in the TIMM50 gene on chromosome 19q13
DOID:0070002
3MC syndrome 2
class of disease
3MC syndrome
3MC syndrome that has material basis in homozygous mutation in the COLEC11 gene on chromosome 2p25
DOID:0060576
3MC syndrome 3
class of disease
3MC syndrome
3MC congenital syndrome associated with the COLEC10 gene on chromosome 8q24
DOID:0060577
4-tert-butylphenol allergic contact dermatitis
class of disease
allergic contact dermatitis
allergic contact dermatitis that has allergic trigger 4-tert-butylphenol
DOID:0040068
4-vinylcyclohexene dioxide respiratory allergy
class of disease
respiratory allergy
respiratory allergy that has allergic trigger 4-vinylcyclohexene dioxide
DOID:0040063
46 XX gonadal dysgenesis
class of disease
gonadal dysgenesis
gonadal dysgenesis that is characterized by the lack of functional ovaries to induce puberty in an otherwise 46,XX female
DOID:14450
C12.706.316.064.249
C12.706.316.309.193
C13.351.875.253.064.249
C13.351.875.253.309.193
C16.131.939.316.064.249
C16.131.939.316.309.193
C19.391.119.064.249
C19.391.119.309.193
46,XX sex reversal 1
class of disease
XX male syndrome
X-linked dominant disease
human disease
DOID:0111761
46,XX sex reversal 2
class of disease
autosomal dominant disease
XX male syndrome
human disease
DOID:0111763
46,XX sex reversal 3
class of disease
XX male syndrome
X-linked dominant disease
human disease
DOID:0111762
46,XX sex reversal 4
class of disease
autosomal dominant disease
XX male syndrome
human disease
DOID:0111764
46,XY sex reversal 1
class of disease
Y-linked disease
XY gonadal dysgenesis
human disease
DOID:0111778
46,XY sex reversal 10
class of disease
hereditary lymphedema
familial hypertrophic cardiomyopathy
46,XY partial gonadal dysgenesis
XY gonadal dysgenesis
autosomal dominant disease
chromosomal deletion syndrome
human disease
DOID:0111775
46,XY sex reversal 2
class of disease
XY gonadal dysgenesis
X-linked disease
human disease
DOID:0111777
46,XY sex reversal 3
class of disease
autosomal dominant disease
XY gonadal dysgenesis
human disease
DOID:0111772
46,XY sex reversal 4
class of disease
XY gonadal dysgenesis
chromosomal deletion syndrome
human disease
DOID:0111771
46,XY sex reversal 5
class of disease
XY gonadal dysgenesis
autosomal recessive disease
human disease
DOID:0111776
46,XY sex reversal 6
class of disease
XY gonadal dysgenesis
autosomal dominant disease
human disease
DOID:0111769
46,XY sex reversal 7
class of disease
autosomal recessive disease
XY gonadal dysgenesis
human disease
DOID:0111774
46,XY sex reversal 8
class of disease
autosomal recessive disease
XY gonadal dysgenesis
human disease
DOID:0111773
46,XY sex reversal 9
class of disease
autosomal dominant disease
XY gonadal dysgenesis
human disease
DOID:0111770
ABCD syndrome
class of disease
autosomal recessive disease
Waardenburg-Shah syndrome
syndrome
Autosomal recessive disease that is characterized by albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness and has material basis in a mutation in the endothelin B receptor gene (EDNRB)
DOID:0050600
ABri amyloidosis
class of disease
cerebral amyloid angiopathy
ITM2B amyloidosis
genetic disease
autosomal dominant disease
human disease
DOID:0070029
ACTH-independent macronodular adrenal hyperplasia 1
class of disease
Cushing syndrome due to macronodular adrenal hyperplasia
human disease
DOID:0111623
ACTH-independent macronodular adrenal hyperplasia 2
class of disease
Cushing syndrome due to macronodular adrenal hyperplasia
human disease
DOID:0111624
AMED syndrome
class of disease
syndrome
autosomal recessive disease
digenic disease
human disease
DOID:0080952
APP-related cerebral amyloid angiopathy
class of disease
cerebral amyloid angiopathy
autosomal dominant disease
A cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of APP on chromosome 21q21.3.
DOID:0070028
Aagenaes syndrome
class of disease
syndrome
primary lymphedema with associated anomalies
genetic vascular anomaly
rare genetic hepatic disease
syndromic lymphedema
rare genetic immune disease
disease
syndrome that is characterized by congenital hypoplasia of lymph vessels, which causes lymphedema of the legs and recurrent cholestasis in infancy, and slow progress to hepatic cirrhosis and giant cell hepatitis with fibrosis of the portal tracts
DOID:6691
Aagenaes syndrome
Achard syndrome
class of disease
syndrome
genetic disease
syndrome that involves arachnodactyly, receding lower jaw, and joint laxity limited to the hands and feet
DOID:6686
Achenbach syndrome
class of disease
skin disease
skin condition characterized by spontaneous focal hemorrhage into the palm or the volar surface of a finger
DOID:6687
Paroxysmal hand hematoma
Acinetobacter infectious disease
class of disease
gram-negative bacterial infection
opportunistic bacterial infectious disease
Human disease
DOID:3091
C01.150.252.400.560.022
Adie syndrome
class of disease
syndrome
abnormal pupillary function
disease
neurological disorder characterized by a tonically dilated pupil
DOID:11549
C10.177.045
C10.292.562.700.250
C11.590.436.200
C11.710.800.180
Adie syndrome
African histoplasmosis
class of disease
histoplasmosis
disease
Human disease
DOID:11315
African iron overload
class of disease
iron overload
HFE hereditary haemochromatosis
hemochromatosis characterized by a predisposition to iron loading that is exacerbated by excessive intake of dietary iron, commonly related to consumption of tradition beer brewed in non-galvanized steel drums
DOID:0111033
African tick-bite fever
class of disease
spotted fever
disease
spotted fever that has material basis in Rickettsia africae, which is transmitted by ticks
DOID:0050035
African tick bite fever
Alkhurma hemorrhagic fever
class of disease
Kyasanur forest disease
Human disease
DOID:0050308
Alkuraya-Kučinskas syndrome
class of disease
cerebral malformation
autosomal recessive disease
syndrome
human disease
DOID:0111555
Alpha-thalassemia mental retardation syndrome
class of disease
rare disease
developmental defect during embryogenesis
designated intractable/rare disease
alpha thalassemia
alpha-thalassemia-related diseases
X-linked dominant disease
X-linked intellectual disability
ATR-X-related syndrome
syndrome with 46,XY disorder of sex development
syndrome with disorder of sex development of gynecological interest
alpha thalassemia that has material basis in mutation in the ATRX gene on Xq21
DOID:0110030
Alpha-thalassemia mental retardation syndrome
Alteración del estado mental
class of disease
schizophrenia
disease
DOID:1229
F03.700.750.600
Alwadei syndrome
class of disease
autosomal recessive non-syndromic intellectual disability
neurodevelopmental disorder
autosomal recessive non-syndromic intellectual disability that has material basis in an autosomal recessive mutation of the RUSC2 gene on chromosome 9p13
DOID:0080239
Alzheimer disease 10
class of disease
Alzheimer's disease
early-onset autosomal dominant Alzheimer disease
Alzheimer's disease that is characterized by an associated with variation in the region 7q36
DOID:0110043
Alzheimer disease 11
class of disease
Alzheimer's disease
early-onset autosomal dominant Alzheimer disease
An Alzheimer's disease that is characterized by an associated with variation in the region 9p22.1.
DOID:0110044
Alzheimer disease 12
class of disease
Alzheimer's disease
early-onset autosomal dominant Alzheimer disease
Alzheimer's disease that is characterized by an associated with variation in the region 8p12-q22
DOID:0110045
Alzheimer disease 13
class of disease
Alzheimer's disease
early-onset autosomal dominant Alzheimer disease
Alzheimer's disease that is characterized by an associated with variation in the region 1q21
DOID:0110046
Alzheimer disease 14
class of disease
Alzheimer's disease
early-onset autosomal dominant Alzheimer disease
Alzheimer's disease that is characterized by an associated with variation in the region 1q25
DOID:0110047
Alzheimer disease 15
class of disease
Alzheimer's disease
early-onset autosomal dominant Alzheimer disease
Alzheimer's disease that is characterized by an associated with variations in the region 3q22-q24
DOID:0110048
Alzheimer disease 16
class of disease
Alzheimer's disease
An Alzheimer's disease that is characterized by an associated with a risk allele in in the PCDH11X gene on chromosome Xq21.3.
DOID:0110036
Alzheimer disease 17
class of disease
Alzheimer's disease
Alzheimer's disease that is characterized by an associated with mutations in the gene TREM2
DOID:0110049
Alzheimer disease 18
class of disease
Alzheimer's disease
Alzheimer's disease that has material basis in a mutation in the ADAM10 gene on chromosome 15q21
DOID:0110050
Alzheimer disease 19
class of disease
Alzheimer's disease
Alzheimer's disease that is characterized by associated variants of the gene PLD3
DOID:0110051
Alzheimer disease 5
class of disease
Alzheimer's disease
early-onset autosomal dominant Alzheimer disease
autosomal dominant disease
human disease
DOID:0110037
Alzheimer disease 6
class of disease
Alzheimer's disease
early-onset autosomal dominant Alzheimer disease
Alzheimer's disease that is characterized by an associated with variation in the region 10q24
DOID:0110038
Alzheimer disease 7
class of disease
Alzheimer's disease
early-onset autosomal dominant Alzheimer disease
Alzheimer's disease that is characterized by an associated with variation in the region 10p13
DOID:0110039
Alzheimer disease 8
class of disease
Alzheimer's disease
early-onset autosomal dominant Alzheimer disease
An Alzheimer's disease that is characterized by an associated with variation in the region 20p12.2-q11.21.
DOID:0110041
Alzheimer's disease 1
class of disease
autosomal dominant disease
Alzheimer's disease
Alzheimer's disease that has material basis in mutation in the gene encoding the amyloid precursor protein on chromosome 21q
DOID:0080348
Alzheimer's disease 9
class of disease
autosomal dominant disease
Alzheimer's disease
early-onset autosomal dominant Alzheimer disease
human disease
DOID:0111364
Ambras type hypertrichosis universalis congenita
class of disease
hypertrichosis
hypertrichosis lanuginosa congenita
human disease
DOID:0111060
American histoplasmosis
class of disease
histoplasmosis
Human disease
DOID:1759
Angelucci's syndrome
class of disease
allergic conjunctivitis
acute conjunctivitis
Human disease
DOID:11203
Arakawa's syndrome I
class of disease
syndrome
disorder of folate metabolism and transport
constitutional megaloblastic anemia due to folate metabolism disorder
vitamin metabolic disorder
autosomal recessive disease
genetic disorder
DOID:0111679
Arenaviridae infectious disease
class of disease
(-)ssRNA virus infectious disease
viral infectious disease
human disease
DOID:3944
C02.782.082
Argyll Robertson pupil
class of disease
abnormal pupillary function
disease
symptom of human disease
DOID:14523
Argyll Robertson pupil
Askin's tumor
class of disease
Ewing sarcoma
Human disease
DOID:0050608
Astrakhan spotted fever
class of disease
spotted fever
Human disease
DOID:0050041
Atlantic cod allergy
class of disease
fish allergy
fish allergy triggered by Gadus morhua
DOID:0060514
Atlantic salmon allergy
class of disease
fish allergy
fish allergy triggered by Salmo salar
DOID:0060515
Axenfeld-Rieger syndrome
class of disease
autosomal dominant disease
eye disease
autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment
DOID:14686
Axenfeld syndrome
Axenfeld-Rieger syndrome type 2
class of disease
Axenfeld-Rieger syndrome
chromosomal deletion syndrome
Axenfeld-Rieger syndrome that has material basis in deletions in the region 13q14
DOID:0110121
B cell and dendritic cell deficiency
class of disease
combined immunodeficiency
human disease
DOID:0111964
B cell deficiency
class of disease
primary immunodeficiency disease
primary immunnodeficiency disease that is caused by a lack of infection-fighting antibody producing B cells (immunoglobulins) or B cells that are not functioning properly
DOID:2115
B cell linker protein deficiency
class of disease
agammaglobulinemia
autosomal recessive disease
Human disease
DOID:0060027
B-cell acute lymphoblastic leukemia
class of disease
acute lymphocytic leukemia
lymphoma
B-cell leukemia
human disease
DOID:0080638
B-cell adult acute lymphocytic leukemia
class of disease
adult acute lymphocytic leukemia
B-cell childhood acute lymphoblastic leukemia
lymphoma
Human disease
DOID:0060592
B-cell childhood acute lymphoblastic leukemia
class of disease
childhood acute lymphocytic leukemia
B-cell acute lymphoblastic leukemia
lymphoma
childhood acute lymphoblastic leukemia that has material basis in B-cells
DOID:0080146
B-cell lymphoma
class of disease
non-Hodgkin lymphoma
leukocyte disease
immune disorder
non-Hodgkin lymphoma that has material basis in B cells
DOID:707
C04.557.386.480.150
C15.604.515.569.480.150
C20.683.515.761.480.150
B-cell lymphomas
B-cell prolymphocytic leukemia
class of disease
prolymphocytic leukemia
human disease
DOID:0081041
B-lymphoblastic leukemia/lymphoma KMT2A rearranged
class of disease
precursor B lymphoblastic lymphoma/leukemia
human disease
DOID:0080644
B-lymphoblastic leukemia/lymphoma with BCR-ABL1
class of disease
precursor B lymphoblastic lymphoma/leukemia
human disease
DOID:0080643
B-lymphoblastic leukemia/lymphoma with ETV6-RUNX1
class of disease
precursor B lymphoblastic lymphoma/leukemia
human disease
DOID:0080645
B-lymphoblastic leukemia/lymphoma with IL3-IGH
class of disease
precursor B lymphoblastic lymphoma/leukemia
human disease
DOID:0080648
B-lymphoblastic leukemia/lymphoma with TCF3-PBX1
class of disease
precursor B lymphoblastic lymphoma/leukemia
human disease
DOID:0080649
B-lymphoblastic leukemia/lymphoma with hyperdiploidy
class of disease
precursor B lymphoblastic lymphoma/leukemia
human disease
DOID:0080646
B-lymphoblastic leukemia/lymphoma with hypodiploidy
class of disease
precursor B lymphoblastic lymphoma/leukemia
human disease
DOID:0080647
B-lymphoblastic leukemia/lymphoma with iAMP21
class of disease
precursor B lymphoblastic lymphoma/leukemia
human disease
DOID:0080651
B-lymphoblastic leukemia/lymphoma, BCR-ABL1–like
class of disease
precursor B lymphoblastic lymphoma/leukemia
human disease
DOID:0080650
BIDS syndrome
class of disease
trichothiodystrophy syndromes
autosomal recessive disease
nonphotosensitive trichothiodystrophy
Human disease
DOID:0050528
Balkan hemorrhagic fever
class of disease
hemorrhagic fever with renal syndrome
Human disease
DOID:0050522
Balkan nephropathy
class of disease
interstitial nephritis
Alport syndrome
interstitial nephritis endemic to the regions along the Danube river, in the modern countries of Croatia, Bosnia and Herzegovina, Serbia, Romania and Bulgaria
DOID:3052
C12.200.777.419.570.643.150
C12.050.351.968.419.570.643.150
C12.950.419.570.643.150
Balo concentric sclerosis
class of disease
demyelinating disease
neurodegeneration
multiple sclerosis
disease
demyelinating disease characterized by the fact that the demyelinated tissues form concentric layers
DOID:0060215
Balo concentric sclerosis
Bardet-Biedl syndrome 1
class of disease
Bardet-Biedl syndrome
Bardet-Biedl syndrome that has material basis in homozygous mutation in the BBS1 gene on chromosome 11q13
DOID:0110123
Barrett's adenocarcinoma
class of disease
esophagus adenocarcinoma
adenocarcinoma arising in Barrett's mucosa
DOID:7941
Barrett's esophagus
class of disease
esophageal disease
disease
esophagus condition
DOID:9206
C04.834.154
C06.405.117.102
Barrett's esophagus
Bartholin's duct cyst
class of disease
Bartholin's gland disease
disease
cyst in a blocked Bartholin's gland
DOID:851
Bartholin's cyst
Bartholin's gland adenocarcinoma
class of disease
Bartholin's gland carcinoma
adenocarcinoma
vulva adenocarcinoma
Human disease
DOID:6316
Bartholin's gland adenoid cystic carcinoma
class of disease
Bartholin's gland carcinoma
Bartholin's gland adenocarcinoma
Human disease
DOID:4879
Bartholin's gland adenoma
class of disease
Bartholin's gland benign neoplasm
benign epithelial neoplasm
benign neoplasms by histologic type
Bartholin's gland disease
adenoma
Human disease
DOID:5382
Bartholin's gland adenomyoma
class of disease
Bartholin's gland benign neoplasm
adenomyoma
Bartholin's gland carcinoma
Bartholin's gland disease
Human disease
DOID:6518
Bartholin's gland adenosquamous carcinoma
class of disease
adenosquamous carcinoma
Bartholin's gland squamous cell carcinoma
Bartholin's gland carcinoma
Bartholin's gland carcinoma that derives from squamous cells and gland-like cells
DOID:5630
Bartholin's gland benign neoplasm
class of disease
vestibular gland benign neoplasm
bartholin gland neoplasm
Human disease
DOID:2068
Bartholin's gland cancer
class of disease
vulvar cancer
Bartholin's gland disease
vulva cancer that is located in Bartholin's gland
DOID:60003
Bartholin's gland carcinoma
class of disease
vulva carcinoma
Bartholin's gland benign neoplasm
Bartholin's gland cancer
disease
vulva carcinoma that has material basis in abnormally proliferating cells derives from epithelial cells and is located in Bartholin's gland
DOID:3999
Bartholin's gland disease
class of disease
female reproductive system disease
Disease that is located in Bartholin's gland
DOID:60002
Bartholin's gland small cell carcinoma
class of disease
Bartholin's gland carcinoma
female reproductive organ cancer
small cell carcinoma
Human disease
DOID:7140
Bartholin's gland squamous cell carcinoma
class of disease
Bartholin's gland carcinoma
squamous cell carcinoma
vulva squamous cell carcinoma
Human disease
DOID:6961
Bartholin's gland transitional cell carcinoma
class of disease
Bartholin's gland carcinoma
transitional cell carcinoma
Human disease
DOID:3998
Bartter disease type 1
class of disease
Bartter disease
A Bartter disease that has material basis in homozygous or compound heterozygous mutation in the sodium-potassium-chloride cotransporter-2 gene (SLC12A1) on chromosome 15q21.
DOID:0110142
Bartter disease type 2
class of disease
Bartter disease
A Bartter disease that has material basis in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24.
DOID:0110143
Bartter disease type 4b
class of disease
Bartter disease
infantile Bartter syndrome with sensorineural deafness
Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes
DOID:0110146
Bartter disease type 5
class of disease
Bartter disease
Bartter disease that has material basis in mutation in the MAGED2 gene on chromosome Xp11
DOID:0110147
Basilicata-Akhtar syndrome
class of disease
X-linked intellectual disability
human disease
DOID:0111838
Beckwith-Wiedemann syndrome
class of disease
syndrome
overgrowth syndrome
disease
syndrome characterized by overgrowth (macrosomia), an increased risk of childhood cancer and congenital malformations
DOID:5572
C16.131.077.133
C16.131.260.080
C16.320.180.080
Beemer-Langer syndrome
class of disease
short rib – polydactyly syndrome
syndrome
syndrome that results in multiple congenital anomalies, including hydrops fetalis, facial and visceral abnormalities, short ribs, and short limbs without polydactyly
DOID:9249
Behcet's syndrome arthropathy
class of disease
arthropathy
Behçet's disease
Human disease
DOID:1670
Bell's palsy
class of disease
symptom or sign
facial paralysis
palsy
disease
facial paralysis resulting from dysfunction in the cranial nerve VII (facial nerve)
DOID:12506
C01.925.256.466.087
C07.465.094
C07.465.299.250
C10.292.319.250
Bell's palsy
Bellini duct carcinoma
class of disease
renal carcinoma
renal cell carcinoma
disease
DOID:4464
Collecting duct carcinoma
Bernard-Soulier syndrome
class of disease
Giant platelet disorder
inherited blood coagulation disease
blood coagulation disease
autosomal recessive disease
disease
Human disease
DOID:2217
C15.378.100.100.080
C15.378.140.120
C15.378.463.080
C16.320.099.080
Blessig's cysts
class of disease
peripheral retinal degeneration
retinoschisis and retinal cysts
Human disease
DOID:12164
Bordetella parapertussis whooping cough
class of disease
pertussis
A pertussis that is a milder disease caused by the bacterium Bordetella parapertussis. The disease has symptom coughing, has symptom sneezing, or has symptom runny nose .
DOID:11750
Borst-Jadassohn intraepidermal carcinoma
class of disease
skin carcinoma
Human disease
DOID:7039
Bowman's membrane folds or rupture
class of disease
corneal disease
Human disease
DOID:11552
Brainstem glioma
class of disease
brain stem cancer
glioma
brain glioma
Human disease
DOID:4202
Brainstem gliomas
Brown's tendon sheath syndrome
class of disease
mechanical strabismus
genetic disease
Human disease
DOID:10235
Brown-Vialetto-Van Laere syndrome
class of disease
autosomal dominant disease
infantile progressive bulbar palsy
Human disease
DOID:0050694
Brown-Vialetto-Van Laere syndrome 1
class of disease
autosomal recessive disease
Brown-Vialetto-Van Laere syndrome
human disease
DOID:0080785
Brugada syndrome 1
class of disease
Brugada syndrome
autosomal dominant disease
Brugada syndrome that has material basis in heterozygous mutation in the SCN5A gene on chromosome 3p22
DOID:0110218
Brugada syndrome 7
class of disease
Brugada syndrome
autosomal dominant disease
Brugada syndrome that has material basis in heterozygous mutation in the SCN3B gene on chromosome 11q24
DOID:0110224
Buruli ulcer disease
class of disease
primary bacterial infectious disease
mycobacterium infectious disease
neglected tropical disease
disease
tropical disease
DOID:0050456
C01.150.252.410.040.552.475.247
C17.800.893.295
Buruli ulcer
Buschke–Ollendorff syndrome
class of disease
osteopetrosis
syndrome
autosomal dominant disease
medical condition
DOID:0111536
Buschke–Ollendorff syndrome
C-P angle neurinoma
class of disease
neurilemmoma
cerebellopontine angle tumor
Human disease
DOID:3199
CADASIL 1
class of disease
CADASIL
autosomal dominant disease
CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13
DOID:0111035
CAKUT1
class of disease
CAKUT
human disease
DOID:0080206
CD3delta deficiency
class of disease
severe combined immunodeficiency
T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta
autosomal recessive disease
primary immunodeficiency disease
A severe combined immunodeficiency that is characterized by the absence of T cells but normal numbers of B cells. CD3D is essential for T cell development.
DOID:0060016
CD3epsilon deficiency
class of disease
severe combined immunodeficiency
autosomal recessive disease
Human disease
DOID:0060017
CD40 ligand deficiency
class of disease
combined immunodeficiency
X-linked hyper IgM syndrome
X-linked recessive disease
Human disease
DOID:0060022
CLOVES syndrome
class of disease
overgrowth syndrome
subcutaneous tissue disease
rare genetic vascular tumor
nevus
complex vascular malformation with associated anomalies
genetic skin vascular disorder
rare genetic subcutaneous tissue disorder
syndrome
PIK3CA-related overgrowth spectrum
CLOVE syndrome is characterized by Congenital Lipomatous Overgrowth, progressive, complex and mixed truncal Vascular malformations, and Epidermal nevi
DOID:0080351
COACH Syndrome
class of disease
syndrome
Joubert syndrome
Joubert syndrome and related disorders
autosomal recessive disease
a rare autosomal recessive disorder characterised by Cerebellar vermis hypoplasia, Oligophrenia (developmental delay/mental retardation), Ataxia, Coloboma, and Hepatic fibrosis.
DOID:0111589
CREST syndrome
class of disease
syndrome
limited scleroderma
disease
syndrome characterized by calcinosis, Raynaud's phenomeno, esophageal dysmotility, sclerodactyly and telangiectasia
DOID:0060218
C06.405.117.119.500.204
C14.907.617.812.500
C14.907.823.225
C17.300.799.801.500
C17.800.784.801.500
C18.452.174.130.204
CREST syndrome
Caplan's syndrome
class of disease
pneumoconiosis
rheumatoid lung disease
disease
pneumoconiosis that results in humans that also have rheumatoid arthritis
DOID:10326
C05.550.114.154.219
C05.799.114.219
C08.381.483.581.300
C08.381.520.702.300
C17.300.775.099.219
C24.800.340
Carrion's disease
class of disease
bartonellosis
disease
infectious disease produced by Bartonella bacilliformis infection
DOID:0050398
Carrion's disease
Cervicocranial syndrome
class of disease
syndrome
neurological disorder
syndrome that involves occipital head aches, nystagmus on head movement, tinnitus, spasms, blurred vision, corneal hyperaesthesia, and corneal ulcers
DOID:6692
C05.116.900.596
Chandler syndrome
class of disease
corneal dystrophy
iridocorneal endothelial syndrome
Human disease
DOID:11554
Charcot-Marie-Tooth disease axonal type 2H
class of disease
Charcot-Marie-Tooth disease type 2
autosomal recessive axonal hereditary motor and sensory neuropathy
autosomal recessive disease
Charcot-Marie-Tooth disease type 2 that has material basis in variation in the region 8q13-q23
DOID:0110166
Charcot-Marie-Tooth disease dominant intermediate A
class of disease
Charcot-Marie-Tooth disease intermediate type
autosomal dominant intermediate Charcot-Marie-Tooth disease
autosomal dominant disease
A Charcot-Marie-Tooth disease intermediate type that has material basis in variation in the region 10q24.1-q25.1.
DOID:0110202
Charcot-Marie-Tooth disease dominant intermediate G
class of disease
Charcot-Marie-Tooth disease intermediate type
human disease
DOID:0080294
Charcot-Marie-Tooth disease intermediate type
class of disease
Charcot–Marie–Tooth disease
Charcot-Marie-Tooth disease characterized by motor conduction velocities above and below 38 m/s
DOID:0050543
Charcot-Marie-Tooth disease type 1
class of disease
Charcot–Marie–Tooth disease
autosomal dominant hereditary demyelinating motor and sensory neuropathy
Charcot-Marie-Tooth disease characterized by demyelination of the peripheral nerve axons
DOID:0050538
Charcot-Marie-Tooth disease type 1G
class of disease
Charcot-Marie-Tooth disease type 1
autosomal dominant disease
human disease
DOID:0111560
Charcot-Marie-Tooth disease type 2A2B
class of disease
Charcot-Marie-Tooth disease type 2
autosomal recessive disease
human disease
DOID:0111557
Charcot-Marie-Tooth disease type 2DD
class of disease
autosomal dominant disease
Charcot-Marie-Tooth disease type 2
human disease
DOID:0111558
Charcot-Marie-Tooth disease type 2EE
class of disease
Charcot-Marie-Tooth disease type 2
autosomal recessive disease
human disease
DOID:0111559
Charcot-Marie-Tooth disease type 3
class of disease
Charcot–Marie–Tooth disease
Human disease
DOID:0050540
Charcot-Marie-Tooth disease type 4
class of disease
Charcot–Marie–Tooth disease
autosomal recessive hereditary demyelinating motor and sensory neuropathy
Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has material basis in autosomal recessive inheritance
DOID:0050541
Charcot-Marie-Tooth disease type 7
class of disease
Charcot–Marie–Tooth disease
Charcot-Marie-Tooth disease that is characterized by optic atrophy followed by retinitis pigmentosa
DOID:0080069
Charcot-Marie-tooth disease type 5
class of disease
Charcot–Marie–Tooth disease
hereditary spastic paraplegia
autosomal dominant disease
Charcot-Marie-Tooth disease that is characterized by pyramidal features including extensor plantar responses, mild increase in tone, and preserved or increased reflexes but no spastic gait
DOID:0080067
Chediak-Higashi syndrome
class of disease
autosomal recessive disease
nervous system heredodegenerative disease
eye degenerative disease
syndrome
disease
rare autosomal recessive disorder related to lysossomal function and the CHS1 gene
DOID:2935
C15.378.553.774.257
C20.673.774.257
C11.270.040.772
Chediak-Higashi syndrome
Clostridioides difficile colitis
class of disease
colitis
Clostridium difficile intestinal infectious disease
disease
colitis characterized by an overgrowth of Clostridioides difficile bacteria
DOID:0060185
C01.150.252.410.222.310
C06.405.205.596.800
C06.405.469.363.800
Pseudomembranous colitis
Clostridium infectious disease
class of disease
bacterial infectious disease
Human disease
DOID:3584
DOID:0050351
C01.150.252.410.222
Coats disease
class of disease
retinal telangiectasia
congenital vitreoretinal dysplasia
secondary glaucoma due to a proliferation and differentiation anomaly
genetic vascular disease
genetic central nervous system and retinal vascular disease
central nervous system and retinal vascular disease
disease
Human disease
DOID:7765
C11.768.748
C14.907.823.502
Coats' disease
Coffin-Siris syndrome 1
class of disease
Coffin-Siris syndrome
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of ARID1B on chromosome 6q25.3.
DOID:0070042
Coffin-Siris syndrome 6
class of disease
Coffin-Siris syndrome
human disease
DOID:0080297
Cogan-Reese syndrome
class of disease
eye disease
iridocorneal endothelial syndrome
eye disease characterized by variable iris atrophy, pigmented and pedunculated nodules located in iris and attachment of the iris to the cornea (peripheral anterior synechiae) and characterized by glaucoma
DOID:0060217
Conn's syndrome
class of disease
hyperaldosteronism
adrenal adenoma
adrenal gland disease
disease
adrenal adenoma characterized by over production of aldosterone
DOID:12028
Primary aldosteronism
Cornelia de Lange syndrome 1
class of disease
Cornelia de Lange syndrome
autosomal dominant disease
Cornelia de Lange syndrome that has material basis in heterozygous mutation in the NIPBL gene, which encodes a component of the cohesin complex, on chromosome 5p13
DOID:0080505
Cornelia de Lange syndrome 2
class of disease
Cornelia de Lange syndrome
X-linked dominant disease
Cornelia de Lange syndrome that has material basis in a mutation in the SMC1A gene, which encodes a subunit of the cohesin complex, on chromosome Xp11
DOID:0080506
Cornelia de Lange syndrome 3
class of disease
Cornelia de Lange syndrome
autosomal dominant disease
A Cornelia de Lange syndrome that has material basis in heterozygous mutation in the SMC3 gene on chromosome 10q25.2.
DOID:0080507
Cornelia de Lange syndrome 4
class of disease
Cornelia de Lange syndrome
autosomal dominant disease
Cornelia de Lange syndrome that has material basis in heterozygous mutation in the RAD21 gene, which encodes a component of the cohesin complex, on chromosome 8q24
DOID:0080508
Cornelia de Lange syndrome 5
class of disease
Cornelia de Lange syndrome
X-linked dominant disease
Cornelia de Lange syndrome that has material basis in by mutation in the HDAC8 gene on chromosome Xq13
DOID:0080509
Cortical blindness
class of disease
visual cortex disease
cerebral visual impairment
human disease
DOID:11831
C10.597.751.941.162.250
C11.966.075.250
C23.888.592.763.941.162.250
Cowden syndrome 1
class of disease
autosomal dominant disease
multiple hamartoma syndrome
syndrome
disease
inherited disorder causing tumor-like growth and increased cancer risk
DOID:6457
Cowden syndrome
Cowper gland carcinoma
class of disease
male reproductive organ cancer
Littre gland carcinoma
carcinoma
male reproductive organ cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the Cowper's gland
DOID:7632
Crohn's colitis
class of disease
Crohn's disease
colitis
inflammatory bowel disease characterized by inflammation located in colon only
DOID:0060192
D-2-hydroxyglutaric aciduria 1
class of disease
D-2-hydroxyglutaric aciduria
autosomal recessive disease
human disease
DOID:0111351
D-2-hydroxyglutaric aciduria 2
class of disease
autosomal dominant disease
D-2-hydroxyglutaric aciduria
human disease
DOID:0111352
D-glycerate dehydrogenase deficiency
class of disease
primary hyperoxaluria
disease
DOID:0111671
D-glyceric aciduria
class of disease
inherited metabolic disorder
autosomal recessive disease
human disease
DOID:0111626
D-mannitol allergy
class of disease
drug allergy
drug allergy that has allergic trigger D-mannitol
DOID:0040019
DIC in newborn
class of disease
disseminated intravascular coagulation
Human disease
DOID:11246
De Barsy syndrome
class of disease
inborn disorder of ornithine or proline metabolism
cutis laxa
autosomal recessive disease
human disease
DOID:0070143
Diamond-Blackfan anemia 1
class of disease
Diamond-Blackfan anemia
autosomal dominant disease
human disease
DOID:0111895
Diamond-Blackfan anemia 10
class of disease
autosomal dominant disease
Diamond-Blackfan anemia
human disease
DOID:0111888
Diamond-Blackfan anemia 11
class of disease
autosomal dominant disease
Diamond-Blackfan anemia
human disease
DOID:0111892
Diamond-Blackfan anemia 12
class of disease
Diamond-Blackfan anemia
autosomal dominant disease
human disease
DOID:0111882
Diamond-Blackfan anemia 13
class of disease
Diamond-Blackfan anemia
autosomal dominant disease
human disease
DOID:0111889
Diamond-Blackfan anemia 15 with mandibulofacial dysostosis
class of disease
Diamond-Blackfan anemia
autosomal dominant disease
human disease
DOID:0111894
Diamond-Blackfan anemia 16
class of disease
Diamond-Blackfan anemia
autosomal dominant disease
human disease
DOID:0111893
Diamond-Blackfan anemia 17
class of disease
autosomal dominant disease
Diamond-Blackfan anemia
human disease
DOID:0111880
Diamond-Blackfan anemia 18
class of disease
Diamond-Blackfan anemia
autosomal dominant disease
human disease
DOID:0111896
Diamond-Blackfan anemia 19
class of disease
autosomal dominant disease
Diamond-Blackfan anemia
human disease
DOID:0111886
Diamond-Blackfan anemia 2
class of disease
autosomal dominant disease
Diamond-Blackfan anemia
human disease
DOID:0111885
Diamond-Blackfan anemia 20
class of disease
autosomal dominant disease
Diamond-Blackfan anemia
human disease
DOID:0111891
Diamond-Blackfan anemia 4
class of disease
autosomal dominant disease
Diamond-Blackfan anemia
human disease
DOID:0111890
Diamond-Blackfan anemia 5
class of disease
Diamond-Blackfan anemia
autosomal dominant disease
human disease
DOID:0111883
Diamond-Blackfan anemia 6
class of disease
Diamond-Blackfan anemia
autosomal dominant disease
human disease
DOID:0111879
Diamond-Blackfan anemia 7
class of disease
autosomal dominant disease
Diamond-Blackfan anemia
human disease
DOID:0111878
Diamond-Blackfan anemia 8
class of disease
Diamond-Blackfan anemia
autosomal dominant disease
human disease
DOID:0111881
Diamond-Blackfan anemia 9
class of disease
Diamond-Blackfan anemia
autosomal dominant disease
human disease
DOID:0111884
Diamond-blackfan anemia 3
class of disease
Diamond-Blackfan anemia
autosomal dominant disease
human disease
DOID:0111887
Dieulafoy lesion
class of disease
stomach disease
disease
Human disease
DOID:12070
Dieulafoy's lesion
Doyne honeycomb retinal dystrophy
class of disease
drusen
genetic disease
autosomal dominant disease
Human disease
DOID:0060745
Ehlers-Danlos syndrome arthrochalasia type 1
class of disease
Ehlers-Danlos syndrome
autosomal dominant disease
human disease
DOID:0080727
Ehlers-Danlos syndrome arthrochalasia type 2
class of disease
autosomal dominant disease
Ehlers-Danlos syndrome
human disease
DOID:0080728
Ehlers-Danlos syndrome cardiac valvular type
class of disease
Ehlers-Danlos syndrome
autosomal recessive disease
human disease
DOID:0080730
Ehlers-Danlos syndrome classic type 2
class of disease
autosomal dominant disease
Ehlers-Danlos syndrome
human disease
DOID:0080726
Ehlers-Danlos syndrome classic-like 1
class of disease
autosomal recessive disease
Ehlers-Danlos syndrome
human disease
DOID:0080731
Ehlers-Danlos syndrome classic-like 2
class of disease
autosomal recessive disease
Ehlers-Danlos syndrome
human disease
DOID:0080732
Ehlers-Danlos syndrome dermatosparaxis type
class of disease
autosomal recessive disease
Ehlers-Danlos syndrome
human disease
DOID:0080733
Ehlers-Danlos syndrome kyphoscoliotic type 1
class of disease
Ehlers-Danlos syndrome
autosomal recessive disease
human disease
DOID:0080734
Ehlers-Danlos syndrome kyphoscoliotic type 2
class of disease
autosomal recessive disease
Ehlers-Danlos syndrome
human disease
DOID:0080735
Ehlers-Danlos syndrome musculocontractural type 1
class of disease
autosomal recessive disease
Ehlers-Danlos syndrome
human disease
DOID:0080736
Ehlers-Danlos syndrome musculocontractural type 2
class of disease
Ehlers-Danlos syndrome
autosomal recessive disease
human disease
DOID:0080737
Ehlers-Danlos syndrome spondylodysplastic type 1
class of disease
autosomal recessive disease
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome progeroid type
human disease
DOID:0080738
Ehlers-Danlos syndrome spondylodysplastic type 3
class of disease
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome progeroid type
human disease
DOID:0080739
Ehlers-Danlos syndrome, periodontal type 2 Edspd2
class of disease
Ehlers-Danlos syndrome, periodontitis type
Ehlers-Danlos syndrome
autosomal dominant disease
human disease
DOID:0080987
Ehrlich tumor carcinoma
class of disease
breast carcinoma
Human disease
DOID:5050
C04.557.470.200.200
C04.619.169
Emery-Dreifuss muscular dystrophy 3, autosomal recessive
class of disease
Emery-Dreifuss muscular dystrophy
autosomal recessive disease
human disease
DOID:0070248
Epstein-Barr virus hepatitis
class of disease
viral hepatitis
viral hepatitis that results in inflammation, located in liver, has material basis in Human herpesvirus 4 and has symptom headache, has symptom fatigue, has symptom fever, has symptom abdominal pain, has symptom nausea, and has symptom jaundice
DOID:0050204
Erdheim-Chester disease
class of disease
non-Langerhans-cell histiocytosis
granulomatous autoinflammatory syndrome
histiocytic and dendritic cell cancer
connective tissue neoplasm
immune disorder
disease
rare disease
DOID:4329
C15.604.250.410.224
Erdheim–Chester disease
Evans' syndrome
class of disease
primary thrombocytopenia
autoimmune hemolytic anemia
hemolytic anemia
autoimmune thrombocytopenia
Human disease
DOID:8931
FTDALS3
class of disease
amyotrophic lateral sclerosis
frontotemporal dementia
behavioral variant of frontotemporal dementia
FTDALS1
amyotrophic lateral sclerosis and frontotemporal dementia
amyotrophic lateral sclerosis that has material basis in mutation in the SQSTM1 gene on chromosome 5q35
DOID:0110068
Fanconi anemia complementation group A
class of disease
Fanconi anemia
genetic disease
autosomal recessive disease
Fanconi anemia that has material basis in homozygous or compound heterozygous mutation in the FANCA gene on chromosome 16q24
DOID:0111095
Fanconi renotubular syndrome 1
class of disease
Fanconi syndrome
autosomal dominant disease
human disease
DOID:0080757
Fanconi renotubular syndrome 2
class of disease
Fanconi syndrome
autosomal recessive disease
human disease
DOID:0080758
Fanconi renotubular syndrome 3
class of disease
Fanconi syndrome
autosomal dominant disease
human disease
DOID:0080759
Fanconi renotubular syndrome 4
class of disease
Fanconi syndrome
autosomal dominant disease
human disease
DOID:0080760
Fanconi renotubular syndrome 5
class of disease
Fanconi syndrome
autosomal recessive disease
human disease
DOID:0080761
Fanconi-like syndrome
class of disease
syndrome
genetic disease
syndrome characterized by pancytopenia, immune deficiency and cutaneous malignancies
DOID:0090066
Far Eastern spotted fever
class of disease
spotted fever
Human disease
DOID:0050046
Foster-Kennedy syndrome
class of disease
papilledema
disease
Human disease
DOID:14555
Fox-Fordyce disease
class of disease
sweat gland disease
disease
chronic blockage of the sweat gland ducts with a secondary, non-bacterial inflammatory response to the secretions and cellular debris in the cysts
DOID:1381
C17.800.946.492.285
Fraser syndrome 1
class of disease
Fraser syndrome
human disease
DOID:0111405
Fraser syndrome 2
class of disease
Fraser syndrome
human disease
DOID:0111407
Fraser syndrome 3
class of disease
Fraser syndrome
human disease
DOID:0111406
French Canadian Leigh disease
class of disease
Leigh disease
human disease
DOID:0111180
Frey syndrome
class of disease
autonomic nervous system disease
human disease
DOID:11599
Frey's syndrome
Friedreich ataxia 1
class of disease
A Friedreich ataxia that has material basis in homozygous or compound heterozygous mutation in FXN on 9q21.1.
DOID:0111218
Friedreich ataxia 2
class of disease
Friedreich ataxia that has material basis in mutation in the 9p23-p11 chromosome region
DOID:0111219
Froelich syndrome
class of disease
hypothalamic disease
hypothalamic disease that is characterized by endocrine dysfunction of the hypothalamic gland resulting in delayed puberty, small testes, and obesity
DOID:6676
Adiposogenital dystrophy
Fuchs' endothelial dystrophy
class of disease
corneal endothelial dystrophy
disease
corneal dystrophy characterized by accumulation of focal outgrowths (guttae) and thickening of Descemet's membrane, leading to corneal edema and loss of vision
DOID:11555
C11.204.236.438
C11.270.162.438
C16.320.290.162.410
Fuchs' dystrophy
Fuchs' heterochromic uveitis
class of disease
uveitis
syndrome
syndrome that is a chronic unilateral (or rarely bilateral) iridocyclitis appearing with the triad of heterochromia, predisposition to cataracts and glaucoma, and keratitic percipitates on the posterior corneal surface
DOID:9375
Fuchs heterochromic iridocyclitis
GM1 gangliosidosis type 1
class of disease
gangliosidosis GM1
GM1 gangliosidosis type 1 is the severe infantile form of GM1 gangliosidosis (see this term) with variable neurological and systemic manifestations
DOID:0080502
GM1 gangliosidosis type 2
class of disease
gangliosidosis GM1
GM1 gangliosidosis that is characterized by slowly progressive generalized neurodegeneration and mild skeletal changes, with onset between 7 months and 3 years of age
DOID:0080501
GM2 gangliosidosis
class of disease
gangliosidosis
nervous system heredodegenerative disease
human disease
DOID:3321
C10.228.140.163.100.435.825.300.300
C16.320.565.189.435.825.300.300
C16.320.565.398.641.803.350.300
C16.320.565.595.554.825.300.300
C18.452.132.100.435.825.300.300
C18.452.584.563.641.803.350.300
C18.452.648.189.435.825.300.300
C18.452.648.398.641.803.350.300
C18.452.648.595.554.825.300.300
GNE myopathy
class of disease
autosomal recessive disease
muscular disease
human disease
DOID:0080718
GRID2-related autosomal dominant spinocerebellar ataxia
class of disease
spinocerebellar ataxia
human disease
DOID:0050988
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
class of disease
frontotemporal lobar degeneration
frontotemporal dementia
primary progressive aphasia
genetic disease
autosomal dominant disease
Human disease
DOID:0060672
Galloway-Mowat syndrome 2
class of disease
Galloway-Mowat syndrome
X-linked recessive disease
human disease
DOID:0080244
Galloway-Mowat syndrome 3
class of disease
Galloway-Mowat syndrome
autosomal recessive disease
human disease
DOID:0080245
Galloway-Mowat syndrome 4
class of disease
Galloway-Mowat syndrome
autosomal recessive disease
human disease
DOID:0080246
Galloway-Mowat syndrome 5
class of disease
Galloway-Mowat syndrome
human disease
DOID:0080247
Gasserian ganglion meningioma
class of disease
meningioma
Human disease
DOID:7635
Gaucher's disease perinatal lethal
class of disease
Gaucher's disease
genetic disease
Gaucher's Disease characterized by perinatal lethality and rapid progression of neurological deterioration that has material basis in an autosomal recessive mutation of GBA on chromosome 1q22
DOID:0110960
Gaucher's disease type I
class of disease
Gaucher's disease
genetic disease
Gaucher's disease characterized by absence of primary central nervous system involvement that has material basis in a mutation of GBA on chromosome 1q22
DOID:0110957
Gaucher's disease type II
class of disease
Gaucher's disease
genetic disease
Gaucher's disease characterized by rapid neurologic deterioration with cranial nerve and extrapyramidal tract involvement that has material basis in an autosomal recessive mutation of GBA on chromosome 1q22
DOID:0110958
Gaucher's disease type III
class of disease
Gaucher's disease
genetic disease
Gaucher's disease characterized by later onset and slower progession of neurological deterioration compared to type II that has material basis in an autosomal recessive mutation of GBA on chromosome 1q22
DOID:0110959
Geleophysic dysplasia 2
class of disease
geleophysic dysplasia
autosomal dominant disease
human disease
DOID:0111726
Gerstmann syndrome
class of disease
neurological disorder
disease
nervous system disease that results from damage located in left parietal lobe, has symptom agraphia, has symptom acalculia, has symptom finger agnosia
DOID:4969
C10.597.606.762.100.300
C23.888.592.604.764.100.300
Gilbert syndrome
class of disease
bilirubin metabolic disorder
disease
metabolic disorder in which the liver processes bilirubin slowly
DOID:2739
C16.320.565.300.528
C18.452.648.300.528
Glanzmann's thrombasthenia
class of disease
blood platelet disease
inherited blood coagulation disease
rare hemorrhagic disorder due to a qualitative platelet defect
disease
human disease
DOID:2219
C15.378.100.100.820
C15.378.140.810
C15.378.463.810
C16.320.099.820
Good syndrome
class of disease
agammaglobulinemia
combined immunodeficiency
agammaglobulinemia that is a condition where there is co-occurrence of deficient cell-mediated immunity and benign thymoma
DOID:0060028
Graves' disease
class of disease
autoimmune disease of endocrine system
autoimmune disease of endocrine system that involves production of excessive amount of thyroid hormones, located in thyroid gland
DOID:12361
C11.675.349.500
C19.874.283.605
C19.874.397.370
C20.111.555
Griscelli syndrome
class of disease
autosomal recessive disease
integumentary system disease
autosomal recessive disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin
DOID:0060831
Griscelli syndrome type 2
class of disease
Griscelli syndrome
A Griscelli syndrome characterized by silvery gray sheen of the hair, hypopigmentation of the skin and immunodeficiency with or without neurologic impairment that has material basis in mutation in the RAB27A gene on chromosome 15q21.3.
DOID:0060833
Griscelli syndrome type 3
class of disease
Griscelli syndrome
Griscelli syndrome characterized by isolated silvery gray sheen of the hair and hypopigmentation of the skin that has material basis in mutation in the MLPH or MYO5A genes
DOID:0060834
Gulf War syndrome
class of disease
syndrome
disease
illlnesses affecting Gulf War Vets
DOID:4491
C24.653
H syndrome
class of disease
histiocytosis
autosomal recessive disease
syndrome
genetic condition
DOID:0111278
HCL-V
class of disease
hairy cell leukemia
Human disease
DOID:713
HELLP syndrome
class of disease
severe pre-eclampsia
disease
severe pre-eclampsia characterized by hemolysis, elevated liver enzyme and low platelet count
DOID:13133
C13.703.395.186
Haemodialysis-associated amyloidosis
class of disease
amyloidosis
Dialytrauma
ABeta2M amyloidosis
acquired metabolic disease
kidney disease
#946;2M) deposits in the musculoskeletal system leading to carpal tunnel syndrome (CTS), chronic arthropathy, cystic bone lesions, destructive osteoarthropathy, and pathologic fractures
DOID:0080928
Heart failure with preserved ejection fraction
class of disease
heart failure
congestive heart failure
congestive heart failure wherein the amount of blood pumped from the heart's left ventricle with each beat (ejection fraction) is greater than 50%
DOID:9775
C14.280.434.611
Heimler syndrome 1
class of disease
deafness-enamel hypoplasia-nail defects syndrome
peroxisomal biogenesis disorder
autosomal recessive disease
human disease
DOID:0080623
Heimler syndrome 2
class of disease
deafness-enamel hypoplasia-nail defects syndrome
peroxisomal biogenesis disorder
autosomal recessive disease
human disease
DOID:0080624
Heinz body anemia
class of disease
congenital hemolytic anemia
congenital nonspherocytic hemolytic anemia
autosomal dominant disease
human disease
DOID:0111363
Henoch-Schoenlein purpura
class of disease
hypersensitivity vasculitis
nonthrombocytopenic purpura
disease
Human disease
DOID:11123
C14.907.940.777
C15.378.100.802.375
C15.378.463.515.580
C20.543.520.600
C23.550.414.950.375
C23.888.885.687.375
Henoch–Schönlein purpura
Her2-receptor negative breast cancer
class of disease
breast cancer
Human disease
DOID:0060080
Her2-receptor positive breast cancer
class of disease
breast cancer
breast carcinoma by gene expression profile
Hormone receptor positive breast tumor
Human disease
DOID:0060079
Hermansky-Pudlak syndrome 1
class of disease
Hermansky-Pudlak syndrome
A Hermansky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the HPS1 gene on chromosome 10q24.
DOID:0060539
Hermansky-Pudlak syndrome 2
class of disease
Hermansky-Pudlak syndrome
A Hermansky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the gene encoding the beta-3A subunit of the AP3 complex (AP3B1) on chromosome 5q14.1.
DOID:0060540
Hermansky-Pudlak syndrome 3
class of disease
Hermansky-Pudlak syndrome
Hermasky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the HPS3 gene on chromosome 3q24
DOID:0060541
Hermansky-Pudlak syndrome 4
class of disease
Hermansky-Pudlak syndrome
A Hermansky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the HPS4 gene on chromosome 22q12.1.
DOID:0060542
Hermansky-Pudlak syndrome 5
class of disease
Hermansky-Pudlak syndrome
Hermansky-Pudlak syndrome that has material basis in homozygous mutation in the HPS5 gene on chromosome 11p14
DOID:0060543
Hermansky-Pudlak syndrome 6
class of disease
Hermansky-Pudlak syndrome
Hermansky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the HPS6 gene on chromosome 10q24
DOID:0060544
Hermansky-Pudlak syndrome 7
class of disease
Hermansky-Pudlak syndrome
A Hermansky-Pudlak syndrome that has material basis in homozygous mutation in the DTNBP1 gene on chromosome 6p22.3.
DOID:0060545
Hermansky-Pudlak syndrome 8
class of disease
Hermansky-Pudlak syndrome
Hermansky-Pudlak syndrome that has material basis in homozygous mutation in the BLOC1S3 gene on chromosome 19q13
DOID:0060546
Hermansky-Pudlak syndrome 9
class of disease
Hermansky-Pudlak syndrome
human disease
DOID:0060547
Hirata disease
class of disease
autoimmune disease of endocrine system
immune disorder
hyperinsulinemic hypoglycemia
autoimmune disease of endocrine system characterized by hypoglycemia caused by antibodies to insulin
DOID:0040100
Hodgkin lymphoma
class of disease
symptom or sign
lymphoma
disease
lymphoma that is marked classically by the presence of Reed-Sternberg cells
DOID:8567
C04.557.386.355
C15.604.515.569.355
C20.683.515.761.355
Hodgkin's lymphoma
Hodgkin's granuloma
class of disease
Hodgkin lymphoma
human disease
DOID:8651
Hodgkin's lymphoma, lymphocytic depletion
class of disease
Hodgkin lymphoma
Human disease
DOID:8628
Hodgkin's lymphoma, lymphocytic-histiocytic predominance
class of disease
Hodgkin lymphoma
Human disease
DOID:8543
Hodgkin's lymphoma, mixed cellularity
class of disease
Hodgkin lymphoma
human disease
DOID:8654
Hodgkin's lymphoma, nodular sclerosis
class of disease
Hodgkin lymphoma
Human disease
DOID:8838
Hodgkin's paragranuloma
class of disease
Hodgkin lymphoma
Human disease
DOID:8642
Horner's syndrome
class of disease
autonomic neuropathy
disease
A disease characterized by miosis (a constricted pupil), partial ptosis (a weak, droopy eyelid), apparent anhydrosis (decreased sweating), with apparent enophthalmos (inset eyeball)
DOID:11486
C10.177.350
C10.597.690.362.500
C11.710.528.500
C23.888.592.708.362.500
Horner's syndrome
IDH-wildtype anaplastic astrocytoma
class of disease
anaplastic astrocytoma
human disease
DOID:0080876
IGSF1 deficiency syndrome
class of disease
central congenital hypothyroidism
X-linked recessive disease
syndrome
X-linked disease characterized by hypothyroidism that is present at birth, delayed testosterone increase in puberty, and testicular enlargement in adulthood that has material basis in mutation of the IGSF1 gene on chromosome Xq26
DOID:0111140
IgG4-related disease
class of disease
autoimmune connective tissue disorder
autoimmune disease
systemic fibroinflammatory disease, associated with elevated serum IgG4 levels in about 60% of cases
DOID:0080356
C20.111.572
IgG4-related disease
Indian plum allergy
class of disease
fruit allergy
fruit allergy triggered by Ziziphus mauritiana plant fruit food product.
DOID:0060507
Indian prawn allergy
class of disease
shrimp allergy
crustacean allergy
crustacean allergy triggered by Fenneropenaeus indicus
DOID:0060527
Indian tick typhus
class of disease
spotted fever
Human disease
DOID:0050042
Israeli tick typhus
class of disease
spotted fever
Human disease
DOID:0050043
Jaccoud's syndrome
class of disease
autoimmune disease
joint disorder
Human disease
DOID:13080
Jaccoud arthropathy
Japanese spotted fever
class of disease
spotted fever
Human disease
DOID:0050050
Jewett-Marshall bladder cancer
class of disease
bladder carcinoma
Human disease
DOID:7315
Joubert syndrome 1
class of disease
Joubert syndrome
Joubert syndrome that has material basis in homozygous mutation in the INPP5E gene on chromosome 9q34
DOID:0110980
Joubert syndrome 10
class of disease
Joubert syndrome
Joubert syndrome with orofaciodigital defect
X-linked recessive disease
A Joubert syndrome that has material basis in X-linked recessive inheritance of mutation in the OFD1 gene on chromosome Xp22.2.
DOID:0110981
Joubert syndrome 13
class of disease
Joubert syndrome
Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the TCTN1 gene on chromosome 12q24
DOID:0110982
Joubert syndrome 14
class of disease
Joubert syndrome
Joubert syndrome with oculorenal defect
Joubert syndrome with ocular defect
human disease
DOID:0110983
Joubert syndrome 15
class of disease
Joubert syndrome
Joubert syndrome with ocular defect
Joubert syndrome characterized by ataxia, hypotonia, delayed psychomotor development, and variable mental retardation that has material basis in homozygous mutation in the CEP41 gene on chromosome 7q32
DOID:0110984
Joubert syndrome 17
class of disease
Joubert syndrome
Joubert syndrome characterized by episodic hyperpnea, abnormal eye movements, ataxia, and global psychomotor retardation that has material basis in compound heterozygous mutation in the C5ORF42 gene on chromosome 5p13
DOID:0110986
Joubert syndrome 18
class of disease
Joubert syndrome
Joubert syndrome with orofaciodigital defect
Joubert syndrome that has material basis in homozygous mutation in the TCTN3 gene on chromosome 10q24
DOID:0110987
Joubert syndrome 20
class of disease
Joubert syndrome
Joubert syndrome with ocular defect
Joubert syndrome that has material basis in compound heterozygous mutation in the TMEM231 gene on chromosome 16q23
DOID:0110989
Joubert syndrome 21
class of disease
Joubert syndrome
Joubert syndrome with Jeune asphyxiating thoracic dystrophy
Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the CSPP1 gene on chromosome 8q13
DOID:0110990
Joubert syndrome 22
class of disease
Joubert syndrome
Joubert syndrome with orofaciodigital defect
Joubert syndrome that has material basis in homozygous mutation in the PDE6D gene on chromosome 2q37
DOID:0110991
Joubert syndrome 23
class of disease
Joubert syndrome
human disease
DOID:0110992
Joubert syndrome 24
class of disease
Joubert syndrome
Joubert syndrome characterized by delayed psychomotor development and molar tooth sign on brain MRI that has material basis in homozygous mutation in the TCTN2 gene on chromosome 12q24
DOID:0110993
Joubert syndrome 25
class of disease
Joubert syndrome
human disease
DOID:0110994
Joubert syndrome 26
class of disease
Joubert syndrome
Joubert syndrome characterized by global developmental delay and cerebellar hypoplasia that has material basis in homozygous mutation in the KIAA0556 gene on chromosome 16p12
DOID:0110995
Joubert syndrome 27
class of disease
Joubert syndrome
Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the B9D1 gene on chromosome 17p11
DOID:0110996
Joubert syndrome 28
class of disease
Joubert syndrome
Joubert syndrome with ocular defect
Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the MKS1 gene on chromosome 17q23
DOID:0110997
Joubert syndrome 29
class of disease
Joubert syndrome
human disease
DOID:0080276
Joubert syndrome 30
class of disease
Joubert syndrome
human disease
DOID:0080275
Joubert syndrome 31
class of disease
Joubert syndrome
human disease
DOID:0080277
Joubert syndrome 6
class of disease
Joubert syndrome
Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the TMEM67 on chromosome 8q22
DOID:0111001
Joubert syndrome 7
class of disease
Joubert syndrome
A Joubert syndrome that has material basis in mutation in the RPGRIP1L gene on chromosome 16q12.2.
DOID:0111002
Joubert syndrome 8
class of disease
Joubert syndrome
A Joubert syndrome that has material basis in mutation in the ARL13B gene on chromosome 3q11.1-q11.2
DOID:0111003
Kallmann syndrome
class of disease
hypogonadotropic hypogonadism
disease
A form of hypogonadotropic hypogonadism which is also accompanied by a total lack or partial loss in the sense of smell. The condition affects both males and females and causes a failure in puberty and infertility.
DOID:3614
C12.706.316.096.750
C13.351.875.253.096.750
C16.131.939.316.096.750
C16.320.467
C19.391.119.096.750
C19.391.482.600
Kallmann syndrome
Kanzaki disease
class of disease
Schindler disease
human disease
DOID:0112319
Kartagener syndrome
class of disease
primary ciliary dyskinesia
situs inversus
disease
primary ciliary dyskinesia that is characterized by sinusitis, bronchiectasis and situs inversus with dextrocardia resulting from dysfunction of the cilia during embryologic development
DOID:0050144
C08.127.384.500
C08.200.531
C08.695.501
C09.150.531
C14.240.400.280.500
C14.280.400.280.500
C16.131.077.245.500.531
C16.131.240.400.280.500
C16.131.740.501
C16.131.810.250.500
C16.320.184.500.531
C16.320.480
Kartagener syndrome
Kawasaki disease
class of disease
lymphadenitis
immune disorder
predominantly medium-vessel vasculitis
disease
human disease in which blood vessels throughout the body become inflamed
DOID:13378
C14.907.940.560
C15.604.560
C17.800.862.560
Kawasaki disease
Kelley–Seegmiller syndrome
class of disease
hypoxanthine-guanine phosphoribosyltransferase deficiency
hyperuricemia
X-linked recessive disease
disease
human disease
DOID:0112127
Kimura disease
class of disease
skin disease
Human disease
DOID:7365
C07.465.815.178
C15.378.553.231.774
C15.604.315.459
King Denborough syndrome
class of disease
autosomal dominant disease
human disease
DOID:0080990
Klatskin's tumor
class of disease
intrahepatic cholangiocarcinoma
disease
Human disease
DOID:4927
DOID:5246
C04.557.470.200.025.450.500
Kleefstra syndrome 1
class of disease
Kleefstra syndrome
autosomal dominant disease
chromosomal deletion syndrome
human disease
DOID:0060352
Kleefstra syndrome 2
class of disease
autosomal dominant disease
Kleefstra syndrome
human disease
DOID:0080598
Klippel-Feil syndrome 1
class of disease
Klippel-Feil syndrome
autosomal dominant disease
human disease
DOID:0080589
Klippel-Feil syndrome 2
class of disease
Klippel-Feil syndrome
autosomal recessive disease
human disease
DOID:0080590
Klippel-Feil syndrome 3, autosomal dominant
class of disease
autosomal dominant disease
Klippel-Feil syndrome
human disease
DOID:0080591
Klüver–Bucy syndrome
class of disease
impulse control disorder
disease
syndrome resulting from bilateral lesions of the medial temporal lobe
DOID:2510
C10.228.140.380.326
F03.615.400.431
Kohler's disease
class of disease
symptom or sign
osteochondrosis
foot diseases
disease
osteochondrosis that results in death and collapse located in navicular bone of foot
DOID:11760
Köhler disease
Korean hemorrhagic fever
class of disease
hemorrhagic fever with renal syndrome
Human disease
DOID:0050200
Kuhnt-Junius degeneration
class of disease
degeneration of macula and posterior pole
human disease
DOID:10873
C11.768.585.439.622
Kunjin encephalitis
class of disease
West Nile encephalitis
Human disease
DOID:0050174
Kuru
class of disease
transmissible spongiform encephalopathy
disease
human disease
DOID:648
C10.228.228.800.435
C10.574.843.625
C01.207.800.435
Kuru (disease)
L-cell glucagon-like peptide producing tumor
class of disease
gastrointestinal neuroendocrine benign tumor
Human disease
DOID:7402
L1 syndrome
class of disease
X-linked intellectual disability
hereditary spastic paraplegia
X-linked complex spastic paraplegia
nervous system heredodegenerative disease
X-linked recessive disease
hereditary spastic paraplegia that is characterized by hydrocephalus, spasticity of the lower limbs, adducted thumbs, aphasia, seizures, agenesis of the corpus callosum and intellectual disability in the mild to moderate range
DOID:0060246
DOID:0110762
LEOPARD syndrome 1
class of disease
LEOPARD syndrome
LEOPARD syndrome that has material basis in heterozygous mutation in the PTPN11 gene on chromosome 12q24
DOID:0080548
LEOPARD syndrome 2
class of disease
LEOPARD syndrome
LEOPARD syndrome that has material basis in heterozygous mutation in the RAF1 gene on chromosome 3p25
DOID:0080549
LEOPARD syndrome 3
class of disease
LEOPARD syndrome
LEOPARD syndrome that has material basis in heterozygous mutation in the BRAF gene on chromosome 7q34
DOID:0080550
Lambert-Eaton myasthenic syndrome
class of disease
neuromuscular junction disease
channelopathy
immune-mediated acquired neuromuscular junction disease
paraneoplastic neurologic syndrome
autoimmune disease of musculoskeletal system
autoimmune disease of peripheral nervous system
disease
an autoimmune, presynaptic disorder of neuromuscular transmission characterized by fluctuating muscle weakness and autonomic dysfunction frequently associated with small-cell lung cancer (SCLC)
DOID:0050214
C04.588.614.550.500.225
C04.730.856.490.225
C10.114.656.150
C10.574.781.588.225
C10.668.758.725.150
C20.111.258.500.150
Langerhans cell sarcoma
class of disease
dendritic cell tumor
leukocyte disease
histiocytic and dendritic cell cancer
sarcoma
histiocytic and dendritic cell cancer that derives from the lymph nodes, derives from the skin, derives from the liver, derives from the spleen and derives from bones
DOID:7146
C04.557.227.500
C15.604.250.390.500
Langerhans-cell histiocytosis
class of disease
histiocytosis
disease
disease involving clonal proliferation of Langerhans cells
DOID:2571
C08.381.483.375
C15.604.250.400
Langerhans cell histiocytosis
Leber congenital amaurosis 1
class of disease
Leber congenital amaurosis
genetic disease
autosomal recessive disease
Leber congenital amaurosis characterized by severe cone-rod dystrophy with photophobia, high hyperopia, and poor but stable vision with no visual improvement and that has material basis in mutation in the GUCY2D gene on chromosome 17p13
DOID:0110078
Leber hereditary optic neuropathy with demyelinating disease of CNS
class of disease
Leber plus disease
human disease
DOID:0111756
Leber optic atrophy and dystonia
class of disease
Leber plus disease
human disease
DOID:0111755
Leber plus disease
class of disease
Leber hereditary optic neuropathy
syndrome
DOID:0111754
Lenz-Majewski hyperostotic dwarfism
class of disease
autosomal dominant disease
syndrome
osteochondrodysplasia
human disease
DOID:0111507
Lewy body dementia
class of disease
synucleinopathy
dementia
type of dementia
DOID:12217
C10.228.140.079.862.400
C10.228.140.380.422
C10.228.662.600.200
C10.574.531
F03.615.400.512
Lewy body dementia
Leydig cell tumor
class of disease
testicular sex cord-stromal neoplasm
sex cord-gonadal stromal tumor
Human disease
DOID:2696
C04.557.475.750.847.249
C04.588.322.762.500.249
C04.588.945.440.915.500.249
C12.294.260.937.500.249
C12.758.409.937.500.249
C19.344.762.500.249
C19.391.829.782.500.249
Li-Fraumeni syndrome 1
class of disease
Li-Fraumeni syndrome
human disease
DOID:0111503
Li-Fraumeni syndrome 2
class of disease
Li-Fraumeni syndrome
human disease
DOID:0111504
Libman–Sacks endocarditis
class of disease
marantic endocarditis
autoimmune disease of cardiovascular system
endocarditis
disease
human disease
DOID:0080740
Lisch epithelial corneal dystrophy
class of disease
epithelial and subepithelial dystrophy
Human disease
DOID:0060450
Littre gland carcinoma
class of disease
male reproductive organ cancer
male urethral cancer
carcinoma
male reproductive organ cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the Littre glands
DOID:6721
Livedoid vasculitis
class of disease
vasculitis
vasculitis with purpuric ulcers
DOID:0040099
C14.907.355.830.573
C17.800.862.406
Livedoid vasculitis
Loeffler endocarditis
class of disease
restrictive cardiomyopathy
non-familial restrictive cardiomyopathy
disease
restrictive cardiomyopathy that affects the endocardium and occurs with white blood cell proliferation, specifically of eosinophils
DOID:396
Loeffler syndrome
class of disease
eosinophilic pneumonia
Acute eosinophilic pneumonia
allergy
disease
Human disease
DOID:9503
Loeys-Dietz syndrome 1
class of disease
Loeys-Dietz syndrome
Loeys-Dietz syndrome that has material basis in heterozygous mutation in the TGFBR1 gene on chromosome 9q22
DOID:0070235
Loeys-Dietz syndrome 2
class of disease
Loeys-Dietz syndrome
Loeys-Dietz syndrome that has material basis in heterozygous mutation in the TGFBR2 gene on chromosome 3p24
DOID:0070234
Loeys-Dietz syndrome 4
class of disease
Loeys-Dietz syndrome
human disease
DOID:0070233
Lown-Ganong-Levine syndrome
class of disease
syndrome
pre-excitation syndrome
genetic cardiac rhythm disease
disease
syndrome that involves pre-excitation of the ventricles due to an accessory pathway providing an abnormal electrical communication from the atria to the ventricles
DOID:13087
C14.280.067.780.560
Lown-Ganong-Levine syndrome
Lynch syndrome
class of disease
autosomal dominant disease
hereditary neoplastic syndromes
colorectal cancer
neoplasm
syndrome
disease
Human disease
DOID:3883
C04.588.274.476.411.307.190
C04.700.250
C06.301.371.411.307.190
C06.405.249.411.307.190
C06.405.469.158.356.190
C06.405.469.491.307.190
C16.320.700.250
C18.452.284.255
Lynch syndrome 1
class of disease
Lynch syndrome
Lynch syndrome that has material basis in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16
DOID:0070271
Lytico-bodig disease
class of disease
amyotrophic lateral sclerosis
progressive supranuclear palsy
neurodegenerative disease with dementia
neurodegeneration
human disease
DOID:0111246
Léri–Weill dyschondrosteosis
class of disease
osteochondrodysplasia
human disease
DOID:0060847
MALT lymphoma
class of disease
marginal zone B-cell lymphoma
primary cutaneous marginal zone lymphoma
non-Hodgkin lymphoma that has material basis in mucosal tissue involved in antibody production
DOID:0050909
C04.557.386.480.150.570
C15.604.515.569.480.150.570
C20.683.515.761.480.150.570
MHC class I deficiency
class of disease
severe combined immunodeficiency
Bare lymphocyte syndrome
Human disease
DOID:0060009
MODY 1
class of disease
maturity-onset diabetes of the young
medical condition
DOID:0111099
MYH9-related disorder
class of disease
blood platelet disease
Inherited giant platelet disorder
A blood platelet disease that has material basis in mutations in the MYH9 gene. It is characterized by thrombocytopenia, enlarged platelets, sensorineural hearing loss and presenile cataract.
DOID:0060651
Maffucci syndrome
class of disease
syndrome
Ollier disease
disease
syndrome characterized by the presence of multiple enchondromas (benign growths of cartilage) associated with multiple cavernous hemangiomas and phleboliths
DOID:0060221
Mahvash Disease
class of disease
endocrine pancreas disease
autosomal recessive disease
human disease
DOID:0112306
Martinez Monasterio Pinheiro syndrome
class of disease
cleft lip and cleft palate
hair diseases
syndactyly
form of Blepharo-cheilo-dontic syndrome with with cleft lip and palate, complete absence of deciduous teeth, hypodontia of permanent teeth, hair alterations, hypertelorism, midface hypoplasia, abnormal EEG, syndactyly, and other findings
DOID:9003731
Masters-Allen syndrome
class of disease
female reproductive system disease
Human disease
DOID:14133
Mayer-Rokitansky-Kuster-Hauser syndrome
class of disease
syndrome
human disease
DOID:0112177
Mayer-Rokitansky-Kuster-Hauser syndrome type 1
class of disease
human disease
DOID:0112178
Meckel syndrome 1
class of disease
Meckel syndrome
Meckel syndrome that has material basis in an autosomal recessive mutation of MKS1 on chromosome 17q22
DOID:0070115
Meckel syndrome 13
class of disease
Meckel syndrome
autosomal recessive disease
human disease
DOID:0080253
Meckel's diverticulitis
class of disease
diverticulitis
diverticulits characterized by the inflammation of a congenital diverticulum, which is a slight bulge of the small intestine present at birth
DOID:8408
Meckel's diverticulum
class of disease
genetic disease
small intestine congenital defect
diverticulum
congenital disorder
disease
congenital disorder of digestive system
DOID:9487
C06.198.859
C16.131.314.556
C23.300.415.750
Meckel's diverticulum
Meckel's diverticulum cancer
class of disease
ileum cancer
Human disease
DOID:10152
Meesmann corneal dystrophy 1
class of disease
Meesmann corneal dystrophy
autosomal dominant disease
human disease
DOID:0080670
Meesmann corneal dystrophy 2
class of disease
Meesmann corneal dystrophy
autosomal dominant disease
human disease
DOID:0080671
Meier-Gorlin syndrome 1
class of disease
Meier-Gorlin syndrome
autosomal recessive disease
Meier-Gorlin syndrome that has material basis in homozygous or compound heterozygous mutation in the ORC1 gene on chromosome 1p32
DOID:0080512
Meige syndrome
class of disease
cranio-facial dystonia
focal, segmental or multifocal dystonia
cranio-facial dystonia that is accompanied by blepharospasm
DOID:3982
C10.228.140.079.590
C10.228.662.300.500
Meige's syndrome
Merkel cell carcinoma
class of disease
skin carcinoma
rare genetic developmental defect during embryogenesis
genetic epidermal disorder
skin tumor or hamartoma
inherited neuroendocrine tumor
genetic nervous system disorder
malignant dermis tumor
dermis disorder
neuroendocrine tumor with other location
nervous system cancer
rare nervous system tumor
disease
rare and highly aggressive skin cancer
DOID:3965
C02.256.721.150
C02.928.216
C04.557.465.625.650.240.325
C04.557.470.200.025.370.325
C04.557.580.625.650.240.325
Merkel cell carcinoma
Middle East respiratory syndrome
class of disease
acute viral respiratory tract infection
coronavirus disease
disease
viral respiratory infection in humans and camels
DOID:0080642
Middle East respiratory syndrome
Milker's nodule
class of disease
viral infectious disease
paravaccinia virus infection
Human disease
DOID:8729
Miller Fisher syndrome
class of disease
symptom or sign
Guillain–Barré syndrome
regional variant of Guillain-Barre syndrome
Guillain-Barre syndrome that manifests as a descending paralysis
DOID:12889
C10.114.750.100.500
C10.228.140.252.500
C10.292.562.350
C10.314.750.450.500
C10.668.829.350.500
C10.668.829.800.750.300.500
C11.590.312
C20.111.258.750.400.500
Miller–Dieker lissencephaly syndrome
class of disease
symptom or sign
syndrome
autosomal dominant
classic lissencephaly
autosomal dominant disease
disease
A syndrome characterized by classical lissencephaly and distinct facial features. Visible and submicroscopic deletions of 17p13.3, including the LIS1 gene, are found in almost 100% of patients.
DOID:0060469
Mitis junctional epidermolysis bullosa
class of disease
junctional epidermolysis bullosa
genetic disease
autosomal recessive disease
human disease
DOID:0060738
Miyoshi muscular dystrophy
class of disease
distal muscular dystrophy
distal muscular dystrophy characterized by autosomal recessive inheritance of distal muscle weakness in the upper and lower limbs that spares the intrinsic muscles of the hands and has onset in young adulthood
DOID:0070198
Miyoshi myopathy
Miyoshi muscular dystrophy 1
class of disease
Miyoshi muscular dystrophy
genetic disease
autosomal recessive disease
Miyoshi muscular dystrophy that has material basis in mutation in the DYSF gene on chromosome 2p13
DOID:0070199
Miyoshi muscular dystrophy 2
class of disease
Miyoshi muscular dystrophy
Miyoshi muscular dystrophy characterized by asymmetric presentation of muscle weakness and atrophy that has material basis in a locus on chromosome 10
DOID:0070200
Monckeberg arteriosclerosis
class of disease
arteriosclerosis
vascular calcification
Human's arterial pathology
DOID:5161
C18.452.174.130.780.500
Monckeberg's arteriosclerosis
Mooren's ulcer
class of disease
corneal ulcer
Human disease
DOID:10439
Morgagni cataract
class of disease
senile cataract
Human disease
DOID:13964
Mullegama-Klein-Martinez syndrome
class of disease
X-linked intellectual disability
human disease
DOID:0111845
Mycoplasma pneumonia
class of disease
atypical pneumonia
bacterial pneumonia
Mycoplasma pneumoniae infection
human disease
DOID:13276
DOID:0050154
C01.150.252.400.610.610.760
C01.150.252.620.500
C08.381.677.540.500
C08.730.610.540.545
C01.748.610.540.545
N,N'-diethylthiourea allergic contact dermatitis
class of disease
allergic contact dermatitis
allergic contact dermatitis that has allergic trigger N,N-diethylthiourea
DOID:0040102
N,N'-diphenylthiourea allergic contact dermatitis
class of disease
allergic contact dermatitis
allergic contact dermatitis that has allergic trigger N,N-diphenylthiourea
DOID:0040101
NK cell deficiency
class of disease
primary immunodeficiency disease
human disease
DOID:0080709
NUT midline carcinoma
class of disease
carcinoma
rare tumor
undifferentiated carcinoma
Human disease
DOID:0060463
NUT midline carcinoma
Nezelof syndrome
class of disease
thymic hypoplasia
primary immunodeficiency disease
autosomal recessive disease
T cell deficiency
Human disease
DOID:2012
Niemann-Pick disease
class of disease
sphingolipidosis
disease
severe metabolic disorders in which sphingomyelin accumulates in lysosomes in cells
DOID:14504
C10.228.140.163.100.435.825.700
C15.604.250.410.625
C16.320.565.189.435.825.700
C16.320.565.398.641.803.730
C16.320.565.595.554.825.700
C18.452.132.100.435.825.700
C18.452.584.687.803.730
C18.452.648.189.435.825.700
C18.452.648.398.641.803.730
C18.452.648.595.554.825.700
Niemann–Pick disease
Niemann-Pick disease type A
class of disease
Niemann-Pick disease
genetic disease
A Niemann-Pick disease characterized by onset in infancy and involvement of neurological tissues that has material basis in an autosomal recessive mutation of SMPD1 on chromosome 11p15.4.
DOID:0070111
Niemann-Pick disease type B
class of disease
Niemann-Pick disease
genetic disease
a Niemann-Pick disease characterized by visceral involvement only and survival into adulthood: material basis in an autosomal recessive mutation of SMPD1 on chromosome 11p15.4
DOID:0070112
C10.228.140.163.100.435.825.700.750
C15.604.250.410.625.750
C16.320.565.189.435.825.700.750
C16.320.565.398.641.803.730.750
C16.320.565.595.554.825.700.750
C18.452.132.100.435.825.700.750
C18.452.584.687.803.730.750
C18.452.648.189.435.825.700.750
C18.452.648.398.641.803.730.750
C18.452.648.595.554.825.700.750
Niemann-Pick disease, type C1
class of disease
Niemann-Pick disease
Niemann–Pick disease, type C
genetic disease
Type C Niemann-Pick disease associated with a mutation in the gene NPC1, encoding Niemann-Pick C1 protein
DOID:0070113
Niemann-Pick disease, type C2
class of disease
Niemann-Pick disease
Niemann–Pick disease, type C
genetic disease
A Niemann-Pick disease that has material basis in an autosomal recessive mutation of NPC2 on chromosome 14q24.3.
DOID:0070114
Nipah virus encephalitis
class of disease
viral encephalitis
Nipah virus infection
viral infectious disease
Human disease
DOID:0050192
Noonan syndrome 1
class of disease
Noonan syndrome
A Noonan syndrome disease type 1 that has material basis in the PTPN11 gene on chromosome 12q24.
DOID:0060578
DOID:0070101
Noonan syndrome 2
class of disease
Noonan syndrome
autosomal recessive disease
Noonan syndrome that has material basis in an autosomal recessive mutation
DOID:0060580
DOID:0070102
Noonan syndrome-like disorder with loose anagen hair 1
class of disease
Noonan syndrome-like disorder with loose anagen hair
human disease
DOID:0080692
Noonan syndrome-like disorder with loose anagen hair 2
class of disease
Noonan syndrome-like disorder with loose anagen hair
human disease
DOID:0080693
Ollier disease
class of disease
syndrome
enchondromatosis
disease
rare nonhereditary sporadic disorder
DOID:4624
Ollier disease
Opitz GBBB syndrome type I
class of disease
X-linked recessive disease
Opitz-GBBB syndrome
human disease
DOID:0080697
Opitz GBBB syndrome type II
class of disease
Opitz-GBBB syndrome
human disease
DOID:0080698
Oropouche fever
class of disease
viral infectious disease
Bunyaviridae infectious disease
disease
Human disease
DOID:0050521
Orthomyxoviridae infectious disease
class of disease
(-)ssRNA virus infectious disease
Human disease
DOID:4493
C01.925.782.620
Orthomyxoviridae infections
Osgood-Schlatter's disease
class of disease
bone inflammation disease
knee disorder
disease
osteochondrosis
DOID:7489
Osgood–Schlatter disease
Pacinian tumor
class of disease
neurofibroma
Human disease
DOID:2669
Paganini-Miozzo syndrome
class of disease
X-linked recessive disease
X-linked intellectual disability
human disease
DOID:0111843
Pancoast tumor
class of disease
lung cancer
pulmonary sulcus neoplasm
disease
tumor of the pulmonary apex
DOID:8007
C04.588.894.797.520.734
C08.381.540.734
C08.785.520.734
Pancoast tumor
Parkinson's disease 21
class of disease
autosomal dominant disease
hereditary late onset Parkinson disease
late onset Parkinson's disease characterized by autosomal dominant inheritance and mean age of onset at 67 years
DOID:0111251
Parkinson's disease 3
class of disease
Parkinson's disease
late onset Parkinson's disease characterized by mean age of onset of 59 years and that has material basis in mutation in a locus in the 2p13 chromosome region
DOID:0111250
Parry–Romberg syndrome
class of disease
facial nerve disease
brain inflammatory disease
inflammatory and autoimmune disease with epilepsy
genetic peripheral neuropathy
rare genetic epilepsy
disease
a rare disease characterized by progressive shrinkage and degeneration of the tissues beneath the skin, usually on only one side of the face (hemifacial atrophy) but occasionally extending to other parts of the body
DOID:1757
C07.465.284
C07.465.299.375
C10.292.319.375
Parry–Romberg syndrome
Partington X-linked mental retardation syndrome
class of disease
X-linked intellectual disability
X-linked recessive disease
syndrome characterized by intellectual disability, focal dystonia of the hands and dysarthria
DOID:14744
Patau syndrome
class of disease
chromosomal disease
total autosomal trisomy
trisomy 13
disease
Human disease
DOID:11665
C10.597.606.360.835
C14.240.400.970
C14.280.400.970
C16.131.240.400.965
C16.320.180.923
C16.131.260.923
C16.131.077.919
Patau syndrome
Pearson syndrome
class of disease
mitochondrial disease
mitochondrial metabolism disease
DOID:0060067
Perrault syndrome 6
class of disease
Perrault syndrome
human disease
DOID:0080256
Peyronie's disease
class of disease
penile disease
fibromatosis
disease
Human disease
DOID:8616
C12.294.494.508
C17.300.715
Peyronie's disease
File:Peyronie disease.jpg
Phlegmonous dacryocystitis
class of disease
dacryocystitis
Human disease
DOID:12997
Plasmodium ovale malaria
class of disease
malaria
malaria characaterized as a relatively mild form caused by a parasite Plasmodium ovale, which is characterized by tertian chills and febrile paroxysms, and that ends spontaneously
DOID:12919
Pleomorphic xanthoastrocytoma
class of disease
astrocytoma
low-grade astrocytoma
Human disease
DOID:4852
Pleomorphic xanthoastrocytoma
Plummer's disease
class of disease
hyperthyroidism
nodular goiter
Human disease
DOID:11277
Posner-Schlossman Syndrome
class of disease
iridocyclitis
Human disease
DOID:9378
Potter's syndrome
class of disease
sequence
renal agenesis
disease
congenital disorder of urinary system
DOID:12594
Prieto syndrome
class of disease
X-linked intellectual disability
X-linked recessive disease
Human disease
DOID:0060805
Prinzmetal's angina
class of disease
Vangina pectoris
coronaropathy
coronary artery vasospasm
disease
cardiac chest pain at rest that occurs in cycles
DOID:0111151
C14.280.647.187.150.150
C14.907.585.187.150.500
C23.888.592.612.233.500.150.150
Pthirus pubis infestation
class of disease
ectoparasitism
lice infestation
disease caused by the pubic louse, Pthirus pubis, a parasitic insect notorious for infesting human pubic hair
DOID:13760
Pubic lice
Qazi Markouizos syndrome
class of disease
syndrome
genetic syndromic intellectual disability
syndrome that is characterized by hypotonia, congenital fiber type disproportion and dysharmonic skeletal maturation
DOID:0050740
Quartan fever
class of disease
malaria
malaria caused by a parasite Plasmodium malariae, which is marked by recurrence of paroxysms at 72-hour intervals
DOID:14324
RASopathy
class of disease
genetic disease
syndrome
Family of genetic conditions caused by mutations affecting Ras genes
DOID:0080690
REM sleep behavior disorder
class of disease
sleep disorder
sleep disorder that involves abnormal behavior including the acting out of violent or dramatic dreams during the sleep phase with rapid eye movement
DOID:9091
C10.886.659.633.700
F03.870.664.633.700
RNASET2-deficient cystic leukoencephalopathy
class of disease
autosomal recessive disease
leukodystrophy
human disease
DOID:0081007
Raynaud disease
class of disease
peripheral vascular disease
Human disease
DOID:10300
C14.907.617.812
Raynaud's disease
Raynaud-Claes syndrome
class of disease
X-linked dominant disease
X-linked intellectual disability
human disease
DOID:0112060
Reye syndrome
class of disease
syndrome
encephalopathy
systemic disease
disease
syndrome characterized by acute brain damage and liver function problems
DOID:14525
C06.552.241.649
C10.228.140.163.780
C18.452.132.780
Reye's syndrome
Rh disease
class of disease
fetal erythroblastosis
blood group incompatibility
problem with Rh+ fetuses in Rh- mothers
DOID:4175
G09.188.114.750
G12.122.780
G12.186.750
Richter's syndrome
class of disease
chronic lymphocytic leukemia
disease
Human disease
DOID:1703
Rickettsia parkeri spotted fever
class of disease
spotted fever
A spotted fever that has material basis in Rickettsia parkeri, which is transmitted by Gulf Coast tick (Amblyomma maculatum). The infection has symptom fever, has symptom headache, has symptom eschar, and has symptom rash.
DOID:0050051
Riedel's fibrosing thyroiditis
class of disease
thyroiditis
disease
thyroid disease
DOID:14351
Riley-Day syndrome
class of disease
hereditary sensory and autonomic neuropathy
primary orthostatic hypotension
rare genetic developmental defect during embryogenesis
other dermis disorder
other genetic dermis disorder
nervous system anomaly with eye involvement
autosomal recessive hereditary sensory and autonomic neuropathy
disease
hereditary sensory and autonomic neuropathy type III (HSAN-III), is a disorder of the autonomic nervous system which affects the development and survival of sensory
DOID:11589
C10.177.575.300
C10.500.310.309
C10.574.500.496.250
C10.668.829.800.175.250
C16.131.666.310.309
C16.320.400.415.309
Familial dysautonomia
Ritscher-Schinzel syndrome 1
class of disease
Ritscher–Schinzel syndrome
genetic disease
Ritscher-Schinzel syndrome that has material basis in homozygous mutation in the KIAA0196 gene on chromosome 8q24
DOID:0060571
Ritter's disease
class of disease
staphylococcal infection
commensal bacterial infectious disease
skin disease
perinatal infectious disease
disease
Human disease
DOID:9063
C01.150.252.410.868.951.770
C01.150.252.819.770.770
C01.800.720.770.770
C17.800.838.765.770.770
Staphylococcal scalded skin syndrome
SAPHO syndrome
class of disease
syndrome
autoinflammatory syndrome with skin involvement
pyogenic autoinflammatory syndrome
disease
variety of inflammatory bone disorders that may be associated with skin changes
DOID:13677
C05.116.099.708.025
SM-AHNMD
class of disease
systemic mastocytosis
Human disease
DOID:4797
SOST-related sclerosing bone dysplasia
class of disease
hyperostosis
genetic disease
autosomal recessive disease
hyperostosis that has material basis in a mutation in the SOST gene which results in overgrowth of endosteal bone producing dense and wide bones throughout the body especially located in skull
DOID:0080036
Sabinas brittle hair syndrome
class of disease
trichothiodystrophy syndromes
genetic disease
nonphotosensitive trichothiodystrophy
human disease
DOID:0111874
Sakati-Nyhan syndrome
class of disease
acrocephalosyndactylia
An acrocephalosyndactylia characterized by abnormalities in the bones of the legs, congenital heart defects and craniofacial defects and craniosynostosis. The patients suffer from cyanosis and other respiratory and breathing infections.
DOID:0060359
Sarcomatoid carcinoma of the lung
class of disease
large-cell lung carcinoma
Sarcomatoid carcinoma
lung carcinoma
medical condition
DOID:0080777
Sarcomatoid carcinoma of lung
Scheuermann's disease
class of disease
osteochondrosis
kyphosis
spinal osteochondrosis
osteochondrosis of genetic origin
spinal disease
disease
osteochondrosis that results in abnormal bone growth and curvature located in thoracic vertebral column
DOID:13300
C05.116.821.500.500
C05.116.900.800.500.500
C05.116.900.808.500
Scheuermann's disease
Schnitzler syndrome
class of disease
type IV hypersensitivity
autoimmune urticaria
unexplained periodic fever syndrome
chronic urticaria
Human disease
DOID:4371
C20.683.780.640.700
Schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma
class of disease
nodular ganglioneuroblastoma
Human disease
DOID:7951
Seckel syndrome 1
class of disease
Seckel syndrome
Seckel syndrome that has material basis in homozygous or compound heterozygous mutation in the ATR gene on chromosome 3q23
DOID:0070007
Sertoli cell tumor
class of disease
testicular sex cord-stromal neoplasm
sex cord-gonadal stromal tumor
Human disease
DOID:3577
C04.557.475.750.847.500
C04.588.322.762.500.500
C04.588.945.440.915.500.500
C12.294.260.937.500.500
C12.758.409.937.500.500
C19.344.762.500.500
C19.391.829.782.500.500
Sertoli cell tumor
Sertoli-Leydig cell tumor
class of disease
testicular sex cord-stromal neoplasm
sex cord-gonadal stromal tumor
Human disease
DOID:2997
C04.557.475.750.847
C04.588.322.455.648
C04.588.322.762.500
C04.588.945.440.915.500
C12.294.260.937.500
C12.758.409.937.500
C13.351.500.056.630.705.648
C13.351.937.418.685.648
C19.344.410.648
C19.344.762.500
C19.391.630.705.648
C19.391.829.782.500
Sezary's disease
class of disease
cutaneous T cell lymphoma
aggressive primary cutaneous T-cell lymphoma
disease
type of cutaneous lymphoma
DOID:8541
C04.557.386.480.750.800.775
C15.604.515.569.480.750.800.775
C15.604.515.841
C20.683.515.761.480.750.800.775
C20.683.515.920
Sézary's disease
Sheehan's syndrome
class of disease
puerperal disorders
necrosis of pituitary
Simmonds' cachexia
hypopituitarism
disease
human disease
DOID:9476
Shukla-Vernon syndrome
class of disease
X-linked recessive disease
syndrome
human disease
DOID:0111841
Shwartzman phenomenon
class of disease
vasculitis
vascular hemostatic disease
Human disease
DOID:3825
C14.907.454.810
C14.907.940.890
C15.378.463.515.810
Simpson-Golabi-Behmel syndrome type 2
class of disease
X-linked recessive disease
Simpson-Golabi-Behmel syndrome
X-linked recessive disease that has material basis in mutation in the OFD1 gene on chromosome Xp22 and is characterized by developmental delay, macrocephaly, and respiratory problems
DOID:0080342
Skene gland carcinoma
class of disease
paraurethral gland cancer
carcinoma
vulva adenocarcinoma
Human disease
DOID:7284
Smarca4-deficient sarcoma of thorax
class of disease
thoracic cancer
human disease
DOID:0080532
Sotos syndrome 1
class of disease
autosomal dominant disease
Sotos syndrome
human disease
DOID:0112103
Sotos syndrome 2
class of disease
Sotos syndrome
autosomal dominant disease
human disease
DOID:0112102
Spinal cord cancer
class of disease
central nervous system cancer
spinal cord disease
spinal cord neoplasm
central nervous system cancer that is located in the spinal cord
DOID:5612
Spirurida infectious disease
class of disease
filariasis
Human disease
DOID:1077
C01.610.335.508.700.750
Stickler syndrome 1
class of disease
Stickler syndrome
autosomal dominant disease
human disease
DOID:0080676
Stickler syndrome type 2
class of disease
Stickler syndrome
autosomal dominant disease
human disease
DOID:0080675
Sudeck's syndrome
class of disease
complex regional pain syndrome
disease
Human disease
DOID:1811
C10.177.195.800
C10.668.829.250.800
Sugarman brachydactyly
class of disease
brachydactyly
brachydactyly characterized by a nonarticulating great toe set dorsal and proximal to the typical position
DOID:0110979
Sweeney-Cox syndrome
class of disease
syndrome
autosomal dominant disease
human disease
DOID:0080538
T cell and NK cell immunodeficiency
class of disease
primary immunodeficiency disease
human disease
DOID:0080710
T cell deficiency
class of disease
primary immunodeficiency disease
Human disease
DOID:11200
DOID:613
T cell, B cell, and NK cell deficiency
class of disease
combined immunodeficiency
human disease
DOID:0111965
T-cell acute lymphoblastic leukemia
class of disease
acute T cell leukemia
lymphoma
acute lymphocytic leukemia
viral infectious disease
T-cell leukemia
Acute lymphoblastic leukemia of T-cell origin. It comprises about 15% of childhood cases and 25% of adult cases. It is more common in males than females. (WHO, 2001)
DOID:5603
DOID:0050523
T-cell adult acute lymphocytic leukemia
class of disease
adult acute lymphocytic leukemia
T-cell leukemia
T-cell acute lymphoblastic leukemia
Human disease
DOID:5602
T-cell childhood acute lymphocytic leukemia
class of disease
childhood acute lymphocytic leukemia
T-cell acute lymphoblastic leukemia
childhood acute lymphoblastic leukemia that has material basis in T-cells
DOID:0080145
T-cell childhood lymphoblastic lymphoma
class of disease
lymphoblastic lymphoma
Precursor T-lymphoblastic lymphoma
lymphoblastic lymphoma that has material basis in T-cells and that occurs during childhood
DOID:0080148
T-cell large granular lymphocyte leukemia
class of disease
chronic lymphocytic leukemia
acquired neutropenia
T-cell leukemia
disease
chronic lymphocytic leukemia that exhibits an unexplained, chronic (> 6 months) elevation in large granular lymphocytes (LGLs) in the peripheral blood
DOID:0050751
C04.557.337.428.580.049
C15.604.515.560.575.049
C20.683.515.528.582.049
T-cell leukemia
class of disease
leukocyte disease
lymphoblastic leukemia
disease
Human disease
DOID:715
C04.557.337.428.580
C15.604.515.560.575
C20.683.515.528.582
Taylor's syndrome
class of disease
uterine disease
disease
Human disease
DOID:9346
Pelvic congestion syndrome
Teebi hypertelorism syndrome 2
class of disease
Hypertelorism, Teebi type
human disease
DOID:0081074
Timothy grass allergy
class of disease
pollen allergy
pollen allergy triggered by Phleum pratense pollen
DOID:0060498
Tn Polyagglutination syndrome
class of disease
genetic disease
hematopoietic system disease
human disease
DOID:0080520
Treacher Collins syndrome 1
class of disease
Treacher Collins syndrome
human disease
DOID:0080789
Treacher Collins syndrome 2
class of disease
Treacher Collins syndrome
autosomal recessive disease
human disease
DOID:0080790
Treacher Collins syndrome 3
class of disease
Treacher Collins syndrome
autosomal recessive disease
human disease
DOID:0080791
Treacher Collins syndrome 4
class of disease
Treacher Collins syndrome
human disease
DOID:0080792
Trichohepatoenteric syndrome 2
class of disease
tricho-hepato-enteric syndrome
human disease
DOID:0111416
Turner syndrome
class of disease
gonadal dysgenesis
X chromosome number anomaly with female phenotype
disease
chromosomal disorder in which a female is partially or completely missing an X chromosome
DOID:3491
C12.050.351.875.253.309.872
C12.050.351.875.253.795.750
C12.200.706.316.309.872
C12.200.706.316.795.750
C14.240.400.980
C14.280.400.980
C16.131.240.400.970
C16.131.260.830.835.750
C16.131.939.316.309.872
C16.131.939.316.795.750
C16.320.180.830.835.750
C19.391.119.309.872
C19.391.119.795.750
C12.800.316.309.872
C12.800.316.795.750
Turner syndrome
Uruguay faciocardiomusculoskeletal syndrome
class of disease
genetic disease
syndrome
cardiomyopathy
human disease
DOID:0112148
Usher syndrome type 1
class of disease
Usher syndrome
Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa
DOID:0110826
Usher syndrome type 1E
class of disease
Usher syndrome type 1
Usher syndrome type 1 that has material basis in variation in the chromosome region 21q21
DOID:0110833
Usher syndrome type 1H
class of disease
Usher syndrome type 1
human disease
DOID:0110835
Usher syndrome type 1K
class of disease
Usher syndrome type 1
An Usher syndrome type 1 that has material basis in variation in the chromosome region 10p11.21-q21.1.
DOID:0110837
Usher syndrome type 2
class of disease
Usher syndrome
Usher syndrome characterized by mild to severe congenital hearing impairment, normal vestibular function and later development of retinitis pigmentosa
DOID:0110827
Usher syndrome type 3
class of disease
Usher syndrome
Usher syndrome characterized by progressive hearing loss typically beginning in late childhood, variable vestibular dysfunction and onset of retinitis pigmentosa by the second decade of life
DOID:0110828
VIPoma
class of disease
neuroendocrine tumor
rare endocrine tumor that overproduces vasoactive intestinal peptide
DOID:5574
C04.557.465.625.650.240.847
C04.557.470.200.025.370.847
C04.588.274.761.500.750
C04.588.322.475.500.750
C06.301.761.500.750
C06.689.667.500.750
C19.344.421.500.750
Van Esch-O'Driscoll syndrome
class of disease
X-linked recessive disease
X-linked intellectual disability
human disease
DOID:0111840
Van Maldergem syndrome 1
class of disease
Van Maldergem syndrome
Van Maldergem syndrome that has material basis in homozygous mutation in the DCHS1 gene on chromosome 11p15
DOID:0080585
Van Maldergem syndrome 2
class of disease
Van Maldergem syndrome
Van Malergem syndrome that has material basis in homozygous or compound heterozygous mutation in the FAT4 gene on chromosome 4q28
DOID:0080586
Verruciform xanthoma
class of disease
xanthomatosis
skin disease
xanthoma
Human disease
DOID:5769
Volkmann's contracture
class of disease
connective tissue disease
disease
permanent flexion contracture of the hand at the wrist, resulting in a claw-like deformity of the hand and fingers
DOID:5587
C05.550.323.734
C05.651.180.531
C05.651.197.734
C14.907.303.531
Volkmann's contracture
WNT4 deficiency
class of disease
partial bilateral aplasia of the mullerian ducts
sex differentiation disease
autosomal dominant disease
human disease
DOID:0111526
Waardenburg syndrome type 1
class of disease
Waardenburg's syndrome
human disease
DOID:0110948
Waardenburg syndrome type 2B
class of disease
Waardenburg's syndrome
human disease
DOID:0110947
Waardenburg syndrome type 2C
class of disease
Waardenburg's syndrome
human disease
DOID:0110951
Waldenström macroglobulinemia
class of disease
B-cell lymphoma
lymphoplasmacytic lymphoma
disease
Type of blood cancer
DOID:0060901
DOID:0050747
C04.557.595.925
C14.907.454.960
C15.378.147.780.925
C15.378.463.515.960
C15.604.515.925
C20.683.780.925
Warburg micro syndrome 1
class of disease
Warburg micro syndrome
Warburg micro syndrome that has material basis in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP1 gene on chromosome 2q21
DOID:0110716
Waterhouse-Friderichsen syndrome
class of disease
adrenal crisis
adrenal gland disease
disease
adrenal gland disease that is characterized by failure of the adrenal gland due to bleeding into the gland
DOID:9931
C01.150.252.223.500.750.500
C01.150.252.400.625.549.449.800
C10.228.228.180.500.750.500
C10.586.625.280.505.904
C15.378.100.802.843
C15.378.463.950
C19.053.500.740
C23.550.414.950.843
C23.888.885.687.843
C01.207.180.500.750.500
Waterhouse–Friderichsen syndrome
Weissenbacher-Zweymuller syndrome
class of disease
Pierre Robin syndrome
osteochondrodysplasia
human disease
DOID:4258
Wernicke encephalopathy
class of disease
encephalopathy
long-term effects of alcohol consumption
thiamine deficiency
disease
presence of neurological symptoms caused by biochemical lesions of the central nervous system after exhaustion of B-vitamin reserves,
DOID:2384
C10.228.140.163.960
C18.452.132.960
C18.654.521.500.133.699.827.822
C25.775.100.625
F03.900.100.875
Whitewater Arroyo hemorrhagic fever
class of disease
viral infectious disease
viral hemorrhagic fever
Human disease
DOID:0050199
Wolf-Hirschhorn syndrome
class of disease
chromosomal deletion syndrome
partial deletion of the short arm of chromosome 4
disease
chromosome abnormality with a distinct craniofacial phenotype and intellectual disability
DOID:0050460
C16.131.077.944
C16.131.260.985
C16.320.180.985
Wolf–Hirschhorn syndrome
Wolffian adnexal neoplasm
class of disease
uterine ligament cancer
Human disease
DOID:7514
Wolffian duct adenocarcinoma
class of disease
cervical adenocarcinoma
mesonephric tumor
clear cell adenocarcinoma
Human disease
DOID:5368
Wolffian duct adenoma
class of disease
reproductive organ benign neoplasm
benign neoplasms by histologic type
benign mesonephroma
adenoma
Human disease
DOID:2616
Wolfram syndrome 1
class of disease
Wolfram syndrome
autosomal recessive disease
Human disease
DOID:0110629
Wolfram syndrome 2
class of disease
Wolfram syndrome
autosomal recessive disease
Human disease
DOID:0110630
Wolfram syndrome, mitochondrial form
class of disease
Wolfram syndrome
human disease
DOID:0080583
Wolman disease
class of disease
lysosomal and lipase deficiency
autosomal recessive inborn error of metabolism that results in the body not producing enough active lysosomal acid lipase (LAL) enzyme
DOID:14497
C16.320.565.398.641.201.500
C16.320.565.595.201.500
C16.614.947
C18.452.584.563.641.201.500
C18.452.648.398.641.201.500
C18.452.648.595.201.500
Lysosomal acid lipase deficiency
X-Linked immunodeficiency 74
class of disease
X-linked recessive disease
T cell deficiency
human disease
DOID:0112063
X-linked Emery-Dreifuss muscular dystrophy 1
class of disease
Emery-Dreifuss muscular dystrophy
X-linked recessive disease
Emery-Dreifuss muscular dystrophy that has material basis in an X-linked recessive mutation of EMD on chromosome Xq28
DOID:0070246
X-linked Emery-Dreifuss muscular dystrophy 6
class of disease
Emery-Dreifuss muscular dystrophy
X-linked recessive disease
An Emery-Dreifuss muscular dystrophy that has material basis in an X-linked recessive mutation of FHL1 on chromosome Xq26.3.
DOID:0070251
X-linked agammaglobulinemia type 2
class of disease
Bruton-type agammaglobulinemia
autosomal recessive disease
B cell deficiency
human disease
DOID:0111999
X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
class of disease
amelogenesis imperfecta
amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region
DOID:0110059
X-linked cardiac valvular dysplasia
class of disease
X-linked disease
heart valve disease
Heart valve dysplasia
human disease
DOID:0111765
X-linked chondrodysplasia punctata
class of disease
chondrodysplasia punctata
X-linked recessive disease
Human disease
DOID:0060292
X-linked chondrodysplasia punctata 2
class of disease
X-linked dominant disease
chondrodysplasia punctata
chondrodysplasia puncata that has material basis in mutation in the gene encoding delta(8)-delta(7) sterol isomerase emopamil-binding protein on chromosome Xp11
DOID:0080352
X-linked chronic granulomatous disease
class of disease
X-linked recessive disease
chronic granulomatous disease
A chronic granulomatous disease characterized by X-linked inheritance that has material basis in mutation in the CYBB gene on chromosome Xp21.1-p11.4.
DOID:0070195
X-linked chronic idiopathic intestinal pseudo-obstruction
class of disease
X-linked recessive disease
neuronal intestinal dysplasia
human disease
DOID:0080681
X-linked cone-rod dystrophy 2
class of disease
cone-rod dystrophy
cone-rod dystrophy that has material basis in variation in the chromosome region Xq27
DOID:0111006
X-linked congenital hemolytic anemia
class of disease
congenital hemolytic anemia
X-linked recessive disease
human disease
DOID:0111846
X-linked congenital myopathy with fiber-type disproportion
class of disease
congenital fiber-type disproportion
A congenital fiber-type disproportion characterized by bilateral ptosis, facial weakness, impaired suckling, generalized hypotonia, and respiratory insufficiency that has material basis in mutation in the chromosome region Xq13.1-q22.1.
DOID:0111226
X-linked deafness 1
class of disease
X-linked nonsyndromic deafness
human disease
DOID:0111739
X-linked deafness 2
class of disease
X-linked nonsyndromic deafness
human disease
DOID:0111737
X-linked deafness 3
class of disease
X-linked nonsyndromic deafness
human disease
DOID:0111736
X-linked deafness 7
class of disease
X-linked nonsyndromic deafness
human disease
DOID:0111738
X-linked disease
class of disease
monogenic disease
monogenic disease that has material basis in mutations in genes on the X chromosome
DOID:0050735
C16.320.322
X-linked dyskeratosis congenita
class of disease
dyskeratosis congenita
X-linked recessive disease
dyskeratosis congenita that has material basis in an X-linked recessive mutation of DKC1 on chromosome Xq28
DOID:0070025
X-linked endothelial corneal dystrophy
class of disease
corneal endothelial dystrophy
posterior corneal dystrophy
X-linked dominant disease
Human disease
DOID:0060446
X-linked exudative vitreoretinopathy 2
class of disease
X-linked disease
exudative vitreoretinopathy
human disease
DOID:0111413
X-linked hyper IgM syndrome
class of disease
hyperimmunoglobulin syndrome
hyper IgM syndrome
X-linked recessive disease
human disease
DOID:6620
X-linked intellectual developmental disorder 108
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0111844
X-linked keratosis follicularis spinulosa decalvans
class of disease
keratosis follicularis spinulosa decalvans
X-linked recessive disease
human disease
DOID:0080754
X-linked lymphoproliferative syndrome 2
class of disease
lymphoproliferative disorders
X-linked lymphoproliferative disease
X-linked recessive disease
Human disease
DOID:0060706
X-linked mental retardation 106
class of disease
non-syndromic X-linked intellectual disability
human disease
DOID:0080240
X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques
class of disease
Olmsted syndrome
X-linked recessive disease
human disease
DOID:0112012
X-linked nephrolithiasis type I
class of disease
renal tubular transport disease
X-linked recessive disease
human disease
DOID:0111798
X-linked recessive hypoparathyroidism
class of disease
hypoparathyroidism, familial isolated
hypoparathyroidism
X-linked disease
human disease
DOID:0111388
X-linked retinitis pigmentosa and sinorespiratory infections
class of disease
syndrome
X-linked disease
human disease
DOID:0112124
X-linked severe congenital neutropenia
class of disease
X-linked recessive disease
severe congenital neutropenia
human disease
DOID:0112128
X-linked sideroblastic anemia
class of disease
Hereditary sideroblastic anemia
X-linked recessive disease
sideroblastic anaemia P
Human disease
DOID:0060063
X-linked spermatogenic failure 1
class of disease
Sertoli cell-only syndrome
Sertoli cell-only syndrome characterized by X-linked inheritance
DOID:0070189
X-linked spermatogenic failure 2
class of disease
azoospermia
X-linked recessive disease
azoospermia characterized by meiotic arrest of spermatocytes and mixed testicular atrophy that has material basis in X-linked inheritance of mutation in the TEX11 gene on chromosome Xq13
DOID:0070185
X-linked spinal muscular atrophy 2
class of disease
X-linked recessive disease
spinal muscular atrophy
human disease
DOID:0111827
X-linked spinocerebellar ataxia 1
class of disease
X-linked recessive disease
X-linked cerebellar ataxia
human disease
DOID:0111829
X-linked spinocerebellar ataxia 2
class of disease
X-linked cerebellar ataxia
human disease
DOID:0111830
X-linked spinocerebellar ataxia 3
class of disease
X-linked cerebellar ataxia
human disease
DOID:0111831
X-linked spinocerebellar ataxia 5
class of disease
X-linked cerebellar ataxia
X-linked recessive disease
human disease
DOID:0111833
XX male syndrome
class of disease
syndrome
anatomical abnormality
disorder of sex development
X chromosome number anomaly with male phenotype
gonadal dysgenesis
disease
rare congenital condition where an individual with a female genotype has phenotypically male characteristics that can vary between cases
DOID:0111760
C12.050.351.875.253.064.124
C12.200.706.316.064.124
C12.800.316.064.124
C16.131.939.316.064.124
C19.391.119.064.124
Y-linked deafness
class of disease
nonsyndromic deafness
Y-linked disease
human disease
DOID:0111757
Y-linked deafness 2
class of disease
Y-linked deafness
human disease
DOID:0111758
Y-linked disease
class of disease
monogenic disease
Y linkage
monogenic disease that has material basis in muations on the Y chromosome
DOID:0050738
C16.320.338
Y-linked spermatogenic failure 1
class of disease
Sertoli cell-only syndrome
Y-linked disease
Sertoli cell-only syndrome that has material basis in deletions in the Yq11 chromosomal region
DOID:0070186
Y-linked spermatogenic failure 2
class of disease
male infertility
Y-linked disease
spermatogenic failure
A male infertility characterized by nonobstroctive azoospermia or oligozoospermia that has material basis in interstitial deletions on the Yq11.221 chromosomal region.
DOID:0070187
Zenker's paralysis
class of disease
peripheral neuropathy
common peroneal nerve lesion
medical condition
DOID:6925
Zollinger–Ellison syndrome
class of disease
syndrome
disease
disease of the digestive tract in which tumors lead to excess acid and peptic ulcers
DOID:0050782
C04.730.713.988
C06.301.371.883
C06.405.249.883
C06.405.469.275.800.924
C06.405.469.965
C06.405.748.586.924
C06.405.748.947
Zollinger–Ellison syndrome
abacavir allergy
class of disease
drug allergy
drug allergy that has allergic trigger abacavir
DOID:0040007
abdominal aortic aneurysm
class of disease
aortic aneurysm
disease
aortic aneurysm that is located in the abdominal aorta
DOID:7693
C14.907.055.239.075
C14.907.109.139.075
Abdominal aortic aneurysm
abdominal obesity-metabolic syndrome
class of disease
autosomal dominant disease
syndrome
Human disease
DOID:0060611
abdominal obesity-metabolic syndrome 3
class of disease
abdominal obesity-metabolic syndrome
abdominal obesity-metabolic syndrome that has material basis in heterozygous mutation in the DYRK1B gene on chromosome 19q13
DOID:0060612
abdominal tuberculosis
class of disease
extrapulmonary tuberculosis
extrapulmonary tuberculosis that is located in gastrointestinal tract, located in peritoneum, located in omentum, located in mesentery, located in liver, located in spleen or located in pancreas
DOID:0050599
Abdominal tuberculosis
abducens nerve neoplasm
class of disease
cranial nerve neoplasm
abducens nerve palsy
Human disease
DOID:14125
abducens nerve palsy
class of disease
cranial nerve palsy
paralytic squint
non-neoplastic or neoplastic disorder affecting the abducens nerve (sixth cranial nerve)
DOID:10865
C10.292.150
Sixth nerve palsy
abnormal pupillary function
class of disease
pupil disorder
Human disease
DOID:11518
abnormal retinal correspondence
class of disease
binocular vision disease
Human disease
DOID:12668
abnormal threshold of rods
class of disease
night blindness
Human disease
DOID:11874
abnormality of glucagon secretion
class of disease
endocrine pancreas disease
Human disease
DOID:14427
acalculous cholecystitis
class of disease
cholecystitis
cystitis
Human disease
DOID:2828
C06.130.564.263.249
acanthocephaliasis
class of disease
parasitic helminthiasis infectious disease
Human disease
DOID:0050254
acantholytic acanthoma
class of disease
acanthoma
Human disease
DOID:4324
acantholytic squamous cell skin carcinoma
class of disease
cutaneous squamous-cell carcinoma
keratinizing squamous cell carcinoma
Human disease
DOID:7643
acantholytic variant squamous cell breast carcinoma
class of disease
breast squamous cell carcinoma
Human disease
DOID:7459
acanthoma
class of disease
squamous cell neoplasm
Human disease
DOID:174
C04.557.470.700.040
C04.588.805.040
acanthosis nigricans
class of disease
pigmentation disorder
disease
A skin condition characterised by dark, velvety patches in body folds and creases.
DOID:3138
C17.800.621.430.530.100
Acanthosis nigricans
accessory nerve disease
class of disease
glossopharyngeal nerve disease
human disease
DOID:339
C10.292.175
Nervus accessorius
accommodative esotropia
class of disease
esotropia
Human disease
DOID:9839
accommodative spasm
class of disease
eye accommodation disease
Human disease
DOID:11637
achalasia
class of disease
esophageal disease
disease
esophageal disease characterized by an inability of the esophagus to move food toward the stomach resulting from the lower esophogeal sphincter not fully relaxing during swallowing
DOID:9164
C06.405.117.119.500.432
Achalasia
achilles bursitis
class of disease
bursitis
foot diseases
Achilles tendinitis
bursitis (inflammation of synovial sac) of bursa situated above the insertion of tendon to calcaneus
DOID:12857
achondrogenesis type IA
class of disease
achondrogenesis
achondrogenesis that results in abnormal ossification of the located in vertebral column or located in spine
DOID:0080054
achondrogenesis type IB
class of disease
achondrogenesis
autosomal recessive disease
achondrogenesis that has material basis in mutation in the SLC26A2 gene which results in umbilical or inguinal hernia and a prominent rounded abdomen
DOID:0080055
achondrogenesis type II
class of disease
achondrogenesis
autosomal dominant disease
spinal disease
achondrogenesis that has material basis in mutations in the COL2A1 gene which results in underdeveloped lungs, hydrops fetalis, a prominent forehead and abnormal ossification of the located in vertebral column or located in pelvis
DOID:0080056
achromatopsia 2
class of disease
achromatopsia
autosomal recessive disease
An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11.
DOID:0110007
achromatopsia 3
class of disease
achromatopsia
autosomal recessive disease
An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the CNGB3 gene on chromosome 8q2.
DOID:0110008
achromatopsia 4
class of disease
achromatopsia
achromatopsia that has material basis in homozygous or compound heterozygous mutation in the GNAT2 gene (139340) on chromosome 1p13
DOID:0110010
achromatopsia 7
class of disease
achromatopsia
autosomal recessive disease
An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the ATF6 gene on chromosome 1q23.
DOID:0110009
acid anhydride respiratory allergy
class of disease
respiratory allergy
respiratory allergy that has allergic trigger acid anhydride
DOID:0040081
acinar cell carcinoma
class of disease
carcinoma
carcinoma that has material basis in abnormally proliferating cells, derives from spindle cells and/or derives from giant cells
DOID:3025
C04.557.470.200.025.215
acinar cell cystadenocarcinoma
class of disease
pancreatic cystadenocarcinoma
cystadenocarcinoma
Human disease
DOID:7729
acinic cell breast carcinoma
class of disease
breast adenocarcinoma
invasive ductal carcinoma
acinar cell carcinoma
Human disease
DOID:5743
acquired angioedema
class of disease
angioedema
human disease
DOID:0080941
acquired color blindness
class of disease
color blindness
human disease
DOID:13912
acquired gastric outlet stenosis
class of disease
pyloric stenosis
Human disease
DOID:14099
acquired generalized lipodystrophy
class of disease
lipodystrophy
complete generalized lipodystrophy
rare skin disease
insulin resistance
acquired lipodystrophy
complete generalized lipodystrophy that is charcterized by generalized disappearance of fat occurring during childhood and adolescence where normal body fat is present at birth
DOID:0080300
acquired hemangioma
class of disease
hemangioma
Human disease
DOID:492
acquired hyperkeratosis
class of disease
keratosis
Human disease
DOID:13072
acquired metabolic disease
class of disease
metabolic disease
human disease
DOID:0060158
acquired night blindness
class of disease
nutritional deficiency disease
night blindness
Human disease
DOID:11491
acquired polycythemia
class of disease
polycythemia
Human disease
DOID:2834
acquired tear duct stenosis
class of disease
lacrimal apparatus disease
Human disease
DOID:13655
acquired thrombocytopenia
class of disease
thrombocytopenia
Human disease
DOID:11126
acquired von Willebrand syndrome
class of disease
blood coagulation disease
von Willebrand's disease
rare hemorrhagic disorder due to an acquired coagulation factor defect
human disease
DOID:0111146
acral lentiginous melanoma
class of disease
skin melanoma
disease
kind of lentiginous skin melanoma
DOID:6367
acrocephalosyndactylia
class of disease
synostosis
craniosynostosis
syndactyly
disease
group of diseases
DOID:12960
C05.116.099.370.894.232.015
C05.116.099.370.894.819.100
C05.660.207.240.100
C05.660.585.800.100
C05.660.906.364.100
C05.660.906.819.100
C16.131.621.207.240.100
C16.131.621.585.800.100
C16.131.621.906.364.100
C16.131.621.906.819.100
Acrocephalosyndactyly
acrodermatitis
class of disease
dermatitis
Foot Dermatoses
dermatitis that selectively affects the hands and feet
DOID:2722
C16.131.831.066
C17.800.174.100
C17.800.804.066
Acrodermatitis
acrodermatitis chronica atrophicans
class of disease
acrodermatitis
Lyme disease
An acrodermatitis characterized by a chronically progressive course, leading to widespread atrophy of the skin. It is a clinical manifestation of Lyme borreliosis.
DOID:0060344
acrofacial dysostosis
class of disease
dysostosis
human disease
DOID:0060379
acropustulosis
class of disease
dermatitis
acrodermatitis
pustulosis
genodermatosis
other epidermal disorder
genetic epidermal disorder
Human disease
DOID:4398
Acropustulosis
acrorenal syndrome
class of disease
syndrome
autosomal recessive disease
Human disease
DOID:0060347
actinic keratosis
class of disease
pre-malignant neoplasm
dermatoheliosis
disease
human disease
DOID:8866
C04.834.450
C17.800.428.570
Actinic keratosis
activated PI3K delta syndrome
class of disease
agammaglobulinemia
combined immunodeficiency
autosomal dominant disease
medical condition
DOID:0111936
active cochlear Meniere's disease
class of disease
Meniere's disease
Human disease
DOID:13492
active cochleovestibular Meniere's disease
class of disease
Meniere's disease
Human disease
DOID:13490
active peptic ulcer disease
class of disease
peptic ulcer disease
stomach bleeding
Human disease
DOID:749
C06.405.227.700
C23.550.414.788.700
active vestibular Meniere's disease
class of disease
Meniere's disease
Human disease
DOID:13491
acute T cell leukemia
class of disease
T-cell leukemia
Human disease
DOID:5603
acute allergic serous otitis media
class of disease
acute serous otitis media
allergy
acute serous otitis media caused by an allergen
DOID:11558
acute apical periodontitis
class of disease
periapical periodontitis
Human disease
DOID:11693
acute asthma
class of disease
asthma
human disease
DOID:0080810
acute basophilic leukemia
class of disease
acute myeloid leukemia
bilineal acute myeloid leukemia
rare acute myeloid leukemia in which the immature cells differentiate towards basophils
DOID:0080795
C04.557.337.539.275.125
acute biphenotypic leukaemia
class of disease
mixed phenotype acute leukemia
acute lymphocytic leukemia
acute leukemia
lymphoma
disease
uncommon type of leukemia which arises in multipotent progenitor cells which have the ability differentiating into both myeloid and lymphoid lineages
DOID:9953
C04.557.337.428.100
C15.604.515.560.100
C20.683.515.528.100
acute canaliculitis
class of disease
acute inflammation of lacrimal passage
canaliculitis
Human disease
DOID:6969
acute cervicitis
class of disease
cervicitis
acute disease
human disease
DOID:10616
acute chest syndrome
class of disease
lung disease
human disease
DOID:1584
C08.381.074
C08.618.009
C15.378.071.141.150.150.219
C15.378.420.155.219
C16.320.070.150.219
C16.320.365.155.219
acute cholangitis
class of disease
ascending cholangitis
Human disease
DOID:14271
acute closed-angle glaucoma
class of disease
primary angle-closure glaucoma
glaucoma
DOID:13862
acute conjunctivitis
class of disease
conjunctivitis
Human disease
DOID:11184
acute contagious conjunctivitis
class of disease
acute conjunctivitis
Human disease
DOID:11213
acute cor pulmonale
class of disease
acute pulmonary heart disease
Human disease
DOID:8517
acute dacryoadenitis
class of disease
dacryoadenitis
Human disease
DOID:952
acute dacryocystitis
class of disease
dacryocystitis
Human disease
DOID:12996
acute diarrhea
class of disease
symptom or sign
diarrhea
diarrhea that is of rapid onset and course characterized by frequent loose or liquid bowel movements. Acute diarrhea is a common cause of death in developing countries and the second most common cause of infant deaths worldwide
DOID:0050140
acute diffuse nephritis
class of disease
diffuse glomerulonephritis
Human disease
DOID:14066
acute disseminated encephalomyelitis
class of disease
encephalomyelitis
encephalomyelitis characterized by inflammation located in brain and located in spinal cord that damages myelin
DOID:639
C10.114.375.225
C10.228.140.695.562.225
C10.314.350.225
C20.111.258.250.350
C23.550.291.500.829.188
acute endometritis
class of disease
endometritis
Human disease
DOID:7528
acute erythroid leukemia
class of disease
acute myeloid leukemia
rare form of acute myeloid leukemia (less than 5% of AML cases) where the myeloproliferation is of erythroblastic precursors.
DOID:0080780
C04.557.337.539.275.325
C15.378.190.636.276
Acute erythroid leukemia
acute ethmoiditis
class of disease
ethmoid sinusitis
acute disease
ethmoid sinusitis which lasts for less than 4 weeks
DOID:9506
acute eustachian salpingitis
class of disease
otosalpingitis
otosalpingitis with a sudden onset and a short course
DOID:10550
acute female pelvic peritonitis
class of disease
peritonitis
pelvic inflammatory diseases
Human disease
DOID:9978
acute frontal sinusitis
class of disease
frontal sinusitis
acute disease
frontal sinusitis which lasts for less than 4 weeks
DOID:14225
acute gonococcal cervicitis
class of disease
acute cervicitis
gonococcal infectious diseases
Human disease
DOID:10615
acute gonococcal cystitis
class of disease
urinary tract infection
gonococcal infectious diseases
Human disease
DOID:13690
acute gonococcal endometritis
class of disease
acute endometritis
gonococcal infectious diseases
Human disease
DOID:7527
acute gonococcal epididymo-orchitis
class of disease
epididymo-orchitis
Human disease
DOID:10802
acute gonococcal prostatitis
class of disease
prostatitis
gonococcal infectious diseases
Human disease
DOID:13943
acute gonococcal salpingitis
class of disease
acute salpingitis
gonococcal infectious diseases
Human disease
DOID:13942
acute hemorrhagic leukoencephalitis
class of disease
acute disseminated encephalomyelitis
acute hemorrhagic encephalitis
acute necrotizing encephalitis
very rare form of acute disseminated encephalomyelitis, characterized by a brief but intense attack of inflammation and necrotizing vasculitis of venules and hemorrhage, and edema
DOID:10992
C10.114.375.225.500
C10.114.375.362
C10.228.140.695.562.225.500
C10.228.140.695.562.375
C10.314.350.225.500
C10.314.350.375
C20.111.258.250.350.500
C20.111.258.250.425
acute hemorrhagic pancreatitis
class of disease
acute pancreatitis
human disease
DOID:0080999
C06.689.750.325
acute hydrops keratoconus
class of disease
keratoconus
eye disease
Human disease
DOID:10125
Corneal hydrops
acute infantile liver failure-multisystemic involvement syndrome
class of disease
liver failure, infantile
autosomal recessive disease
human disease
DOID:0080717
acute infection of pinna
class of disease
otitis externa
Human disease
DOID:10520
acute inflammation of lacrimal passage
class of disease
lacrimal apparatus disease
Human disease
DOID:6970
acute kidney tubular necrosis
class of disease
acute kidney injury
disease
medical condition involving the death of tubular epithelial cells that form the renal tubules of the kidneys
DOID:12556
C12.050.351.968.419.780.050.500
C12.200.777.419.780.050.500
C12.950.419.780.050.500
acute laryngitis
class of disease
laryngitis
respiratory disease
DOID:9396
acute laryngopharyngitis
class of disease
upper respiratory tract disease
laryngopharyngitis
respiratory disease
DOID:11195
acute leukemia
class of disease
leukemia
lymphoblastic leukemia
disease
human disease
DOID:12603
Acute leukemias
acute lymphocytic leukemia
class of disease
acute leukemia
lymphoblastic leukemia
disease
leukemia that is characterized by over production of lymphoblasts.
DOID:9952
Acute lymphoblastic leukemia
acute maxillary sinusitis
class of disease
maxillary sinusitis
acute disease
maxillary sinusitis which lasts for less than 4 weeks
DOID:2050
acute megakaryoblastic leukemia
class of disease
acute myeloid leukemia
leukemia
bilineal acute myeloid leukemia
leukemia that derives from blood-forming tissue in which megakaryocytes proliferate in the bone marrow and circulate in the blood in large numbers
DOID:8761
C04.557.337.539.275.450
acute monocytic leukemia
class of disease
monocytic leukemia
acute myeloid leukemia
disease
Human disease
DOID:8864
C04.557.337.539.275.484
Acute monocytic leukemia
acute myeloid leukemia
class of disease
acute leukemia
myeloid leukemia
disease
myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells
DOID:9119
C04.557.337.539.275
Acute myeloid leukemia
acute myeloid leukemia with BCR-ABL1
class of disease
acute myeloid leukemia
human disease
DOID:0080976
acute myocardial infarction
class of disease
myocardial infarction
acute coronary syndrome
human disease
DOID:9408
acute myocarditis
class of disease
myocarditis
human disease
DOID:3951
acute necrotizing encephalitis
class of disease
encephalitis
Human disease
DOID:5222
acute orbital inflammation
class of disease
orbital disease
inflammation
human disease
DOID:11230
acute pancreatitis
class of disease
pancreatitis
disease
Human disease
DOID:2913
Acute pancreatitis
acute pericementitis
class of disease
periodontitis
Human disease
DOID:10423
acute perichondritis of pinna
class of disease
perichondritis of auricle
human disease
DOID:221
acute poststreptococcal glomerulonephritis
class of disease
glomerulonephritis
Human disease
DOID:14064
acute proliferative glomerulonephritis
class of disease
glomerulonephritis
proliferative glomerulonephritis
disease
Human disease
DOID:13138
Acute proliferative glomerulonephritis
acute promyelocytic leukemia
class of disease
symptom or sign
acute myeloid leukemia
bilineal acute myeloid leukemia
disease
acute myeloid leukemia characterized by accumulation of promyelocytes in the bone marrow and by a translocation between chromosomes 15 and 17
DOID:0060318
C04.557.337.539.275.700
Acute promyelocytic leukemia
acute pulmonary heart disease
class of disease
cor pulmonale
Human disease
DOID:8514
acute retinal necrosis syndrome
class of disease
retinitis
Human disease
DOID:3611
C11.768.773.674
acute retrobulbar neuritis
class of disease
optic neuritis
Human disease
DOID:14155
acute salpingitis
class of disease
salpingitis
Human disease
DOID:10973
acute salpingo-oophoritis
class of disease
salpingo-oophoritis
acute salpingitis
Human disease
DOID:10971
acute serous otitis media
class of disease
acute transudative otitis media
serous glue ear
acute transudative otitis media with thin, watery and sterile effusion
DOID:11557
acute sphenoidal sinusitis
class of disease
sphenoid sinusitis
acute disease
sphenoid sinusitis which lasts for less than 4 weeks
DOID:13046
acute stress disorder
class of disease
anxiety disorder
stress-related disorders
disease
psychological response to a terrifying, traumatic, or surprising experience
DOID:6088
F03.950.750.550
acute thyroiditis
class of disease
thyroiditis
Human disease
DOID:14353
acute tympanitis
class of disease
tympanic membrane disease
myringitis
Human disease
DOID:13790
acute vascular insufficiency of intestine
class of disease
intestinal disease
Human disease
DOID:8590
adamantinoid basal cell epithelioma
class of disease
basal-cell carcinoma
Human disease
DOID:4290
adamantinoma
class of disease
bone cancer
disease
bone cancer that is located in almost exclusively in the long bones
DOID:2776
C04.588.149.030
C05.116.231.030
Adamantinoma
adamantinous craniopharyngioma
class of disease
craniopharyngioma
Human disease
DOID:3846
adenocarcinoma
class of disease
carcinoma
disease
carcinoma that has material basis in abnormally proliferating cells, derives from epithelial cells, which originate in glandular tissue
DOID:299
C04.557.470.200.025
Adenocarcinomas
adenocarcinoma in situ
class of disease
in situ carcinoma
adenocarcinoma
Human disease
DOID:4943
C04.557.470.200.025.014
C04.557.470.200.240.124
C23.149.249
adenocarcinoma of the lung
class of disease
lung cancer
adenocarcinoma
non-small cell lung carcinoma that derives from epithelial cells of glandular origin
DOID:3910
C04.557.470.200.025.022
C04.588.894.797.520.055
adenofibroma
class of disease
benign neoplasms by histologic type
fibroma
cell type benign neoplasm that is composed of glandular and fibrous tissues, with a relatively large proportion of glands
DOID:2683
C04.557.450.565.590.595.050
C04.557.470.625.050
adenoid basal cell carcinoma
class of disease
basal-cell carcinoma
tonsil cancer
Human disease
DOID:4294
adenoid cystic carcinoma
class of disease
cancer
cylindroma
carcinoma
tonsil cancer
type of cancer
DOID:0080202
C04.557.470.200.025.220
Adenoid cystic carcinoma
adenoid hypertrophy
class of disease
upper respiratory tract disease
upper respiratory tract disease characterized by the unusual growth of the adenoid tonsil; has symptom snoring, has symptom hyponasality, has symptom otitis media with effusion, has symptom mouth breathing
DOID:0060311
Adenoid hypertrophy
adenoiditis
class of disease
upper respiratory tract disease
nasopharyngitis
inflammation of the adenoid tissue
DOID:0050145
adenoma
class of disease
benign neoplasms by histologic type
disease
cell type benign neoplasm that is composed of epithelial tissue in which tumor cells form glands or glandlike structures
DOID:657
C04.557.470.035
Adenomas
adenomatoid tumor
class of disease
benign neoplasm
benign mesothelioma
type of tumor
DOID:746
C04.557.470.035.200
C04.557.470.660.200
Adenomatoid tumors
adenomyoma
class of disease
carcinosarcoma
carcinoma
carcinosarcoma that has material basis in gland and muscle components
DOID:2609
C04.557.435.110
Adenomyomas
adenomyoma of uterine corpus
class of disease
adenomyoma
uterine corpus cancer
carcinosarcoma of the corpus uteri
uterine benign neoplasm
Human disease
DOID:4994
adenomyosis
class of disease
endometriosis
uterine disease
disease
extension of endometrial tissue into the myometrium
DOID:288
C13.351.500.852.113
Adenomyosis of the uterus
adenosarcoma
class of disease
carcinosarcoma
carcinosarcoma that derives from simultaneously or consecutively in mesodermal tissue and glandular epithelium
DOID:1974
C04.557.435.135
C04.557.450.795.135
adenosquamous bile duct carcinoma
class of disease
squamous cell carcinoma
bile duct cancer
human disease
DOID:5624
adenosquamous breast carcinoma
class of disease
breast squamous cell carcinoma
adenosquamous carcinoma
breast cancer
squamous cell carcinoma
Human disease
DOID:5623
adenosquamous carcinoma
class of disease
squamous cell carcinoma
disease
squamous cell carcinoma that contains squamous cells and gland-like cells
DOID:4830
C04.557.435.250
C04.557.470.200.150
Adenosquamous carcinoma
adenosquamous cell lung carcinoma
class of disease
adenosquamous carcinoma
squamous cell carcinoma of the lung
squamous cell carcinoma
lung cancer
Human disease
DOID:4829
adenosquamous gallbladder carcinoma
class of disease
gallbladder squamous cell carcinoma
adenosquamous carcinoma
squamous cell carcinoma
gallbladder cancer
gallbladder carcinoma
gallbladder carcinoma that derives from squamous cells and gland-like cells
DOID:5627
adenosquamous pancreas carcinoma
class of disease
adenosquamous carcinoma
squamous cell carcinoma of pancreas
squamous cell carcinoma
pancreatic cancer
pancreatic ductal carcinoma that derives from squamous cells and gland-like cells
DOID:5637
adenosquamous prostate carcinoma
class of disease
adenosquamous carcinoma
squamous cell carcinoma
prostate cancer
prostate carcinoma that derives from squamous cells and gland-like cells
DOID:5634
adenoviral keratoconjunctivitis
class of disease
viral conjunctivitis
keratoconjunctivitis
adenovirus infection
common and highly contagious viral infection of the eye
DOID:13014
Adenoviral keratoconjunctivitis
adhesions of uterus
class of disease
gynatresia
uterine disease
disease
adhesions or fibrosis of endometrium of uterus
DOID:13812
Asherman's syndrome
adhesive otitis media
class of disease
ear disease
otitis media
adhesive middle ear disease
An auditory system disease that is characterized by a thin retracted ear drum becomes sucked into the middle-ear space and stuck (i.e., adherent) to the ossicles and other bones of the middle ear.
DOID:11235
adiposis dolorosa
class of disease
lipomatosis
subcutaneous tissue disease
rare condition characterized by generalized obesity and fatty tumors in the adipose tissue.
DOID:3928
C17.800.463.249
C18.452.584.718.500
Adiposis dolorosa
adjustment disorder
class of disease
mental disorder
disease
human disease
DOID:507
F03.950.500
Adjustment disorder
adolescence-adult electroclinical syndrome
class of disease
electroclinical syndrome
absence seizure
electroclinical syndrome with onset in adolescence and adulthood
DOID:0050705
adrenal adenoma
class of disease
endocrine organ benign neoplasm
adrenal gland disease
benign epithelial neoplasm
benign neoplasm of adrenal gland
adenoma
disease
endocrine organ benign neoplasm, a benign tumor of the glandular type (adenoma) in the adrenal gland
DOID:656
adrenal carcinoma
class of disease
adrenal gland cancer
carcinoma
adrenal cancer that is located in the cortex (steroid hormone-producing tissue) of the adrenal gland and that has material basis in abnormally proliferating cells derives from epithelial cells
DOID:3950
adrenal cortex cancer
class of disease
adrenal gland cancer
adrenal cortex neoplasm
adrenal cortex disease
Human disease
DOID:660
Cancers of adrenal glands
adrenal cortex disease
class of disease
adrenal gland disease
disease involving the adrenal cortex
DOID:3952
C19.053.098
adrenal cortical adenocarcinoma
class of disease
adrenocortical carcinoma
adenocarcinoma
adrenalcortical carcinoma that originating in the cortex of the adrenal gland and derives from epithelial cells of glandular origin
DOID:3959
adrenal cortical hypofunction
class of disease
adrenal cortex disease
primary adrenal insufficiency
Human disease
DOID:10493
adrenal gland cancer
class of disease
endocrine gland cancer
adrenal gland neoplasm
adrenal gland disease
endocrine gland cancer located in the adrenal glands which are located above the kidneys
DOID:3953
adrenal gland disease
class of disease
endocrine system disease
endocrine disease
DOID:9553
C19.053
Diseases and disorders of adrenal glands/hormones
adrenal gland ganglioneuroblastoma
class of disease
adrenal gland cancer
adrenal neuroblastoma
peripheral nervous system ganglioneuroblastoma
malignant peripheral nerve neoplasm
Human disease
DOID:8140
adrenal gland hyperfunction
class of disease
adrenal cortex disease
Human disease
DOID:3947
C19.053.800
adrenal gland pheochromocytoma
class of disease
phaeochromocytoma
malignant pheochromocytoma
adrenal medulla cancer that is characterized by overproduction of adrenaline
DOID:0050892
adrenal medulla cancer
class of disease
adrenal gland cancer
adrenal medulla neoplasm
adrenal gland cancer that is located in the adrenal medulla
DOID:5719
adrenal medulla carcinoma
class of disease
adrenal medulla cancer
carcinoma
adrenal medulla cancer that has material basis in abnormally proliferating cells derives from epithelial cells
DOID:7379
adrenal neuroblastoma
class of disease
adrenal gland cancer
nervous system cancer
adrenal medulla cancer
endocrine gland cancer
neuroblastoma
adrenal gland cancer that derives from immature neuroblastic cells
DOID:5718
Neuroblastoma of the adrenal glands
adrenal rest tumor
class of disease
endocrine organ benign neoplasm
Human disease
DOID:1786
C04.557.470.035.232
adrenocortical adenoma
class of disease
adrenal adenoma
adrenal adenoma that is a benign tumor of the adrenal cortex
DOID:0050891
C04.588.322.078.265.500
C19.053.098.265.500
C19.053.347.500.500
C19.344.078.265.500
Adrenocortical adenoma
adult acute lymphocytic leukemia
class of disease
acute lymphocytic leukemia
Human disease
DOID:5604
adult acute monocytic leukemia
class of disease
acute monocytic leukemia
acute monocytic leukemia occurring in adults
DOID:0080149
adult astrocytic tumour
class of disease
astrocytoma
Human disease
DOID:3076
adult botryoid rhabdomyosarcoma
class of disease
botryoid embryo rhabdomyosarcoma
Human disease
DOID:6847
adult brain ependymoma
class of disease
brain ependymoma
Human disease
DOID:7750
adult brain stem glioma
class of disease
Brainstem glioma
brain stem cancer
Human disease
DOID:4813
adult brainstem astrocytoma
class of disease
adult brain stem glioma
brain stem astrocytic neoplasm
Human disease
DOID:5922
adult brainstem gliosarcoma
class of disease
adult brain stem glioma
human disease
DOID:4812
adult brainstem mixed glioma
class of disease
adult brain stem glioma
Human disease
DOID:5921
adult central nervous system choriocarcinoma
class of disease
choriocarcinoma
central nervous system cancer
central nervous system adult germ cell tumor
central nervous system choriocarcinoma
nervous system cancer
central nervous system disease
Human disease
DOID:6634
adult central nervous system embryonal carcinoma
class of disease
central nervous system adult germ cell tumor
central nervous system embryonal carcinoma
Human disease
DOID:7233
adult central nervous system germinoma
class of disease
central nervous system germinoma
central nervous system adult germ cell tumor
Human disease
DOID:7867
adult central nervous system immature teratoma
class of disease
adult central nervous system teratoma
central nervous system immature teratoma
Human disease
DOID:6018
adult central nervous system mature teratoma
class of disease
adult central nervous system teratoma
central nervous system mature teratoma
Human disease
DOID:6016
adult central nervous system mixed germ cell tumor
class of disease
central nervous system adult germ cell tumor
mixed germ cell tumor of central nervous system
Human disease
DOID:7945
adult central nervous system primitive neuroectodermal neoplasm
class of disease
central nervous system primitive neuroectodermal neoplasm
Human disease
DOID:3865
adult central nervous system teratoma
class of disease
central nervous system teratoma
central nervous system adult germ cell tumor
Human disease
DOID:6015
adult cerebellar neoplasm
class of disease
cerebellum cancer
Human disease
DOID:5056
adult choroid plexus cancer
class of disease
choroid plexus neoplasm
Human disease
DOID:3542
adult cystic teratoma
class of disease
cystic teratoma
Human disease
DOID:7079
adult dermatomyositis
class of disease
dermatomyositis
Dermatomyositis in an adult
DOID:14202
adult endodermal sinus tumor
class of disease
endodermal sinus tumor
endodermal sinus tumor that occurs in adults
DOID:5348
adult ependymoblastoma
class of disease
ependymoblastoma
adult central nervous system primitive neuroectodermal neoplasm
Human disease
DOID:7631
adult epithelioid sarcoma
class of disease
epithelioid sarcoma
Human disease
DOID:8282
adult extraosseous chondrosarcoma
class of disease
extraosseous chondrosarcoma
Human disease
DOID:7902
adult extraosseous osteosarcoma
class of disease
bone cancer
extraosseous osteosarcoma
osteosarcoma
adult sarcoma of soft tissue and extraosseous osteosarcoma that is located in the soft tissues without direct attachment to the skeletal system and results in the production of osteoid, bone, or chondroid material
DOID:7827
adult familial myoclonic epilepsy 1
class of disease
benign adult familial myoclonic epilepsy
autosomal dominant disease
human disease
DOID:0111690
adult familial myoclonic epilepsy 3
class of disease
benign adult familial myoclonic epilepsy
autosomal dominant disease
human disease
DOID:0111695
adult fibrosarcoma
class of disease
fibrosarcoma
conventional fibrosarcoma
Human disease
DOID:3516
adult hepatocellular carcinoma
class of disease
hepatocellular carcinoma
hepatocellular carcinoma is characterized by hepatic mass, abdominal pain and, in advanced stages, jaundice, cachexia and liver failure and often develops in the setting of chronic necro-inflammation
DOID:0070328
adult hypophosphatasia
class of disease
hypophosphatasia
A hypophosphatasia that has material basis in a heterozygous mutation of ALPL on chromosome 1p36.12.
DOID:0110913
adult infiltrating astrocytic neoplasm
class of disease
adult astrocytic tumour
Human disease
DOID:7656
adult intracranial malignant hemangiopericytoma
class of disease
connective tissue neoplasm
Human disease
DOID:6333
adult leptomeningeal melanoma
class of disease
meningeal melanoma
Human disease
DOID:6090
adult liposarcoma
class of disease
liposarcoma
Human disease
DOID:5693
adult lymphoma
class of disease
lymphoma
Human disease
DOID:5825
adult malignant hemangiopericytoma
class of disease
hemangiopericytoma
hemangiopericytoma, malignant
Human disease
DOID:6332
adult malignant mesenchymoma
class of disease
malignant mesenchymoma
Human disease
DOID:5894
adult malignant schwannoma
class of disease
malignant peripheral nerve sheath tumor
childhood malignant schwannoma
Human disease
DOID:8369
adult medulloblastoma
class of disease
medulloblastoma
Human disease
DOID:3864
adult mesenchymal chondrosarcoma
class of disease
mesenchymal chondrosarcoma
adult sarcoma of soft tissue and mesenchymal chondrosarcoma that is located in the cartilage
DOID:4547
adult myxoid chondrosarcoma
class of disease
myxoid chondrosarcoma
adult sarcoma of soft tissue and myxoid chondrosarcoma that is composed of multiple lobules of chondroblast-like cells, arranged in cords and strands, embedded in a myxoid stroma, and separated by fibrous septa
DOID:6495
adult oligodendroglioma
class of disease
oligodendroglioma
Human disease
DOID:3186
adult papillary meningioma
class of disease
rhabdoid meningioma
papillary meningioma
Human disease
DOID:7826
adult pineal parenchymal tumor
class of disease
pinealoma
Human disease
DOID:5031
adult pineoblastoma
class of disease
adult pineal parenchymal tumor
pinealoblastoma
Human disease
DOID:6648
adult pleomorphic rhabdomyosarcoma
class of disease
pleomorphic rhabdomyosarcoma
Human disease
DOID:8251
adult spinal cord ependymoma
class of disease
spinal cord ependymoma
Human disease
DOID:7788
adult spinal cord glioblastoma multiforme
class of disease
spinal cord glioma
Human disease
DOID:7806
adult teratoma
class of disease
teratoma
benign teratoma
Human disease
DOID:5565
adult type testicular granulosa cell tumor
class of disease
testicular granulosa cell tumor
Human disease
DOID:8394
adult vagina botryoid rhabdomyosarcoma
class of disease
vagina botryoid rhabdomyosarcoma
adult botryoid rhabdomyosarcoma
Human disease
DOID:6848
adult xanthogranuloma
class of disease
non-Langerhans-cell histiocytosis
xanthogranuloma
Human disease
DOID:7875
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
class of disease
leukodystrophy
autosomal dominant disease
Leukoencephalopathy with neuroaxonal spheroids
leukodystrophy that is characterized by progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy and has material basis in heterozygous mutation in the CSF1R gene on chromosome 5q32
DOID:0080523
adult-onset severe asthma
class of disease
chronic asthma
human disease
DOID:0080816
adult-onset type II citrullinemia
class of disease
citrullinemia
human disease
DOID:0070342
advanced sleep phase syndrome 1
class of disease
advanced sleep phase syndrome
advanced sleep phase syndrome that has material basis in heterozygous mutation in the PER2 gene on chromosome 2q37
DOID:0110011
afferent loop syndrome
class of disease
postgastrectomy syndrome
Human disease
DOID:8438
C06.405.469.531.099
C23.550.767.050
aflatoxins-related hepatocellular carcinoma
class of disease
hepatocellular carcinoma
Human disease
DOID:5022
agammaglobulinemia 5
class of disease
autosomal dominant disease
agammaglobulinemia
human disease
DOID:0080588
age related macular degeneration 1
class of disease
age related macular degeneration
human disease
DOID:0110014
age related macular degeneration 10
class of disease
age related macular degeneration
hereditary retinal dystrophy
An age related macular degeneration associated with variation in the genomic region 9:112,100,000-127,500,000 (GRCh38). TLR4 has been put forth as a candidate gene.
DOID:0110022
age related macular degeneration 13
class of disease
age related macular degeneration
hereditary retinal dystrophy
age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25
DOID:0110025
age related macular degeneration 14
class of disease
age related macular degeneration
hereditary retinal dystrophy
age related macular degeneration associated with variation at or near the C2 and CFB genes on chromosome 6p21
DOID:0110026
age related macular degeneration 15
class of disease
age related macular degeneration
hereditary retinal dystrophy
age related macular degeneration conferred by variation in the C9 gene on chromosome 5p13
DOID:0110027
age related macular degeneration 5
class of disease
age related macular degeneration
hereditary retinal dystrophy
age related macular degeneration onferred by heterozygous mutation in the ERCC6 gene on chromosome 10q11
DOID:0110028
aggressive digital papillary adenocarcinoma
class of disease
papillary adenocarcinoma
skin carcinoma
adenocarcinoma
sweat gland carcinoma
medical condition
DOID:5590
aggressive periodontitis
class of disease
periodontitis
periodontitis characterized by rapid attachment loss and bone destruction
DOID:1474
C07.465.714.533.161
aggressive systemic mastocytosis
class of disease
systemic mastocytosis
Human disease
DOID:4798
agoraphobia
class of disease
phobia
disease
phobic disorder involving the specific anxiety about being in a place or situation where escape is difficult or embarrassing or where help may be unavailable
DOID:593
F03.080.100
agraphia
class of disease
symptom or sign
writing disorder
aphasia
disease
disease that results in the loss of the ability to write
DOID:0060223
C10.597.606.150.500.050
C23.888.592.604.150.500.050
C10.597.606.150.550.700.125
C23.888.592.604.150.550.700.125
F03.625.374.188.700.125
F03.625.562.700.125
ainhum
class of disease
connective tissue disease
foot diseases
genetic disease
autoamputation
disease
Human disease
DOID:11329
C05.116.264.143
Ainhum
akinetic mutism
class of disease
encephalopathy
brain disease characterized by marked reduction of nearly all motor functions including facial expressions, gestures and speech output, but with some degree of alertness
DOID:4267
C10.228.140.042
akinetopsia
class of disease
agnosia
visual perception
motion perception
agnosia that is a loss of motion perception
DOID:0060130
alastrim
class of disease
smallpox
milder form of smallpox
DOID:9153
alcohol abuse
class of disease
substance abuse
alcohol consumption
alcohol-related disorders
substance abuse that involves the recurring use of alcoholic beverages despite negative consequences
DOID:1574
Alcohol abuse
alcohol dependence
class of disease
non-controlled substance abuse
alcoholism
alcohol abuse
human disease
DOID:0050741
alcohol-induced mental disorder
class of disease
long-term effects of alcohol consumption
non-controlled substance abuse
substance-induced psychosis
nental and behavioural disorders due to use of alcohol
DOID:251
alcohol-induced psychotic disorder
class of disease
alcohol-induced mental disorder
substance-induced psychosis
organic psychotic states due mainly to excessive consumption of alcoholic beverages
DOID:252
C25.723.809.750
C25.775.100.087.750
alcohol-related birth defect
class of disease
fetal alcohol spectrum disorders
fetal alcohol spectrum disorder that results in damage to organs, bones, or muscles due to prenatal alcohol exposure
DOID:0050668
alcohol-related neurodevelopmental disorder
class of disease
fetal alcohol spectrum disorders
human disease
DOID:0050667
alcoholic cardiomyopathy
class of disease
extrinsic cardiomyopathy
long-term effects of alcohol consumption
alcohol and health
disease in which the chronic long-term abuse of alcohol (i.e., ethanol) leads to heart failure
DOID:12935
C14.280.238.057
C25.775.100.087.250
alcoholic gastritis
class of disease
gastritis
long-term effects of alcohol consumption
chronic gastritis
human disease
DOID:8680
alcoholic hepatitis
class of disease
hepatitis
alcoholic liver disease
disease
hepatitis (inflammation of the liver) due to excessive intake of alcohol
DOID:12351
C06.552.380.290
C06.552.645.490
C25.775.100.087.645.490
Alcoholic hepatitis
alcoholic liver cirrhosis
class of disease
liver cirrhosis
alcoholic liver disease
Human disease
DOID:14018
C06.552.630.380
C06.552.645.590
C25.775.100.087.645.550
Alcoholic cirrhosis
alcoholic neuropathy
class of disease
inflammatory and toxic neuropathy
polyneuropathy
long-term effects of alcohol consumption
nervous system alcohol-induced disorders
disease
Human disease
DOID:14183
C10.668.829.800.050
C10.720.112.400
C25.723.705.150.400
C25.775.100.087.193.400
alcoholic pancreatitis
class of disease
pancreatitis
long-term effects of alcohol consumption
alcohol and health
human disease
DOID:4988
C06.689.750.660
C25.775.100.087.730
alcuronium bromide allergy
class of disease
drug allergy
drug allergy that has allergic trigger alcuronium bromide
DOID:0040077
aleukemic leukemia
class of disease
leukemia
leukemia that arises from changes in the tissues forming white blood cells and characterized by a normal or decreased number of white blood cells in the circulating blood
DOID:6004
aleukemic leukemia cutis
class of disease
aleukemic leukemia
Leukemia cutis
Human disease
DOID:6003
aleukemic monocytic leukemia cutis
class of disease
aleukemic leukemia cutis
Human disease
DOID:6958
alexithymia
class of disease
agnosia
disease
subclinical deficiency in understanding, processing, or describing emotions
DOID:0060131
algoneurodystrophy
class of disease
complex regional pain syndrome
Human disease
DOID:14022
allergic asthma
class of disease
respiratory allergy
asthma
extrinsic asthma
asthma with a basis in a pathological type I hypersensitivity reaction
DOID:9415
Asthma
allergic conjunctivitis
class of disease
symptom or sign
chronic conjunctivitis
eye allergy
allergy
chronic conjunctivitis that is an inflammation of the conjunctiva
DOID:11204
C11.187.183.200
C20.543.480.200
Allergic conjunctivitis
allergic contact dermatitis
class of disease
allergic dermatitis
contact dermatitis
disease
medical condition
DOID:3042
C17.800.174.255.100
C17.800.815.255.100
C20.543.418.150
Allergic contact dermatitis
allergic contact dermatitis of eyelid
class of disease
noninfectious dermatoses of eyelid
allergic contact dermatitis
Eyelid dermatitis
Human disease
DOID:1895
allergic rhinitis
class of disease
symptom or sign
rhinitis
respiratory allergy
disease
human disease
DOID:4481
C08.460.799.315
C08.674.453
C09.603.799.315
C20.543.480.680.443
Allergic rhinitis
allescheriosis
class of disease
primary systemic mycosis
Pseudallescheriasis
primary systemic mycosis that results in systemic fungal infection, has material basis in Pseudallescheria boydii, which results in formation of abscesses
DOID:11186
alopecia areata
class of disease
symptom or sign
alopecia
autoimmune disease
autoimmune skin disease
condition in which hair is lost from some or all areas of the body
DOID:986
C17.800.329.937.122.147
Alopecia areata
alopecia-intellectual disability syndrome
class of disease
genetic syndromic intellectual disability
syndrome
human disease
DOID:0080627
alopecia-mental retardation syndrome 1
class of disease
autosomal recessive disease
alopecia-intellectual disability syndrome
human disease
DOID:0080628
alopecia-mental retardation syndrome 2
class of disease
alopecia-intellectual disability syndrome
autosomal recessive disease
human disease
DOID:0080629
alopecia-mental retardation syndrome 4
class of disease
alopecia-intellectual disability syndrome
autosomal recessive disease
human disease
DOID:0080950
alpha chain disease
class of disease
heavy chain disease
intestinal neoplasm
heavy chain disease that results from an overproduction of alpha antibodies (IgA)
DOID:0060126
C04.557.386.390
C06.301.371.411.512
C06.405.249.411.512
C06.405.469.491.505
C15.378.147.780.490.512
C15.604.515.435.512
C20.683.515.512
C20.683.780.490.512
alpha-thalassemia-myelodysplastic syndrome
class of disease
Acquired hemolytic anemia
alpha-thalassemia-related diseases
myelodysplastic syndrome
syndrome
human disease
DOID:0112125
alternating esotropia
class of disease
esotropia
Human disease
DOID:9888
alternating exotropia
class of disease
exotropia
Human disease
DOID:1142
alveolar osteitis
class of disease
periostitis
disease
human disease
DOID:13585
C07.465.227
alveolar rhabdomyosarcoma
class of disease
rhabdomyosarcoma
human disease
DOID:4051
C04.557.450.590.550.660.665
C04.557.450.795.550.660.665
alveoli adenoma
class of disease
lung adenoma
bronchial neoplasm
benign neoplasms by histologic type
adenoma
Human disease
DOID:8003
Alveolar adenoma
amblyopia
class of disease
symptom or sign
eye disease
visual impairment
disease
human disease
DOID:10376
C10.228.140.055
C10.597.751.941.073
C11.966.073
C23.888.592.763.941.073
Amblyopia
amelanotic melanoma
class of disease
melanoma
human disease
DOID:4359
C04.557.465.625.650.510.515
C04.557.580.625.650.510.515
C04.557.665.510.515
amelogenesis imperfecta type 1B
class of disease
amelogenesis imperfecta
autosomal dominant disease
amelogenesis imperfecta that has material basis in heterozygous mutation in the enamelin gene (ENAM) on chromosome 4q13
DOID:0110052
amelogenesis imperfecta type 2A6
class of disease
amelogenesis imperfecta
human disease
DOID:0080960
amelogenesis imperfecta type 3B
class of disease
amelogenesis imperfecta
autosomal dominant disease
amelogenesis imperfecta type 3
human disease
DOID:0080243
amelogenesis imperfecta type 3C
class of disease
amelogenesis imperfecta type 3
autosomal recessive disease
human disease
DOID:0111722
amenorrhea
class of disease
female reproductive system disease
hypomenorrhea
disease
absence of a menstrual period in a woman of reproductive age
DOID:13938
C23.550.568.500
ametropic amblyopia
class of disease
amblyopia
refractive error
Human disease
DOID:10377
amino acid metabolic disorder
class of disease
inherited metabolic disorder
inherited metabolic disorder that is characterized by impaired synthesis and degradation of amino acids
DOID:9252
C16.320.565.100
C18.452.648.100
amnesia
class of disease
symptom or sign
cognitive disorder
memory disorder
psychopathological syndrome
disease
cognitive disorder where the memory is disturbed or lost and involves the loss of memories previously established, loss of the ability to create new memories, continuous high blood pressure and severe shock may also cause amnesia
DOID:10914
C10.597.606.525.100
C23.888.592.604.529.100
F01.700.625.100
F03.615.200
amodiaquine allergy
class of disease
drug allergy
drug allergy that has allergic trigger amodiaquine
DOID:0040022
amoxicillin allergy
class of disease
beta-lactam allergy
beta-lactam allergy that has allergic trigger amoxicillin
DOID:0040004
amphetamine-related disorders
class of disease
substance abuse
stimulant use disorder
negative health consequences of substance abuse that involves the recurring use of amphetamines
DOID:670
C25.775.225
F03.900.225
ampulla of Vater adenocarcinoma
class of disease
ampulla of Vater carcinoma
duodenum adenocarcinoma
extrahepatic bile duct adenocarcinoma
adenocarcinoma
ampulla of Vater carcinoma that derives from epithelial cells of glandular origin
DOID:3502
ampulla of Vater adenosquamous carcinoma
class of disease
ampulla of Vater squamous cell carcinoma
adenosquamous bile duct carcinoma
squamous cell carcinoma
ampulla of Vater cancer
ampulla of Vater carcinoma that derives from squamous cells and gland-like cells
DOID:5628
ampulla of Vater cancer
class of disease
duodenum cancer
ampulla of Vater neoplasm
bile duct cancer
Human disease
DOID:10020
ampulla of Vater carcinoma
class of disease
ampulla of Vater cancer
small intestine carcinoma
duodenum cancer
extrahepatic bile duct carcinoma
carcinoma
ampulla of Vater cancer that has material basis in abnormally proliferating cells derives from epithelial cells
DOID:4932
Carcinoma of the ampulla of Vater
ampulla of Vater clear cell adenocarcinoma
class of disease
ampulla of Vater adenocarcinoma
bile duct clear cell adenocarcinoma
Human disease
DOID:5308
ampulla of Vater mucinous adenocarcinoma
class of disease
ampulla of Vater adenocarcinoma
bile duct mucinous adenocarcinoma
Human disease
DOID:3693
ampulla of Vater neoplasm
class of disease
duodenal neoplasm
bile duct disease
biliary tract neoplasm
Human disease
DOID:10022
ampulla of Vater small cell carcinoma
class of disease
ampulla of Vater carcinoma
liver neuroendocrine carcinoma
small cell carcinoma
Human disease
DOID:7136
ampulla of Vater squamous cell carcinoma
class of disease
ampulla of Vater carcinoma
squamous cell bile duct carcinoma
squamous cell carcinoma of the small intestine
squamous cell carcinoma
ampulla of Vater carcinoma that derives from epithelial squamous cells
DOID:5527
ampullary signet ring cell adenocarcinoma
class of disease
ampulla of Vater adenocarcinoma
bile duct signet ring cell carcinoma
Human disease
DOID:3501
amusia
class of disease
agnosia
auditory agnosia
music-specific disorders
loss of the ability to recognize musical notes, rhythms, and intervals
DOID:0060132
amyloid tumor
class of disease
mesenchymal cell neoplasm
connective tissue benign neoplasm
amyloidosis
Human disease
DOID:6755
amyloidosis
class of disease
systemic disease
proteostasis deficiency
acquired metabolic disease
disease
metabolic disease involving abnormal deposited amyloid proteins
DOID:9120
C18.452.845.500
Amyloidosis
amyotrohpic lateral sclerosis type 22
class of disease
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis that has material basis in mutation in the TUBA4A gene on chromosome 2q35
DOID:0060355
amyotrophic lateral sclerosis type 1
class of disease
amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis
The most common type of familial ALS that has material basis in mutation in the SOD1 gene on chromosome 21
DOID:0060193
amyotrophic lateral sclerosis type 10
class of disease
amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis
amyotrophic lateral sclerosis and frontotemporal dementia
human disease
DOID:0060201
amyotrophic lateral sclerosis type 11
class of disease
amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis
human disease
DOID:0060202
amyotrophic lateral sclerosis type 12
class of disease
amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis
amyotrophic lateral sclerosis that has material basis in mutation in the OPTN gene on chromosome 10
DOID:0060203
amyotrophic lateral sclerosis type 13
class of disease
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis where a mutation that has material basis in the ATXN2 gene on chromosome 12 contributes to suscepitbility
DOID:0060204
amyotrophic lateral sclerosis type 14
class of disease
amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis
amyotrophic lateral sclerosis and frontotemporal dementia
amyotrophic lateral sclerosis that has material basis in mutation in the VCP gene on chromosome 9
DOID:0060205
amyotrophic lateral sclerosis type 15
class of disease
amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis
amyotrophic lateral sclerosis that has material basis in mutation in the UBQLN2 gene on chromosome X
DOID:0060206
amyotrophic lateral sclerosis type 18
class of disease
amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis
amyotrophic lateral sclerosis that has material basis in mutation in the PFN1 gene on chromosome 17
DOID:0060209
amyotrophic lateral sclerosis type 19
class of disease
amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis
amyotrophic lateral sclerosis that has material basis in mutation in the ERBB4 gene on chromosome 2
DOID:0060210
amyotrophic lateral sclerosis type 2
class of disease
amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis
human disease
DOID:0060194
amyotrophic lateral sclerosis type 20
class of disease
amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis
amyotrophic lateral sclerosis with juvenile onset that has material basis in mutation in the HNRNPA1 gene on chromosome 12
DOID:0060211
amyotrophic lateral sclerosis type 21
class of disease
amyotrophic lateral sclerosis
nervous system heredodegenerative disease
amyotrophic lateral sclerosis that has material basis in mutation in the MATR3 gene on chromosome 5
DOID:0060212
amyotrophic lateral sclerosis type 23
class of disease
amyotrophic lateral sclerosis
human disease
DOID:0080225
amyotrophic lateral sclerosis type 3
class of disease
amyotrophic lateral sclerosis
human disease
DOID:0060195
amyotrophic lateral sclerosis type 6
class of disease
amyotrophic lateral sclerosis
sporadic amyotrophic lateral sclerosis
amyotrophic lateral sclerosis and frontotemporal dementia
human disease
DOID:0060198
amyotrophic lateral sclerosis type 7
class of disease
amyotrophic lateral sclerosis
human disease
DOID:0060199
amyotrophic lateral sclerosis type 8
class of disease
amyotrophic lateral sclerosis
human disease
DOID:0050752
amyotrophic lateral sclerosis type 9
class of disease
amyotrophic lateral sclerosis
human disease
DOID:0060200
amyotrophic lateral sclerosis-parkinsonism/dementia complex 1
class of disease
neurodegeneration
A neurodegenerative disease characterized by chronic, progressive amyotrophic lateral sclerosis and parkinsonism-dementia. Susceptibility to this disease is influenced by heterozygous mutation in TRPM7 on 15q21.2.
DOID:0111246
amyotrophic neuralgia
class of disease
brachial plexus neuropathy
neurodegeneration
human disease
DOID:10383
anaerobic meningitis
class of disease
bacterial meningitis
anaerobic infection
human disease
DOID:14559
anal Buschke-Lowenstein tumor
class of disease
anal squamous cell carcinoma
verrucous carcinoma
giant condyloma acuminatum
Human disease
DOID:7175
anal Paget's disease
class of disease
anus adenocarcinoma
extramammary Paget's disease
rare genetic intestinal disease
inherited digestive tract tumor
rare epithelial tumor of rectum
Human disease
DOID:3446
Anal Paget's disease
anal canal Paget's disease
class of disease
anal canal adenocarcinoma
extramammary Paget's disease
anal Paget's disease
Human disease
DOID:8119
anal canal adenocarcinoma
class of disease
anus adenocarcinoma
anal canal cancer
adenocarcinoma
anal canal cancer that derives from epithelial cells of glandular origin
DOID:3692
anal canal cancer
class of disease
large intestine cancer
large intestine cancer that is located in the terminal part of the large intestine
DOID:0050688
anal canal carcinoma
class of disease
carcinoma
anal canal cancer
anal canal cancer that derives from epithelial cells
DOID:6126
anal canal squamous cell carcinoma
class of disease
squamous cell carcinoma
anal squamous cell carcinoma
anal canal cancer
anal canal cancer that derives from epithelial squamous cells
DOID:7177
anal cancer
class of disease
anus neoplasm
anal canal cancer
anal disease
large intestine cancer
disease
Is a rare disease which it is caused in most of the cases by the infection of the Human Papilloma Virus (HPV).
DOID:14110
Anal cancer
anal carcinoma
class of disease
anal cancer
carcinoma
anus cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the anus
DOID:4908
anal carcinoma in situ
class of disease
anal carcinoma
rectum carcinoma in situ
in situ carcinoma
Anal dysplasia
Human disease
DOID:9087
anal colloid adenocarcinoma
class of disease
anus adenocarcinoma
rectum mucinous adenocarcinoma
anus carcinoma that derives from epithelial cells of glandular origin located in the anal colloid
DOID:3691
anal disease
class of disease
anorectal disorder
rectal disease
human disease
DOID:3128
C06.405.469.860.101
Diseases and disorders of anus and anal canal
anal fistula
class of disease
rectal disease
anus disease characterized by an abnormal connection between the epithelialised surface of the anal canal and the perianal skin
DOID:0060328
C06.267.550.600
C06.405.469.471.600
C06.405.469.860.752
C23.300.575.185.550.600
Anal fistula
anal gland adenocarcinoma
class of disease
anus adenocarcinoma
anus carcinoma that derives from epithelial cells of glandular origin located in the anal gland
DOID:7531
anal margin basal cell carcinoma
class of disease
anal margin carcinoma
basal-cell carcinoma
Human disease
DOID:4283
anal margin carcinoma
class of disease
anal carcinoma
skin carcinoma
skin cancer
anal carcinoma that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the anal margin (where the canal meets the outside skin at the anus)
DOID:4284
anal margin squamous cell carcinoma
class of disease
anal margin carcinoma
squamous cell carcinoma
Human disease
DOID:12239
anal neuroendocrine tumor
class of disease
anus neoplasm
rectum neuroendocrine neoplasm
Human disease
DOID:5545
anal spasm
class of disease
anal disease
Human disease
DOID:11374
anal squamous cell carcinoma
class of disease
anal carcinoma
rectum squamous cell carcinoma
squamous cell carcinoma
anal carcinoma that arises near the squamocolumnar junction
DOID:5525
anal stricture
class of disease
anorectal anomalies
anal disease
human disease
DOID:11014
C06.198.025
C16.131.314.047
anaplastic astrocytoma
class of disease
astrocytoma
astrocytoma that is characterized by cells with regular, round to oval nuclei
DOID:3078
Anaplastic astrocytoma
anaplastic ependymoma
class of disease
ependymoma
grade III glioma
Human disease
DOID:5889
Anaplastic ependymoma
anaplastic large-cell lymphoma
class of disease
T-cell lymphoma
non-Hodgkin lymphoma
non-Hodgkin lymphoma involving aberrant T-cells
DOID:0050744
C04.557.386.480.750.399
C15.604.515.569.480.750.600
C20.683.515.761.480.750.399
anaplastic oligodendroglioma
class of disease
oligodendroglioma
human disease
DOID:7154
Anaplastic oligodendroglioma
anaplastic thyroid cancer
class of disease
thyroid cancer
large cell carcinoma
undifferentiated carcinoma
thyroid carcinoma
form of thyroid cancer
DOID:0080522
anatomical narrow angle borderline glaucoma
class of disease
borderline glaucoma
chronic closed-angle glaucoma
Human disease
DOID:13327
anauxetic dysplasia
class of disease
spondyloepimetaphyseal dysplasia
human disease
DOID:0080942
anauxetic dysplasia 2
class of disease
autosomal recessive disease
anauxetic dysplasia
human disease
DOID:0080962
androgen insensitivity syndrome
class of disease
pseudohermaphroditism
sex differentiation disease
disease
sex differentiation condition involving hormonal resistance due to androgen receptor dysfunction in a karyotypically male person
DOID:4674
C12.706.316.096.500
C13.351.875.253.096.500
C16.131.939.316.096.500
C16.320.322.061
C19.391.119.096.500
Androgen insensitivity syndrome
androgenic alopecia
class of disease
baldness
androgen-dependent syndrome
disease
hair loss due to susceptibility of hair follicles to androgenic miniaturization
DOID:0050801
Androgenic alopecia
anemia
class of disease
symptom or sign
hematopoietic system disease
cytopenia
hemic system symptom
disease
decrease in number of red blood cells
DOID:2355
C15.378.071
Anemias
anemia of prematurity
class of disease
neonatal anemia
premature infant disease
Human disease
DOID:11243
anencephaly
class of disease
nervous system malformations
disease
absence of a major portion of the brain, skull, and scalp that occurs during embryonic development
DOID:0060668
C10.500.680.196
C16.131.085.197
C16.131.666.680.196
Anencephaly
aneruptive fever
class of disease
spotted fever
A spotted fever that has material basis in Rickettsia helvetica, which is transmitted by ticks (Ixodes sp). The infection has symptom fever, has symptom headache, has symptom myalgia.
DOID:0050484
aneurysm of heart
class of disease
heart disease
aneurysm
disease
Human disease
DOID:9768
C14.280.358
C14.907.055.608
Heart aneurysms
aneurysm-osteoarthritis syndrome
class of disease
Loeys-Dietz syndrome
human disease
DOID:0070237
angiodysplasia
class of disease
vascular disease
disease
vascular disease that is characterized as a small vascular malformation of the gut
DOID:2494
C14.907.075
Angiodysplasia
angiodysplasia of intestine
class of disease
intestinal disease
angiodysplasia
Human disease
DOID:10846
angioid streaks
class of disease
retinal disease
rare genetic eye disease
genetic disease
Human disease
DOID:13401
C11.768.094
angioid streaks of choroid
class of disease
choroidal sclerosis
angioid streaks
nervous system heredodegenerative disease
genetic vascular disease
choroid disease
retinal degeneration
angioid streaks that involves the optic choroid
DOID:979
angioimmunoblastic T-cell lymphoma
class of disease
T-cell lymphoma
peripheral T-cell lymphoma
immunoblastic lymphadenopathy
peripheral T-cell lymphoma characterized by autoimmune features and poor prognosis
DOID:0111147
angiokeratoma
class of disease
skin hemangioma
benign cutaneous lesion of capillaries, resulting in small marks of red to blue color and characterized by hyperkeratosis
DOID:479
C04.557.645.115
Angiokeratoma
angiokeratoma circumscriptum
class of disease
skin benign neoplasm
angiokeratoma
Human disease
DOID:5949
angiokeratoma of Fordyce
class of disease
skin benign neoplasm
angiokeratoma
disease
sebaceous glands that are present in most individuals
DOID:664
Fordyce's spots
angiokeratoma of Mibelli
class of disease
angiokeratoma
Human disease
DOID:5948
angiolipoma
class of disease
lipoma
lipoma that is a painful subcutaneous nodule, having all other features of a typical lipoma
DOID:3616
C04.557.450.550.100
Angiolipoma
angioma serpiginosum
class of disease
skin hemangioma
skin hemangioma characterized by the presence of small red dots that cluster together to form a linear or snake-like array or ring-shaped pattern located in the blood vessels of the skin
DOID:4028
angiomatous meningioma
class of disease
meningioma
Human disease
DOID:6548
angiomyolipoma
class of disease
benign neoplasms by histologic type
disease
cell type benign neoplasm that from perivascular epithelioid cells
DOID:3314
C04.557.450.550.125
C04.557.450.692.249
Angiomyolipomas
angiomyoma
class of disease
benign perivascular tumor
vascular disease
Human disease
DOID:4265
C04.557.450.590.450.125
angiosarcoma
class of disease
vascular tissue neoplasm
vascular cancer
disease
malignant Vascular tumor that results in rapidly proliferating, extensively infiltrating anaplastic cells derives from blood vessels and derived from the lining of irregular blood-filled spaces
DOID:0001816
Angiosarcoma
angle-closure glaucoma
class of disease
glaucoma
human disease
DOID:13550
C11.525.381.056
angular blepharoconjunctivitis
class of disease
blepharoconjunctivitis
blepharoconjunctivitis that is characterized by fissuring, scaling, maceration and erythema of the lateral or medial canthal area
DOID:2455
angular cheilitis
class of disease
symptom or sign
cheilitis
disease
cheilitis characterized by inflammation of one or both of the corners of the mouth
DOID:0060312
Angular cheilitis
anhidrosis
class of disease
hypohidrosis
disease
Human disease
DOID:11156
animal phobia
class of disease
specific phobia
disease
specific phobia that involves a fear caused by the presence or thought of a specific animal that poses little or no danger at all
DOID:600
aniseikonia
class of disease
refractive error
dysmetropsia
disease
Human disease
DOID:0050304
DOID:12274
C11.744.116
anismus
class of disease
symptom or sign
focal dystonia
constipation
failure of the normal relaxation of pelvic floor muscles during attempted defecation
DOID:0050839
anisometropia
class of disease
refractive error
disease
human disease
DOID:12273
C11.744.126
ankyloglossia
class of disease
tongue disease
genetic nervous system disorder
genetic disease
congenital disorder of tongue mobility
DOID:0060604
C07.160
Ankyloglossia
ankylosing spondylitis 1
class of disease
ankylosing spondylitis
human disease
DOID:0080603
ankylosing spondylitis 2
class of disease
ankylosing spondylitis
autosomal dominant disease
human disease
DOID:0080604
ankylosing spondylitis 3
class of disease
ankylosing spondylitis
human disease
DOID:0080605
ankylosis
class of disease
arthropathy
joint stiffness
disease
Human disease
DOID:227
C05.550.069
Ankylosis
anodontia
class of disease
tooth agenesis
tooth agenesis
tooth abnormality
tooth pathology
disease
human disease
DOID:13714
C07.650.800.100
C07.793.700.100
C16.131.850.800.100
anomic aphasia
class of disease
symptom or sign
aphasia
clinical sign
disease
type of aphasia
DOID:4541
C10.597.606.150.500.090
C23.888.592.604.150.500.090
anorexia nervosa
class of disease
eating disorder
disease
type of eating disorder
DOID:8689
F03.400.128
Anorexia nervosa
anosognosia
class of disease
agnosia
disease
Unawareness of one's own illness, symptoms or impairments
DOID:0060133
anovulation
class of disease
ovarian disease
disease
human disease
DOID:3781
C13.351.500.056.630.050
C19.391.630.050
G08.686.784.690.080
anterior cerebral artery infarction
class of disease
cerebral infarction
cerebral artery occlusion
Human disease
DOID:3528
C10.228.140.300.150.477.200.400
C10.228.140.300.510.200.325
C10.228.140.300.775.200.200.400
C14.907.253.092.477.200.400
C14.907.253.560.200.325
C14.907.253.855.200.200.400
C23.550.513.355.250.200.400
C23.550.717.489.250.200.400
anterior compartment syndrome
class of disease
compartment syndrome
disease
DOID:3933
C05.651.180.063
C14.907.303.063
anterior corneal pigmentation
class of disease
corneal deposit
Human disease
DOID:12307
anterior dislocation of lens
class of disease
globe disease
lens subluxation
Human disease
DOID:2460
anterior horn cell disease
class of disease
spinal muscular atrophy
Human disease
DOID:4873
anterior ischemic optic neuropathy
class of disease
ischemic optic neuropathy
optic nerve disease
Human disease
DOID:12010
anterior optic tract meningioma
class of disease
optic nerve tumor
visual pathway meningioma
Human disease
DOID:6334
anterior scleritis
class of disease
scleritis
Human disease
DOID:13794
anterior segment dysgenesis 1
class of disease
corneal opacification and other ocular anomalies
autosomal dominant disease
human disease
DOID:0080606
anterior segment dysgenesis 2
class of disease
autosomal recessive disease
corneal opacification and other ocular anomalies
human disease
DOID:0080607
anterior segment dysgenesis 3
class of disease
autosomal dominant disease
corneal opacification and other ocular anomalies
human disease
DOID:0080608
anterior segment dysgenesis 4
class of disease
corneal opacification and other ocular anomalies
autosomal dominant disease
human disease
DOID:0080609
anterior segment dysgenesis 5
class of disease
corneal opacification and other ocular anomalies
human disease
DOID:0080610
anterior spinal artery syndrome
class of disease
syndrome
cerebrovascular disease
vascular myelopathy
artery disease
Human disease
DOID:6712
C10.228.854.785.650.100
C14.907.790.550.100
anterior urethral cancer
class of disease
urethral cancer
female urethral cancer
Human disease
DOID:8272
anterior uveitis
class of disease
uveitis
panuveitis
Human disease
DOID:1407
C11.941.879.780.880
anterograde amnesia
class of disease
amnesia
loss of the ability to create new memories after the onset of amnesia
DOID:5340
C10.597.606.525.100.075
C23.888.592.604.529.100.075
F01.700.625.100.075
F03.615.200.137
anterolateral myocardial infarction
class of disease
myocardial infarction
Human disease
DOID:5845
anteroseptal myocardial infarction
class of disease
myocardial infarction
Human disease
DOID:5855
anthracosilicosis
class of disease
pneumoconiosis
anthracosis
human disease
DOID:10324
C08.381.483.581.062.500
C08.381.483.581.760.125
C08.381.520.702.062.500
C08.381.520.702.760.125
C24.800.834.201
anthracosis
class of disease
occupational disease
pneumoconiosis
disease
human disease
DOID:10327
C08.381.483.581.062
C08.381.520.702.062
Black lung disease
anti-basement membrane glomerulonephritis
class of disease
Goodpasture syndrome
Human disease
DOID:4780
antidepressant abuse
class of disease
substance abuse
abuse of medicaments
substance abuse that involves the recurring use of antidepressant drugs despite negative consequences
DOID:11718
antisocial personality disorder
class of disease
Cluster B personality disorders
personality disorder
disease
Personality disorder that involves a pervasive pattern of disregard for other people
DOID:10939
F03.675.050
Antisocial personality disorder
antisynthetase syndrome
class of disease
autoimmune disease
idiopathic inflammatory myopathy
human disease
DOID:0080744
anuria
class of disease
symptom or sign
kidney disease
oliguria
urological symptom
lack of urine
DOID:2983
C12.050.351.968.419.078
C12.200.777.934.141
C12.200.777.419.078
C12.050.351.968.934.070
C12.950.419.078
C12.950.934.070
anus adenocarcinoma
class of disease
anal carcinoma
adenocarcinoma
anal carcinoma that originating in the cortex of the adrenal gland and derives from epithelial cells of glandular origin
DOID:3447
anus basaloid carcinoma
class of disease
anal squamous cell carcinoma
basaloid squamous cell carcinoma
Human disease
DOID:7174
anus leiomyoma
class of disease
leiomyoma
benign neoplasm of anus
rectum leiomyoma
anus neoplasm
Human disease
DOID:5134
anus leiomyosarcoma
class of disease
anus sarcoma
leiomyosarcoma
rectum leiomyosarcoma
human disease
DOID:5267
anus lymphoma
class of disease
anal cancer
lymphoma
Human disease
DOID:14139
anus neoplasm
class of disease
intestinal neoplasm
anal disease
intestinal benign neoplasm
Human disease
DOID:4551
C04.588.274.476.411.307.790.040
C06.301.371.411.307.790.040
C06.405.249.411.307.790.040
C06.405.469.491.307.790.040
C06.405.469.860.101.163
C06.405.469.860.180.500.040
anus rhabdomyosarcoma
class of disease
anus sarcoma
rhabdomyosarcoma
rectum rhabdomyosarcoma
anal cancer
rhabdomyosarcoma and sarcoma of the anus that is located in the anus
DOID:4066
anus sarcoma
class of disease
anal cancer
sarcoma
intestinal benign neoplasm
sarcoma and malignant neoplasm of anus that is located in the anus
DOID:4067
anxiety disorder
class of disease
cognitive disorder
disease
cognitive disorder with an excessive, irrational dread of everyday situations
DOID:2030
F03.080
Anxiety disorders
aorta angiosarcoma
class of disease
angiosarcoma
aortic disease
human disease
DOID:4510
aorta atresia
class of disease
aortic disease
aortic disease that is characterized by an absence of an opening from the left ventricle of the heart into the aorta
DOID:14037
aortic aneurysm
class of disease
aortic disease
aneurysm
clinical sign
disease
aorta to greater than 1.5 times normal size
DOID:3627
C14.907.055.239
C14.907.109.139
Aortic aneurysms
aortic atherosclerosis
class of disease
atherosclerosis
Human disease
DOID:10230
aortic disease
class of disease
artery disease
artery disease characterized by degeneration of the cells composing the aortic wall
DOID:520
C14.907.109
aortic malignant tumor
class of disease
vascular cancer
aortic disease
Human disease
DOID:8352
aortic valve disease
class of disease
heart valve disease
aortic disease
Human disease
DOID:62
C14.280.484.048
Aortic valve diseases
aortic valve disease 1
class of disease
familial bicuspid aortic valve
bicuspid aortic valve disease that has material basis in heterozygous mutation in the NOTCH1 gene on chromosome 9q34
DOID:0080333
aortic valve disease 2
class of disease
familial bicuspid aortic valve
autosomal dominant disease
bicuspid aortic valve disease that has material basis in heterozygous mutation in the SMAD6 gene on chromosome 15q22
DOID:0080334
aortic valve insufficiency
class of disease
aortic valve disease
valve insufficiency
disease
aortic valve disease that is characterized by leaking of the aortic valve of the heart causes blood to flow in the reverse direction during ventricular diastole, from the aorta into the left ventricle
DOID:57
C14.280.484.095
Aortic valve insufficiency
aortic valve prolapse
class of disease
aortic valve disease
heart valve prolapse
Human disease
DOID:5232
C14.280.484.400.100
aortitis
class of disease
aortic disease
inflammation of the aortic wall
DOID:519
C14.907.109.320
C14.907.940.080
Aortitis
aphasia
class of disease
symptom or sign
language disorder
neurological symptom
specific language impairment-5
disease
Inability to spoke
DOID:0060046
C10.597.606.150.500.800.100
C23.888.592.604.150.500.800.100
Aphasia
aphthous stomatitis
class of disease
symptom or sign
clinical sign
stomatitis
lesions in mouth
disease
stomatitis characterized by the repeated formation of benign and non-contagious mouth ulcers
DOID:9663
C07.465.864.750
Aphthous ulcer
apical granuloma
class of disease
disease
periapical periodontitis
granuloma
tooth disease
DOID:4617
C07.320.830.700.740
C07.465.714.306.700.740
C07.465.714.533.487.740
apical myocardial infarction
class of disease
myocardial infarction
Human disease
DOID:5848
apocrine adenocarcinoma
class of disease
apocrine sweat gland cancer
sweat gland carcinoma
adenocarcinoma
Apocrine gland carcinoma
apocrine sweat gland cancer that derives from epithelial cells of glandular origin
DOID:4933
apocrine adenoma
class of disease
apocrine sweat gland neoplasm
Human disease
DOID:3895
apocrine adenosis of breast
class of disease
non-proliferative fibrocystic change of the breast
Human disease
DOID:5999
apocrine sweat gland cancer
class of disease
sweat gland cancer
apocrine sweat gland neoplasm
Human disease
DOID:4934
apocrine sweat gland neoplasm
class of disease
sweat gland neoplasm
apocrine sweat gland disease
Human disease
DOID:5876
apolipoprotein C-3 deficiency
class of disease
cholesterol-ester transfer protein deficiency
autosomal dominant disease
human disease
DOID:0111370
appendiceal neoplasm
class of disease
intestinal neoplasm
appendix disease
cecal neoplasm
intestinal benign neoplasm
Human disease
DOID:11240
C04.588.274.476.411.184.290
C06.301.371.411.184.290
C06.405.249.411.184.290
C06.405.469.110.417.290
C06.405.469.491.184.290
Appendiceal neoplasms
appendix cancer
class of disease
intestinal cancer
appendiceal neoplasm
appendix disease
cancer that is located in the appendix
DOID:11239
Appendiceal cancer
appendix disease
class of disease
gastrointestinal system disease
cecal disease
gastrointestinal system disease that is located in the appendix
DOID:60000
Diseases and disorders of appendix
appendix lymphoma
class of disease
appendix cancer
primary organ-specific lymphoma
human disease
DOID:11241
apperceptive agnosia
class of disease
visual agnosia
agnosia
agnosia that is a loss of the ability to distinguish visual shapes
DOID:0060134
apple allergy
class of disease
fruit allergy
fruit allergy triggered by Malus domestica plant fruit food product.
DOID:0060504
apricot allergy
class of disease
fruit allergy
fruit allergy triggered by Prunus armeniaca plant fruit food product.
DOID:0060505
aqueous misdirection
class of disease
glaucoma
Human disease
DOID:11149
arcus senilis
class of disease
corneal degeneration
rare genetic eye disease
genetic disease
disease
Human disease
DOID:11342
C11.204.299.070
Arcus senilis
ariboflavinosis
class of disease
nutritional deficiency disease
vitamin deficiency
vitamin B deficiency
disease
Human disease
DOID:8454
C18.654.521.500.133.699.713
arrhythmogenic right ventricular dysplasia 1
class of disease
arrhythmogenic right ventricular cardiomyopathy
autosomal dominant disease
arrhythmogenic right ventricular dysplasia that has material basis in heterozygous mutation in the TGFB3 gene on chromosome 14q24
DOID:0110070
arrhythmogenic right ventricular dysplasia 3
class of disease
arrhythmogenic right ventricular cardiomyopathy
autosomal dominant disease
arrhythmogenic right ventricular dysplasia associated with variation in the region 14q12-q22
DOID:0110072
arrhythmogenic right ventricular dysplasia 4
class of disease
arrhythmogenic right ventricular cardiomyopathy
autosomal dominant disease
An arrhythmogenic right ventricular dysplasia associated with variation in the region 2q32.1-q32.3.
DOID:0110073
arrhythmogenic right ventricular dysplasia 6
class of disease
arrhythmogenic right ventricular cardiomyopathy
arrhythmogenic right ventricular dysplasia associated with variation in the region 10p14-p12
DOID:0110075
arterial hypertension
class of disease
symptom or sign
vascular disease
artery disease
clinical sign
hypertension
disease
long term medical condition with elevated arterial blood pressure
DOID:10763
C14.907.489
Hypertension
arteriolosclerosis
class of disease
arteriosclerosis
coronary artery disease
Human disease
DOID:5162
C14.907.137.126.056
Arteriolosclerosis
arteriosclerosis
class of disease
artery disease
disease
thickening, hardening and loss of elasticity of the walls of arteries
DOID:2349
C14.907.137.126
Atherosclerosis
arteriosclerosis obliterans
class of disease
arteriosclerosis
peripheral artery disease
coronary artery disease
human disease
DOID:5160
C14.907.137.126.114
arteriosclerotic cardiovascular disease
class of disease
arteriosclerosis
coronary artery disease
human disease
DOID:2348
arteritic anterior ischemic optic neuropathy
class of disease
anterior ischemic optic neuropathy
Human disease
DOID:0050863
artery disease
class of disease
vascular disease
type of vascular disease
DOID:0050828
arthrogryposis multiplex congenita-4
class of disease
autosomal recessive disease
human disease
DOID:0080980
arthrogryposis, renal dysfunction, and cholestasis 1
class of disease
arthrogryposis–renal dysfunction–cholestasis syndrome
human disease
DOID:0111353
arthrogryposis, renal dysfunction, and cholestasis 2
class of disease
arthrogryposis–renal dysfunction–cholestasis syndrome
human disease
DOID:0111354
arthropathy
class of disease
joint disorder
bone disease
disease
disease of a joint
DOID:381
C05.550
Arthropathies
arthus reaction
class of disease
type III hypersensitivity
Human disease
DOID:1556
C20.543.520.100
articulation disorder
class of disease
speech disorder
language disorder
speech disorder that involves mispronouncing speech sounds by omitting, distorting, substituting, or adding sounds which can make speech difficult to understand
DOID:4186
C10.597.606.150.500.800.150
C23.888.592.604.150.500.800.150
asbestos-related lung carcinoma
class of disease
lung carcinoma
Human disease
DOID:7596
asbestosis
class of disease
pneumoconiosis
asbestos-related disease
disease
pneumoconiosis caused by inhalation and retention of asbestos fibers
DOID:10320
C08.381.483.581.125
C08.381.520.702.125
C24.800.127
Asbestosis
ascending cholangitis
class of disease
symptom or sign
non-neoplastic bile duct disorder
inflammatory disease
bile duct disease
disease
bile duct disease that is an inflammation of the bile duct
DOID:9446
C06.130.120.200
Ascending cholangitis
ascending cholangitis
class of disease
ascending cholangitis
Human disease
DOID:14270
ascending colon cancer
class of disease
plump cancer
Human disease
DOID:218
aseptic meningitis
class of disease
meningitis
non-infectious meningitis
disease
meningitis caused by anything other than bacteria
DOID:12157
C10.586.625.220
aspergillosis
class of disease
opportunistic mycosis
disease
infectious disease of humans, birds and other animals
DOID:13564
C01.150.703.080
Aspergillosis
asphyxia neonatorum
class of disease
respiratory disease
perinatal respiratory disorder
disease
Respiratory failure in the newborn. (Dorland, 27th ed)
DOID:11088
C16.614.092
asphyxiating thoracic dysplasia
class of disease
osteochondrodysplasia
autosomal recessive disease
bone development disease
human disease
DOID:0050592
Asphyxiating thoracic dysplasia
asphyxiating thoracic dystrophy 1
class of disease
asphyxiating thoracic dysplasia
autosomal recessive disease
asphyxiating thoracic dystrophy associated with variation in the region 15q13
DOID:0110085
aspiration pneumonia
class of disease
symptom or sign
bacterial pneumonia
disease
bronchopneumonia that develops due to the entrance of foreign materials into the lungs
DOID:0050152
C08.381.677.529
C08.730.610.529
Aspiration pneumonia
aspiration pneumonitis
class of disease
pneumonia
aspiration pneumonia
disease
chemical pneumonitis or aspiration pneumonitis caused by aspiration during anaesthesia, especially during pregnancy
DOID:3240
aspirin-induced respiratory disease
class of disease
intrinsic asthma
salicylate sensitivity
human disease
DOID:0080822
associative agnosia
class of disease
visual agnosia
agnosia
agnosia that is a loss of the ability to recognize visual scenes or classes of objects but retain the abilty to describe them
DOID:0060136
astereognosia
class of disease
agnosia
tactile agnosia
agnosia that is the loss of the ability to recognize objects by touch based on its texture, size and weight
DOID:0060150
asthma
class of disease
bronchospasm
disease
long-term disease involving inflamed airways
DOID:2841
C08.127.108
C08.381.495.108
C08.674.095
C20.543.480.680.095
Asthma
astigmatism
class of disease
symptom or sign
refractive error
disease
astigmatism
refractive error characterized by the optics of the eye to focus a point object into a sharp focused image on the retina, has_symptom blurred vision.
DOID:11782
C11.744.212
Astigmatism (eye)
astroblastoma
class of disease
astrocytoma
glial tumor derived from the astroblast, a type of cell that closely resembles spongioblastoma and astrocytes
DOID:7305
Astroblastoma
astrocytoma
class of disease
glioma
cerebrum cancer
central nervous system cancer
disease
type of cancer of the brain originating in a particular kind of glial cells, star-shaped brain cells in the cerebrum called astrocytes
DOID:3069
C04.557.465.625.600.380.080
C04.557.470.670.380.080
C04.557.580.625.600.380.080
Astrocytic tumors
asymmetric motor neuropathy
class of disease
motor neuritis
Human disease
DOID:7559
asymptomatic dengue
class of disease
dengue fever
asymptomatic disease
A dengue disease that results in infection, has material basis in Dengue virus [NCBITaxon:12637] with four serotypes (Dengue virus 1, 2, 3 and 4), which are transmitted by Aedes mosquito bite. The infection has no manifestations of symptoms.
DOID:0050143
asymptomatic neurosyphilis
class of disease
tertiary neurosyphilis
tertiary neurosyphilis that results in mild meningitis
DOID:10035
asynchronous multifocal osteogenic sarcoma
class of disease
multifocal osteogenic sarcoma
Human disease
DOID:6697
ataxia and polyneuropathy, adult-onset
class of disease
genetic disease
mitochondrial disease
human disease
DOID:0111750
ataxia with oculomotor apraxia type 3
class of disease
autosomal recessive cerebellar ataxia
oculomotor apraxia
spinocerebellar ataxia with axonal neuropathy type 2
human disease
DOID:0060557
ataxic cerebral palsy
class of disease
cerebral palsy
A cerebral palsy that is caused by damage to the cerebellum, which affects muscle coordination, particularly in the limb. Some individuals suffer from hypotonia, tremors, difficulty with visual and/or auditory processing.
DOID:0050670
atheroembolism of kidney
class of disease
cholesterol embolism
kidney disease
Human disease
DOID:1460
atherosclerosis
class of disease
arteriosclerotic cardiovascular disease
arteriosclerosis
disease
human disease
DOID:1936
C14.907.137.126.307
Atherosclerosis
atopic dermatitis
class of disease
symptom or sign
dermatitis
allergic contact dermatitis
disease
type of inflammation of the skin
DOID:3310
C16.320.850.210
C17.800.174.193
C17.800.815.193
C17.800.827.210
C20.543.480.343
Atopic dermatitis
atopic dermatitis 2
class of disease
atopic dermatitis
atopic dermatitis conferred by variation in the FLG gene on chromosome 1q21
DOID:0110098
atopic dermatitis 3
class of disease
atopic dermatitis
atopic dermatitis associated with variation in the region 20p
DOID:0110099
atopic dermatitis 4
class of disease
atopic dermatitis
An atopic dermatitis associated with variation in the region 17q25.3.
DOID:0110100
atopic dermatitis 5
class of disease
atopic dermatitis
atopic dermatitis associated with variation in the region 13q12-q14
DOID:0110101
atopic dermatitis 6
class of disease
atopic dermatitis
atopic dermatitis associated with variation in the region 5q31-q33
DOID:0110102
atopic dermatitis 7
class of disease
atopic dermatitis
An atopic dermatitis associated with variation in the region 11q13.5.
DOID:0110103
atopic dermatitis 8
class of disease
atopic dermatitis
An atopic dermatitis associated with variation in the region 4q22.1.
DOID:0110104
atopic dermatitis 9
class of disease
atopic dermatitis
atopic dermatitis associated with variation in the region 3p24
DOID:0110105
atrial heart septal defect 1
class of disease
atrial heart septal defect
atrial heart septal defect type 1 associated with variation in the region 5p
DOID:0110106
atrophic gastritis
class of disease
gastritis
chronic gastritis
Human disease
DOID:8929
C06.405.205.697.394
C06.405.748.398.394
Atrophic gastritis
atrophic muscular disease
class of disease
neuromuscular disease
muscle tissue disease
muscular disease
neuromuscular disease characterized by an abnormal reduction in the muscle volume and atrophy
DOID:913
C05.651.534
C10.668.491.175
atrophic nonflaccid tympanic membrane
class of disease
tympanic membrane disease
Tympanic membrane retraction
Human disease
DOID:12546
atrophic vaginitis
class of disease
vaginitis
disease
inflammation of the vagina due to the thinning and shrinking of the tissues, as well as decreased lubrication
DOID:11968
C13.351.500.894.906.316
Atrophic vaginitis
atrophic vulva
class of disease
vulvar disease
Human disease
DOID:14275
atrophodermia vermiculata
class of disease
keratosis pilaris atropicans
Dermatological condition
DOID:0080756
atrophy of prostate
class of disease
prostate disease
Human disease
DOID:2301
atypical Gaucher's disease due to saposin c deficiency
class of disease
Gaucher's disease
genetic disease
A Gaucher's disease that has material basis in an autosomal recessive mutation of PSAP on chromosome 10q22.1.
DOID:0110961
atypical autism
class of disease
autism spectrum disorder
pervasive developmental disorder
disease
autism spectrum disorder that involves some autistic symptoms occuring after age 3 with an abscence of all the traits necessary for a diagnosis of autism
DOID:0060042
atypical breast papilloma
class of disease
breast duct papilloma
Human disease
DOID:8227
atypical choroid plexus papilloma
class of disease
choroid plexus neoplasm
papilloma
cerebrovascular benign neoplasm
Human disease
DOID:3544
atypical chronic myeloid leukemia
class of disease
myelodysplastic/myeloproliferative neoplasm
chronic myeloid leukemia
A myelodysplastic myeloproliferative neoplasm characterized by the principal involvement of the neutrophil series with leukocytosis and multilineage dysplasia. The neoplastic cells do not have a Philadelphia chromosome or the BCR/ABL fusion gene.
DOID:0060597
C04.557.337.539.300
C15.378.190.615.500
atypical depressive disorder
class of disease
mood disorder
disease
depression characterized by improved mood in response to positive events
DOID:12294
Atypical depression
atypical follicular adenoma
class of disease
follicular adenoma
Human disease
DOID:8292
atypical hereditary sensory neuropathy
class of disease
hereditary sensory and autonomic neuropathy
hereditary sensory neuropathy characterized by late onset of sensory ataxia without ulcerating acropathy or autonomic abnormalities
DOID:0070160
atypical lipomatous tumor
class of disease
liposarcoma
Human disease
DOID:5690
atypical neurofibroma
class of disease
neurofibroma
Human disease
DOID:5153
atypical polypoid adenomyoma
class of disease
adenomyoma
Human disease
DOID:4993
auditory agnosia
class of disease
agnosia
music-specific disorders
agnosia that is a loss of the ability to distinguishing environmental and non-verbal auditory cues including difficulty distinguishing speech from non-speech sounds even though hearing is usually normal
DOID:0060137
auricular cancer
class of disease
ear neoplasms
human disease
DOID:5101
autoimmune atherosclerosis
class of disease
autoimmune disease of cardiovascular system
autoimmune disease of cardiovascular system that is characterized by a build up of plaque in the arteries
DOID:0040096
autoimmune cardiomyopathy
class of disease
autoimmune disease of cardiovascular system
heart disease
immune disorder
cardiomyopathy
autoimmune disease of cardiovascular system that is characterized by deterioration of the function of the heart muscle
DOID:0040095
autoimmune cholangitis
class of disease
autoimmune hepatitis
ascending cholangitis
human disease
DOID:0080742
autoimmune disease
class of disease
hypersensitivity
disease
immune disorder
primary immunodeficiency disease
type of human disease
DOID:417
C20.111
Autoimmune diseases and disorders
autoimmune disease of blood
class of disease
autoimmune disease
hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the blood
DOID:0060050
autoimmune disease of cardiovascular system
class of disease
autoimmune disease
cardiovascular disease
hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the cardiovascular system.
DOID:0060051
autoimmune disease of central nervous system
class of disease
autoimmune disease of the nervous system
central nervous system disease
autoimmune disease of the central nervous system
DOID:0060004
autoimmune disease of endocrine system
class of disease
autoimmune disease
endocrine system disease
hypersensitivity reaction type II disease that is the abnormal functioning of the immune system resulting in production of antibodies or T cells against cells and/or tissues in the endocrine system
DOID:0060005
autoimmune disease of exocrine system
class of disease
autoimmune disease
immune system disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the exocrine system
DOID:0060029
autoimmune disease of eyes, ear, nose and throat
class of disease
autoimmune disease of the nervous system
sensory system disease
hypersensitivity reaction type II disease of the eyes, ears, nose and throat
DOID:0060030
autoimmune disease of gastrointestinal tract
class of disease
autoimmune disease
gastrointestinal system disease
hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the gastrointestinal tract
DOID:0060031
autoimmune disease of musculoskeletal system
class of disease
autoimmune disease
musculoskeletal disorder
autoimmune disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the musculoskeletal system
DOID:0060032
autoimmune disease of peripheral nervous system
class of disease
autoimmune disease of the nervous system
peripheral neuropathy
autoimmune disease of the nervous system that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the peripheral nervous system
DOID:0060033
autoimmune disease of the nervous system
class of disease
autoimmune disease
nervous system disease
neurological disorder
A disorder characterized by the degeneration of the nervous system due to autoimmunity. Representative examples include multiple sclerosis, Guillain-Barre syndrome, and myasthenia gravis.
DOID:438
C10.114
C20.111.258
autoimmune disease of urogenital tract
class of disease
autoimmune disease
reproductive system disease
urinary system disease
hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the urogenital tract
DOID:0060049
autoimmune gastritis
class of disease
autoimmune disease of gastrointestinal tract
stomach disease
gastritis
autoimmune disease of gastrointestinal tract that is located in the stomach
DOID:0040090
autoimmune glomerulonephritis
class of disease
autoimmune disease of urogenital tract
immune disorder
rare urogenital disease
glomerulonephritis
human disease
DOID:0040094
autoimmune myocarditis
class of disease
autoimmune cardiomyopathy
myocarditis
autoimmune disease of cardiovascular system
DOID:0080767
autoimmune neuropathy
class of disease
autoimmune disease of central nervous system
autoimmune disease of centreal nervous system caused by an autoimmune response
DOID:0060499
autoimmune optic neuritis
class of disease
autoimmune disease of peripheral nervous system
optic neuritis
autoimmune disease of peripheral nervous system that is located in the neuron projection bundle connecting eye with brain
DOID:0040089
autoimmune pancreatitis
class of disease
chronic pancreatitis
IgG4-related disease
autoimmune disease of endocrine system
pancreas disease
type of chronic pancreatitis
DOID:0040091
C06.689.750.830.500
C20.111.296
C23.550.291.500.750.500
autoimmune peripheral neuropathy
class of disease
autoimmune disease of peripheral nervous system
autoimmune disease of peripheral nervous system that results in peripheral neuropathy
DOID:0040087
autoimmune polyendocrine syndrome
class of disease
autoimmune disease of endocrine system
polyglandular dysfunction
disease
autoimmune disease of endocrine system with auto-reactivity against endocrine organs
DOID:14040
C19.787
C20.111.750
autoimmune polyendocrine syndrome type 2
class of disease
autoimmune polyendocrine syndrome
An autoimmune polyendocrine syndrome that is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs. It is more heterogeneous and has not been linked to one gene.
DOID:0050168
autoimmune skin disease
class of disease
autoimmune disease
skin disease
rheumatic disease
cellulitis
rare skin disease
immune disorder
autoimmune disease of musculoskeletal system
connective tissue disease
hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the skin and connective tissue
DOID:0060039
autoimmune thyroiditis
class of disease
autoimmune disease of endocrine system
thyroiditis
disease
autoimmune disease of endocrine system that involves inflammation located in thyroid gland caused by the immune system reacting against its own tissues
DOID:7188
C19.874.871.102
C20.111.809
autoimmune vasculitis
class of disease
autoimmune disease of cardiovascular system
immune disorder
vasculitis
autoimmune disease of cardiovascular system that is characterized by inflammation of the blood vessels
DOID:0040097
autonomic nervous system benign neoplasm
class of disease
peripheral nervous system benign neoplasm
autonomic nervous system neoplasm
human disease
DOID:0080321
autonomic nervous system disease
class of disease
peripheral neuropathy
human disease
DOID:11465
Diseases and disorders of autonomic nervous system
autonomic nervous system neoplasm
class of disease
peripheral nervous system neoplasm
autonomic nervous system disease
peripheral nervous system neoplasm that is located in the autonomic nervous system
DOID:2621
autonomic neuropathy
class of disease
autonomic nervous system disease
polyneuropathy
human disease
DOID:11504
autonomic peripheral neuropathy
class of disease
peripheral neuropathy
autonomic neuropathy
Human disease
DOID:0060054
autosomal dominant Aarskog syndrome
class of disease
Aarskog syndrome
autosomal dominant disease
human disease
DOID:0111825
autosomal dominant Emery-Dreifuss muscular dystrophy 2
class of disease
Emery-Dreifuss muscular dystrophy
autosomal dominant disease
Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of LMNA on chromosome 1q22
DOID:0070247
autosomal dominant Emery-Dreifuss muscular dystrophy 4
class of disease
Emery-Dreifuss muscular dystrophy
autosomal dominant disease
An Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of SYNE1 on chromosome 6q25.2.
DOID:0070249
autosomal dominant Emery-Dreifuss muscular dystrophy 5
class of disease
Emery-Dreifuss muscular dystrophy
autosomal dominant disease
An Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of SYNE2 on chromosome 14q23.2.
DOID:0070250
autosomal dominant Emery-Dreifuss muscular dystrophy 7
class of disease
Emery-Dreifuss muscular dystrophy
autosomal dominant disease
An Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of TMEM43 on chromosome 3p25.1.
DOID:0070252
autosomal dominant Kenny-Caffey syndrome
class of disease
Kenny-Caffey syndrome
autosomal dominant disease
human disease
DOID:0080723
autosomal dominant Parkinson disease 1
class of disease
hereditary late onset Parkinson disease
autosomal dominant disease
human disease
DOID:0060367
autosomal dominant Parkinson's disease 22
class of disease
autosomal dominant disease
hereditary late onset Parkinson disease
A late onset Parkinson's disease that has material basis in heterozygous mutation in the CHCHD2 gene on chromosome 7p11.2
DOID:0080504
autosomal dominant Wolfram syndrome
class of disease
Wolfram syndrome
autosomal dominant disease
Wolfram syndrome that is characterized by congenital progressive hearing impairment, diabetes mellitus, and optic atrophy and that has material basis in autosomal dominant inheritance of a heterozygous mutation in the WFS1 gene on chromosome 4p16
DOID:0080584
autosomal dominant centronuclear myopathy
class of disease
centronuclear myopathy
centronuclear myopathy that has material basis in autosomal dominant inheritance
DOID:0111217
autosomal dominant chondrodysplasia punctata
class of disease
chondrodysplasia punctata
autosomal dominant disease
Human disease
DOID:0060293
autosomal dominant craniodiaphyseal dysplasia
class of disease
autosomal dominant disease
craniodiaphyseal dysplasia
human disease
DOID:0080807
autosomal dominant craniometaphyseal dysplasia
class of disease
autosomal dominant disease
craniometaphyseal dysplasia
human disease
DOID:0080801
autosomal dominant cutis laxa
class of disease
cutis laxa
autosomal dominant disease
cutis laxa characterized by autosomal dominant inheritance of skin that is loose, hanging, wrinkled and lacking in elasticity
DOID:0070142
autosomal dominant cutis laxa 1
class of disease
autosomal dominant cutis laxa
autosomal dominant cutis laxa that has material basis in heterozygous mutations in the ELN gene on chromosome 7q11
DOID:0070130
autosomal dominant cutis laxa 2
class of disease
autosomal dominant cutis laxa
autosomal dominant cutis laxa that has material basis in heterozygous mutation in the FBLN5 gene on chromosome 14q32
DOID:0070136
autosomal dominant disease
class of disease
autosomal genetic disease
genetic disease characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease
DOID:0050736
autosomal dominant distal hereditary motor neuropathy
class of disease
Distal hereditary motor neuropathies
spinal muscular atrophy
autosomal dominant disease
Autosomal dominant form of distal hereditary motor neuropathy
DOID:0111198
autosomal dominant dyskeratosis congenita 1
class of disease
dyskeratosis congenita
autosomal dominant disease
A dyskeratosis congenita that has material basis in an autosomal dominant mutation of TERC on chromosome 3q26.2.
DOID:0070014
autosomal dominant dyskeratosis congenita 2
class of disease
dyskeratosis congenita
autosomal dominant disease
A dyskeratosis congenita that has material basis in an autosomal dominant mutation of TERT on chromosome 5p15.33.
DOID:0070016
autosomal dominant dyskeratosis congenita 3
class of disease
dyskeratosis congenita
autosomal dominant disease
dyskeratosis congenita that has material basis in an autosomal dominant mutation of TINF2 on chromosome 14q12
DOID:0070018
autosomal dominant dyskeratosis congenita 4
class of disease
dyskeratosis congenita
autosomal dominant disease
A dyskeratosis congenita that has material basis in an autosomal dominant mutation of RTEL1 on chromosome 20q13.33.
DOID:0070020
autosomal dominant dyskeratosis congenita 6
class of disease
dyskeratosis congenita
autosomal dominant disease
A dyskeratosis congenita that has material basis in an autosomal dominant mutation of ACD on chromosome 16q22.1.
DOID:0070023
autosomal dominant hyaline body myopathy
class of disease
hyaline body myopathy
autosomal dominant disease
A hyaline body myopathy that has material basis in heterozygous mutation in MYH7 on 14q11.2.
DOID:0111269
autosomal dominant hypocalcemia
class of disease
hypocalcaemia
autosomal dominant disease
metal metabolism disorder
calcium metabolism disease characterized by autosomal dominant inheritance of variable degrees of hypocalcemia with normal to low levels of parathyroid hormone
DOID:0090109
autosomal dominant keratitis-ichthyosis-deafness syndrome
class of disease
autosomal dominant disease
keratitis–ichthyosis–deafness syndrome
syndrome
autosomal dominant disease characterized by congenital deafness, keratopachydermia and constrictions of fingers and toes that has material basis in heterozygous mutation in the GJB2 gene on chromosome 13q
DOID:0060871
autosomal dominant limb-girdle muscular dystrophy type 1
class of disease
autosomal dominant limb-girdle muscular dystrophy
autosomal dominant limb-girdle muscular dystrophy that has material basis in heterozygous mutation in the DNAJB6 gene on chromosome 7q36
DOID:0110305
autosomal dominant limb-girdle muscular dystrophy type 1H
class of disease
autosomal dominant limb-girdle muscular dystrophy
An autosomal dominant limb-girdle muscular dystrophy that has material basis in with variation in the region 3p25.1-p23.
DOID:0110303
autosomal dominant mental retardation 45
class of disease
autosomal dominant non-syndromic intellectual disability
human disease
DOID:0080236
autosomal dominant mental retardation 46
class of disease
autosomal dominant non-syndromic intellectual disability
human disease
DOID:0080237
autosomal dominant mental retardation 47
class of disease
autosomal dominant non-syndromic intellectual disability
human disease
DOID:0080238
autosomal dominant mental retardation 48
class of disease
autosomal dominant non-syndromic intellectual disability
human disease
DOID:0080235
autosomal dominant mental retardation 49
class of disease
autosomal dominant non-syndromic intellectual disability
human disease
DOID:0080234
autosomal dominant mental retardation 50
class of disease
autosomal dominant non-syndromic intellectual disability
human disease
DOID:0080233
autosomal dominant mental retardation 51
class of disease
autosomal dominant non-syndromic intellectual disability
human disease
DOID:0080232
autosomal dominant mental retardation 52
class of disease
autosomal dominant non-syndromic intellectual disability
human disease
DOID:0080231
autosomal dominant mental retardation 53
class of disease
autosomal dominant non-syndromic intellectual disability
human disease
DOID:0080228
autosomal dominant mental retardation 54
class of disease
autosomal dominant non-syndromic intellectual disability
human disease
DOID:0080230
autosomal dominant mental retardation 55
class of disease
autosomal dominant disease
syndromic intellectual disability
human disease
DOID:0080227
autosomal dominant mental retardation 56
class of disease
autosomal dominant disease
syndromic intellectual disability
human disease
DOID:0080226
autosomal dominant microcephaly
class of disease
autosomal dominant disease
microcephaly
human disease
DOID:14725
autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques
class of disease
autosomal dominant disease
Olmsted syndrome
human disease
DOID:0112013
autosomal dominant nocturnal frontal lobe epilepsy 1
class of disease
autosomal dominant nocturnal frontal lobe epilepsy
autosomal dominant nocturnal frontal lobe epilepsy that has material basis in heterozygous mutation in the CHRNA4 gene on chromosome 20q13
DOID:0060682
autosomal dominant nocturnal frontal lobe epilepsy 2
class of disease
autosomal dominant nocturnal frontal lobe epilepsy
autosomal dominant nocturnal frontal lobe epilepsy that has material basis in variation in the chromosome region 15q24
DOID:0060683
autosomal dominant nocturnal frontal lobe epilepsy 5
class of disease
autosomal dominant nocturnal frontal lobe epilepsy
autosomal dominant nocturnal frontal lobe epilepsy that has material basis in heterozygous mutation in the KCNT1 gene on chromosome 9q34
DOID:0060686
autosomal dominant non-syndromic intellectual disability 1
class of disease
autosomal dominant non-syndromic intellectual disability
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of MBD5 on chromosome 2q23.1.
DOID:0070031
autosomal dominant non-syndromic intellectual disability 2
class of disease
autosomal dominant non-syndromic intellectual disability
autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of DOCK8 on chromosome 9p24
DOID:0070032
autosomal dominant nonsyndromic deafness 1
class of disease
autosomal dominant nonsyndromic deafness
autosomal dominant nonsyndromic deafness that is characterized by low frequency progressive hearing loss and has material basis in mutation in the DIAPH1 gene on chromosome 5q31
DOID:0110541
autosomal dominant nonsyndromic deafness 18
class of disease
autosomal dominant nonsyndromic deafness
autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 3q22
DOID:0110549
autosomal dominant nonsyndromic deafness 30
class of disease
autosomal dominant nonsyndromic deafness
autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 15q25-q26
DOID:0110560
autosomal dominant nonsyndromic deafness 33
class of disease
autosomal dominant nonsyndromic deafness
autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 13q34
DOID:0110562
autosomal dominant nonsyndromic deafness 47
class of disease
autosomal dominant nonsyndromic deafness
autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 9p22-p21
DOID:0110570
autosomal dominant nonsyndromic deafness 52
class of disease
autosomal dominant nonsyndromic deafness
An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 5q31.1-q32.
DOID:0110578
autosomal dominant nonsyndromic deafness 71
class of disease
autosomal dominant nonsyndromic deafness
human disease
DOID:0080267
autosomal dominant nonsyndromic deafness 72
class of disease
autosomal dominant nonsyndromic deafness
human disease
DOID:0080268
autosomal dominant nonsyndromic deafness 77
class of disease
autosomal dominant nonsyndromic deafness
human disease
DOID:0112168
autosomal dominant nonsyndromic deafness 79
class of disease
autosomal dominant nonsyndromic deafness
human disease
DOID:0112160
autosomal dominant optic atrophy and cataract
class of disease
autosomal dominant optic atrophy
optic atrophy
autosomal dominant disease
gene (19q13.32).
DOID:0111433
autosomal dominant optic atrophy plus syndrome
class of disease
autosomal dominant optic atrophy
syndrome
autosomal dominant disease
human disease
DOID:0111340
autosomal dominant osteopetrosis 1
class of disease
osteopetrosis
autosomal dominant disease
human disease
DOID:0110937
autosomal dominant progressive external ophthalmoplegia 1
class of disease
autosomal dominant disease
chronic progressive external ophthalmoplegia
human disease
DOID:0111521
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6
class of disease
autosomal dominant disease
chronic progressive external ophthalmoplegia
human disease
DOID:0111519
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
class of disease
chronic progressive external ophthalmoplegia
autosomal dominant disease
human disease
DOID:0111517
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3
class of disease
autosomal dominant disease
chronic progressive external ophthalmoplegia
human disease
DOID:0111520
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4
class of disease
chronic progressive external ophthalmoplegia
autosomal dominant disease
human disease
DOID:0111525
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5
class of disease
chronic progressive external ophthalmoplegia
autosomal dominant disease
human disease
DOID:0111518
autosomal dominant sensory ataxia 1
class of disease
hereditary ataxia
autosomal dominant disease
human disease
DOID:0111170
autosomal dominant severe congenital neutropenia
class of disease
severe congenital neutropenia
autosomal dominant disease
human disease
DOID:0112130
autosomal dominant spondyloepiphyseal dysplasia tarda
class of disease
autosomal dominant disease
spondyloepiphyseal dysplasia tarda
human disease
DOID:0112285
autosomal dominant thrombophilia due to protein C deficiency
class of disease
protein C deficiency
human disease
DOID:0111909
autosomal dominant woolly hair
class of disease
woolly hair
autosomal dominant disease
human disease
DOID:0111573
autosomal genetic disease
class of disease
monogenic disease
monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes
DOID:0050739
Autosomal diseases
autosomal hemophilia A
class of disease
blood coagulation disease
autosomal genetic disease
hemophilia A
human disease
DOID:0111823
autosomal recessive Alport syndrome
class of disease
Alport syndrome
autosomal recessive disease
Alport syndrome that has material -basis in homozygous or compound heterozygous mutation in the COL4A3 or the COL4A4 gene, both of which map to chromosome 2q
DOID:0110033
autosomal recessive Kenny-Caffey syndrome
class of disease
Kenny-Caffey syndrome
autosomal recessive disease
human disease
DOID:0080722
autosomal recessive Robinow syndrome
class of disease
Robinow syndrome
autosomal recessive disease
Human disease
DOID:0060764
autosomal recessive centronuclear myopathy
class of disease
centronuclear myopathy
autosomal recessive disease
inherited neuromuscular disorder defined by numerous centrally placed nuclei on muscle biopsy and clinical features of a congenital myopathy
DOID:0111216
autosomal recessive chronic granulomatous disease cytochrome b-negative
class of disease
autosomal recessive disease
chronic granulomatous disease
A chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the CYBA gene on chromosome 16q24.2.
DOID:0070193
autosomal recessive chronic granulomatous disease cytochrome b-positive type I
class of disease
chronic granulomatous disease
autosomal recessive disease
A chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the NCF1 gene on chromosome 7q11.23.
DOID:0070192
autosomal recessive chronic granulomatous disease cytochrome b-positive type II
class of disease
autosomal recessive disease
chronic granulomatous disease
chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the NCF2 gene on chromosome 1q25
DOID:0070191
autosomal recessive chronic granulomatous disease cytochrome b-positive type III
class of disease
autosomal recessive disease
chronic granulomatous disease
chronic granulomatous disease characterized by that autosomal recessive inheritance has material basis in mutation in the NCF4 gene on chromosome 22q12
DOID:0070194
autosomal recessive congenital bilateral absence of vas deferens
class of disease
autosomal recessive disease
congenital bilateral aplasia of the vas deferens
human disease
DOID:0111864
autosomal recessive congenital ichthyosis
class of disease
autosomal recessive disease
congenital ichthyosis
skin disease that is characterized by autosomal recessive inheritance and abnormal skin scaling over the whole body due to a defect in keratinization
DOID:0060655
autosomal recessive congenital ichthyosis 1
class of disease
autosomal recessive congenital ichthyosis
An autosomal recessive congenital ichthyosis characterized by lamellar ichthyosis, ectropion, eclabium and hyperkeratosis that has material basis in homozygous or compound heterozygous mutation in the TGM1 gene on chromosome 14q11.2.
DOID:0060656
autosomal recessive congenital ichthyosis 13
class of disease
autosomal recessive congenital ichthyosis
human disease
DOID:0080257
autosomal recessive congenital ichthyosis 14
class of disease
autosomal recessive congenital ichthyosis
human disease
DOID:0080258
autosomal recessive congenital ichthyosis 7
class of disease
autosomal recessive congenital ichthyosis
Human disease
DOID:0060716
autosomal recessive craniometaphyseal dysplasia
class of disease
autosomal recessive disease
craniometaphyseal dysplasia
human disease
DOID:0080802
autosomal recessive cutis laxa type 2, classic type
class of disease
cutis laxa
autosomal recessive disease
autosomal recessive cutis laxa type 2
cutis laxa characterized by generalized skin wrinkling, sparse subcutaneous fat, dysmorphic progeroid facial features and severe hypotonia
DOID:0070141
autosomal recessive cutis laxa type I
class of disease
cutis laxa
autosomal recessive disease
cutis laxa characterized by wrinkled, redundant and sagging inelastic skin and severe systemic manifestations particulary in the lungs, vasculature, and gastrointestinal and genitourinary systems
DOID:0070144
autosomal recessive cutis laxa type IA
class of disease
autosomal recessive cutis laxa type I
autosomal recessive cutis laxa type I that has material basis in homozygous or compound heterozygous mutation in the FBLN5 gene on chromosome 14q32
DOID:0070135
autosomal recessive cutis laxa type IB
class of disease
autosomal recessive cutis laxa type I
human disease
DOID:0070133
autosomal recessive cutis laxa type IC
class of disease
autosomal recessive cutis laxa type I
autosomal recessive cutis laxa type I that has material basis in homozygous or compound heterozygous mutation in the LTBP4 gene on chromosome 19q13
DOID:0070139
autosomal recessive cutis laxa type IIA
class of disease
autosomal recessive cutis laxa type 2, classic type
autosomal recessive cutis laxa type II classic type that has material basis in homozygous or compound heterozygous mutations in the ATP6V0A2 gene on chromosome 12q24
DOID:0070134
autosomal recessive cutis laxa type IIB
class of disease
cutis laxa
autosomal recessive disease
autosomal recessive cutis laxa type 2
A cutis laxa characterized by progeroid features that has material basis in homozygous or compound heterozygous mutation in the PYCR1 gene on chromosome 17q25.3.
DOID:0070137
autosomal recessive cutis laxa type IIIA
class of disease
De Barsy syndrome
human disease
DOID:0070132
autosomal recessive cutis laxa type IIIB
class of disease
De Barsy syndrome
autosomal recessive cutis laxa type III that has material basis in homozygous or compound heterozygous mutation in the PYCR1 gene on chromosome 17q25
DOID:0070138
autosomal recessive disease
class of disease
autosomal genetic disease
disease
genetic disease characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop
DOID:0050737
Autosomal recessive diseases
autosomal recessive distal hereditary motor neuronopathy
class of disease
autosomal recessive disease
spinal muscular atrophy
spinal muscular atrophy that has material basis in autosomal recessive inheritance
DOID:0111197
autosomal recessive dyskeratosis congenita 4
class of disease
dyskeratosis congenita
autosomal recessive disease
A dyskeratosis congenita that has material basis in an autosomal recessive mutation of TERT on chromosome 5p15.33.
DOID:0070021
autosomal recessive dyskeratosis congenita 5
class of disease
dyskeratosis congenita
autosomal recessive disease
A dyskeratosis congenita that has material basis in an autosomal recessive mutation of RTEL1 on chromosome 20q13.33.
DOID:0070022
autosomal recessive dyskeratosis congenita 6
class of disease
dyskeratosis congenita
autosomal recessive disease
human disease
DOID:0070024
autosomal recessive early-onset Parkinson disease 23
class of disease
young-onset Parkinson disease
autosomal recessive disease
early-onset Parkinson disease that has material basis in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22
DOID:0060896
autosomal recessive hyaline body myopathy
class of disease
hyaline body myopathy
autosomal recessive disease
A hyaline body myopathy that has material basis in compound heterozygous or homozygous mutation in MYH7 on 14q11.2.
DOID:0111268
autosomal recessive intellectual developmental disorder-72
class of disease
syndromic intellectual disability
human disease
DOID:0080765
autosomal recessive isolated ectopia lentis 2
class of disease
isolated ectopia lentis
autosomal recessive disease
isolated ectopia lentis that has material basis in homozygous or compound heterozygous mutation in the ADAMTSL4 gene on chromosome 1q21
DOID:0111149
autosomal recessive limb-girdle muscular dystrophy
class of disease
limb-girdle muscular dystrophy
autosomal recessive disease
limb-girdle muscular dystrophy has material basis in autosomal recessive inheritance
DOID:0110274
autosomal recessive limb-girdle muscular dystrophy type 2B
class of disease
autosomal recessive limb-girdle muscular dystrophy
autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the gene encoding the skeletal muscle protein dysferlin (DYSF) on chromosome 2p13
DOID:0110276
autosomal recessive limb-girdle muscular dystrophy type 2C
class of disease
autosomal recessive limb-girdle muscular dystrophy
sarcoglycanopathy
qualitative or quantitative defects of gamma-sarcoglycan
neuromuscular disease with dilated cardiomyopathy
autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous mutation in the gamma-sarcoglycan gene (SGCG) on chromosome 13q12
DOID:0110277
autosomal recessive limb-girdle muscular dystrophy type 2Z
class of disease
disorder of O-xylosylglycan synthesis
autosomal recessive limb-girdle muscular dystrophy
An autosomal recessive condition caused by mutation(s) in the POGLUT1 gene, encoding protein O-glucosyltransferase 1. It is characterized by progressive muscular dystrophy, primarily affecting the proximal muscles, resulting in difficulty walking.
DOID:0080762
autosomal recessive nonsyndromic deafness 100
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0111638
autosomal recessive nonsyndromic deafness 106
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0080261
autosomal recessive nonsyndromic deafness 107
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0080262
autosomal recessive nonsyndromic deafness 108
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0080263
autosomal recessive nonsyndromic deafness 109
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0111639
autosomal recessive nonsyndromic deafness 110
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0111644
autosomal recessive nonsyndromic deafness 111
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0111640
autosomal recessive nonsyndromic deafness 112
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0111637
autosomal recessive nonsyndromic deafness 113
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0111636
autosomal recessive nonsyndromic deafness 114
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0111642
autosomal recessive nonsyndromic deafness 115
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0111643
autosomal recessive nonsyndromic deafness 1A
class of disease
autosomal recessive nonsyndromic deafness
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has material basis in mutation in the GJB2 gene on chromosome 13q12
DOID:0110475
autosomal recessive nonsyndromic deafness 27
class of disease
autosomal recessive nonsyndromic deafness
autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 2q23-q31
DOID:0110485
autosomal recessive nonsyndromic deafness 4
class of disease
autosomal recessive nonsyndromic deafness
autosomal recessive nonsyndromic deafness that has material basis in mutation in the SLC26A4 gene on chromosome 7q22
DOID:0110498
autosomal recessive nonsyndromic deafness 40
class of disease
autosomal recessive nonsyndromic deafness
An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 22q11.21-q12.1.
DOID:0110499
autosomal recessive nonsyndromic deafness 5
class of disease
autosomal recessive nonsyndromic deafness
autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 14q12
DOID:0110507
autosomal recessive nonsyndromic deafness 57
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0111635
autosomal recessive nonsyndromic deafness 94
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0111641
autosomal recessive nonsyndromic deafness 99
class of disease
autosomal recessive nonsyndromic deafness
human disease
DOID:0111634
autosomal recessive osteopetrosis 1
class of disease
osteopetrosis
autosomal recessive disease
An osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the TCIRG1 gene on chromosome 11q13.2.
DOID:0110942
autosomal recessive osteopetrosis 3
class of disease
osteopetrosis
autosomal recessive disease
renal tubular acidosis
osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the CA2 gene on chromosome 8q21
DOID:0110941
autosomal recessive pericentral pigmentary retinopathy
class of disease
retinitis pigmentosa
autosomal recessive disease
retinitis pigmentosa that is characterized autosomal recessive inheritance of pigmentary retinal degeneration with onset in the infancy but slower rates of progression than other forms of retinopathy
DOID:0110422
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2
class of disease
autosomal recessive disease
chronic progressive external ophthalmoplegia
human disease
DOID:0111515
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3
class of disease
chronic progressive external ophthalmoplegia
autosomal recessive disease
human disease
DOID:0111523
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4
class of disease
chronic progressive external ophthalmoplegia
autosomal recessive disease
human disease
DOID:0111516
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5
class of disease
autosomal recessive disease
chronic progressive external ophthalmoplegia
human disease
DOID:0111524
autosomal recessive pseudohypoaldosteronism type 1
class of disease
pseudohypoaldosteronism
autosomal recessive disease
human disease
DOID:0060854
autosomal recessive pyridoxine-refractory sideroblastic anemia 3
class of disease
pyridoxine-refractory autosomal recessive sideroblastic anemia
autosomal recessive disease
sideroblastic anaemia P
sideroblastic anemia that is characterized by homozygous or compound heterozygous mutation in the GLRX5 gene on chromosome 14q32
DOID:0080343
autosomal recessive spinocerebellar ataxia 23
class of disease
autosomal recessive cerebellar ataxia
human disease
DOID:0111613
autosomal recessive spinocerebellar ataxia 24
class of disease
autosomal recessive cerebellar ataxia
human disease
DOID:0111615
autosomal recessive spinocerebellar ataxia 27
class of disease
autosomal recessive cerebellar ataxia
human disease
DOID:0111616
autosomal recessive spinocerebellar ataxia 3
class of disease
autosomal recessive cerebellar ataxia
human disease
DOID:0111612
autosomal recessive spinocerebellar ataxia 4
class of disease
autosomal recessive cerebellar ataxia
human disease
DOID:0111611
autosomal recessive spinocerebellar ataxia 6
class of disease
autosomal recessive cerebellar ataxia
human disease
DOID:0111617
autosomal recessive spinocerebellar ataxia 8
class of disease
autosomal recessive cerebellar ataxia
human disease
DOID:0111618
autosomal recessive spondyloepiphyseal dysplasia tarda
class of disease
spondyloepiphyseal dysplasia tarda
autosomal recessive disease
human disease
DOID:0112293
autosomal recessive type IV Ehlers-Danlos syndrome
class of disease
Ehlers-Danlos syndrome
autosomal recessive disease
Human disease
DOID:14759
autosomal-mitochondrial sensorineural deafness
class of disease
digenic disease
sensorineural hearing loss
human disease
DOID:0111752
autotopagnosia
class of disease
agnosia
form of agnosia
DOID:0060138
avoidant personality disorder
class of disease
personality disorder
disease
severe form of social anxiety
DOID:1509
Avoidant personality disorder
axial osteomalacia
class of disease
osteosclerosis
osteomalacia
genetic disease
osteosclerosis that results in coarsening located in trabecular bone
DOID:0080039
axillary adentis
class of disease
lymphadenitis
Human disease
DOID:4640
axonal neuropathy
class of disease
peripheral neuropathy
Human disease
DOID:7319
azoospermia
class of disease
male infertility
oligospermia
disease
male infertility disease characterized by the absence of any measurable level of sperm in semen
DOID:14227
C12.200.294.430.380
C12.100.500.430.380
C12.100.750.700.380
Azoospermia
aztreonam allergy
class of disease
beta-lactam allergy
beta-lactam allergy that has allergic trigger aztreonam
DOID:0040037
bacillary angiomatosis
class of disease
bartonellosis
angiomatosis
disease
human disease
DOID:0060345
C01.150.252.400.126.100.075
C01.150.252.819.150
C01.800.720.150
C14.907.077.060
C17.800.838.765.150
C17.800.862.060
background diabetic retinopathy
class of disease
diabetic retinopathy
Human disease
DOID:13208
bacterial esophagitis
class of disease
esophagitis
bacterial infectious disease
An acute bacterial infection that affects the esophagus. Symptoms include severe pain on swallowing and retrosternal pain. Endoscopic examination reveals esophageal mucosal ulcerations and pseudomembranous formations.
DOID:13921
bacterial gastritis
class of disease
gastritis
bacterial infectious disease
chronic gastritis
Gastritis resulting from bacteria
DOID:4033
bacterial sepsis
class of disease
bacterial infectious disease
sepsis
bacterial infectious disease has material basis in Bacteria
DOID:0040085
bacteriuria
class of disease
urinary system disease
disease
medical term denoting the presence of bacteria in urine
DOID:1412
C01.915.219
C12.200.777.892.219
C12.050.351.968.892.219
C12.950.892.219
bagassosis
class of disease
extrinsic allergic alveolitis
silicosis
DOID:12522
balanitis
class of disease
symptom or sign
penile disease
inflammatory disease
disease
infectious or non-infectious inflammation of the glans penis
DOID:13033
C12.294.494.136
Balanitis
File:Inflammation of the glans penis and the preputial mucosa.jpg
balanitis xerotica obliterans
class of disease
balanitis
Human disease
DOID:13477
C12.294.494.136.500
Balanitis xerotica obliterans
balanoposthitis
class of disease
penile disease
balanitis
posthitis
human disease
DOID:13031
Balanoposthitis
baldness
class of disease
hair diseases
hairstyle
hair anomaly
absence
disease
state where most or all of hair from the head has been lost or intentionally removed
DOID:987
Baldness
balloon cell malignant melanoma
class of disease
skin melanoma
Human disease
DOID:10044
band keratopathy
class of disease
corneal degeneration
Human disease
DOID:11164
Band keratopathy
barbiturate abuse
class of disease
substance abuse
substance abuse that involves the recurring use of barbiturate drugs despite negative consequences
DOID:8519
barbiturate dependence
class of disease
barbiturate abuse
substance dependence
drug dependence that involves the continued use of barbiturates despite problems related to use of the substance
DOID:2575
basal ganglia cerebrovascular disease
class of disease
basal ganglia disease
cerebrovascular disease
Human disease
DOID:10991
C10.228.140.079.127
C10.228.140.300.100
C14.907.253.061
basal ganglia disease
class of disease
encephalopathy
brain disease that is characterized by dysfunction of the basal ganglia which help start and control movement
DOID:679
C10.228.140.079
basal-cell carcinoma
class of disease
skin cancer
skin carcinoma
basal-cell neoplasm
disease
subtype of basal-cell carcinoma most commonly occurring on the sun-exposed areas of the head and neck
DOID:2513
C04.557.470.200.165
C04.557.470.565.165
Basal-cell carcinoma
basaloid large cell carcinoma of the lung
class of disease
large-cell lung carcinoma
squamous cell carcinoma of the lung
basaloid carcinoma
human disease
DOID:7045
basaloid squamous cell carcinoma
class of disease
squamous cell carcinoma
basaloid carcinoma
basal-cell carcinoma
Human disease
DOID:5522
basaloid squamous cell skin carcinoma
class of disease
basaloid squamous cell carcinoma
keratinizing squamous cell carcinoma
skin cancer
squamous cell carcinoma
Human disease
DOID:7049
basidiobolomycosis
class of disease
subcutaneous mycosis
zygomycosis
Human disease
DOID:0050278
basilar artery insufficiency
class of disease
transient cerebral isolation
vertebrobasilar insufficiency
syndrome
artery disease
human disease
DOID:223
basilar artery occlusion
class of disease
occlusion precerebral artery
artery disease
Human disease
DOID:13446
basosquamous carcinoma
class of disease
basal-cell carcinoma
Human disease
DOID:5063
C04.557.470.200.170
C04.557.470.565.170
baylisascariasis
class of disease
parasitic helminthiasis infectious disease
spinal cord disease
eye disease
intestinal disease
encephalopathy
Human disease
DOID:0050259
benign adult familial myoclonic epilepsy
class of disease
myoclonic epilepsy
adolescence-adult electroclinical syndrome
human disease
DOID:0111689
benign blood vessel neoplasm
class of disease
vascular neoplasm
cardiovascular organ benign neoplasm
benign neoplasm arising from arteries or veins
DOID:60006
Benign vascular neoplasms
benign breast adenomyoepithelioma
class of disease
breast benign neoplasm
Human disease
DOID:1641
benign breast phyllodes tumor
class of disease
breast benign neoplasm
phyllodes tumor
Human disease
DOID:1631
benign deep fibrous histiocytoma
class of disease
immune system organ benign neoplasm
sclerosing hemangioma
Human disease
DOID:4419
benign dermal neurilemmoma
class of disease
skin benign neoplasm
Human disease
DOID:7181
benign eccrine breast spiradenoma
class of disease
breast benign neoplasm
Human disease
DOID:1616
benign ependymoma
class of disease
benign glioma
ependymoma
human disease
DOID:4844
benign epilepsy with centrotemporal spikes
class of disease
childhood electroclinical syndrome
epilepsy syndrome
the most common epilepsy syndrome in childhood which usually subsides with age
DOID:3329
C10.228.140.490.360.280
C10.228.140.490.493.250
benign essential hypertension
class of disease
essential hypertension
Human disease
DOID:10913
benign fibrous mesothelioma
class of disease
benign mesothelioma
solitary fibrous tumor of the pleura
human disease
DOID:2653
C04.557.450.565.590.797.750
C04.588.894.797.640.800
benign hypertensive renal disease
class of disease
renal hypertension
Human disease
DOID:11520
benign intermediate mesothelioma
class of disease
benign mesothelioma
human disease
DOID:5884
benign lymphoepithelial lesion of salivary gland
class of disease
salivary gland disease
disease
Human disease
DOID:12899
benign mammary dysplasia
class of disease
breast benign neoplasm
Human disease
DOID:9504
Benign mammary dysplasias
benign mastocytoma
class of disease
benign neoplasms by histologic type
human disease
DOID:4658
benign mediastinal neurilemmoma
class of disease
benign neurilemmoma
mediastinal neurilemmoma
benign neoplasm of mediastinum
Human disease
DOID:7922
benign mediastinal psammomatous neurilemmoma
class of disease
benign mediastinal neurilemmoma
Human disease
DOID:7921
benign meningioma
class of disease
meningioma
benign neoplasm of meninges
central nervous system organ benign neoplasm
Human disease
DOID:4587
benign mesothelioma
class of disease
angiomyolipoma
cell type benign neoplasm that has material basis in mesothelium
DOID:2645
benign neonatal seizures
class of disease
neonatal period electroclinical syndrome
Human disease
DOID:14264
C10.228.140.490.370
C16.614.258
benign neoplasm
class of disease
disease of cellular proliferation
neoplasm
disease
disease of cellular proliferation that results in abnormal growths in the body which lack the ability to metastasize
DOID:0060072
Benign neoplasms
benign neoplasm of exocrine pancreas
class of disease
pancreatic exocrine neoplasm
benign neoplasm of pancreas
endocrine organ benign neoplasm
benign neoplasm that involves the exocrine pancreas
DOID:0080781
benign neoplasm of lymph node
class of disease
lymph node neoplasm
immune system organ benign neoplasm
benign neoplasm that involves the lymph node
DOID:0080617
Benign neoplasms of lymph nodes
benign neoplasms by histologic type
class of disease
benign neoplasm
neoplasms by histologic type
benign neoplasm that is classified by the type of cell or tissue from which it is derived
DOID:0060084
benign neurilemmoma
class of disease
neurilemmoma
Human disease
DOID:955
benign ovarian sex cord-stromal tumor
class of disease
ovarian sex cord-stromal tumor
sex cord-stromal benign neoplasm
sex cord-stromal tumor arising from the ovary, without metastatic potential
DOID:0080370
benign parathyroid gland neoplasm
class of disease
parathyroid neoplasm
endocrine organ benign neoplasm
parathyroid gland disease
benign neoplasm that involves the parathyroid gland
DOID:60008
Benign neoplasms of parathyroid gland
benign paroxysmal positional nystagmus
class of disease
peripheral vertigo
disease
human disease
DOID:13941
C09.218.568.900.883.500
C10.597.951.500
C23.888.592.958.500
benign pericardial teratoma
class of disease
mature teratoma
benign neoplasm of pericardium
rare circulatory system disease
cardiovascular organ benign neoplasm
pericardium disease
Human disease
DOID:8012
benign peritoneal mesothelioma
class of disease
peritoneal benign neoplasm
human disease
DOID:1789
benign perivascular tumor
class of disease
cardiovascular organ benign neoplasm
perivascular tumor
Human disease
DOID:5238
benign pleural mesothelioma
class of disease
pleural cancer
respiratory system benign neoplasm
pleural disease
benign neoplasms by histologic type
human disease
DOID:5157
benign prostate phyllodes tumor
class of disease
male reproductive organ benign neoplasm
prostate phyllodes tumor
Human disease
DOID:2885
benign recurrent intrahepatic cholestasis 1
class of disease
benign recurrent intrahepatic cholestasis
autosomal recessive disease
benign recurrent intrahepatic cholestasis characterized by typically autosomal recessive inheritance that has material basis in mutation in the ATP8B1 gene on chromosome 18q
DOID:0070231
benign recurrent intrahepatic cholestasis 2
class of disease
benign recurrent intrahepatic cholestasis
autosomal recessive disease
benign recurrent intrahepatic cholestasis characterized by autosomal recessive inheritance that has material basis in mutation in the ABCB11 gene on chromosome 2q31
DOID:0070232
benign renovascular hypertension
class of disease
benign secondary hypertension
renal hypertension
renovascular hypertension
Human disease
DOID:13145
benign secondary hypertension
class of disease
secondary hypertension
Human disease
DOID:13143
benign shuddering attacks
class of disease
movement disorders
myoclonus
Human disease
DOID:1713
benign struma ovarii
class of disease
struma ovarii
ovarian benign neoplasm
Human disease
DOID:5209
benign teratoma
class of disease
germ cell benign neoplasm
human disease
DOID:0080602
benign vaginal carcinosarcoma
class of disease
vaginal benign neoplasm
Human disease
DOID:135
benzo[d]isothiazol-3-one allergic contact dermatitis
class of disease
allergic contact dermatitis
allergic contact dermatitis that has allergic trigger benzo[d]isothiazol-3-one
DOID:0040075
benzoic acid allergic contact dermatitis
class of disease
allergic contact dermatitis
allergic contact dermatitis that has allergic trigger benzoic acid
DOID:0040057
benzylpenicillin allergy
class of disease
beta-lactam allergy
beta-lactam allergy that has allergic trigger benzylpenicillin
DOID:0040003
beriberi
class of disease
nutritional deficiency disease
thiamine deficiency
disease
nutritional thiamine deficiency disease in humans
DOID:13725
C18.654.521.500.133.699.827.223
Beriberi
berylliosis
class of disease
pneumoconiosis
occupational lung disease
Beryllium poisoning
respiratory allergy
disease
pneumoconiosis that involves allergic response located in lungs caused by inhalation of beryllium compounds
DOID:10322
C08.381.483.581.225
C08.381.520.702.225
C24.800.225
Berylliosis
beta-lactam allergy
class of disease
drug allergy
drug allergy triggered by a beta-lactam
DOID:0060519
beta-thalassemia intermedia
class of disease
beta thalassemia
Beta-thalassemia (BT) intermedia is a form of BT (see this term) characterized by mild to moderate anemia which does not or only occasionally requires transfusion
DOID:0080772
beta-thalassemia major
class of disease
beta thalassemia
Beta-thalassemia (BT) major is a severe early-onset form of BT (see this term) characterized by severe anemia requiring regular red blood cell transfusions
DOID:0080771
bicipital tenosynovitis
class of disease
tenosynovitis
Human disease
DOID:14192
bilateral breast cancer
class of disease
breast carcinoma
breast carcinoma that is characterized by an individual having breast cancer in both breasts, either simultaneously or at different times
DOID:6741
bilateral frontoparietal polymicrogyria
class of disease
autosomal recessive disease
human disease
DOID:0080922
bilateral hyperactive labyrinth
class of disease
labyrinthine dysfunction
Human disease
DOID:14165
bilateral optic nerve hypoplasia
class of disease
autosomal dominant disease
optic nerve disease
optic nerve hypoplasia
human disease
DOID:0111531
bilateral renal aplasia
class of disease
renal agenesis
renal agenesis that is characterized by the absence of both kidneys at birth
DOID:0080200
bile duct adenocarcinoma
class of disease
bile duct carcinoma
adenocarcinoma of liver and intrahepatic biliary tract
adenocarcinoma
bile duct carcinoma that derives from epithelial cells of glandular origin
DOID:4896
bile duct adenoma
class of disease
liver neoplasm
biliary tract neoplasm
bile duct disease
gastrointestinal adenoma
benign neoplasms by histologic type
adenoma
adenoma and biliary tract cancer that results in a small firm white nodule with multiple bile ducts that are located in a fibrous stroma
DOID:5381
C04.557.470.035.085
bile duct cancer
class of disease
biliary tract cancer
bile duct neoplasm
bile duct disease
biliary tract cancer that is located in the bile duct
DOID:4606
bile duct carcinoma
class of disease
bile duct cancer
carcinoma
bile duct cancer that has material basis in abnormally proliferating cells derives from epithelial cells
DOID:4897
bile duct carcinoma in situ
class of disease
in situ carcinoma
biliary tract neoplasm
bile duct disease
Human disease
DOID:0050613
bile duct clear cell adenocarcinoma
class of disease
bile duct adenocarcinoma
clear cell adenocarcinoma
extrahepatic bile duct adenocarcinoma
Human disease
DOID:7032
bile duct cystadenocarcinoma
class of disease
bile duct adenocarcinoma
bile duct cystadenoma
Human disease
DOID:4075
bile duct cystadenoma
class of disease
bile duct adenoma
bile duct disease
biliary tract neoplasm
benign neoplasms by histologic type
Human disease
DOID:5384
bile duct disease
class of disease
biliary tract disease
Human disease
DOID:4138
C06.130.120
bile duct mucinous adenocarcinoma
class of disease
bile duct adenocarcinoma
extrahepatic bile duct adenocarcinoma
mucinous adenocarcinoma
Human disease
DOID:3698
bile duct mucoepidermoid carcinoma
class of disease
mucoepidermoid carcinoma
bile duct mucinous adenocarcinoma
bile duct cancer
Human disease
DOID:4681
bile duct rhabdomyosarcoma
class of disease
bile duct sarcoma
rhabdomyosarcoma
bile duct cancer
rhabdomyosarcoma and sarcoma of bile duct that is located in the bile duct
DOID:3254
bile duct sarcoma
class of disease
bile duct cancer
sarcoma
sarcoma and malignant tumor of extrahepatic bile duct that is located in the bile duct
DOID:4064
bile duct signet ring cell carcinoma
class of disease
signet ring cell adenocarcinoma
bile duct carcinoma
extrahepatic bile duct adenocarcinoma
Human disease
DOID:3494
bile reflux
class of disease
biliary tract disease
Human disease
DOID:12237
C06.130.140
C06.405.748.240.140
biliary dyskinesia
class of disease
gallbladder disease
common bile duct disease
gallbladder disease characterized by altered tonus of the sphincter of Oddi, disturbance in the coordination of contraction of the biliary ducts, and/or reduction in the speed of emptying of the biliary tree
DOID:4140
C06.130.120.250.098
biliary papillomatosis
class of disease
biliary tract neoplasm
papilloma
biliary tract neoplasm characterized by multiple papillary tumors in the intrahepatic and/or extrahepatic biliary tree
DOID:5468
Intraductal papillary neoplasm of the bile duct
biliary reflux
class of disease
duodenal disease
stomach disease
gastroesophageal reflux disease
human disease
DOID:4071
C06.405.469.275.700
C06.405.748.240
Biliary reflux
biliary tract cancer
class of disease
hepatobiliary system cancer
biliary tract neoplasm
gastrointestinal system cancer that results in malignant growth located in the gallbladder or located in the bile duct
DOID:4607
Biliary tract cancers
biliary tract disease
class of disease
biliary disease
hepatobiliary disease
disease involving the biliary tree
DOID:9741
C06.130
biliary tract intraductal papillary mucinous neoplasm
class of disease
biliary tract neoplasm
human disease
DOID:5469
biliary tract neoplasm
class of disease
hepatobiliary neoplasm
biliary tract disease
hepatobiliary neoplasm located in the biliary tract
DOID:0050625
C04.588.274.120
C06.130.320
C06.301.120
Biliary tract neoplasms
bilirubin metabolic disorder
class of disease
inherited metabolic disorder
hyperbilirubinemia
inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism
DOID:2741
C16.320.565.300
C18.452.648.300
binocular vision disease
class of disease
strabismus
vision disorder
human disease
DOID:12667
biotin deficiency
class of disease
nutritional deficiency disease
vitamin deficiency
disease
nutritional deficiency disease that is characterized by thinning of the hair (often with loss of hair color), and red scaly rash around the eyes, nose, and mouth
DOID:0050810
biotinidase deficiency
class of disease
multiple carboxylase deficiency
disorder of other vitamins and cofactors metabolism and transport
rare genetic epilepsy
rare hereditary metabolic disease with peripheral neuropathy
multiple carboxylase deficiency that involves a deficiency in biotinidase
DOID:856
C16.320.565.100.620.100
C16.320.565.202.720.100
C18.452.648.100.620.100
C18.452.648.202.720.100
biphasic synovial sarcoma
class of disease
synovial sarcoma
Human disease
DOID:5492
bipolar I disorder
class of disease
bipolar disorder
disease
bipolar disorder that is characterized by at least one manic or mixed episode
DOID:14042
bipolar II disorder
class of disease
bipolar disorder
disease
bipolar disorder that is characterized by at least one hypomanic episode and at least one major depressive episode; with this disorder, depressive episodes are more frequent and more intense than manic episodes
DOID:0060166
bipolar disorder
class of disease
mood disorder
human mental illness characterized by mood changes
DOID:3312
F03.084.500
Bipolar disorder
bird fancier's lung
class of disease
extrinsic allergic alveolitis
rare allergic respiratory disease
extrinsic allergic alveolitis which is caused by inhalation of antigens from avian excreta, symptoms are abrupt onset of dyspnea, cough, malaise, and fever after exposure to antigen
DOID:13891
C08.381.483.125.125
C08.674.055.125
C20.543.480.680.075.125
C24.125
birdshot chorioretinopathy
class of disease
uveitis
white dot syndrome
posterior uveitis
non-infectious posterior uveitis
human disease
DOID:0111079
C11.768.773.348.500
C11.941.160.478.400.500
C11.941.879.780.900.300.318.500
C11.941.879.780.900.650.250
C20.111.303
Birdshot chorioretinopathy
bizarre leiomyoma
class of disease
leiomyoma
Human disease
DOID:5127
black piedra
class of disease
superficial mycosis
disease
superficial mycosis that is a superficial fungal infection of the hair shaft caused by Piedraia hortae
DOID:12711
Black piedra
bladder adenocarcinoma
class of disease
bladder carcinoma
adenocarcinoma
bladder carcinoma that derives from epithelial cells of glandular origin
DOID:3711
Adenocarcinomas of the urinary bladder
bladder benign neoplasm
class of disease
urinary system benign neoplasm
bladder disease
human disease
DOID:0050623
bladder calculus
class of disease
urolithiasis
bladder disease
stone found in the urinary bladder
DOID:11355
C12.777.829.720
C12.777.967.500.925
C13.351.968.829.521
C13.351.968.967.500.925
C23.300.175.850.875
Urinary bladder stones
bladder cancer
class of disease
urinary system cancer
bladder disease
bladder neoplasm
disease
urinary system cancer that results in malignant growth located in the urinary bladder
DOID:11054
Urinary bladder cancer
bladder carcinoma
class of disease
bladder cancer
carcinoma
urinary bladder cancer that has material basis in abnormally proliferating cells derives from epithelial cells
DOID:4007
bladder carcinoma in situ
class of disease
non-invasive bladder urothelial carcinoma
bladder flat intraepithelial lesion
carcinoma in situ of breast and genitourinary system
bladder disease
in situ carcinoma
Human disease
DOID:9053
bladder clear cell adenocarcinoma
class of disease
bladder adenocarcinoma
clear cell adenocarcinoma
Human disease
DOID:5306
bladder colloid adenocarcinoma
class of disease
bladder adenocarcinoma
Human disease
DOID:3710
bladder colonic type adenocarcinoma
class of disease
bladder adenocarcinoma
Human disease
DOID:6594
bladder diffuse clear cell adenocarcinoma
class of disease
bladder clear cell adenocarcinoma
Human disease
DOID:6210
bladder disease
class of disease
urinary system disease
urinary system disease that is located in the bladder
DOID:365
C12.777.829
C13.351.968.829
Diseases and disorders of the urinary bladder
bladder diverticulum
class of disease
bladder disease
diverticulum
genetic disease
Human disease
DOID:11353
Bladder diverticulum
bladder dome cancer
class of disease
bladder cancer
human disease
DOID:11820
bladder exstrophy
class of disease
bladder disease
bladder exstrophy-epispadias-cloacal exstrophy complex
disease
congenital disorder of urinary system
DOID:0080174
C12.706.132
C12.777.829.132
C13.351.875.132
C13.351.968.829.132
C16.131.939.132
Bladder exstrophy
bladder exstrophy-epispadias-cloacal exstrophy complex
class of disease
congenital disorder
urinary system disease
physical disorder that is characterized as a spectrum of anomalies involving the urinary tract, genital tract, musculoskeletal system and sometimes the intestinal tract
DOID:0080173
bladder flat intraepithelial lesion
class of disease
bladder benign neoplasm
bladder cancer
Human disease
DOID:5429
bladder hepatoid adenocarcinoma
class of disease
bladder adenocarcinoma
hepatoid adenocarcinoma
Human disease
DOID:8097
bladder lateral wall cancer
class of disease
bladder cancer
Human disease
DOID:11593
bladder leiomyoma
class of disease
bladder benign neoplasm
leiomyoma
Human disease
DOID:13109
bladder lymphoma
class of disease
bladder cancer
primary organ-specific lymphoma
lymphoma
human disease
DOID:11821
bladder mixed adenocarcinoma
class of disease
bladder adenocarcinoma
Human disease
DOID:8096
bladder neck cancer
class of disease
bladder cancer
human disease
DOID:11809
bladder neck obstruction
class of disease
urinary tract obstruction
bladder disease
bladder outlet obstruction
Human disease
DOID:13948
C12.777.767.700.962
C12.777.829.760
C13.351.968.767.700.850
C13.351.968.829.601
bladder papillary clear cell adenocarcinoma
class of disease
bladder clear cell adenocarcinoma
Human disease
DOID:8051
bladder papillary transitional cell neoplasm
class of disease
urinary tract papillary transitional cell benign neoplasm
bladder cancer
Human disease
DOID:5432
bladder sarcoma
class of disease
bladder cancer
sarcoma
sarcoma and malignant neoplasm of urinary bladder that is located in the bladder
DOID:11812
bladder signet ring cell adenocarcinoma
class of disease
bladder adenocarcinoma
signet ring cell adenocarcinoma
Human disease
DOID:6481
bladder squamous cell carcinoma
class of disease
bladder carcinoma
squamous cell carcinoma
carcinoma of bladder that is manifested in squamous cells of the bladder
DOID:3742
bladder squamous papilloma
class of disease
bladder benign neoplasm
Human disease
DOID:13110
bladder transitional cell papilloma
class of disease
bladder papillary transitional cell neoplasm
transitional papilloma
urinary tract non-invasive transitional cell neoplasm
urinary system benign neoplasm
Human disease
DOID:6933
bladder trigone cancer
class of disease
bladder cancer
bladder dome cancer
Human disease
DOID:11813
bladder tubulo-cystic clear cell adenocarcinoma
class of disease
bladder clear cell adenocarcinoma
Human disease
DOID:8050
bladder urachal adenocarcinoma
class of disease
bladder urachal carcinoma
bladder adenocarcinoma
urachal cancer
Human disease
DOID:7694
bladder urachal carcinoma
class of disease
bladder carcinoma
urachal cancer
Human disease
DOID:5958
bladder urachal squamous cell carcinoma
class of disease
bladder urachal carcinoma
bladder squamous cell carcinoma
squamous cell carcinoma
Human disease
DOID:5957
bladder urachal urothelial carcinoma
class of disease
bladder urachal carcinoma
bladder urothelial carcinoma
Human disease
DOID:7244
bladder urothelial carcinoma
class of disease
bladder carcinoma
transitional cell carcinoma
bladder carcinoma that has material basis in transitional cells located in the lining of the bladder
DOID:4006
bladder urothelial papillary carcinoma
class of disease
bladder urothelial carcinoma
bladder papillary transitional cell neoplasm
papillary transitional carcinoma
Human disease
DOID:6975
bladder verrucous squamous cell carcinoma
class of disease
bladder squamous cell carcinoma
verrucous carcinoma
Human disease
DOID:3741
blastema predominant kidney Wilms' tumor
class of disease
nephroblastoma
Human disease
DOID:5182
blastoma
class of disease
cell type cancer
disease
A cell type cancer that has material basis in abnormally proliferating cells derived from precursor cells called blast cells.
DOID:0070003
Blastomas
blepharitis
class of disease
symptom or sign
eyelid disease
eye inflammation
inflammatory disease
disease
eyelid disease that is characterized by often chronic inflammation of the eyelid, generally the part where eyelashes grow
DOID:9423
C11.338.133
Blepharitis
blepharochalasis
class of disease
eyelid disease
eyelid disease that is characterized by exacerbations and remissions of eyelid edema, which results in a stretching and subsequent atrophy of the eyelid tissue, leading to the formation of redundant folds over the lid margins
DOID:348
blepharocheilodontic syndrome 1
class of disease
Blepharo-cheilo-odontic syndrome
blepharocheilodontic syndrome that has material basis in heterozygous mutation in the CDH1 gene on chromosome 16q22
DOID:0080345
blepharocheilodontic syndrome 2
class of disease
Blepharo-cheilo-odontic syndrome
blepharocheilodontic syndrome that has material basis in heterozygous mutation in the CTNND1 gene on chromosome 11q12
DOID:0080346
blepharoconjunctivitis
class of disease
blepharitis
conjunctivitis
blepharitis that is characterized by the dual combination of conjunctivitis with blepharitis
DOID:2456
blepharophimosis
class of disease
eyelid disease
congenital physical abnormality
disease
Human disease
DOID:10348
C11.250.090
C11.338.190
C16.131.384.190
Blepharophimosis
blepharospasm
class of disease
focal dystonia
cranio-facial dystonia
disease
focal dystonia that is characterized by the involuntary, forcible contraction of the muscles controlling eye blinks
DOID:529
C11.338.250
blind hypertensive eye
class of disease
eye degenerative disease
glaucoma
human disease
DOID:11776
blind loop syndrome
class of disease
intestinal disease
small intestinal bacterial overgrowth
intestinal disease characterized by a dysbalance of the bacterial flora of the small intestine, causing derangement to the normal physiological processes of digestion and absorption
DOID:10606
C06.405.469.637.145
C18.452.603.145
blindness
class of disease
symptom or sign
visual impairment
eye disease
vision symptom
sensory disability
complete or nearly complete lack of vision; visual acuity worse than 3/60
DOID:1432
C10.597.751.941.162
C11.966.075
C23.888.592.763.941.162
Visual impairment
blood coagulation disease
class of disease
symptom or sign
hematopoietic system disease
hemic system symptom
disease
condition in which the blood’s ability to coagulate (form clots) is impaired
DOID:1247
C15.378.100
blood group incompatibility
class of disease
hematopoietic system disease
transfusion incident
Human disease
DOID:4176
G09.188.114
G12.186
blood platelet disease
class of disease
hematopoietic system disease
blood coagulation disease
disorder of platelet function
DOID:2218
C15.378.140
blood protein disease
class of disease
hematopoietic system disease
human disease
DOID:620
C15.378.147
blue toe syndrome
class of disease
foot diseases
cyanosis
cholesterol embolism
Human disease
DOID:14121
C14.907.355.350.454.500.200
C14.907.617.249
blunt duct adenosis of breast
class of disease
microglandular adenosis
non-proliferative fibrocystic change of the breast
Human disease
DOID:5996
body dysmorphic disorder
class of disease
somatoform disorder
hypochondriasis
disease
mental disorder
DOID:0060163
F03.875.149
Body dysmorphic disorder
bone Ewing's sarcoma
class of disease
Ewing sarcoma
peripheral primitive neuroectodermal tumor that is located in bone
DOID:3368
bone ameloblastoma
class of disease
bone benign neoplasm
ameloblastoma
bone benign neoplasm that has material basis in odontogenic epithelium and is located in bone
DOID:0050895
bone angioendothelial sarcoma
class of disease
osteosarcoma
vascular bone neoplasm
bone sarcoma
Human disease
DOID:3351
bone benign neoplasm
class of disease
connective tissue benign neoplasm
bone disease
bone neoplasm
musculoskeletal system benign neoplasm
connective tissue benign neoplasm that is located in bone
DOID:0060094
DOID:0060120
bone cancer
class of disease
connective tissue neoplasm
bone disease
rare tumor
rare bone disease
musculoskeletal system cancer
bone neoplasm
connective tissue cancer that is located in bone and is characterized by uncontrolled cellular proliferation that destroys normal bone tissue
DOID:184
Cancers of bone and articular cartilage
bone carcinoma
class of disease
bone cancer
carcinoma
bone cancer that has material basis in abnormally proliferating cells derives from epithelial cells
DOID:2762
bone chondrosarcoma
class of disease
chondrosarcoma
chondrosarcoma that is located in bone
DOID:0050897
bone deterioration disease
class of disease
bone structure disease
bone structure disease that results in change or damage of structure located in bone
DOID:0080007
bone development disease
class of disease
bone disease
bone disease that results in abnormal growth and development located in bone or located in cartilage
DOID:0080006
C05.116.099
bone disease
class of disease
connective tissue disease
medical condition which affects the bone
DOID:0080001
C05.116
Osteopathies
bone epithelioid hemangioma
class of disease
bone benign neoplasm
histiocytoid hemangioma
Human disease
DOID:6610
bone giant cell sarcoma
class of disease
malignant giant cell tumor
bone sarcoma
malignant giant cell tumor that is composed of multinucleated giant cells
DOID:4719
bone inflammation disease
class of disease
bone disease
inflammation
disease
inflammation of bone
DOID:3342
C05.116.680
bone leiomyosarcoma
class of disease
osteosarcoma
leiomyosarcoma
Human disease
DOID:3367
bone lymphoma
class of disease
bone cancer
primary organ-specific lymphoma
lymphoma
bone cancer and lymphoma by site that results in lymphoma starting in the bone
DOID:6759
bone marrow disease
class of disease
hematopoietic system disease
bone disease
human disease
DOID:4961
C15.378.190
bone osteosarcoma
class of disease
osteosarcoma
Human disease
DOID:3376
bone peripheral neuroepithelioma
class of disease
bone Ewing's sarcoma
Human disease
DOID:4388
bone remodeling disease
class of disease
bone disease
bone disease that results in formation or resorption abnormalities located in bone
DOID:0080005
bone resorption disease
class of disease
bone remodeling disease
human disease
DOID:0080011
bone sarcoma
class of disease
sarcoma
bone cancer
bone neoplasm
a sarcoma that arises from the bone, for example osteosarcoma and chondrosarcoma
DOID:0080639
bone squamous cell carcinoma
class of disease
bone carcinoma
squamous cell carcinoma
bone carcinoma that derives from squamous epithelial cells
DOID:0050896
bone structure disease
class of disease
bone disease
spinal disease
bone disease that has material basis in an abnormality in the location or function of the skeletal structure
DOID:0080010
borderline glaucoma
class of disease
glaucoma
Human disease
DOID:9283
borderline personality disorder
class of disease
personality disorder
disease
personality disorder characterized by variability of moods and unstable relationships
DOID:10930
F03.675.100
Borderline personality disorder
botryoid embryo rhabdomyosarcoma
class of disease
embryonal rhabdomyosarcoma
Human disease
DOID:3255
bowel dysfunction
class of disease
intestinal disease
Human disease
DOID:9779
bowel obstruction
class of disease
intestinal disease
disease
Human disease
DOID:8437
C06.405.469.531
Intestinal obstruction
brachial plexus lesion
class of disease
brachial plexus neuropathy
nerve injury
neck injury
disease
brachial plexus neuropathy characterized by an abnormality, usually caused by disease or trauma, located in the brachial plexus
DOID:8443
Brachial plexus injury
brachial plexus neoplasm
class of disease
nerve plexus neoplasm
brachial plexus neuropathy
central nervous system cancer
neoplasm (disease) that involves the brachial nerve plexus
DOID:5913
brachial plexus neuritis
class of disease
neuritis
brachial plexus neuropathy
An inflammatory process affecting the brachial plexus. It results in severe pain in the upper extremity and shoulder, upper arm weakness and loss of sensation in the upper arm.
DOID:3689
C10.668.829.100.500
C10.668.829.650.250
brachial plexus neuropathy
class of disease
plexopathy
peripheral neuropathy
brachial plexus disorder characterized by regional paresthesia, pain and muscle weakness, and limited movement in the arm or hand
DOID:3690
C10.668.829.100
Brachial plexus neuropathies
brachydactyly
class of disease
dysostosis
hand congenital deformity
disease
bone development disease characterized by short fingers and toes
DOID:0050581
C05.660.585.262
C16.131.621.585.262
Brachydactyly
brachydactyly type A1B
class of disease
brachydactyly type A1
A brachydactyly type A1 characterized by shortened middle phalanges of all the digits and shortened proximal phalanges of the thumbs and big toes but normal stature that has material basis in variation in the chromosome region 5p13.3-p13.2.
DOID:0110974
bradyopsia
class of disease
retinal disease
genetic vitreous-retinal disease
retinal disease characterized by the slower than usual adaptation of the eyes to changing light conditions; can have material basis in mutations in the RGS9 or the R9AP genes
DOID:0050335
brain angioma
class of disease
hemangioma
central nervous system organ benign neoplasm
encephalopathy
cerebrovascular disease
Human disease
DOID:5393
brain cancer
class of disease
central nervous system cancer
brain tumor
encephalopathy
cancer
central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain
DOID:1319
brain compression
class of disease
encephalopathy
Human disease
DOID:11457
brain ependymoma
class of disease
brain glioma
ependymal tumor
bone cancer
spinal disease
Human disease
DOID:7497
brain germinoma
class of disease
brain cancer
central nervous system germinoma
germ cell cancer
Human disease
DOID:2127
brain glioblastoma multiforme
class of disease
brain glioma
Human disease
DOID:3073
brain glioma
class of disease
brain cancer
glioma
brain cancer that has material basis in glial cells
DOID:0060108
Brain gliomas
brain infarction
class of disease
cerebrovascular disease
brain ischemia
Human disease
DOID:3454
C10.228.140.300.150.477
C10.228.140.300.775.200
C14.907.253.092.477
C14.907.253.855.200
C23.550.513.355.250
C23.550.717.489.250
brain ischemia
class of disease
ischemia
cerebrovascular disease
stroke
disease
insufficient blood flow to the brain
DOID:2316
C10.228.140.300.150
C14.907.253.092
Brain ischemia
brain meningioma
class of disease
brain cancer
meningioma
Human disease
DOID:0060106
brain oligodendroglioma
class of disease
brain glioma
oligodendroglioma
brain glioma that has material basis in oligodendrocytes
DOID:3187
brain sarcoma
class of disease
brain cancer
central nervous system sarcoma
Human disease
DOID:2132
brain small vessel disease
class of disease
encephalopathy
human disease
DOID:0112313
brain small vessel disease 3
class of disease
brain small vessel disease
autosomal recessive disease
human disease
DOID:0112315
brain stem angioblastoma
class of disease
brain stem cancer
hemangioblastoma
benign neoplasm of brain stem
carcinoma
Human disease
DOID:6501
brain stem astrocytic neoplasm
class of disease
Brainstem glioma
brain astrocytoma
Human disease
DOID:4860
brain stem cancer
class of disease
infratentorial cancer
brain stem neoplasm
Human disease
DOID:4203
brain stem ependymoma
class of disease
Brainstem glioma
brain ependymoma
ependymal tumor
Human disease
DOID:5508
brain stem infarction
class of disease
brain infarction
brain stem stroke syndrome
human disease
DOID:3523
C10.228.140.300.150.477.100
C10.228.140.300.775.200.100
C14.907.253.092.477.100
C14.907.253.855.200.100
brain stem medulloblastoma
class of disease
brain stem cancer
medulloblastoma
brain stem cancer that begins in the lower part of the brain on the floor of the skull
DOID:0050899
brainstem intraparenchymal clear cell meningioma
class of disease
clear cell meningioma
Human disease
DOID:4209
branch retinal artery occlusion
class of disease
retinal artery occlusion
Human disease
DOID:13094
branchiootorenal syndrome 1
class of disease
branchiootorenal syndrome
human disease
DOID:0111423
branchiootorenal syndrome 2
class of disease
branchiootorenal syndrome
human disease
DOID:0111424
brawny scleritis
class of disease
anterior scleritis
Human disease
DOID:14287
breast adenocarcinoma
class of disease
breast carcinoma
adenocarcinoma
breast carcinoma that originates in the milk ducts and/or lobules (glandular tissue) of the breast
DOID:3458
breast adenoid cystic carcinoma
class of disease
breast carcinoma
breast adenocarcinoma
invasive breast carcinoma
Human disease
DOID:4877
breast adenoma
class of disease
breast benign neoplasm
benign neoplasms by histologic type
adenoma
Human disease
DOID:1625
breast adenomyoepithelial adenosis
class of disease
microglandular adenosis
Human disease
DOID:7312
breast adenomyoepithelioma
class of disease
breast myoepithelial neoplasm
breast myoepithelial neoplasm that affects the breast and is characterized by biphasic proliferation of both epithelial and myoepithelial cells
DOID:1642
breast angiomatosis
class of disease
angiomatosis
capillary disease
breast disease
Human disease
DOID:1637
breast angiosarcoma
class of disease
breast sarcoma
inherited soft tissue tumor
inherited gynecological tumor
rare genetic vascular tumor
angiosarcoma
angiosarcoma and sarcoma of breast and vascular neoplasm of breast that is located in the cells that line the blood vessels within the breast or underarm area
DOID:4511
breast apocrine adenoma
class of disease
breast adenoma
hidradenoma
benign neoplasm of sweat gland
apocrine adenoma
benign epithelial skin neoplasm
Human disease
DOID:7540
breast apocrine carcinoma
class of disease
breast adenocarcinoma
apocrine adenocarcinoma
Human disease
DOID:6581
breast apocrine carcinoma in situ
class of disease
breast carcinoma in situ
Human disease
DOID:8428
breast benign neoplasm
class of disease
symptom or sign
thoracic benign neoplasm
breast disease
breast neoplasm
non-metastasizing neoplasm arising from the breast parenchyma
DOID:0060082
breast cancer
class of disease
symptom or sign
thoracic cancer
breast disease
breast neoplasm
disease
cancer that originates in the mammary gland
DOID:1612
Breast cancer
breast capillary hemangioma
class of disease
breast hemangioma
Human disease
DOID:6491
breast carcinoma
class of disease
breast cancer
A breast cancer that has material basis in abnormally proliferating cells derives from epithelial cells.
DOID:3459
Breast carcinomas
breast carcinoma in situ
class of disease
in situ carcinoma
carcinoma in situ of breast and genitourinary system
breast disease
Human disease
DOID:8791
C04.557.470.200.240.187
C04.588.180.130
C17.800.090.500.130
breast columnar cell mucinous carcinoma
class of disease
breast mucinous carcinoma
Human disease
DOID:8130
breast cystic hypersecretory carcinoma
class of disease
breast secretory carcinoma
Human disease
DOID:7537
breast disease
class of disease
thoracic disease
disease
thoracic disease that is located in the breast
DOID:3463
C17.800.090
Diseases and disorders of the breast
breast duct papilloma
class of disease
intraductal papillary breast neoplasm
papilloma
Human disease
DOID:1626
breast ductal adenoma
class of disease
breast adenoma
Human disease
DOID:7538
DOID:5397
breast ductal carcinoma
class of disease
breast carcinoma
ductal carcinoma
breast carcinoma that derives from the lining of milk ducts
DOID:3007
C04.557.470.200.025.232.500
C04.557.470.615.132.500
C04.588.180.390
C17.800.090.500.390
Breast ductal carcinomas
breast epithelioid hemangioma
class of disease
breast hemangioma
histiocytoid hemangioma
Human disease
DOID:6492
breast fibroadenoma
class of disease
breast benign neoplasm
adenoma
disease
breast benign neoplasm comprised of fibrous and glandular tissues
DOID:1618
C04.557.450.565.590.595.350
C04.557.470.625.350
Breast fibroadenomas
breast fibrocystic disease
class of disease
symptom or sign
breast benign neoplasm
benign mammary dysplasia
Human disease
DOID:10354
C17.800.090.750
Fibrocystic breast changes
breast fibrosarcoma
class of disease
breast sarcoma
fibrosarcoma
Human disease
DOID:6001
breast giant fibroadenoma
class of disease
breast fibroadenoma
Human disease
DOID:7223
breast granular cell tumor
class of disease
breast cancer
Human disease
DOID:3011
breast hemangioma
class of disease
breast benign neoplasm
hemangioma
Human disease
DOID:476
breast hemangiopericytoma
class of disease
breast sarcoma
hemangiopericytoma
hemangiopericytoma that is manifested in the breast
DOID:5370
breast implant-associated anaplastic large cell lymphoma
class of disease
peripheral T-cell lymphoma
human disease
DOID:0070333
breast intracanalicular fibroadenoma
class of disease
breast fibroadenoma
Human disease
DOID:2656
breast intraductal papillomatosis
class of disease
breast papillomatosis
intraductal papillomatosis
intraductal breast papilloma
Human disease
DOID:7511
breast intraductal proliferative lesion
class of disease
intraductal breast neoplasm
Human disease
DOID:6839
breast juvenile papillomatosis
class of disease
breast papillomatosis
Human disease
DOID:6641
breast large cell neuroendocrine carcinoma
class of disease
inherited gynecological tumor
rare genetic respiratory disease
inherited neuroendocrine tumor
invasive breast carcinoma
breast carcinoma
Human disease
DOID:6657
breast leiomyoma
class of disease
breast benign neoplasm
leiomyoma
Human disease
DOID:1623
breast leiomyosarcoma
class of disease
breast sarcoma
inherited gynecological tumor
inherited soft tissue tumor
Human disease
DOID:5285
breast liposarcoma
class of disease
breast sarcoma
Human disease
DOID:5701
breast lobular carcinoma
class of disease
breast carcinoma
Lobular carcinoma
breast carcinoma that derives from breast lobules (milk glands)
DOID:0050938
C04.557.470.200.025.305
C04.557.470.615.305
C04.588.180.437
C17.800.090.500.437
breast lymphoma
class of disease
breast cancer
inherited gynecological tumor
genetic hematologic disease
lymphoma
Human disease
DOID:5826
breast malignant eccrine spiradenoma
class of disease
breast cancer
inherited gynecological tumor
inherited skin tumor
genetic epidermal disorder
malignant spiradenoma
breast adenocarcinoma
Human disease
DOID:7983
breast malignant phyllodes tumor
class of disease
breast cancer
breast fibroepithelial neoplasm
phyllodes tumor
malignant phyllodes tumor
Human disease
DOID:3016
breast medullary carcinoma
class of disease
breast adenocarcinoma
invasive ductal carcinoma
Human disease
DOID:5605
breast metaplastic carcinoma
class of disease
breast carcinoma
Metaplastic carcinoma
invasive breast carcinoma
Human disease
DOID:4680
breast mucinous carcinoma
class of disease
breast adenocarcinoma
invasive ductal carcinoma
Human disease
DOID:3610
Mucinous breast carcinoma
breast mucinous cystadenocarcinoma
class of disease
breast mucinous carcinoma
mucinous cystadenocarcinoma
Human disease
DOID:3609
breast mucoepidermoid carcinoma
class of disease
breast metaplastic carcinoma
breast adenocarcinoma
mucoepidermoid carcinoma
Human disease
DOID:4679
breast myoepithelial carcinoma
class of disease
breast carcinoma
invasive breast carcinoma
myoepithelial carcinoma
Human disease
DOID:6776
breast myoepithelial neoplasm
class of disease
breast cancer
Human disease
DOID:3004
breast myoepitheliosis
class of disease
breast myoepithelial neoplasm
Human disease
DOID:7521
breast neuroendocrine neoplasm
class of disease
breast benign neoplasm
Human disease
DOID:3009
breast osteosarcoma
class of disease
breast sarcoma
extraosseous osteosarcoma
Human disease
DOID:7787
breast papillary carcinoma
class of disease
breast carcinoma
breast papillary neoplasm
Human disease
DOID:5592
breast papillomatosis
class of disease
breast benign neoplasm
papillomatosis
Human disease
DOID:1634
breast pericanalicular fibroadenoma
class of disease
breast fibroadenoma
Human disease
DOID:2639
breast rhabdomyosarcoma
class of disease
breast sarcoma
Human disease
DOID:4060
breast sarcoma
class of disease
breast cancer
breast cancer that has material basis in abnormally proliferating cells derives from mesenchymal cells
DOID:3017
breast scirrhous carcinoma
class of disease
breast carcinoma
invasive ductal carcinoma
Human disease
DOID:7578
breast secretory carcinoma
class of disease
breast adenocarcinoma
invasive ductal carcinoma
secretory carcinoma
Human disease
DOID:4922
breast signet ring cell adenocarcinoma
class of disease
breast adenocarcinoma
signet ring cell adenocarcinoma
invasive breast carcinoma
Human disease
DOID:3503
breast squamous cell carcinoma
class of disease
breast metaplastic carcinoma
squamous cell carcinoma
Human disease
DOID:5514
brittle cornea syndrome 2
class of disease
autosomal recessive disease
corneal disease
Ehlers-Danlos syndrome
human disease
DOID:0080729
broad ligament malignant neoplasm
class of disease
uterine adnexa cancer
Human disease
DOID:10744
bronchial mucus gland adenoma
class of disease
bronchus adenoma
Human disease
DOID:7030
bronchial neoplasm
class of disease
respiratory system benign neoplasm
bronchospasm
human disease
DOID:3906
C04.588.894.797.520.109
C08.127.265
C08.785.520.100
bronchiectasis 1
class of disease
bronchiectasis
autosomal dominant disease
bronchiectasis that has material basis in mutation in the gene encoding the beta subunit of the epithelial sodium channel on chromosome 16p12
DOID:0080526
bronchiectasis 2
class of disease
autosomal dominant disease
bronchiectasis
bronchiectasis that has material basis in mutation in the gene encoding the alpha subunit of the epithelial sodium channel
DOID:0080527
bronchiectasis 3
class of disease
autosomal dominant disease
bronchiectasis
bronchiectasis that has material basis in mutation in the gene encoding the gamma subunit of the epithelial sodium channel
DOID:0080528
bronchiolitis
class of disease
symptom or sign
lung disease
bronchospasm
respiratory syncytial virus infectious disease
respiratory signs and symptoms
disease
blockage of the small airways in the lungs due to a viral infection
DOID:2942
C08.127.446.135
C08.381.495.146.135
C08.730.099.135
C01.748.099.135
Bronchiolitis
bronchiolo-alveolar adenocarcinoma
class of disease
adenocarcinoma of the lung
lung adenocarcinoma characterized by a predominantly lepidic pattern and 5 mm or less invasion in greatest dimension
DOID:4926
C04.557.470.200.025.022.500
C04.588.894.797.520.055.500
Bronchiolo-alveolar carcinoma
bronchitis
class of disease
symptom or sign
bronchospasm
chronic obstructive pulmonary disease
respiratory signs and symptoms
disease
inflammation of the large airways in the lungs
DOID:6132
C08.127.446
C08.381.495.146
C08.730.099
Bronchitis
bronchospasm
class of disease
lower respiratory tract disease
bronchial disease
disease
lower respiratory tract disease that affects the airways leading into the lungs
DOID:1176
C08.127.321
bronchus adenoma
class of disease
lung adenoma
bronchial neoplasm
respiratory tract papilloma
benign neoplasms by histologic type
adenoma
Human disease
DOID:5391
bronchus cancer
class of disease
respiratory system cancer
lung cancer
bronchospasm
respiratory system cancer that is located in the bronchus
DOID:1325
bronchus carcinoma
class of disease
bronchus cancer
carcinoma
bronchus cancer that has material basis in epithelial cells
DOID:3904
C04.588.894.797.520.109.220
C08.381.540.140
C08.785.520.100.220
brown shrimp allergy
class of disease
shrimp allergy
crustacean allergy
crustacean allergy triggered by Farfantepenaeus aztecus
DOID:0060525
bruxism
class of disease
symptom or sign
sleep disorder
parafunctional habit
disease
disorder that involves involuntarily grinding or clenching of the teeth
DOID:2846
C07.793.099
Bruxism
bubonic plague
class of disease
plague
lymph node disease
disease
human and animal disease
DOID:10773
Bubonic plague
bulbomembranous urethral cancer
class of disease
male urethral cancer
Human disease
DOID:8259
bulbospinal polio
class of disease
paralytic poliomyelitis
spinal cord disease
Human disease
DOID:0050514
bullous keratopathy
class of disease
corneal edema
keratopathy
cornea blistering
Human disease
DOID:11031
bullous pemphigoid
class of disease
autoimmune skin disease
pemphigoid
bullous skin disease
disease
autoimmune disease of skin and connective tissue characterized by large blisters
DOID:8506
C17.800.865.690
C20.111.730
Bullous pemphigoid
bullous retinoschisis
class of disease
retinoschisis
Human disease
DOID:12108
bullous skin disease
class of disease
dermatitis
cellulitis
autoimmune skin disease
connective tissue disease
An autoimmune disease of skin and connective tissue that is characterized by blisters filled with a watery fluid, located in skin. The disease is associated with the amount of gluten ingested.
DOID:8502
buphthalmos
class of disease
hydrophthalmos
disease
Human disease
DOID:11211
Buphthalmos
burning mouth syndrome
class of disease
symptom or sign
mouth disease
dysesthesia
glossalgia
rare headache disorder
burning sensation
disease
Human disease
DOID:4331
C07.465.114
Burning mouth syndrome
bursitis
class of disease
symptom or sign
arthropathy
synovial, tendon or bursa disorder
inflammation
disease
human disease
DOID:2965
C05.550.251
Bursitis
byssinosis
class of disease
pneumoconiosis
disease
human disease of the respiratory system
DOID:10323
C08.381.483.581.275
C24.800.323
C08.381.520.702.275
calcaneal spur
class of disease
osteophyte
foot diseases
exostosis
exostosis that results in an abnomal growth located in calcaneus
DOID:210
C05.116.540.310.600
C05.360.400
Calcaneal spur
calcaneonavicular coalition
class of disease
synostosis
tarsal-carpal coalition syndrome
synostosis characterized by the fusion of carpal and tarsal bones, which causes stiffness and immobility of the hands and the feet
DOID:14762
calcific tendinitis
class of disease
tendinitis
calcium deposits in tendon and bursa
disorder characterized by deposits of hydroxyapatite (a crystalline calcium phosphate) in any tendon of the body
DOID:14181
Calcific tendinitis
calcinosis
class of disease
calcium metabolism disease
ectopic calcification
disease
calcium metabolism disease that is the result of the formation of calcium deposits in any soft tissue
DOID:182
C18.452.174.130
Calcinosis
calciphylaxis
class of disease
calcinosis
systemic disease
vascular disease
Human disease
DOID:4734
C18.452.174.130.186
Calciphylaxis
calcium metabolism disease
class of disease
mineral metabolism disease
Disorders in the processing of calcium in the body: its absorption, transport, storage, and utilization
DOID:10575
C18.452.174
calcium oxalate nephrolithiasis
class of disease
nephrolithiasis
human disease
DOID:0080652
cancer
class of disease
disease of cellular proliferation
neoplasm
tumor
disease
group of diseases involving abnormal cell growth and spread
DOID:162
cancer of exocrine pancreas
class of disease
pancreatic cancer
pancreatic exocrine neoplasm
Human disease
DOID:1795
cancerophobia
class of disease
nosophobia
overwhelming, irrational, and persistent fear of being diagnosed with cancer
DOID:602
candidal paronychia
class of disease
candidiasis
paronychia
nail disease
Human disease
DOID:14512
cannabis abuse
class of disease
substance abuse
effects of cannabis
cannabis consumption
substance abuse that involves the recurring use of cannabis despite negative consequences
DOID:9505
C25.775.635
F03.900.635
cannabis dependence
class of disease
hallucinogen dependence
effects of cannabis
drug dependence that involves the continued use of cannabis despite problems related to use of the substance
DOID:1849
capillariasis
class of disease
parasitic helminthiasis infectious disease
intestinal disease
liver disease
lung disease
disease
disease caused by nematodes of the genus Capillaria
DOID:12474
capillary disease
class of disease
vascular disease
microangiopathy
vascular disease that is located in the capillaries
DOID:1271
capillary hemangioma
class of disease
symptom or sign
capillary disease
skin hemangioma
most common variant of hemangioma, dull red, firm, dome-shaped hemangioma, usually located on the head and neck, which grows rapidly caused by proliferation of immature capillary vessels
DOID:2725
C04.557.645.375.380
Cutaneous capillary hemangioma
capillary leak syndrome
class of disease
capillary disease
urticarial syndrome
disease
human disease
DOID:14400
C14.907.218
capillary lymphangioma
class of disease
capillary disease
lymphangioma
Human disease
DOID:2286
carbamazepine allergy
class of disease
drug allergy
drug allergy that has allergic trigger carbamazepine
DOID:0040006
carbapenem allergy
class of disease
drug allergy
beta-lactam allergy
drug allergy that has allergic trigger carbapenems
DOID:0040032
carbohydrate metabolic disorder
class of disease
inherited metabolic disorder
carbohydrate metabolism disease
inherited metabolic disorder that affect the catabolism and anabolism of carbohydrates
DOID:2978
C16.320.565.202
C18.452.648.202
Disorders of carbohydrate metabolism
carbohydrate metabolism disease
class of disease
acquired metabolic disease
acquired metabolic disease that is characterized by abnormal carbohydrate metabolism
DOID:0050013
carbuncle
class of disease
гнійне захворювання
pyoderma
human disease
DOID:2176
C01.150.252.410.868.951.270.200
C01.150.252.819.770.270.200
C01.800.720.770.270.200
C17.800.838.765.770.270.200
Carbuncles
carcinoma of supraglottis
class of disease
supraglottis cancer
Human disease
DOID:7763
carcinosarcoma
class of disease
malignant mixed tumor
disease
mixed cell type cancer that has material basis in carcinomatous (epithelial tissue) and sarcomatous (connective tissue) components
DOID:4236
C04.557.435.290
C04.557.450.795.290
Carcinosarcoma
cardia cancer
class of disease
stomach cancer
human disease
DOID:10548
cardiac granular cell neoplasm
class of disease
cardiovascular organ benign neoplasm
benign neoplasm of epicardium
Human disease
DOID:5044
cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies
class of disease
genetic disease
genetic syndromic intellectual disability
rare syndrome with cardiac malformations
syndrome
autosomal dominant disease
human disease
DOID:0111697
cardiac sarcoidosis
class of disease
sarcoidosis
heart disease
Human disease
DOID:13405
cardiac tuberculosis
class of disease
cardiovascular tuberculosis
heart disease
human disease
DOID:0060570
cardiac valvular defect, developmental
class of disease
genetic disease
congenital disorder
Heart valve dysplasia
human disease
DOID:0080633
cardiofaciocutaneous syndrome 1
class of disease
autosomal dominant disease
cardiofaciocutaneous syndrome
human disease
DOID:0111460
cardiofaciocutaneous syndrome 2
class of disease
autosomal dominant disease
cardiofaciocutaneous syndrome
human disease
DOID:0111461
cardiofaciocutaneous syndrome 3
class of disease
cardiofaciocutaneous syndrome
autosomal dominant disease
human disease
DOID:0111462
cardiofaciocutaneous syndrome 4
class of disease
cardiofaciocutaneous syndrome
autosomal dominant disease
human disease
DOID:0111463
cardiomyopathy, infantile hypertrophic
class of disease
genetic disease
hypertrophic cardiomyopathy
human disease
DOID:0111753
cardiovascular organ benign neoplasm
class of disease
organ system benign neoplasm
cardiovascular neoplasm
cardiovascular disease
organ system benign neoplasm disease located in the blood, heart, blood vessels or the lymphatic system
DOID:0060091
carotenemia
class of disease
acquired metabolic disease
Human disease
DOID:9969
carotid artery disease
class of disease
cerebrovascular disease
artery disease
human disease
DOID:3407
C10.228.140.300.200
C14.907.253.123
carotid artery dissection
class of disease
carotid artery disease
dissection
disease
Human disease
DOID:9348
carotid artery occlusion
class of disease
occlusion precerebral artery
carotid artery stenosis
carotid artery disease
Vascular occlusion
human disease
DOID:807
carotid artery stenosis
class of disease
carotid artery disease
peripheral artery disease
narrowing or constriction of the inner surface (lumen) of the carotid artery, usually caused by atherosclerosis
DOID:13001
C10.228.140.300.200.360
C14.907.137.230
C14.907.253.123.360
Carotid artery stenosis
carotid artery thrombosis
class of disease
carotid artery disease
intracranial thrombosis
Human disease
DOID:3410
C10.228.140.300.200.355
C14.907.253.123.355
C14.907.253.566.206
C14.907.355.590.213.206
carp allergy
class of disease
fish allergy
fish allergy triggered by Cyprinus carpio
DOID:0060516
cartilage cancer
class of disease
connective tissue neoplasm
chondropathy
cartilage tumor
Human disease
DOID:0060102
carvone allergic contact dermatitis
class of disease
allergic contact dermatitis
allergic contact dermatitis that has allergic trigger (-)-carvone
DOID:0040064
cascade stomach
class of disease
stomach disease
Human disease
DOID:12234
cataract 1 multiple types
class of disease
cataract
autosomal dominant disease
cataract that has material basis in heterozygous mutation in the gene encoding the alpha-8 subunit of the gap junction protein (GJA8) on chromosome 1q21
DOID:0110231
cataract 24
class of disease
cataract
autosomal dominant disease
cataract that has material basis in variation in the region 17p13
DOID:0110257
cataract 26 multiple types
class of disease
cataract
cataract that has material basis in variation in the region 9q13-q22
DOID:0110246
cataract 27
class of disease
cataract
cataract that has material basis in mutation in the region 2p12
DOID:0110233
cataract 28
class of disease
cataract
human disease
DOID:0110244
cataract 29
class of disease
cataract
autosomal dominant disease
cataract that has material basis in variation in the region 2pter-p24
DOID:0110232
cataract 3 multiple types
class of disease
cataract
autosomal dominant disease
cataract that has material basis in heterozygous mutation in the beta-B2-crystallin gene (CRYBB2) on chromosome 22q11
DOID:0110269
cataract 37
class of disease
cataract
autosomal dominant disease
A cataract that has material basis in variation in the region 12q24.2-q24.3.
DOID:0110252
cataract 4 multiple types
class of disease
cataract
autosomal dominant disease
cataract that has material basis in heterozygous mutation in the gamma-D-crystallin gene (CRYGD) on chromosome 2q33
DOID:0110234
cataract 47
class of disease
autosomal dominant disease
cataract
human disease
DOID:0070353
cataract 48
class of disease
cataract
autosomal recessive disease
human disease
DOID:0070354
cataract 9 multiple types
class of disease
cataract
autosomal recessive disease
autosomal dominant disease
cataract that has material basis in heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22
DOID:0110266
catecholaminergic polymorphic ventricular tachycardia 1
class of disease
catecholaminergic polymorphic ventricular tachycardia
catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal dominant inheritance and has material basis in heterozygous mutation in the RYR2 gene on chromosome 1q43
DOID:0060675
cauda equina intradural extramedullary astrocytoma
class of disease
cauda equina neoplasm
Human disease
DOID:4846
cauda equina neoplasm
class of disease
spinal cord neoplasm
nerve root neoplasm
Human disease
DOID:4847
cauda equina syndrome
class of disease
peripheral neuropathy
syndrome
disease
nerve damage at the end of the spinal cord
DOID:11577
C10.668.829.550.350
C10.668.829.800.750.150
Cauda equina syndrome
causalgia
class of disease
complex regional pain syndrome
human disease
DOID:3222
C10.177.195.200
C10.668.829.250.200
C10.668.829.600.200
cavernous hemangioma
class of disease
symptom or sign
vascular hemostatic disease
disease
human disease
DOID:483
C04.557.645.375.385
C14.907.454.385
C15.378.463.515.385
Cavernous hemangiomas
cavernous hemangioma of orbit
class of disease
cavernous hemangioma
hemangioma of orbit
Human disease
DOID:14463
cavernous sinus thrombosis
class of disease
cerebral venous sinus thrombosis
disease
Human disease
DOID:3575
C10.228.140.300.525.425.500.375
C14.907.253.566.350.500.375
C14.907.355.590.213.350.500.375
cecal disease
class of disease
intestinal disease
intestinal disease located in the cecum
DOID:1518
C06.405.469.110
cecum adenoma
class of disease
cecal benign neoplasm
benign neoplasms by histologic type
adenoma
cecal benign neoplasm that has material basis in epithelial tissue with glandular origin
DOID:0050910
cecum cancer
class of disease
large intestine cancer
cecal neoplasm
cecal disease
large intestine cancer that is located in the cecum
DOID:1521
cecum lymphoma
class of disease
cecum cancer
lymphoma
human disease
DOID:1522
cefaclor allergy
class of disease
cephalosporin allergy
cephalosporin allergy that has allergic trigger cefaclor
DOID:0040023
cefixime allergy
class of disease
cephalosporin allergy
cephalosporin allergy that has allergic trigger cefixime
DOID:0040030
cefotaxime allergy
class of disease
cephalosporin allergy
cephalosporin allergy that has allergic trigger cefotaxime
DOID:0040020
cefotiam allergy
class of disease
cephalosporin allergy
cephalosporin allergy that has allergic trigger cefotiam
DOID:0040103
ceftazidime allergy
class of disease
cephalosporin allergy
cephalosporin allergy that has allergic trigger ceftazidime
DOID:0040024
ceftriaxone allergy
class of disease
cephalosporin allergy
cephalosporin allergy that has allergic trigger ceftriaxone
DOID:0040005
cefuroxime allergy
class of disease
cephalosporin allergy
cephalosporin allergy that has allergic trigger cefuroxime
DOID:0040025
celery allergy
class of disease
vegetable allergy
human disease
DOID:0070335
celiac disease
class of disease
symptom or sign
autoimmune disease of gastrointestinal tract
gluten-related disorder
disease
long term autoimmune disorder caused by a reaction to gluten
DOID:10608
C06.405.469.637.250
C18.452.603.250
Coeliac disease
cell type cancer
class of disease
cancer
cancer that is classified by the type of cell from which it is derived
DOID:0050687
Cancers by histological type
cellular congenital mesoblastic nephroma
class of disease
congenital mesoblastic nephroma
Human disease
DOID:8082
cellular ependymoma
class of disease
benign ependymoma
An ependymoma which shows conspicuous cellularity without a significant increase in mitotic rate. (Adapted from WHO)
DOID:5500
cellular leiomyoma
class of disease
leiomyoma
Human disease
DOID:5139
cellular myxoid liposarcoma
class of disease
liposarcoma
myxoid liposarcoma
Human disease
DOID:5692
cellular neurofibroma
class of disease
neurofibroma
Human disease
DOID:5152
cellular phase chronic idiopathic myelofibrosis
class of disease
myelofibrosis
chronic idiopathic myelofibrosis
Human disease
DOID:8106
cellular schwannoma
class of disease
neurilemmoma
neurilemmoma with a predominantly cellular growth but no Verocay bodies
DOID:3196
central breast papilloma
class of disease
breast duct papilloma
Human disease
DOID:8224
central conducting lymphatic anomaly
class of disease
lymphatic system disease
autosomal dominant disease
human disease
DOID:0081030
central corneal ulcer
class of disease
corneal ulcer
Human disease
DOID:9910
central epithelioid sarcoma
class of disease
epithelioid sarcoma
Human disease
DOID:7492
central gyrate choroidal dystrophy
class of disease
partial central choroid dystrophy
human disease
DOID:9820
central nervous system adult germ cell tumor
class of disease
central nervous system germ cell tumor
Human disease
DOID:5349
central nervous system angiosarcoma
class of disease
central nervous system sarcoma
central nervous system sarcoma that is located in the inner lining of blood vessels
DOID:4504
central nervous system cancer
class of disease
nervous system cancer
central nervous system neoplasm
central nervous system disease
nervous system cancer that is located in the central nervous system
DOID:3620
central nervous system childhood germ cell tumor
class of disease
central nervous system germ cell tumor
germ cell cancer
pediatric germ cell tumor
Human disease
DOID:6052
central nervous system chondroma
class of disease
chondroma
central nervous system organ benign neoplasm
soft tissue chondroma
Human disease
DOID:3813
central nervous system disease
class of disease
neurological disorder
nervous system disease
nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system
DOID:331
C10.228
Diseases and disorders of the central nervous system
central nervous system embryonal carcinoma
class of disease
central nervous system germ cell tumor
embryonal carcinoma
primary germ cell tumor of central nervous system
Human disease
DOID:7232
central nervous system endodermal sinus tumor
class of disease
central nervous system germ cell tumor
malignant mixed tumor
sarcoma
germ cell cancer
primary germ cell tumor of central nervous system
Human disease
DOID:5343
central nervous system fibrosarcoma
class of disease
central nervous system sarcoma
fibrosarcoma
Human disease
DOID:6451
central nervous system germ cell tumor
class of disease
central nervous system cancer
extragonadal germ cell tumor
germ cell cancer
Human disease
DOID:4439
central nervous system germinoma
class of disease
central nervous system germ cell tumor
germinoma
germ cell cancer
Human disease
DOID:4438
central nervous system hemangioma
class of disease
hemangioma
central nervous system organ benign neoplasm
hemangioma arising from the brain and spinal cord
DOID:501
central nervous system hematologic cancer
class of disease
central nervous system cancer
hematologic cancer
hematologic cancer and central nervous system neoplasm that is located in the central nervous system
DOID:5772
central nervous system immature teratoma
class of disease
central nervous system teratoma
Human disease
DOID:6019
central nervous system leiomyoma
class of disease
central nervous system organ benign neoplasm
leiomyoma
Human disease
DOID:5126
central nervous system leiomyosarcoma
class of disease
central nervous system mesenchymal non-meningothelial tumor
leiomyosarcoma
malignant central nervous system mesenchymal, non-meningothelial neoplasm
Human disease
DOID:5254
central nervous system leukemia
class of disease
leukemia
central nervous system hematologic cancer
central nervous system cancer
hematologic cancer located in the central nervous system
DOID:12969
central nervous system lipoma
class of disease
central nervous system organ benign neoplasm
lipoma
human disease
DOID:6293
central nervous system lymphoma
class of disease
lymphoma
central nervous system hematologic cancer
hematologic cancer that has material basis in lymphoma located in central nervous system
DOID:3234
central nervous system mature teratoma
class of disease
central nervous system teratoma
mature teratoma
Human disease
DOID:6017
central nervous system melanocytic neoplasm
class of disease
central nervous system neoplasm
melanocytic tumor
central nervous system cancer
Human disease
DOID:4955
central nervous system organ benign neoplasm
class of disease
nervous system benign neoplasm
central nervous system neoplasm
central nervous system disease
Human disease
DOID:0060090
central nervous system origin vertigo
class of disease
central nervous system disease
encephalopathy
vertigo
Human disease
DOID:2479
central nervous system osteosarcoma
class of disease
central nervous system mesenchymal non-meningothelial tumor
extraosseous osteosarcoma
malignant central nervous system mesenchymal, non-meningothelial neoplasm
Human disease
DOID:7994
central nervous system primitive neuroectodermal neoplasm
class of disease
central nervous system cancer
neuroectodermal tumor
Embryonal tumors of the central nervous system
primitive neuroectodermal tumor
Human disease
DOID:0060103
Primitive neuroectodermal tumor
central nervous system rhabdomyosarcoma
class of disease
central nervous system sarcoma
rhabdomyosarcoma
nervous system cancer
central nervous system disease
Human disease
DOID:4048
central nervous system sarcoma
class of disease
central nervous system cancer
sarcoma
human disease
DOID:2133
central nervous system teratoma
class of disease
central nervous system germ cell tumor
primary germ cell tumor of central nervous system
sarcoma
germ cell cancer
Human disease
DOID:3640
central nervous system vasculitis
class of disease
vasculitis
central nervous system disease
disease
Human disease
DOID:525
C10.114.875
C10.228.140.300.850
C14.907.253.946
C14.907.940.907
C20.111.258.962
central neurocytoma
class of disease
neurocytoma
cerebral ventricle cancer
Human disease
DOID:14174
Central neurocytoma
central pontine myelinolysis
class of disease
demyelinating disease
demyelinating disease of central nervous system
demyelination disease that is characterized by severe damage to the myelin sheath of the pons' nerve cells and has symptom acute paralysis, has symptom dysphagia, and has symptom dysarthria
DOID:636
C10.228.140.163.560
C10.314.500
C18.452.132.560
Central pontine myelinolysis
central precocious puberty
class of disease
endocrine system disease
human disease
DOID:0112308
central precocious puberty 1
class of disease
autosomal dominant disease
human disease
DOID:0112310
central pterygium
class of disease
progressive peripheral pterygium
Human disease
DOID:13473
central retinal artery occlusion
class of disease
retinal artery occlusion
retinal artery occlusion characterized by blockage of blood flow through the central retinal artery
DOID:13098
Central retinal artery occlusion
central retinal vein occlusion
class of disease
retinal vein occlusion
Human disease
DOID:2450
central sleep apnea
class of disease
sleep apnea
sleep apnea that is characterized by a malfunction of the basic neurological controls for breathing rate and the failure to give the signal to inhale, causing the individual to miss one or more cycles of breathing
DOID:9220
C08.618.085.852.800
C10.886.425.800.750.800
centronuclear myopathy 1
class of disease
An autosomal dominant centronuclear myopathy characterized by slowly progressive muscle wasting and weakness involving mainly the limb girdle, trunk, and neck muscles that has material basis in heterozygous mutation in DNM2 on 19p13.2.
DOID:0111223
centronuclear myopathy 2
class of disease
centronuclear myopathy
autosomal recessive centronuclear myopathy
An autosomal recessive centronuclear myopathy that has material basis in homozygous or compound heterozygous mutation in BIN1 on 2q14.3.
DOID:0111220
centronuclear myopathy 4
class of disease
autosomal dominant centronuclear myopathy
An autosomal dominant centronuclear myopathy that has material basis in heterozygous mutation in CCDC78 on 16p13.3.
DOID:0111224
centronuclear myopathy 5
class of disease
autosomal recessive centronuclear myopathy
autosomal recessive centronuclear myopathy characterized by severe neonatal hypotonia, respiratory insufficiency, and difficulty feeding that has material basis in homozygous or compound heterozygous mutation in SPEG on 2q35
DOID:0111222
centronuclear myopathy 6 with fiber-type disproportion
class of disease
congenital fiber-type disproportion
A congenital fiber-type disproportion characterized by onset in infancy or early childhood of slowly progressive centronuclear myopathy that has material basis in homozygous or compound heterozygous mutation in ZAK on 2q31.1.
DOID:0111221
centronuclear myopathy X-linked
class of disease
centronuclear myopathy
centronuclear myopathy that has material basis in X-linked inheritance of mutations in MTM1 on Xq28
DOID:0111225
cephalosporin allergy
class of disease
drug allergy
beta-lactam allergy
drug allergy that has allergic trigger cephalosporin
DOID:0040021
cercarial dermatitis
class of disease
schistosomiasis
skin disease
human disease
DOID:11302
Schistosome cercarial dermatitis
cerebellar angioblastoma
class of disease
cerebellum cancer
hemangioblastoma
benign neoplasm of cerebellum
carcinoma
Human disease
DOID:6500
Cerebellar hemangioblastoma
cerebellar astrocytoma
class of disease
cerebellum cancer
brain astrocytoma
glioma
Human disease
DOID:4848
cerebellar ataxia
class of disease
cerebellar disease
hereditary ataxia
cerebellar disease characterized by ataxia originating in the cerebellum.
DOID:0050753
C10.228.140.252.190
C10.597.350.090.500
C23.888.592.350.090.200
Cerebellar ataxia
cerebellar ataxia type 48
class of disease
spinocerebellar ataxia
human disease
DOID:0111746
cerebellar hyplasia/atrophy, epilepsy, and global developmental delay
class of disease
syndrome
neurodevelopmental disorder
human disease
DOID:0070339
cerebellar hypoplasia
class of disease
neurological disorder
rare disorder in which the cerebellum is either missing entirely or is smaller than usual
DOID:0070338
Cerebellar hypoplasia
cerebellar liponeurocytoma
class of disease
cerebellum cancer
neuronal tumor
Human disease
DOID:6458
cerebellar medulloblastoma
class of disease
cerebellum cancer
medulloblastoma
cerebellum cancer that begins in the lower part of the brain on the floor of the skull
DOID:0060104
cerebellar vermis medulloblastoma
class of disease
cerebellar medulloblastoma
medulloblastoma
Human disease
DOID:3860
cerebellopontine angle meningioma
class of disease
cerebellopontine angle tumor
meningioma
brain meningioma
Human disease
DOID:6337
cerebellopontine angle primitive neuroectodermal
class of disease
cerebellopontine angle tumor
Human disease
DOID:4787
cerebellopontine angle tumor
class of disease
brain stem neoplasm
brain stem cancer
Human disease
DOID:3200
cerebellum cancer
class of disease
infratentorial cancer
cerebellar disease
infratentorial neoplasm
Human disease
DOID:4205
C04.588.614.250.195.411.211
C10.228.140.211.500.200
C10.228.140.252.200
C10.551.240.250.400.300
cerebral amyloid angiopathy
class of disease
amyloidosis
amyloidosis where amyloid protein progressively deposits in cerebral blood vessel walls with subsequent degenerative vascular changes
DOID:9246
C10.228.140.300.510.200.200
C14.907.253.560.200.200
C18.452.845.500.100
Cerebral amyloid angiopathy
cerebral angioma
class of disease
brain angioma
benign neoplasm of cerebrum
Human disease
DOID:6621
cerebral arterial disease
class of disease
intracranial arterial disease
artery disease
Human disease
DOID:3527
C10.228.140.300.510.200
C14.907.253.560.200
cerebral arteriovenous malformation
class of disease
rare genetic vascular tumor
rare nervous system tumor
central nervous system vascular malformation
rare genetic epilepsy
genetic central nervous system and retinal vascular disease
central nervous system organ benign neoplasm
hemangioma
encephalopathy
cerebrovascular disease
arteriovenous malformation that is located in the brain
DOID:0060688
C10.228.140.300.520
C10.500.190.500
C14.240.850.750.295
C14.240.850.875.500
C14.907.150.295
C14.907.253.560.400
C16.131.240.850.750.295
C16.131.240.850.875.500
C16.131.666.190.500
Cerebral arteriovenous malformation
cerebral arteritis
class of disease
central nervous system vasculitis
cerebrovascular disease
arteritis
Human disease
DOID:11390
cerebral artery occlusion
class of disease
cerebral infarction
cerebrovascular disease
human disease
DOID:10127
cerebral atherosclerosis
class of disease
atherosclerosis
intracranial arteriosclerosis
type of atherosclerosis where build-up of plaque in the blood vessels of the brain occurs
DOID:12720
cerebral cavernous angioma
class of disease
central nervous system cavernous hemangioma
cerebrovascular disease
vascular anomaly of the central nervous system characterized by dilated blood-filled capillaries lacking structural support
DOID:0060669
cerebral cavernous malformation 1
class of disease
cerebral cavernous angioma
cerebral cavernous malformation that has material basis in heterozygous mutation in the KRIT1 gene on chromosome 7q21
DOID:0080491
cerebral convexity meningioma
class of disease
cerebral meningioma
Human disease
DOID:6114
cerebral creatine deficiency syndrome
class of disease
amino acid metabolic disorder
Human disease
DOID:0050798
cerebral degeneration
class of disease
disease
encephalopathy
neurodegeneration
human disease
DOID:1443
Cerebral atrophy
cerebral edema
class of disease
encephalopathy
disease
human disease
DOID:4724
C10.228.140.187
Cerebral edema
cerebral hemisphere lipoma
class of disease
central nervous system lipoma
benign neoplasm of cerebrum
intracranial lipoma
Human disease
DOID:6291
cerebral infarction
class of disease
brain infarction
disease
type of ischemic stroke resulting from a blockage in the blood vessels supplying blood to the brain
DOID:3526
C10.228.140.300.150.477.200
C10.228.140.300.775.200.200
C14.907.253.092.477.200
C14.907.253.855.200.200
C23.550.513.355.250.200
C23.550.717.489.250.200
Cerebral infarction
cerebral lipidosis
class of disease
cerebral degeneration
lipid storage disease
encephalopathy
metabolic disease with dementia
Human disease
DOID:10742
cerebral lymphoma
class of disease
cerebrum cancer
central nervous system lymphoma
lymphoma
central nervous system hematologic cancer
cerebrum cancer that affects the lymph cells and derives from the brain
DOID:5815
cerebral malaria
class of disease
malaria
malaria that involves neurologic damage resulting from blockage of the blood vessels, caused due to the infection of the red blood cells by Plasmodium species
DOID:14069
C01.207.205.300.500
C01.610.105.300.500
C01.610.752.530.620
C01.920.875.620
C10.228.228.205.300.500
Cerebral malaria
cerebral meningioma
class of disease
cerebrum cancer
meningioma
Human disease
DOID:6112
cerebral neuroblastoma
class of disease
brain cancer
cerebrum cancer
intracranial primitive neuroectodermal tumor
Human disease
DOID:4164
cerebral palsy
class of disease
encephalopathy
cerebral degeneration
palsy
disease
group of permanent movement disorders that appear in early childhood
DOID:1969
C10.228.140.140.254
Cerebral palsy
cerebral primitive neuroectodermal tumor
class of disease
cerebrum cancer
primitive neuroectodermal tumor
Human disease
DOID:7398
cerebral sarcoidosis
class of disease
sarcoidosis
neurosarcoidosis
Human disease
DOID:13403
cerebral venous sinus thrombosis
class of disease
venous thrombosis
intracranial thrombosis
stroke
disease
presence of acute thrombosis (a blood clot) in the dural venous sinuses, which drain blood from the brain.
DOID:3572
C10.228.140.300.525.425.500
C14.907.253.566.350.500
C14.907.355.590.213.350.500
Cerebral venous sinus thrombosis
cerebral ventricle cancer
class of disease
cerebrum cancer
cerebral ventricle neoplasm
cerebrum cancer that is located in the cerebral ventricles
DOID:3541
cerebritis
class of disease
encephalopathy
brain inflammatory disease
Human disease
DOID:3431
cerebrooculofacioskeletal syndrome
class of disease
Cockayne syndrome
human disease
DOID:0080910
cerebrooculofacioskeletal syndrome 1
class of disease
human disease
DOID:0080911
cerebrovascular benign neoplasm
class of disease
cardiovascular organ benign neoplasm
cerebrovascular disease
cardiovascular organ benign neoplasm that is located in the cerebrovascular system
DOID:60007
cerebrovascular disease
class of disease
central nervous system disease
vascular disease
encephalopathy
central nervous system and retinal vascular disease
disease
artery disease that is characterized by dysfunction of the blood vessels supplying the brain
DOID:6713
C10.228.140.300
C14.907.253
Cerebrovascular diseases
cerebrum cancer
class of disease
supratentorial cancer
neoplasm of cerebral hemisphere
supratentorial cancer that is located in the cerebrum
DOID:368
ceruminoma
class of disease
apocrine sweat gland neoplasm
ceruminous tumor
apocrine adenoma
Human disease
DOID:7549
cervical Mullerian papilloma
class of disease
cervical benign neoplasm
Human disease
DOID:9442
cervical Wilms' tumor
class of disease
cervical carcinosarcoma
cervical carcinosarcoma is located in the cervix with morphological features resembling Wilms tumor of the kidney
DOID:5190
cervical adenocarcinoma
class of disease
cervix carcinoma
adenocarcinoma
cervix carcinoma that derives from epithelial cells of glandular origin
DOID:3702
Adenocarcinoma of the cervix
cervical adenofibroma
class of disease
cervical benign neoplasm
Human disease
DOID:5476
cervical adenoid basal carcinoma
class of disease
cervix carcinoma
Human disease
DOID:6428
cervical adenoid cystic carcinoma
class of disease
cervix carcinoma
adenoid cystic carcinoma of the cervix uteri
Human disease
DOID:4867
cervical adenoma malignum
class of disease
cervical mucinous adenocarcinoma
Human disease
DOID:6627
cervical adenomyoma
class of disease
adenomyoma
cervical uterine cancer
cervical benign neoplasm
Human disease
DOID:4995
cervical adenosarcoma
class of disease
cervical carcinosarcoma
malignant mixed epithelial and mesenchymal tumor of cervix uteri
adenosarcoma
cervical carcinosarcoma that is located in the cervix
DOID:4111
cervical adenosquamous carcinoma
class of disease
adenosquamous carcinoma
cervical squamous cell carcinoma
squamous cell carcinoma
cervical uterine cancer
cervical carcinoma that derives from squamous cells and gland-like cells
DOID:5636
cervical alveolar soft part sarcoma
class of disease
cervical uterine cancer
alveolar soft part sarcoma and cervical soft tissue tumor and malignant neoplasm of cervix uteri that is located in the cervix
DOID:4442
cervical atypical polypoid adenomyoma
class of disease
cervical adenomyoma
Human disease
DOID:8179
cervical basaloid squamous cell carcinoma
class of disease
cervical squamous cell carcinoma
basaloid squamous cell carcinoma
Human disease
DOID:7046
cervical benign neoplasm
class of disease
uterine benign neoplasm
cervix disease
uterine cervix neoplasm
Human disease
DOID:0060110
cervical carcinosarcoma
class of disease
cervical uterine cancer
malignant mixed epithelial and mesenchymal tumor of cervix uteri
Human disease
DOID:4112
cervical clear cell adenocarcinoma
class of disease
cervical adenocarcinoma
clear cell adenocarcinoma
Human disease
DOID:5303
cervical dystonia
class of disease
focal dystonia
human disease
DOID:0050840
cervical endometrial stromal sarcoma
class of disease
cervix endometrial stromal tumor
Human disease
DOID:4520
cervical endometrioid adenocarcinoma
class of disease
cervical adenocarcinoma
endometrial carcinoma
Human disease
DOID:5830
cervical incompetence
class of disease
abnormality of organs and soft tissues of pelvis complicating pregnancy, childbirth, or the puerperium
cervix disease
disease
cervix disease that is characterized by the beginning of dilation and effacement of a pregnant woman's cervix before her pregnancy has reached term
DOID:9681
DOID:9678
C12.050.351.500.852.593.120
C12.050.703.039.089.339
C12.100.250.852.593.120
cervical keratinizing squamous cell carcinoma
class of disease
cervical squamous cell carcinoma
keratinizing squamous cell carcinoma
Human disease
DOID:7483
cervical large cell neuroendocrine carcinoma
class of disease
cervix carcinoma
Human disease
DOID:6659
cervical lymphoepithelioma-like carcinoma
class of disease
cervical squamous cell carcinoma
Human disease
DOID:7598
cervical mucinous adenocarcinoma
class of disease
cervical adenocarcinoma
mucinous adenocarcinoma
Human disease
DOID:3701
cervical neuroblastoma
class of disease
extracranial neuroblastoma
extracranial neuroblastoma that has material basis in immature nerve cells
DOID:0050935
cervical non-keratinizing squamous cell carcinoma
class of disease
cervical squamous cell carcinoma
Human disease
DOID:7961
cervical polyp
class of disease
cervix disease
Uterine polyp
cervix disease characterized by a benign polyp on the surface of the cervical canal
DOID:0060325
Cervical polyp
cervical serous adenocarcinoma
class of disease
cervical adenocarcinoma
serous cystadenocarcinoma
Human disease
DOID:5752
cervical spinal canal and spinal cord meningioma
class of disease
spinal canal and spinal cord meningioma
Human disease
DOID:7915
cervical squamous cell carcinoma
class of disease
cervix carcinoma
squamous cell carcinoma
cervix carcinoma that has material basis in squamous cells of the cervix
DOID:3744
cervical uterine cancer
class of disease
uterine cancer
cervix disease
uterine cervix neoplasm
disease
cancer arising from the cervix
DOID:4362
Cervical cancer
cervical verrucous carcinoma
class of disease
cervical squamous cell carcinoma
papillary carcinoma of the cervix uteri
verrucous carcinoma
Human disease
DOID:3743
cervicitis
class of disease
cervix disease
disease
inflammation of the uterine cervix
DOID:2568
C13.351.500.852.593.150
Cervicitis
cervicomedullary junction neoplasm
class of disease
infratentorial cancer
Spinal cord cancer
Human disease
DOID:4707
cervix carcinoma
class of disease
cervical uterine cancer
carcinoma
cervical cancer that is located in the cervix uteri or located in the cervical area and that has material basis in abnormally proliferating cells derives from epithelial cells
DOID:2893
cervix disease
class of disease
uterine disease
human disease
DOID:2253
C13.351.500.852.593
Diseases and disorders of cervix uteri
cervix endometrial stromal tumor
class of disease
cervical uterine cancer
Human disease
DOID:4521
cervix endometriosis
class of disease
cervix disease
endometriosis
Human disease
DOID:361
cervix erosion
class of disease
cervix disease
disease
ectropion
DOID:3456
C13.351.500.852.593.112
Cervical ectropion
cervix melanoma
class of disease
cervical uterine cancer
mucosal melanoma
Human disease
DOID:4413
cervix small cell carcinoma
class of disease
cervix carcinoma
small cell carcinoma
Human disease
DOID:6740
cervix squamous papilloma
class of disease
cervical benign neoplasm
papilloma
Human disease
DOID:9445
cervix uteri carcinoma in situ
class of disease
cervical intraepithelial neoplasia
cervix disease
uterus carcinoma in situ
Human disease
DOID:8991
cheilitis
class of disease
lip disease
inflammation
inflammation of the lips
DOID:1762
C07.465.409.215
Cheilitis
chemical colitis
class of disease
colitis
colitis caused by introduction of various chemicals
DOID:0060186
cherry allergy
class of disease
fruit allergy
fruit allergy triggered by Prunus avium plant fruit food product.
DOID:0060506
chest wall bone cancer
class of disease
bone cancer
chest wall lymphoma
bone cancer and malignant neoplasm of chest wall that is located in the chest wall
DOID:6579
chest wall lymphoma
class of disease
malignant neoplasm of chest wall
thoracic cancer
lymphoma
thoracic cancer that is located in the chest wall
DOID:6758
chest wall parachordoma
class of disease
parachordoma
chest wall lymphoma
neoplasm of chest wall
mesenchymal cell neoplasm
Human disease
DOID:8043
chiasmal syndrome
class of disease
optic nerve disease
encephalopathy
optic nerve disease that is characterized by lesions of the optic chiasm, manifesting as various impairments of the sufferer's visual field according to the location of the lesion along the optic nerve
DOID:5655
chicken egg allergy
class of disease
egg allergy
egg allergy triggered by Gallus gallus eggs
DOID:0060492
chief cell adenoma
class of disease
parathyroid adenoma
Human disease
DOID:7607
childhood absence epilepsy
class of disease
symptom or sign
absence seizure
childhood electroclinical syndrome
Idiopathic generalized epilepsy
generalized seizure
childhood electroclinical syndrome characterized by the occurrence of typical absence seizures, starting between the age of four and ten years
DOID:1825
childhood acute lymphocytic leukemia
class of disease
acute lymphocytic leukemia
childhood leukemia
acute lymphocytic leukemia occuring during childhood
DOID:0080144
childhood acute megakaryoblastic leukemia
class of disease
acute megakaryoblastic leukemia
disease
DOID:0080794
childhood acute myeloid leukemia
class of disease
childhood leukemia
bilineal acute myeloid leukemia
acute myeloid leukemia
Acute myeloid leukemia occurring in childhood
DOID:0070323
childhood asthma
class of disease
asthma
chronic asthma
human disease
DOID:0080815
childhood botryoid rhabdomyosarcoma
class of disease
botryoid embryo rhabdomyosarcoma
Childhood Rhabdomyosarcoma
rare childhood malignant neoplasm
Human disease
DOID:6786
childhood brain germinoma
class of disease
brain germinoma
childhood central nervous system germinoma
Human disease
DOID:7429
childhood brain meningioma
class of disease
brain meningioma
rare childhood malignant neoplasm
pediatric meningioma
Human disease
DOID:6939
childhood brain stem glioma
class of disease
childhood brain stem neoplasm
Brainstem glioma
rare childhood malignant neoplasm
Human disease
DOID:6383
childhood brain stem neoplasm
class of disease
brain stem neoplasm
childhood cancer
childhood infratentorial neoplasm
brain stem cancer
Human disease
DOID:4206
childhood brainstem astrocytoma
class of disease
childhood brain stem glioma
brain stem astrocytic neoplasm
human disease
DOID:6386
childhood central nervous system germinoma
class of disease
central nervous system germinoma
malignant childhood germ cell neoplasm
Human disease
DOID:8078
childhood central nervous system immature teratoma
class of disease
central nervous system immature teratoma
Human disease
DOID:6654
childhood central nervous system mature teratoma
class of disease
central nervous system mature teratoma
pediatric central nervous system tumor
Human disease
DOID:6423
childhood central nervous system mixed germ cell tumor
class of disease
central nervous system childhood germ cell tumor
malignant childhood germ cell neoplasm
mixed germ cell tumor of central nervous system
rare childhood malignant neoplasm
brain cancer
Human disease
DOID:7516
childhood central nervous system primitive neuroectodermal neoplasm
class of disease
central nervous system primitive neuroectodermal neoplasm
childhood cancer
Human disease
DOID:3870
childhood cerebellar astrocytic neoplasm
class of disease
cerebellar astrocytoma
childhood cerebellar neoplasm
juvenile astrocytoma
Human disease
DOID:6286
childhood cerebellar neoplasm
class of disease
cerebellum cancer
childhood infratentorial neoplasm
Human disease
DOID:5059
childhood cerebral astrocytoma
class of disease
cerebrum cancer
juvenile astrocytoma
Human disease
DOID:7007
childhood choriocarcinoma of the ovary
class of disease
choriocarcinoma of ovary
rare childhood malignant neoplasm
non-gestational ovarian choriocarcinoma
malignant childhood germ cell neoplasm
pediatric ovarian germ cell tumor
Human disease
DOID:8336
childhood choriocarcinoma of the testis
class of disease
choriocarcinoma of the testis
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
pediatric testicular germ cell tumor
Human disease
DOID:6160
childhood choroid plexus cancer
class of disease
childhood cancer
childhood choroid plexus neoplasm
choroid plexus neoplasm
Human disease
DOID:3545
childhood disintegrative disease
class of disease
pervasive developmental disorder
disease
neurodevelopmental condition
DOID:13487
childhood electroclinical syndrome
class of disease
electroclinical syndrome
Epilepsy in children
absence seizure
electroclinical syndrome with onset in childhood between one and 12 years of age
DOID:0050704
childhood embryonal testis carcinoma
class of disease
embryonal testis carcinoma
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
pediatric testicular germ cell tumor
embryonal testis carcinoma that occurs in children
DOID:6162
childhood endodermal sinus tumor
class of disease
endodermal sinus tumor
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
endodermal sinus tumor that occurs in children
DOID:5342
childhood extraosseous osteosarcoma
class of disease
extraosseous osteosarcoma
pediatric osteosarcoma
Human disease
DOID:7297
childhood germ cell brain tumor
class of disease
central nervous system childhood germ cell tumor
brain cancer
Human disease
DOID:7430
childhood hypophosphatasia
class of disease
hypophosphatasia
A hypophosphatasia that has material basis in an autosomal recessive mutation of ALPL on chromosome 1p36.12.
DOID:0110915
childhood immature teratoma of ovary
class of disease
immature teratoma of ovary
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
childhood teratoma of the ovary
Human disease
DOID:7037
childhood infratentorial neoplasm
class of disease
brain stem cancer
infratentorial cancer
childhood neoplasm
childhood brain tumor
Human disease
DOID:4207
childhood intracortical osteosarcoma
class of disease
pediatric osteosarcoma
intracortical osteogenic sarcoma
human disease
DOID:7612
childhood kidney angiomyolipoma
class of disease
childhood kidney neoplasm
kidney angiomyolipoma
Human disease
DOID:8410
childhood kidney cell carcinoma
class of disease
renal cell carcinoma
rare childhood malignant neoplasm
childhood malignant kidney neoplasm
Human disease
DOID:4454
childhood kidney neoplasm
class of disease
kidney neoplasm
childhood neoplasm
kidney cancer
Human disease
DOID:3675
childhood leukemia
class of disease
leukemia
childhood cancer
rare childhood malignant neoplasm
bone marrow cancer
leukemia that occurs in children
DOID:7757
childhood malignant hemangiopericytoma
class of disease
hemangiopericytoma
hemangiopericytoma, malignant
Human disease
DOID:7731
childhood malignant mesenchymoma
class of disease
malignant mesenchymoma
childhood cancer
Human disease
DOID:5893
childhood malignant schwannoma
class of disease
malignant peripheral nerve sheath tumor
neurilemmoma
rare childhood malignant neoplasm
Human disease
DOID:7732
childhood mature teratoma of the ovary
class of disease
childhood teratoma of the ovary
mature teratoma of the ovary
Human disease
DOID:6229
childhood mediastinal neurogenic tumor
class of disease
malignant mediastinal neurogenic neoplasm
childhood neoplasm
Human disease
DOID:4690
childhood medulloblastoma
class of disease
medulloblastoma
childhood infratentorial neoplasm
Human disease
DOID:3869
childhood multilocular cystic kidney neoplasm
class of disease
kidney benign neoplasm
childhood kidney neoplasm
multiloculated renal cyst
A childhood renal Wilms cancer that occurs in children. It encompasses two histologically distinct but grossly indistinguishable lesions: cystic nephroma and cystic partially differentiated nephroblastoma (CPDN).
DOID:7762
childhood oligodendroglioma
class of disease
oligodendroglioma
Human disease
DOID:3183
childhood onset epileptic encephalopathy
class of disease
generalized epilepsy
Epilepsy in children
An idiopathic generalized epilepsy characterized by onset of multiple seizure types in the first few years of life and associated with poor prognosis. Affected individuals have cognitive regression and intellectual disability.
DOID:0060475
childhood optic nerve glioma
class of disease
optic nerve glioma
human disease
DOID:6576
childhood ovarian embryonal carcinoma
class of disease
ovarian embryonal carcinoma
pediatric ovarian germ cell tumor
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
ovarian embryonal carcinoma that occurs in childhood
DOID:8036
childhood ovarian endodermal sinus tumor
class of disease
ovarian endodermal sinus tumor
pediatric ovarian germ cell tumor
childhood endodermal sinus tumor
Human disease
DOID:6083
childhood parosteal osteogenic sarcoma
class of disease
juxtacortical osteosarcoma
pediatric osteosarcoma
Human disease
DOID:5809
childhood pilocytic astrocytoma
class of disease
pilocytic astrocytoma
Human disease
DOID:6812
childhood pleomorphic rhabdomyosarcoma
class of disease
pleomorphic rhabdomyosarcoma
Childhood Rhabdomyosarcoma
rare childhood malignant neoplasm
Human disease
DOID:7463
childhood spinal cord tumor
class of disease
Spinal cord cancer
childhood cancer
Human disease
DOID:3637
childhood teratocarcinoma of the testis
class of disease
childhood testicular mixed germ cell tumor
Human disease
DOID:6474
childhood teratoma of the ovary
class of disease
ovarian germ cell teratoma
pediatric ovarian germ cell tumor
Human disease
DOID:6230
childhood testicular mixed germ cell tumor
class of disease
mixed testicular germ cell tumor
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
pediatric testicular germ cell tumor
Human disease
DOID:6161
childhood type dermatomyositis
class of disease
dermatomyositis
Human disease
DOID:14203
childhood vagina botryoid rhabdomyosarcoma
class of disease
vagina botryoid rhabdomyosarcoma
childhood botryoid rhabdomyosarcoma
Human disease
DOID:6787
chloramine T respiratory allergy
class of disease
metal allergy
respiratory allergy
respiratory allergy that has allergic trigger chloramine T
DOID:0040062
chlorhexidine allergy
class of disease
drug allergy
drug allergy that has allergic trigger chlorhexidine
DOID:0040026
cholangiocarcinoma
class of disease
bile duct adenocarcinoma
disease
bile duct adenocarcinoma that has material basis in bile duct epithelial cells.
DOID:4947
C04.557.470.200.025.450
Cholangiocarcinoma
cholangiolocellular carcinoma
class of disease
intrahepatic cholangiocarcinoma
rare parenchymal liver disease
Human disease
DOID:7642
cholecystitis
class of disease
symptom or sign
ascending cholangitis
disease
cholangitis that is characterized by an inflammation that is located in the gallbladder
DOID:1949
C06.130.564.263
Cholecystitis
cholecystolithiasis
class of disease
gallbladder disease
gallstone
Human disease
DOID:11151
C06.130.409.178
C06.130.564.332
choledochal cyst
class of disease
bile duct disease
disease
congenital disorder of digestive system
DOID:899
C04.182.198
C06.130.120.127
C06.198.184
C16.131.314.184
Choledochal cysts
choledocholithiasis
class of disease
gallbladder disease
common bile duct disease
endocrine system disease
disease
Human disease
DOID:11755
C06.130.120.250.174
C06.130.409.267
Choledocholithiasis
cholelithiasis
class of disease
gallbladder disease
disease
Human disease
DOID:10211
C06.130.409
Cholelithiasis
cholestasis
class of disease
bile duct disease
disease
Human disease
DOID:13580
C06.130.120.135
Cholestasis
cholesteatoma
class of disease
keratosis
disease
keratosis characterized by keratinizing squamous epithelium located in middle ear and/or mastoid, subepithelial connective tissue and by the progressive accumulation of keratin debris with or without surrounding inflammatory reaction
DOID:869
C17.800.428.260
Cholesteatoma
cholesterol embolism
class of disease
vascular disease
embolism
vascular disease with blood vessel obstruction resulting from the release of cholesterol
DOID:1461
C14.907.355.350.454.500
Cholesterol embolism
choline deficiency disease
class of disease
nutritional deficiency disease
Human disease
DOID:8456
C18.654.521.500.133.699.160
cholinergic urticaria
class of disease
physical urticaria
disease
urticaria induced by sweating
DOID:14443
chondroblastic osteosarcoma
class of disease
osteosarcoma
Human disease
DOID:3372
chondroblastoma
class of disease
connective tissue neoplasm
connective tissue benign neoplasm
benign neoplasms by histologic type
disease
Human disease
DOID:2649
C04.557.450.565.250
Chondroblastoma
chondrodysplasia with joint dislocations gPAPP type
class of disease
autosomal recessive disease
osteochondrodysplasia
human disease
DOID:0112224
chondroid chordoma
class of disease
chordoma
chordoma that histologically derives from chordoma, derives from chondroma, and derives from chondrosarcoma
DOID:4152
chondroid lipoma
class of disease
lipoma
lipoma that is a deep-seated, firm, yellow tumors that characteristically occur on the legs of women
DOID:10208
chondroid syringoma of the vulva
class of disease
eccrine mixed tumor of skin
vulvar benign neoplasm
Human disease
DOID:2078
chondroma
class of disease
benign neoplasms by histologic type
cartilage tumor
disease
cell type benign neoplasm that is a cartilaginous tumor encapsulated with a lobular growing pattern
DOID:2602
C04.557.450.565.265
Chondroma
chondromalacia
class of disease
articular cartilage disease
DOID:2557
chondropathy
class of disease
osteochondropathy
connective tissue disease
disease
human disease
DOID:1222
C05.182
C17.300.182
Chondropathies
chordoid meningioma
class of disease
clear cell meningioma
Human disease
DOID:8368
chordoma
class of disease
notochordal cancer
disease
notochordal cancer that derives from cellular remnants of the notochord
DOID:3302
C04.557.465.220
Chordoma
chorea gravidarum
class of disease
choreatic disease
complications of pregnancy
disease
Human disease
DOID:14483
C10.228.140.079.294
C10.228.662.262.249.500
C13.703.141
chorioamnionitis
class of disease
placenta disease
disease
placenta disease that is an inflammation of the fetal membranes (amnion and chorion) due to a bacterial infection
DOID:0050697
C13.703.277.030
C13.703.420.339.260
C13.703.590.268
C16.300.030
Chorioamnionitis
chorioangioma
class of disease
placenta disease
uterine benign neoplasm
hemangioma
Human disease
DOID:277
Chorangioma
choriocarcinoma
class of disease
placenta cancer
trophoblastic neoplasm
disease
Human disease
DOID:3594
C04.557.465.955.207
C04.557.470.200.025.455
C04.850.908.208
C13.703.720.949.208
Choriocarcinoma
choriocarcinoma of ovary
class of disease
malignant ovarian germ cell neoplasm
non-gestational choriocarcinoma
choriocarcinoma
Human disease
DOID:5550
choriocarcinoma of the testis
class of disease
non-gestational choriocarcinoma
testicular non-seminomatous germ cell cancer
choriocarcinoma
Human disease
DOID:5551
chorioretinal scar
class of disease
retinal disease
scar
Human disease
DOID:11086
chorioretinitis
class of disease
symptom or sign
eye disease
uveitis
disease
inflammation of the choroid
DOID:8886
C11.768.773.348
C11.941.160.478.400
C11.941.879.780.900.300.318
Chorioretinitis
choroid cancer
class of disease
uveal cancer
choroid neoplasm
choroid disease
Human disease
DOID:12759
choroid disease
class of disease
uveal disease
human disease
DOID:1417
C11.941.160
choroid plexus carcinoma
class of disease
choroid plexus neoplasm
carcinoma
choroid plexus cancer that has material basis in epithelial cells of the choroid plexus
DOID:5648
Choroid plexus carcinoma
choroid plexus meningioma
class of disease
choroid plexus neoplasm
meningioma
cerebral meningioma
Human disease
DOID:4584
choroid plexus neoplasm
class of disease
cerebral ventricle neoplasm
cerebral ventricle cancer
cerebral ventricle neoplasm that is located in the plexus located in the ventricles of the brain
DOID:3540
C04.588.614.250.195.205.200
C10.228.140.211.280.300
C10.551.240.250.200.200
Choroid plexus cancers
choroid plexus papilloma
class of disease
papilloma
choroid plexus neoplasm
cerebrovascular benign neoplasm
Benign brain tumor
DOID:2626
C04.588.614.250.195.205.200.500
C10.228.140.211.280.300.500
C10.551.240.250.200.200.500
Choroid plexus papilloma
choroidal sclerosis
class of disease
eye degenerative disease
choroid disease
neurodegenerative disease that involves the optic choroid
DOID:980
choroiditis
class of disease
choroid disease
uveitis
inflammation of the choroid
DOID:11406
C11.941.160.478
C11.941.879.780.900.300
chromium allergic contact dermatitis
class of disease
allergic contact dermatitis
metal allergy
allergic contact dermatitis that has allergic trigger chromium atom
DOID:0040056
chromophobe renal cell carcinoma
class of disease
renal cell carcinoma
renal cell carcinoma that has material basis in chromophobe cell that appear pale when viewed under microscope, but that are larger and display different features than clear cells
DOID:4471
Chromophobe renal cell carcinoma
chromosomal deletion syndrome
class of disease
chromosomal disease
Human disease
DOID:0060388
C23.550.210.050.500.500
G05.365.590.029.530.175
G05.365.590.175.050.500.500
G05.365.590.762.180
G05.558.800.180
G05.700.131.500.500
Chromosome deletion
chromosomal duplication syndrome
class of disease
chromosomal disease
Human disease
DOID:0060429
C23.550.210.182
chromosome 10q23 deletion syndrome
class of disease
chromosomal deletion syndrome
partial monosomy of the long arm of chromosome 10
Human disease
DOID:0060389
chromosome 13q14 deletion syndrome
class of disease
chromosomal deletion syndrome
autosomal dominant disease
Human disease
DOID:0060391
chromosome 17p13.1 deletion syndrome
class of disease
chromosomal deletion syndrome
classical lissencephalies and subcortical band heterotopias
autosomal dominant disease
partial monosomy of the short arm of chromosome 17
Human disease
DOID:0060402
chromosome 18p deletion syndrome
class of disease
chromosomal deletion syndrome
autosomal dominant disease
human disease
DOID:0060406
chromosome 18q deletion syndrome
class of disease
chromosomal deletion syndrome
partial deletion of the long arm of chromosome 18
autosomal dominant disease
human disease
DOID:0060407
Distal 18q-
chromosome 19p13.13 deletion syndrome
class of disease
chromosomal deletion syndrome
autosomal dominant disease
partial deletion of the short arm of chromosome 19
Human disease
DOID:0060426
chromosome 1q41-q42 deletion syndrome
class of disease
chromosomal deletion syndrome
Human disease
DOID:0060412
chromosome 3-linked frontotemporal dementia
class of disease
frontotemporal dementia
A frontotemporal dementia that has material basis in heterozygous mutation in CHMP2B on 3p11.2.
DOID:0111227
chromosome Xp11.22 duplication syndrome
class of disease
partial duplication of the short arm of chromosome X
non-syndromic X-linked intellectual disability
human disease
DOID:0112037
chronic NK-cell lymphocytosis
class of disease
type IV hypersensitivity
mature T-cell neoplasm
Human disease
DOID:7465
chronic apical periodontitis
class of disease
periapical periodontitis
Human disease
DOID:11269
chronic asthma
class of disease
asthma
human disease
DOID:0080809
chronic atticoantral disease
class of disease
chronic purulent otitis media
Human disease
DOID:14248
chronic cervicitis
class of disease
cervicitis
Human disease
DOID:1513
chronic cholangitis
class of disease
ascending cholangitis
Human disease
DOID:9439
chronic closed-angle glaucoma
class of disease
primary angle-closure glaucoma
Human disease
DOID:14445
chronic conjunctivitis
class of disease
conjunctivitis
Human disease
DOID:2475
chronic cystitis
class of disease
cystitis
chronic condition
Recurrent infections of the urinary bladder
DOID:1680
Chronic cystitis
chronic dacryoadenitis
class of disease
dacryoadenitis
Human disease
DOID:949
chronic dacryocystitis
class of disease
chronic inflammation of lacrimal passage
dacryocystitis
Human disease
DOID:9937
chronic duodenal ileus
class of disease
duodenal obstruction
Human disease
DOID:13687
chronic eosinophilic leukemia
class of disease
chronic leukemia
eosinophilic leukemia
human disease
DOID:0080367
chronic ethmoiditis
class of disease
ethmoid sinusitis
chronic rhinosinusitis
ethmoid sinusitis which lasts for 12 weeks or more
DOID:9312
chronic eustachian salpingitis
class of disease
otosalpingitis
otosalpingitis which is persistent and long-lasting
DOID:1999
chronic fatigue syndrome
class of disease
symptom or sign
syndrome
primary immunodeficiency disease
disease
medical condition involving extreme fatigue and a wide range of other symptoms
DOID:8544
C02.330
C05.651.310
C10.228.440.600
C10.668.364
chronic follicular conjunctivitis
class of disease
chronic conjunctivitis
Human disease
DOID:13326
chronic frontal sinusitis
class of disease
frontal sinusitis
chronic condition
frontal sinusitis which lasts for 12 weeks or more. This causes steady headache, localized tenderness and intermittent, purulent nasal and postnasal drainage.
DOID:10790
chronic fungal otitis externa
class of disease
otomycosis
fungal infectious disease
otomycosis which is persistent and long-lasting or recurrent
DOID:10519
chronic gastritis
class of disease
gastritis
stomach disease
Inflammation of the stomach that is chronic in nature
DOID:4029
chronic gonococcal salpingitis
class of disease
chronic salpingitis
gonococcal infectious diseases
Human disease
DOID:12718
chronic gonorrhea of cervix
class of disease
chronic cervicitis
gonococcal infectious diseases
Human disease
DOID:1512
chronic inducible urticaria
class of disease
chronic urticaria
human disease
DOID:0080748
C17.800.862.945.533.500
C20.543.480.904.533.500
C23.550.291.500.360.500
chronic inflammation of lacrimal passage
class of disease
chronic inflammatory response
lacrimal apparatus disease
Human disease
DOID:9935
chronic inflammatory demyelinating polyneuritis
class of disease
inflammatory and toxic neuropathy
chronic inflammatory demyelinating polyradiculoneuropathy
demyelinating polyneuropathy
An immunologic inflammatory disorder characterized by loss of myelin in the peripheral nerves. Patients present with progressive weakness and loss of sensory function in the legs and arms.
DOID:2536
chronic interstitial cystitis
class of disease
interstitial cystitis
chronic cystitis
human disease
DOID:1678
chronic intestinal vascular insufficiency
class of disease
intestinal disease
Human disease
DOID:8633
chronic lacrimal gland enlargement
class of disease
dacryoadenitis
Human disease
DOID:12809
chronic laryngitis
class of disease
laryngitis
A laryngitis in which symptoms last longer than three weeks. Gastroesophageal reflux, and lingering bronchitis can cause the disease.
DOID:11797
chronic leukemia
class of disease
leukemia
broad type of leukemia; disjoint with acute leukemia
DOID:1036
Chronic leukemias
chronic lymphocytic leukemia
class of disease
symptom or sign
lymphoblastic leukemia
chronic leukemia
small lymphocytic lymphoma
lymphoma
leukemia
disease
lymphoblastic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood
DOID:1040
C04.557.337.428.080.125
C15.604.515.560.080.125
C20.683.515.528.080.125
C15.378.508.428.080.125
C23.550.291.500.483
Chronic lymphocytic leukemia
chronic lymphocytic leukemia and small lymphocytic lymphoma
class of disease
chronic lymphocytic leukemia
chronic lymphocytic leukemia that is characterized by the presence of immature lymphocytes in the blood and bone marrow and/or in the lymph nodes
DOID:6354
chronic maxillary sinusitis
class of disease
maxillary sinusitis
chronic condition
maxillary sinusitis which lasts for 12 weeks or more
DOID:10792
chronic meningitis
class of disease
meningitis
Human disease
DOID:10341
chronic metabolic polyneuropathy
class of disease
chronic polyneuropathy
Human disease
DOID:7441
chronic monocytic leukemia
class of disease
monocytic leukemia
chronic myelomonocytic leukemia
human disease
DOID:8593
chronic myeloid leukemia
class of disease
myeloid leukemia
chronic leukemia
disease
myeloid leukemia that is characterized by over production of white blood cells
DOID:8552
C04.557.337.539.250
C15.378.190.636.370
Chronic myeloid leukemia
chronic myelomonocytic leukemia
class of disease
monocytic leukemia
chronic myeloid leukemia
chronic leukemia
chronic leukemia characterized by monocytosis, increased monocytes in the bone marrow, variable degrees of dysplasia, but an absence of immature granulocytes in the blood
DOID:0080188
C04.557.337.539.522
C15.378.190.615.510
C15.378.508.539.522
C23.550.291.500.495
Chronic myelomonocytic leukemia
chronic neutrophilic leukemia
class of disease
myeloproliferative disorders
chronic leukemia
chronic leukemia characterized by neutrophilic leukocytosis with no detectable Philadelphia chromosome or BCR/ABL fusion gene
DOID:0080187
C15.378.190.636.380
chronic obstructive pulmonary disease
class of disease
obstructive lung disease
disease
lung disease involving long-term poor airflow
DOID:3083
C08.381.495.389
C23.550.291.500.875
Chronic obstructive pulmonary disease
chronic orbital inflammation
class of disease
orbital disease
chronic inflammatory response
Human disease
DOID:1397
chronic perichondritis of pinna
class of disease
perichondritis of auricle
pinna disease
perichondritis of auricle which is persistent and long-lasting
DOID:14243
chronic polyneuropathy
class of disease
polyneuropathy
Human disease
DOID:5221
chronic pulmonary eosinophilia
class of disease
eosinophilic pneumonia
An eosinophilic pneumonia which slowly progresses over weeks to months. Life-threatening shortness of breath can develop if the condition is not treated. Individuals are often diagnosed with asthma before the advent of this disease.
DOID:9502
chronic pulmonary heart disease
class of disease
cor pulmonale
Human disease
DOID:12326
chronic purulent otitis media
class of disease
suppurative otitis media
chronic otitis media
suppurative otitis media which is persistent and long-lasting
DOID:14247
chronic pyelonephritis
class of disease
pyelonephritis
Human disease
DOID:1076
Chronic pyelonephritis
chronic rapidly progressive glomerulonephritis
class of disease
glomerulonephritis
rapidly progressive glomerulonephritis
Human disease
DOID:11036
chronic rheumatic pericarditis
class of disease
pericarditis
rheumatic heart disease
human disease
DOID:1869
DOID:14044
chronic salpingitis
class of disease
salpingitis
Human disease
DOID:5731
chronic salpingo-oophoritis
class of disease
salpingo-oophoritis
Human disease
DOID:12265
chronic sphenoidal sinusitis
class of disease
sphenoid sinusitis
chronic condition
sphenoid sinusitis which lasts for 12 weeks or more
DOID:10793
chronic spontaneous urticaria
class of disease
chronic urticaria
idiopathic urticaria
human disease
DOID:0080749
Chronic spontaneous urticaria
chronic subinvolution of uterus
class of disease
uterine disease
Human disease
DOID:13811
chronic toxic polyneuropathy
class of disease
chronic polyneuropathy
Human disease
DOID:7825
chronic tubotympanic suppurative otitis media
class of disease
chronic purulent otitis media
suppurative otitis media
Human disease
DOID:14435
chronic tympanitis
class of disease
tympanic membrane disease
myringitis
Human disease
DOID:11217
chronic ulcer of skin
class of disease
symptom or sign
skin disease
ulcer
human disease
DOID:8549
chronic urticaria
class of disease
urticaria
urticaria with symptoms lasting for more than 6 weeks
DOID:0080747
C17.800.862.945.533
C20.543.480.904.533
chronic venous insufficiency
class of disease
venous insufficiency
disease
Human disease
DOID:0050853
Chronic venous insufficiency
chronic wasting disease
class of disease
animal disease
transmissible spongiform encephalopathy
animal disease
DOID:3530
C10.228.228.800.858
C10.574.843.925
C22.955
C01.207.800.858
Chronic wasting disease
chylocele of tunica vaginalis
class of disease
male reproductive system disease
Human disease
DOID:10835
cicatricial ectropion
class of disease
ectropion
Human disease
DOID:12782
cicatricial entropion
class of disease
entropion
Human disease
DOID:13113
cicatricial lagophthalmos
class of disease
lagophthalmos
Human disease
DOID:13038
cicatricial pemphigoid
class of disease
bullous skin disease
pemphigoid
eye inflammation
autoimmune disease of musculoskeletal system
autoimmune blistering disease
DOID:11656
C11.187.482
C17.800.865.670
ciliary body cancer
class of disease
iris cancer
ciliary body neoplasm
ciliary body disease
Human disease
DOID:4352
ciliary body disease
class of disease
iris disease
Human disease
DOID:4353
citrullinemia type I
class of disease
citrullinemia
medical condition
DOID:0070340
classic congenital mesoblastic nephroma
class of disease
congenital mesoblastic nephroma
Human disease
DOID:8083
classic pulmonary blastoma
class of disease
pulmonary blastoma
Human disease
DOID:4767
classic type lipoma
class of disease
lipoma
Human disease
DOID:10193
classic variant of chromophobe renal cell carcinoma
class of disease
chromophobe renal cell carcinoma
Human disease
DOID:6605
clear cell acanthoma
class of disease
skin benign neoplasm
acanthoma
Human disease
DOID:172
clear cell adenocarcinoma
class of disease
adenocarcinoma
clear cell carcinoma
adenocarcinoma that derives from epithelial cells which have clear cytoplasm
DOID:4468
C04.557.470.200.025.045
clear cell adenofibroma
class of disease
adenofibroma
benign neoplasm characterized by the presence of glandular structures which contain clear cells and a fibrotic stroma
DOID:5477
clear cell adenoma
class of disease
adenoma
adenoma that is composed of cells with a clear cytoplasm located in ovary
DOID:5390
clear cell basal cell carcinoma
class of disease
basal-cell carcinoma
Human disease
DOID:4293
clear cell carcinoma
class of disease
carcinoma
connective tissue benign neoplasm
clear-cell tumor
sarcoma
carcinoma (i.e. not a sarcoma) showing clear cells
DOID:4233
clear cell chondrosarcoma
class of disease
chondrosarcoma
Human disease
DOID:5867
C04.557.450.565.280.140
C04.557.450.795.300.140
clear cell cystadenofibroma
class of disease
cystadenofibroma
clear cell adenofibroma
benign neoplasm characterized by the presence of cystic glandular and fibrous tissues and clear cells
DOID:5895
clear cell ependymoma
class of disease
benign ependymoma
ependymoma, often supratentorial in location, characterized by the presence of ependymal cells with a perinuclear halo
DOID:5507
clear cell hidradenoma
class of disease
hidradenoma
clear cell adenoma
Human disease
DOID:5443
clear cell meningioma
class of disease
meningioma
Human disease
DOID:4210
clear cell squamous cell skin carcinoma
class of disease
cutaneous squamous-cell carcinoma
clear cell carcinoma
keratinizing squamous cell carcinoma
Human disease
DOID:8288
clear cell variant infiltrating bladder urothelial carcinoma
class of disease
invasive bladder transitional cell carcinoma
Human disease
DOID:6476
clear-cell ovarian carcinoma
class of disease
ovarian carcinoma
clear cell carcinoma
ovarian clear cell tumor
ovarian carcinoma that has material basis in cells with clear cytoplasm and glycogen secreting hob nail cells
DOID:0050934
DOID:5305
Clear-cell ovarian carcinoma
cleft lip
class of disease
lip disease
cleft lip and cleft palate
human disease
DOID:9296
C07.465.409.225
C07.465.525.164
C07.650.525.164
C16.131.850.525.164
cleft palate
class of disease
cleft lip and cleft palate
orofacial cleft characterized by a fissure of the soft and/or hard palate, due to faulty fusion of the two plates of the skull that form the hard palate
DOID:674
C05.500.460.185
C05.660.207.540.460.185
C07.320.440.185
C07.465.525.185
C07.650.500.460.185
C07.650.525.185
C16.131.621.207.540.460.185
C16.131.850.500.460.185
C16.131.850.525.185
Cleft palate
cleft soft palate
class of disease
cleft palate
Cleft velum is a fissure type embryopathy that affects in varying degrees the soft palate
DOID:0110214
clitoris cancer
class of disease
clitoris neoplasm
human disease
DOID:2401
cloacogenic carcinoma
class of disease
anal squamous cell carcinoma
anal canal carcinoma
Human disease
DOID:7173
co-trimoxazole allergy
class of disease
drug allergy
drug allergy that has allergic trigger co-trimoxazole
DOID:0040070
cobalt allergic asthma
class of disease
allergic asthma
cobalt allergy
metal allergy
allergic asthma that has allergic trigger cobalt atom
DOID:0040054
cobalt allergic contact dermatitis
class of disease
allergic contact dermatitis
cobalt allergy
metal allergy
allergic contact dermatitis that has allergic trigger cobalt atom
DOID:0040053
cobblestone retinal degeneration
class of disease
peripheral retinal degeneration
Human disease
DOID:12166
cocaine dependence
class of disease
cocaine-related disorder
substance dependence
substance abuse
disease
drug dependence that is a psychological dependency on the regular use of cocaine
DOID:9975
DOID:809
coccidioidomycosis
class of disease
primary systemic mycosis
disease
fungal infection
DOID:13450
C01.150.703.203
Coccidioidomycosis
coenurosis
class of disease
parasitic helminthiasis infectious disease
Coenurosis
skin disease
central nervous system disease
Human disease
DOID:0050251
cognitive disorder
class of disease
mental disorder
organic brain syndrome
disease of mental health that affects cognitive functions including memory processing, perception and problem solving
DOID:1561
F03.615.250
Neurocognitive disorders
cold-induced sweating syndrome 1
class of disease
cold-induced sweating syndrome
human disease
DOID:0080329
cold-induced sweating syndrome 2
class of disease
cold-induced sweating syndrome
cold-induced sweating syndrome that has material basis in compound heterozygous mutation in the CLCF1 gene on chromosome 11q13
DOID:0080330
cold-induced sweating syndrome 3; CISS3
class of disease
cold-induced sweating syndrome
human disease
DOID:0080331
colitis
class of disease
inflammatory bowel diseases
colonic disease
disease
inflammation of the colon or the large intestine
DOID:0060180
C06.405.205.265
C06.405.469.158.188
Colitis
collagen disease
class of disease
connective tissue disease
group of diseases affecting connective tissue
DOID:854
C17.300.200
Collagen diseases
collagenous colitis
class of disease
microscopic colitis
disease
colitis characterized by a distinctive thickening of the subepithelial collagen table
DOID:0060183
C06.405.205.265.173.500
C06.405.469.158.188.173.500
Collagenous colitis
colloid adenoma
class of disease
follicular adenoma
Human disease
DOID:8419
colloid carcinoma of the pancreas
class of disease
pancreatic carcinoma
Human disease
DOID:7717
coloboma of optic nerve
class of disease
coloboma
optic nerve disease
visual pathway disease
rare defect of the optic nerve that causes moderate to severe visual field defects.
DOID:11975
colon adenocarcinoma
class of disease
colon carcinoma
adenocarcinoma
colon carcinoma that derives from epithelial cells of glandular origin
DOID:234
colon adenoma
class of disease
colonic benign neoplasm
benign neoplasms by histologic type
colorectal adenoma
adenoma
colonic benign neoplasm that has material basis in epithelial tissue with glandular origin
DOID:0050912
colon carcinoma
class of disease
plump cancer
carcinoma
colon cancer that has material basis in abnormally proliferating cells derives_from epithelial cells
DOID:1520
colon leiomyoma
class of disease
leiomyoma
colonic benign neoplasm
colonic disease
Human disease
DOID:10656
Colonic leiomyoma
colon lymphoma
class of disease
plump cancer
lymphoma
colorectal lymphoma
Human disease
DOID:1523
colon signet ring adenocarcinoma
class of disease
colon adenocarcinoma
Human disease
DOID:3033
colonic benign neoplasm
class of disease
intestinal benign neoplasm
colonic neoplasm
lymphangioma
colonic disease
intestinal benign neoplasm that is located in the colon
DOID:235
colonic disease
class of disease
intestinal disease
pathological processes in the colon or large intestine
DOID:5353
C06.405.469.158
Diseases and disorders of colon
colonic lymphangioma
class of disease
colonic benign neoplasm
Human disease
DOID:10657
color agnosia
class of disease
agnosia
visual agnosia
agnosia that is a loss of the ability to recognize a color, while being able to perceive or distinguish it
DOID:0060139
color blindness
class of disease
vision disorder
colour vision deficiency
blindness
disease
inability or decreased ability to see colour, or perceive colour differences, under normal lighting conditions
DOID:13399
C10.597.751.941.256
C11.966.256
C23.888.592.763.941.256
C11.270.151.500
Color blindness
colorectal adenocarcinoma
class of disease
colorectal carcinoma
adenocarcinoma
colorectal cancer that derives from epithelial cells of glandular origin
DOID:0050861
Colorectal adenocarcinoma
colorectal adenoma
class of disease
colonic benign neoplasm
gastrointestinal adenoma
colorectal polyp
intestinal benign neoplasm
adenoma
human disease
DOID:0050860
C04.557.470.035.215
colorectal cancer
class of disease
colorectal neoplasm
large intestine cancer
disease
cancer of the colon or rectum
DOID:9256
Colorectal cancer
colorectal carcinoma
class of disease
colorectal cancer
carcinoma
colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa
DOID:0080199
columnar cell variant papillary carcinoma
class of disease
papillary thyroid cancer
Human disease
DOID:7088
combat disorder
class of disease
acute stress disorder
post-traumatic stress disorder
disease
acute stress disorder that involves neurotic reactions to unusual, severe, or overwhelming military stress
DOID:6950
F03.950.750.249
Combat stress reaction
combined T cell and B cell immunodeficiency
class of disease
combined immunodeficiency
human disease
DOID:628
combined cellular and humoral immune defects with granulomas
class of disease
autosomal recessive disease
combined immunodeficiency
human disease
DOID:0112253
combined oxidative phosphorylation deficiency 10
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111480
combined oxidative phosphorylation deficiency 11
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111481
combined oxidative phosphorylation deficiency 13
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111467
combined oxidative phosphorylation deficiency 14
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111477
combined oxidative phosphorylation deficiency 15
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111491
combined oxidative phosphorylation deficiency 16
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111469
combined oxidative phosphorylation deficiency 17
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111496
combined oxidative phosphorylation deficiency 18
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111484
combined oxidative phosphorylation deficiency 19
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111476
combined oxidative phosphorylation deficiency 2
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111483
combined oxidative phosphorylation deficiency 20
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111478
combined oxidative phosphorylation deficiency 21
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111465
combined oxidative phosphorylation deficiency 22
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111498
combined oxidative phosphorylation deficiency 23
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111500
combined oxidative phosphorylation deficiency 24
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111485
combined oxidative phosphorylation deficiency 27
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111489
combined oxidative phosphorylation deficiency 3
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111486
combined oxidative phosphorylation deficiency 31
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111488
combined oxidative phosphorylation deficiency 32
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111492
combined oxidative phosphorylation deficiency 33
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
DOID:0111495
combined oxidative phosphorylation deficiency 34
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111497
combined oxidative phosphorylation deficiency 35
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111464
combined oxidative phosphorylation deficiency 36
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111482
combined oxidative phosphorylation deficiency 37
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111499
combined oxidative phosphorylation deficiency 38
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111466
combined oxidative phosphorylation deficiency 39
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111475
combined oxidative phosphorylation deficiency 4
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111494
combined oxidative phosphorylation deficiency 40
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0112117
combined oxidative phosphorylation deficiency 41
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0112119
combined oxidative phosphorylation deficiency 42
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0112118
combined oxidative phosphorylation deficiency 43
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0112116
combined oxidative phosphorylation deficiency 45
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0112113
combined oxidative phosphorylation deficiency 46
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0112115
combined oxidative phosphorylation deficiency 47
class of disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0112114
combined oxidative phosphorylation deficiency 48
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0112112
combined oxidative phosphorylation deficiency 49
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0112110
combined oxidative phosphorylation deficiency 5
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111473
combined oxidative phosphorylation deficiency 50
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0112111
combined oxidative phosphorylation deficiency 51
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0112137
combined oxidative phosphorylation deficiency 6
class of disease
combined oxidative phosphorylation deficiency
X-linked recessive disease
human disease
DOID:0111502
combined oxidative phosphorylation deficiency 7
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111487
combined oxidative phosphorylation deficiency 8
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111479
combined oxidative phosphorylation deficiency 9
class of disease
autosomal recessive disease
combined oxidative phosphorylation deficiency
human disease
DOID:0111472
combined thymoma
class of disease
thymoma
Human disease
DOID:3281
comedocarcinoma
class of disease
intraductal carcinoma
disease
carcinoma that is in situ
DOID:5670
commensal Klebsiella infectious disease
class of disease
klebsiellosis
Human disease
DOID:0050479
commensal bacterial infectious disease
class of disease
bacterial infectious disease
Human disease
DOID:0050339
common bile duct disease
class of disease
bile duct disease
Human disease
DOID:4137
C06.130.120.250
common bile duct neoplasm
class of disease
biliary tract neoplasm
common bile duct disease
human disease
DOID:4608
C04.588.274.120.250.250
C06.130.120.120.280
C06.130.120.250.280
C06.130.320.120.280
C06.301.120.250.250
common peroneal nerve lesion
class of disease
mononeuritis of lower limb
Human disease
DOID:12527
common wart
class of disease
viral infectious disease
wart
viral infectious disease that results in infection located in skin, has material basis in human papillomavirus (types 2 and 4)
DOID:11165
Verruca vulgaris
communicating hydrocephalus
class of disease
hydrocephalus
abnormal accumulation of cerebrospinal fluid within the ventricles of the brain that occurs as a consequence of impaired cerebrospinal fluid reabsorption by the arachnoid granulations
DOID:1573
compartment syndrome
class of disease
ischemia
disease
condition in which increased pressure within one of the body's compartments results in insufficient blood supply to tissue within that space
DOID:682
C05.651.180
C14.907.303
Compartment syndrome
complement component 5 deficiency
class of disease
complement deficiency
Human disease
DOID:8158
complement component 6 deficiency
class of disease
complement deficiency
Human disease
DOID:0060299
complement component 7 deficiency
class of disease
complement deficiency
Human disease
DOID:0060300
complement deficiency
class of disease
primary immunodeficiency disease
metabolic disease
primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation
DOID:626
Complement deficiencies
complete generalized lipodystrophy
class of disease
lipodystrophy
lipodystrophy that is characterized by complete loss of adipose tissue
DOID:0080298
complex cortical dysplasia with other brain malformations
class of disease
encephalopathy
autosomal dominant disease
human disease
DOID:0090131
complex partial seizure
class of disease
symptom or sign
focal epilepsy
focal seizure
human disease
DOID:12382
C10.228.140.490.360.260
composite lymphoma
class of disease
B-cell lymphoma
lymphoma that begins in cells of the immune system in which different types of lymphoma cells occur at the same time
DOID:5820
C04.557.386.150
C04.557.435.295
C15.604.515.569.150
C20.683.515.761.150
conduct disorder
class of disease
specific developmental disorder
behavioral disorder
disease
specific developmental disorder marked by a pattern of repetitive behavior wherein the rights of others or social norms are violated
DOID:12995
F03.625.094.300
cone-rod dystrophy
class of disease
retinal degeneration
monogenic disease
retinal degeneration that characterized by progressive deterioration of the cone and rod photoreceptor cells
DOID:0050572
C11.270.152
C11.768.585.658.250
C16.320.290.152
cone-rod dystrophy 1
class of disease
cone-rod dystrophy
A cone-rod dystrophy that has material basis in variation in the chromosome region 18q21.1-q21.3.
DOID:0111009
cone-rod dystrophy 17
class of disease
cone-rod dystrophy
cone-rod dystrophy that has material basis in variation in the chromosome region 10q26
DOID:0111023
cone-rod dystrophy 8
class of disease
cone-rod dystrophy
cone-rod dystrophy that has material basis in variation in the chromosome region 1q12-q24
DOID:0111014
congenital Zika virus infection
class of disease
Zika virus infection
vertically transmitted infection
syndrome
infectious embryofetopathy
human disease
DOID:0080180
congenital aphakia
class of disease
lens disease
aphakia
Human disease
DOID:11367
congenital bile acid synthesis defect
class of disease
steroid inherited metabolic disorder
bile acid synthesis defect with cholestasis and malabsorption
congenital disorder
steroid inherited metabolic disorder characterized by abnormal conversion of cholesterol into bile acids which occurs predominantly in the liver
DOID:0050674
congenital chylothorax
class of disease
pleural disease
chylothorax
rare genetic respiratory disease
primary interstitial lung disease specific to childhood due to alveolar vascular disorder
pleural disease characterized by the accumulation of chyle within the pleural space leading to respiratory distress, malnutrition and immunological compromise, either immediately after birth or within the first few weeks of life
DOID:0060646
congenital diarrhea
class of disease
diarrhea
congenital disorder
diarrhea characterized by frequent loose or liquid bowel movements where the disease is present from birth
DOID:0060774
congenital disorder
class of disease
disease
condition present at birth regardless of cause; human disease or disorder developed prior to birth
DOID:0080015
DOID:0060035
C16
Congenital diseases and disorders
congenital disorder of glycosylation 1cc
class of disease
X-linked recessive disease
congenital disorder of glycosylation type I
human disease
DOID:0111839
congenital disorder of glycosylation type I
class of disease
congenital disorder of glycosylation
congenital disorder of glycosylation involve disrupted synthesis of the lipid-linked oligosaccharide precursor
DOID:0050570
congenital disorder of glycosylation type IIa
class of disease
congenital disorder of glycosylation type II
autosomal recessive disease
A congenital disorder of glycosylation type II that has material basis in an autosomal recessive mutation of MGAT2 on chromosome 14q21.3.
DOID:0070253
congenital disorder of glycosylation type IIq
class of disease
congenital disorder of glycosylation type II
autosomal recessive disease
A congenital disorder of glycosylation type II that has material basis in an autosomal recessive mutation of COG2 on chromosome 1q42.2.
DOID:0070269
congenital disorder of glycosylation type Ia
class of disease
congenital disorder of glycosylation type I
autosomal recessive disease
human disease
DOID:0080552
congenital dyserythropoietic anemia type I
class of disease
congenital dyserythropoietic anemia
Congenital dyserythropoietic anemiatype I (CDA I) is a hematologic disorder of erythropoiesis characterized by moderate to severe macrocytic anemia occasionally associated with limb or nail deformities and scoliosis
DOID:0111396
congenital dyserythropoietic anemia type II
class of disease
congenital dyserythropoietic anemia
autosomal recessive disease
medical condition
DOID:0111401
congenital dyserythropoietic anemia type III
class of disease
congenital dyserythropoietic anemia
medical condition
DOID:0111399
congenital dyserythropoietic anemia type IV
class of disease
congenital dyserythropoietic anemia
autosomal dominant disease
medical condition
DOID:0111400
congenital dyserythropoietic anemia type Ia
class of disease
autosomal recessive disease
congenital dyserythropoietic anemia type I
human disease
DOID:0111398
congenital dyserythropoietic anemia type Ib
class of disease
autosomal recessive disease
congenital dyserythropoietic anemia type I
human disease
DOID:0111397
congenital fiber-type disproportion
class of disease
congenital myopathy
Human disease
DOID:0080102
Congenital fiber type disproportion
congenital fibrosarcoma
class of disease
pediatric fibrosarcoma
Human disease
DOID:8418
congenital generalized lipodystrophy type 1
class of disease
congenital generalized lipodystrophy
A congenital generalized lipodystrophy that has material basis in an autosomal recessive mutation of AGPAT2 on chromosome 9q34.3.
DOID:0111135
congenital granular cell tumor
class of disease
mesenchymal cell neoplasm
Human disease
DOID:8303
congenital heart block
class of disease
congenital heart disease
genetic cardiac rhythm disease
atrioventricular block
heart conduction disease
atrioventricular block characterized by the presence of conduction system disease of any form, which is diagnosed on or before 28 days of life
DOID:990
congenital hemolytic anemia
class of disease
symptom or sign
hemolytic anemia
congenital anemia
Human disease
DOID:589
C15.378.071.141.150
C16.320.070
congenital hypogammaglobulinemia
class of disease
B cell deficiency
agammaglobulinemia
Human disease
DOID:14177
congenital hypoplastic anemia
class of disease
aplastic anemia
congenital anemia
congenital bone marrow failure syndromes
congenital disorder
Human disease
DOID:1342
C15.378.071.085.080
C15.378.190.223.500.500
C16.320.077
congenital hypothyroidism
class of disease
hypothyroidism
congenital disorder
hypothyroidism that is present at birth
DOID:0050328
C05.116.099.343.347
C05.116.132.256
C16.320.240.625
C19.297.155
C19.874.482.281
Congenital hypothyroidism
congenital intrinsic factor deficiency
class of disease
vitamin B12 deficiency
inborn disorder of cobalamin metabolism and transport
vitamin B12 deficiency anemia
congenital disorder
vitamin B12 deficiency that is characterized by megaloblastic anemia due to the absence of gastric intrinsic factor which results in abnormal vitamin B12 absorption
DOID:0050734
congenital lactase deficiency
class of disease
lactase deficiency
carbohydrate metabolic disorder
disorder of carbohydrate absorption and transport
congenital intestinal disease due to an enzymatic defect
metabolic disease with intestinal involvement
autosomal recessive disease
rare severe gastrointestinal disorder in newborns primarily reported in Finland
DOID:0111646
congenital limbs-face contractures-hypotonia-developmental delay syndrome
class of disease
syndrome
autosomal dominant disease
human disease
DOID:0081048
congenital megabladder
class of disease
bladder disease
autosomal dominant disease
Megacystis
human disease
DOID:0112014
congenital mesoblastic nephroma
class of disease
mesoblastic nephroma
kidney cancer
Human disease
DOID:4773
congenital muscular dystrophy
class of disease
muscular dystrophy
autosomal recessive disease
disease
human disease
DOID:0050557
congenital muscular dystrophy 1B
class of disease
congenital muscular dystrophy
genetic disease
autosomal recessive disease
congenital muscular dystrophy characterized by autosomal recessive inheritance of proximal muscle weakness, muscle hypertrophy, and early respiratory failure that has material basis in variation in the chromosome region 1q42
DOID:0110634
congenital muscular dystrophy merosin-positive
class of disease
congenital muscular dystrophy
genetic disease
autosomal recessive disease
human disease
DOID:0110638
congenital muscular dystrophy with cataracts and intellectual disability
class of disease
congenital muscular dystrophy
genetic disease
autosomal recessive disease
human disease
DOID:0080197
congenital muscular dystrophy-dystroglycanopathy A14
class of disease
congenital muscular dystrophy-dystroglycanopathy type A
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in in GMPPB on 3p21.31.
DOID:0111233
congenital muscular dystrophy-dystroglycanopathy A7
class of disease
congenital muscular dystrophy-dystroglycanopathy type A
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in ISPD on 7p21.2-p21.1.
DOID:0111234
congenital muscular dystrophy-dystroglycanopathy type A
class of disease
muscular dystrophy-dystroglycanopathy
muscular dystrophy-dystroglycanopathy characterized by cobblestone lissencephaly, muscle weakness, and brain and eye anomalies that has material basis in autosomal recessive inheritance a defect in alpha-dystroglycan post-translational processing
DOID:0111229
congenital muscular dystrophy-dystroglycanopathy type A1
class of disease
congenital muscular dystrophy-dystroglycanopathy type A
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMT1 on 9q34.13.
DOID:0111237
congenital muscular dystrophy-dystroglycanopathy type A10
class of disease
congenital muscular dystrophy-dystroglycanopathy type A
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in RXYLT1 on 12q14.2.
DOID:0111239
congenital muscular dystrophy-dystroglycanopathy type A11
class of disease
congenital muscular dystrophy-dystroglycanopathy type A
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in B3GALNT2 on 1q42.3.
DOID:0111230
congenital muscular dystrophy-dystroglycanopathy type A12
class of disease
congenital muscular dystrophy-dystroglycanopathy type A
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMK on 8p11.21.
DOID:0111235
congenital muscular dystrophy-dystroglycanopathy type A13
class of disease
congenital muscular dystrophy-dystroglycanopathy type A
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in B4GAT1 on 11q13.2.
DOID:0111238
congenital muscular dystrophy-dystroglycanopathy type A3
class of disease
congenital muscular dystrophy-dystroglycanopathy type A
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMGNT1 on 1p34.1.
DOID:0111236
congenital muscular dystrophy-dystroglycanopathy type A5
class of disease
congenital muscular dystrophy-dystroglycanopathy type A
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in FKRP on 19q13.32.
DOID:0111241
congenital muscular dystrophy-dystroglycanopathy type A6
class of disease
congenital muscular dystrophy-dystroglycanopathy type A
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in LARGE on 22q12.3.
DOID:0111242
congenital muscular dystrophy-dystroglycanopathy type A8
class of disease
congenital muscular dystrophy-dystroglycanopathy type A
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMGNT2 on 3p22.1.
DOID:0111231
congenital muscular dystrophy-dystroglycanopathy type A9
class of disease
congenital muscular dystrophy-dystroglycanopathy type A
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in DAG1 on 3p21.31.
DOID:0111232
congenital myasthenic syndrome 10
class of disease
congenital myasthenic syndrome
genetic disease
autosomal recessive disease
human disease
DOID:0110668
congenital myasthenic syndrome 1A
class of disease
congenital myasthenic syndrome
genetic disease
autosomal dominant disease
human disease
DOID:0110663
congenital nongoitrous hypothryoidism 1
class of disease
hypothyroidism, congenital, nongoitrous
genetic disease
autosomal recessive disease
congenital hypothyroidism that has material basis in mutation in the TSHR gene on chromosome 14q31
DOID:0070126
congenital nongoitrous hypothryoidism 2
class of disease
hypothyroidism, congenital, nongoitrous
congenital hypothyroidism due to developmental anomaly
congenital thyroid malformation without hypothyroidism
thyroid hormone resistance syndrome
genetic disease
autosomal dominant disease
congenital hypothyroidism that has material basis in heterozygous mutation in the PAX8 gene on chromosome 2q13
DOID:0070124
congenital nongoitrous hypothryoidism 3
class of disease
hypothyroidism, congenital, nongoitrous
genetic disease
autosomal dominant disease
A congenital hypothyroidism characterized by autosomal dominant inheritance of resistance to thyrotropin that has material basis in variation in the chromosome region 15q25.3-q26.1.
DOID:0070127
congenital nongoitrous hypothryoidism 4
class of disease
hypothyroidism, congenital, nongoitrous
genetic disease
autosomal recessive disease
congenital hypothyroidism characterized by a permanent thyroid deficiency present at birth and resulting from deficiency in TSH synthesis that has material basis in homozygous mutation in the TSHB gene on chromosome 1p13
DOID:0070123
congenital nongoitrous hypothryoidism 5
class of disease
hypothyroidism, congenital, nongoitrous
genetic disease
autosomal dominant disease
congenital hypothyroidism
congenital hypothyroidism that has material basis in heterozygous mutation in the NKX2-5 gene on chromosome 5q35
DOID:0070125
congenital nongoitrous hypothryoidism 6
class of disease
hypothyroidism, congenital, nongoitrous
genetic disease
autosomal dominant disease
A congenital hypothyroidism that has material basis in heterozygous mutation in the THRA gene on chromosome 17q21.1.
DOID:0070128
congenital nongoitrous hypothyroidism 7
class of disease
autosomal recessive disease
hypothyroidism, congenital, nongoitrous
human disease
DOID:0111836
congenital nongoitrous hypothyroidism 8
class of disease
autosomal dominant disease
hypothyroidism, congenital, nongoitrous
human disease
DOID:0111837
congenital nongoitrous hypothyroidism 9
class of disease
X-linked recessive disease
hypothyroidism, congenital, nongoitrous
human disease
DOID:0111835
congenital nystagmus 1
class of disease
autosomal genetic disease
congenital nystagmus
human disease
DOID:0111790
congenital nystagmus 2
class of disease
congenital nystagmus
autosomal dominant disease
human disease
DOID:0111792
congenital nystagmus 3
class of disease
autosomal dominant disease
congenital nystagmus
human disease
DOID:0111793
congenital nystagmus 4
class of disease
congenital nystagmus
autosomal dominant disease
human disease
DOID:0111794
congenital nystagmus 5
class of disease
X-linked dominant disease
congenital nystagmus
human disease
DOID:0111796
congenital nystagmus 6
class of disease
congenital nystagmus
human disease
DOID:0111795
congenital nystagmus 7
class of disease
autosomal dominant disease
congenital nystagmus
human disease
DOID:0111791
congenital ptosis
class of disease
ptosis
ptosis characterized by eyelid drop present at birth
DOID:0060261
congenital stationary night blindness
class of disease
hereditary night blindness
night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves
DOID:0050534
congenital stationary night blindness 1A
class of disease
congenital stationary night blindness
X-linked recessive disease
A congenital stationary night blindness that has material basis in mutation in the NYX gene on chromosome Xp11.4.
DOID:0110870
congenital stationary night blindness 2A
class of disease
congenital stationary night blindness
X-linked recessive disease
A congenital stationary night blindness that has material basis in mutation in the CACNA1F gene on chromosome Xp11.23.
DOID:0110871
congenital structural myopathy
class of disease
muscular disease
human disease
DOID:422
C05.651.575
C10.668.491.550
congenital symmetric circumferential skin creases 1
class of disease
autosomal dominant disease
human disease
DOID:0112242
congestive heart failure
class of disease
heart disease
heart failure
human disease
DOID:6000
conidiobolomycosis
class of disease
subcutaneous mycosis
Human disease
DOID:0050279
conjugate gaze palsy
class of disease
strabismus
disease
Human disease
DOID:12445
conjunctival cancer
class of disease
ocular cancer
conjunctival neoplasm
conjunctival disease
Human disease
DOID:5467
conjunctival concretion
class of disease
conjunctival deposit
Human disease
DOID:11988
conjunctival degeneration
class of disease
conjunctival disease
conjunctival degenerations and deposits
eye degenerative disease
Human disease
DOID:10139
conjunctival deposit
class of disease
conjunctival disease
conjunctival degenerations and deposits
Human disease
DOID:11653
conjunctival disease
class of disease
eye disease
Human disease
DOID:4251
C11.187
conjunctival folliculosis
class of disease
acute conjunctivitis
Human disease
DOID:11219
conjunctival pigmentation
class of disease
pigmentation disorder
Human disease
DOID:12304
conjunctival pterygium
class of disease
conjunctival degeneration
pterygium
human disease
DOID:10526
conjunctival vascular disease
class of disease
conjunctival disease
Human disease
DOID:10989
conjunctivochalasis
class of disease
conjunctival disease
Human disease
DOID:4250
Conjunctivochalasis
connective tissue benign neoplasm
class of disease
musculoskeletal system benign neoplasm
connective tissue disease
connective tissue neoplasm
musculoskeletal system benign neoplasm that is located in connective tissue
DOID:0060123
connective tissue disease
class of disease
musculoskeletal disorder
skin and connective tissue diseases
musculoskeletal system disease that affects tissues such as skin, tendons, and cartilage
DOID:65
C17.300
Connective tissue diseases
connective tissue neoplasm
class of disease
musculoskeletal system cancer
connective tissue disease
connective and soft tissue neoplasms
musculoskeletal system cancer that is located in connective tissue
DOID:201
C04.557.450.565
C17.300.680
constant exophthalmos
class of disease
orbital disease
exophthalmos
Human disease
DOID:9945
constipation
class of disease
symptom or sign
bowel dysfunction
clinical sign
feces and droppings symptom
disease
bowel dysfunction that is characterized by infrequent or difficult evacuation of feces
DOID:2089
C23.888.821.150
Constipation
constrictive pericarditis
class of disease
pericarditis
heart disorder in which the pericardial sac becomes thickened and fibrotic, tightening the myocardium and impeding the normal myocardial function
DOID:11481
C14.280.720.595
Constrictive pericarditis
contact blepharoconjunctivitis
class of disease
blepharoconjunctivitis
Human disease
DOID:13999
contact dermatitis
class of disease
dermatitis
eczema
disease
human disease
DOID:2773
C17.800.174.255
C17.800.815.255
Contact dermatitis
contact lens corneal edema
class of disease
corneal edema
Human disease
DOID:11034
conus medullaris neoplasm
class of disease
Spinal cord cancer
Human disease
DOID:3641
conventional angiosarcoma
class of disease
angiosarcoma
Human disease
DOID:4512
conventional central osteosarcoma
class of disease
bone osteosarcoma
Human disease
DOID:3378
conventional fibrosarcoma
class of disease
fibrosarcoma
Human disease
DOID:3517
conventional leiomyosarcoma
class of disease
leiomyosarcoma
Human disease
DOID:5253
conventional malignant hemangiopericytoma
class of disease
hemangiopericytoma
hemangiopericytoma, malignant
Human disease
DOID:6197
conversion disorder
class of disease
symptom or sign
somatoform disorder
functional neurologic disorder
disease
physical illness or symptoms caused by serious emotional stress
DOID:1768
F03.875.300
cor pulmonale
class of disease
congestive heart failure
disease
human disease
DOID:8515
C14.280.832
Pulmonary heart disease
core binding factor acute myeloid leukemia
class of disease
acute myeloid leukemia
human disease
DOID:0080796
cork-handlers' disease
class of disease
extrinsic allergic alveolitis
An extrinsic allergic alveolitis caused by inhalation of cork dust containing the antigens produced by the fungus Penicillium glabrum. The symptoms include dyspnea, wheezing cough, fever and asthenia.
DOID:840
cornea cancer
class of disease
ocular cancer
cornea neoplasm
corneal disease
Human disease
DOID:6199
cornea plana
class of disease
corneal disease
Human disease
DOID:0060287
cornea squamous cell carcinoma
class of disease
cornea cancer
squamous cell carcinoma
Human disease
DOID:13538
corneal abscess
class of disease
deep keratitis
Human disease
DOID:11543
corneal argyrosis
class of disease
corneal disease
argyria
Human disease
DOID:13447
corneal degeneration
class of disease
corneal disease
eye degenerative disease
Human disease
DOID:1237
corneal deposit
class of disease
corneal disease
Human disease
DOID:11547
corneal disease
class of disease
eye disease
human disease
DOID:10124
C11.204
Disorders of sclera and cornea
corneal dystrophy
class of disease
corneal disease
human disease
DOID:2566
C11.204.236
C11.270.162
C16.320.290.162
Corneal dystrophy
corneal ectasia
class of disease
corneal disease
Human disease
DOID:1436
corneal edema
class of disease
corneal disease
Human disease
DOID:11030
C11.204.267
corneal endothelial dystrophy
class of disease
corneal dystrophy
Human disease
DOID:0060443
corneal granular dystrophy
class of disease
epithelial-stromal TGFBI dystrophy
autosomal dominant disease
Human disease
DOID:12318
Granular corneal dystrophy
corneal neovascularization
class of disease
keratitis
neovascularization
Human disease
DOID:11382
C11.204.290
Corneal neovascularization
corneal opacification and other ocular anomalies
class of disease
sclerocornea
genetic disease
monogenic disease
eye disease
sclerocornea that has material basis in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25 and is characterized by corneal opacifiaction, cataract, microcornea, microphthalmia, and anterior segment dysgenesis
DOID:0060648
corneal staphyloma
class of disease
corneal disease
staphyloma
Human disease
DOID:12753
corneal ulcer
class of disease
symptom or sign
keratitis
corneal disease
eye ulceration
cornea symptom
disease
area of epithelial tissue loss from corneal surface; associated with inflammatory cells in the cornea and anterior chamber
DOID:8463
C01.539.375.177
C11.204.564.225
C11.294.177
Corneal ulcer
coronary aneurysm
class of disease
aneurysm
aneurysm of heart
coronary artery disease
Human disease
DOID:3362
C14.280.647.250.250
C14.907.055.395
C14.907.585.250.250
Coronary aneurysm
coronary artery anomaly
class of disease
coronary artery disease
vascular malformation
congenital heart disease
Human disease
DOID:11843
C14.240.400.210
C14.280.400.210
C16.131.240.400.210
Coronary artery anomalies
coronary artery disease
class of disease
artery disease
cardiovascular disease
disease
disease characterized by plaque building up in the arteries of the heart
DOID:3393
C14.280.647.250.260
C14.907.137.126.339
C14.907.585.250.260
Coronary artery disease
coronary artery vasospasm
class of disease
coronary artery disease
vasospasm
disease
Human disease
DOID:11840
C14.280.647.250.295
C14.907.585.250.295
coronary restenosis
class of disease
coronary stenosis
restenosis
Human disease
DOID:4247
C14.280.647.250.285.200
C14.907.585.250.285.200
coronary stenosis
class of disease
coronary artery disease
Human disease
DOID:4248
C14.280.647.250.285
C14.907.585.250.285
coronary thrombosis
class of disease
coronary artery disease
thrombosis
arterial thrombosis
disease
disease: formation of a blood clot inside a blood vessel of the heart, which clot may then restrict blood flow within the heart, leading to heart tissue damage, or a myocardial infarction, also known as a heart attack
DOID:11847
C14.280.647.250.290
C14.907.355.830.220
C14.907.585.250.290
Cardiac thrombosis
corpus callosum lipoma
class of disease
cerebral hemisphere lipoma
Human disease
DOID:6294
corpus callosum oligodendroglioma
class of disease
brain oligodendroglioma
oligodendroglioma
brain oligodendroglioma located in the corpus callosum
DOID:0050901
corpus luteum cyst
class of disease
ovarian cyst
human disease
DOID:13050
cortical deafness
class of disease
sensorineural hearing loss
agnosia
central auditory disease
auditory agnosia
agnosia that is a loss of the ability to perceive any auditory information but whose hearing is intact
DOID:0060140
cortical senile cataract
class of disease
senile cataract
human disease
DOID:13574
cortical thymoma
class of disease
dendritic cell thymoma
Human disease
DOID:6530
corticosteroid allergy
class of disease
drug allergy
steroids allergy
drug allergy that has allergic trigger corticosteroid
DOID:0040014
corticosterone methyloxidase deficiency 1
class of disease
autosomal recessive disease
adrenal gland disease
human disease
DOID:0080626
cortisone reductase deficiency
class of disease
endocrine system disease
hyperandrogenism
endocrine system disease characterized by failure to regenerate the active glucocorticoid cortisol from cortisone resulting in adrenal hyperandrogenism
DOID:0090139
costochondritis
class of disease
chondropathy
syndrome
disease
human disease
DOID:14021
cough variant asthma
class of disease
asthma
chronic asthma
asthma that is characterized by chronic nonproductive cough without shortness of breath
DOID:12323
C08.127.108.784
C08.381.495.108.750
C08.674.095.784
C20.543.480.680.095.688
cow milk allergy
class of disease
milk allergy
milk allergy triggered by Bos taurus milk
DOID:0060521
cranial nerve III tumor
class of disease
third cranial nerve disease
cranial nerve neoplasm
peripheral nervous system neoplasm
Human disease
DOID:2817
cranial nerve disease
class of disease
peripheral neuropathy
neuropathy that is located in one of the twelve cranial nerves
DOID:5656
C10.292
cranial nerve neoplasm
class of disease
nervous system neoplasm
cranial nerve disease
central nervous system cancer
Human disease
DOID:338
C04.588.614.300
C04.588.614.596.240
C10.292.225
C10.551.360
C10.551.775.250
Cranial nerve neoplasms
cranial nerve palsy
class of disease
symptom or sign
cranial nerve disease
palsy
eye symptom
Human disease
DOID:3817
cranial pseudosarcomatous fasciitis
class of disease
pseudosarcomatous fibromatosis
Human disease
DOID:7326
cranio-facial dystonia
class of disease
focal dystonia
focal dystonia that is characterized as dystonia that affects the muscles of the head, face, and neck
DOID:0050845
craniodiaphyseal dysplasia
class of disease
osteosclerosis
osteosclerosis that results in increased calcium concentration located in skull which decreases the size of cranium foramina and cervical spinal canal
DOID:0080032
cranioectodermal dysplasia 1
class of disease
Sensenbrenner syndrome
human disease
DOID:0080803
cranioectodermal dysplasia 2
class of disease
Sensenbrenner syndrome
human disease
DOID:0080804
cranioectodermal dysplasia 3
class of disease
Sensenbrenner syndrome
human disease
DOID:0080805
cranioectodermal dysplasia 4
class of disease
Sensenbrenner syndrome
human disease
DOID:0080806
craniopharyngioma
class of disease
central nervous system organ benign neoplasm
Rathke's pouch tumor
type of brain tumor derived from pituitary gland embryonic tissue that occurs most commonly in children, but also affects adults
DOID:3840
C04.557.465.625.200
C04.557.580.625.200
Craniopharyngiomas
craniosynostosis
class of disease
synostosis
rare disease
craniofacial disease
disease
premature fusion of bones in the skull
DOID:2340
C05.116.099.370.894.232
C05.660.207.240
C05.660.906.364
C16.131.621.207.240
C16.131.621.906.364
Craniosynostosis
crater-like holes of optic disc
class of disease
visual pathway disease
Human disease
DOID:13295
Optic pit
crescentic glomerulonephritis
class of disease
acute proliferative glomerulonephritis
Human disease
DOID:13139
cribriform carcinoma
class of disease
breast carcinoma
Human disease
DOID:5675
cribriform variant testicular seminoma
class of disease
testis seminoma
Human disease
DOID:7269
critical illness polyneuropathy
class of disease
inflammatory and toxic neuropathy
polyneuropathy
Human disease
DOID:14402
crustacean allergy
class of disease
shellfish allergy
seafood allergy
shellfish allergy triggered by Crustacea
DOID:0060524
cryptococcal meningitis
class of disease
cryptococcosis
fungal meningitis
fungal meningitis that has material basis in Crypococcus fungal infection
DOID:0080159
DOID:12052
C01.150.703.181.500.500
C01.150.703.248.290
C10.228.228.198.500.500
C10.586.625.300.500
C01.207.198.500.500
Meningeal cryptococcosis
cryptophthalmos
class of disease
eyelid disease
congenital disorder
congenital abnormality characterized by the presence of a continuous layer of skin extending over the eyeballs and the absence of eyelids and the palpebral fissure
DOID:0111716
cryptorchidism
class of disease
congenital disorder
testicular disease
male reproductive system disease
genetic disease
sex differentiation disease
disease
defective mammal development
DOID:11383
C12.200.294.829.258
C12.200.706.258
C16.131.939.258
C19.391.829.258
C12.100.500.829.258
C12.800.258
Cryptorchidism
cutaneous Paget's disease
class of disease
skin carcinoma
extramammary Paget's disease
skin carcinoma that is characterized by infiltration of the skin by neoplastic large cells with abundant pale cytoplasm and large nuclei with prominent nucleoli
DOID:3450
cutaneous T cell lymphoma
class of disease
peripheral T-cell lymphoma
genetic disease
cutaneous lymphoma
disease
non-Hodgkin's lymphoma that has material basis in a mutation of T cells
DOID:0060061
C04.557.386.480.750.800
C15.604.515.569.480.750.800
C20.683.515.761.480.750.800
Cutaneous T-cell lymphoma
cutaneous candidiasis
class of disease
symptom or sign
dermatomycosis
candidiasis
skin disease
candidiasis that is characterized by Candida infection located in the skin
DOID:0080161
C01.150.703.160.132
C01.150.703.302.105
C01.800.200.105
C17.800.838.208.170
Candidiasis of the skin
cutaneous diphtheria
class of disease
pyoderma
diphtheria
pyoderma that is a milder form of diphtheria restricted to the skin producing shallow skin ulcers is caused by direct physical contact of individuals infected with Corynebacterium diphtheriae as the bacteria releases the diphtheria toxin
DOID:12275
cutaneous endometriosis
class of disease
endometriosis
human disease
DOID:11430
cutaneous ganglioneuroma
class of disease
skin benign neoplasm
ganglioneuroma
Human disease
DOID:2425
cutaneous leiomyosarcoma
class of disease
skin sarcoma
Human disease
DOID:5273
Cutaneous leiomyosarcoma
cutaneous liposarcoma
class of disease
skin sarcoma
Human disease
DOID:5712
cutaneous lupus erythematosus
class of disease
lupus erythematosus
skin disease
lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight
DOID:0050169
C17.300.475
C17.800.480
cutaneous mastocytosis
class of disease
mastocytosis
skin disease
human disease
DOID:3663
C04.557.450.565.465.500
C17.800.508.473
cutaneous meningioma
class of disease
skin benign neoplasm
ectopic meningioma
skin cancer
Human disease
DOID:8006
cutaneous mucoepidermoid carcinoma
class of disease
skin benign neoplasm
mucoepidermoid carcinoma
skin carcinoma
Human disease
DOID:4683
cutaneous small-vessel vasculitis
class of disease
hypersensitivity vasculitis
skin disease
microvasculitis
allergy
disease
hypersensitivity vasculitis that results in inflammation of small blood vessels, characterized clinically by palpable purpura, which is a slightly elevated purpuric rash over one or more areas of the skin
DOID:11450
Cutaneous small-vessel vasculitis
cutaneous squamous-cell carcinoma
class of disease
skin carcinoma
squamous cell carcinoma
disease
skin carcinoma that has material basis in squamous cells
DOID:3151
Squamous-cell carcinoma of the skin
cyclophosphamide allergy
class of disease
drug allergy
drug allergy that has allergic trigger cyclophosphamide
DOID:0040027
cycloplegia
class of disease
eye accommodation disease
disease
paralysis of the ciliary muscle of the eye, resulting in a loss of accommodation
DOID:10033
cyclothymia
class of disease
bipolar disorder
disease
persistent instability of mood that involves recurrent hypomanic and dysthymic episodes, but no full manic episodes or full major depressive episodes
DOID:845
F03.600.500
cyclotropia
class of disease
strabismus
Human disease
DOID:9838
cylindrical spirals myopathy
class of disease
congenital myopathy
Human disease
DOID:0080103
cystadenocarcinoma
class of disease
cystic neoplasm
malignant cystadenoma
disease
adenocarcinoma that derives from epithelial cells originating in glandular tissue, in which cystic accumulations of retained secretions are formed
DOID:3111
C04.557.470.200.025.480
C04.557.470.590.480
cystadenofibroma
class of disease
adenofibroma
ovarian benign neoplasm
adenofibroma composed of epithelial ovarian tissue
DOID:5482
C04.557.450.565.590.595.050.500
C04.557.470.590.482
C04.557.470.625.050.500
cystadenoma
class of disease
adenoma
adenoma that is a cystic
DOID:2634
C04.557.470.035.320
C04.557.470.590.485
Cystadenomas
cystathioninuria
class of disease
sulfuraminoacidemia
amino acid metabolic disorder
genetic disease
amino acid metabolic disorder characterized by elevated plasma and urinary cystathionine levels that has material basis in homozygous or compound heterozygous mutation in the CTH gene on chromosome 1p31
DOID:0090142
cystic basal cell carcinoma
class of disease
basal-cell carcinoma
Human disease
DOID:4302
cystic echinococcosis
class of disease
echinococcosis
lung disease
bone disease
heart disease
liver disease
encephalopathy
Human disease
DOID:1495
cystic kidney disease
class of disease
renal cyst
kidney disease
congenital or acquired kidney disorder characterized by the presence of renal cysts
DOID:2975
C12.777.419.403
C13.351.968.419.403
Cystic kidney diseases
cystic lymphangioma
class of disease
lymphangioma
Cystic lymphatic malformation
hygroma
human disease
DOID:3081
C04.557.375.450.450
Cystic hygroma
cystic nephroma
class of disease
kidney benign neoplasm
nephroma
disease
Human disease
DOID:2673
Cystic nephroma
cystic teratoma
class of disease
teratoma
benign teratoma
Human disease
DOID:2660
cystinuria
class of disease
amino acid metabolic disorder
ureteral disease
bladder disease
kidney disease
disease
amino acid metabolic disorder that involves the formation of cystine stones in the kidneys, ureter, and bladder
DOID:9266
C12.777.419.815.885.250
C13.351.968.419.815.885.250
C16.320.565.861.885.250
C18.452.648.861.885.250
Cystine crystals in urine
cystitis
class of disease
symptom or sign
bladder disease
inflammation
inflammatory disease
disease
human disease
DOID:1679
C12.200.777.829.495
C12.050.351.968.829.495
C12.950.829.495
Cystitis
cystitis cystica
class of disease
cystitis
human disease
DOID:7138
Cystitis cystica
cystoid macular edema
class of disease
macular retinal edema
Human disease
DOID:4447
cystoid macular retinal degeneration
class of disease
degeneration of macula and posterior pole
Human disease
DOID:14245
cytochrome P450 oxidoreductase deficiency
class of disease
steroid inherited metabolic disorder
autosomal recessive disease
human disease
DOID:0080925
cytomegalovirus retinitis
class of disease
cytomegaloviral disease
retinitis
viral eye infection
disease
retinitis that has material basis in Cytomegalovirus
DOID:0080160
C01.375.725.270
C01.925.256.466.245.150
C11.294.800.270
C11.768.773.360
C01.925.325.270
Cytomegalovirus retinitis
dacryoadenitis
class of disease
lacrimal apparatus disease
disease
human disease
DOID:950
dacryocystitis
class of disease
acute inflammation of lacrimal passage
disease
infection of the lacrimal sac
DOID:9938
C11.496.221
Dacryocystitis
dacryocystocele
class of disease
chronic inflammation of lacrimal passage
Human disease
DOID:9939
deafness, aminoglycoside-induced
class of disease
drug-induced hearing loss
human disease
DOID:0111734
dedifferentiated liposarcoma
class of disease
liposarcoma
liposarcoma that is characterized as a high-grade tumor that occurs when a lower-grade tumor changes and creates new high-grade cells
DOID:0080531
deep angioma
class of disease
hemangioma
Human disease
DOID:469
deep corneal vascularisation
class of disease
corneal neovascularization
Human disease
DOID:12087
deep keratitis
class of disease
keratitis
human disease
DOID:9858
deep leiomyoma
class of disease
leiomyoma
Human disease
DOID:5128
deficiency anemia
class of disease
anemia
nutritional deficiency disease
Human disease
DOID:13121
Nutritional anemias
degeneration of macula and posterior pole
class of disease
macular degeneration
human disease
DOID:2007
degenerative disc disease
class of disease
Intervertebral disc disorder
bone deterioration disease
bone deterioration disease that has material basis in gradual dehydration and tears located in intervertebral disc
DOID:90
C05.116.900.153
Degenerative disc disease
degenerative myopia
class of disease
eye degenerative disease
myopia
Excessive axial myopia associated with complications (especially posterior staphyloma and choroidal neovascularization) that can lead to blindness
DOID:11829
C11.744.636.500
dehydrated hereditary stomatocytosis
class of disease
hereditary stomatocytosis
hemolytic anemia
DOID:0111575
dehydrated hereditary stomatocytosis 1
class of disease
dehydrated hereditary stomatocytosis
autosomal dominant disease
human disease
DOID:0111576
dehydration polycythemia
class of disease
acquired polycythemia
hemoconcentration
Human disease
DOID:2833
delayed sleep phase disorder
class of disease
sleep disorder
circadian rhythm sleep disorder
disease
chronic mismatch between a person's normal daily rhythm, compared to other people and societal norms
DOID:0111141
delta chain disease
class of disease
heavy chain disease
heavy chain disease that results from an overproduction of delta antibody (IgD)
DOID:0060129
delta thalassemia
class of disease
thalassemia
beta thalassemia
autosomal dominant disease
type of thalassemia
DOID:0080773
C15.378.071.141.150.875.575
C15.378.420.826.200
C16.320.070.875.575
C16.320.365.826.575
delusional disorder
class of disease
symptom or sign
psychosis
disease
mental disease
DOID:778
dementia
class of disease
symptom or sign
cognitive disorder
organic brain syndrome
clinical sign
disability affecting intellectual abilities
disease
long-term brain disorder causing personality changes and impaired memory, reasoning, and social function
DOID:1307
C10.228.140.380
F03.615.400
Dementia
demyelinating disease
class of disease
neurological disorder
neurodegeneration
central nervous system disease
disease
type of neurological disease where the myelin sheath of neurons is damaged
DOID:3213
C10.314
Demyelinating diseases
demyelinating polyneuropathy
class of disease
polyneuropathy
spinal cord disease
demyelinating disease
Polyneuropathy that is characterized by demyelination of axons
DOID:5214
dendritic cell deficiency
class of disease
primary immunodeficiency disease
human disease
DOID:0111963
dendritic cell sarcoma
class of disease
histiocytic and dendritic cell cancer
sarcoma
dendritic cell tumor
histiocytic and dendritic cell cancer that is mainly located in lymph nodes
DOID:7849
dendritic cell thymoma
class of disease
thymoma
leukocyte disease
hematologic cancer
Human disease
DOID:3282
dengue shock syndrome
class of disease
dengue fever
dengue hemorrhagic fever
Human disease
DOID:0050125
dental abscess
class of disease
symptom or sign
tooth pathology
abscess
tooth disease characterized by a localized collection of pus associated with a tooth
DOID:0060324
Tooth abscess
dental caries
class of disease
teeth hard tissue disease
caries
deformation of teeth made by acids from bacteria
DOID:216
C07.793.720.210
Dental caries
dental enamel hypoplasia
class of disease
teeth hard tissue disease
Human disease
DOID:693
C07.650.800.255
C07.793.700.255
C16.131.850.800.255
Enamel hypoplasia
dental fluorosis
class of disease
tooth pathology
fluoride toxicity
disease
human disease
DOID:13711
C07.793.330
Dental fluorosis
dental pulp calcification
class of disease
dental pulp disease
Human disease
DOID:5608
C07.793.237.252
dental pulp disease
class of disease
tooth pathology
connective tissue disease
disease involving the dental pulp
DOID:5330
C07.793.237
dental pulp necrosis
class of disease
dental pulp disease
Human disease
DOID:11623
C07.793.237.315
C23.550.717.182
dentin caries
class of disease
dental caries
Human disease
DOID:10461
dentine erosion
class of disease
dental erosion
Human disease
DOID:13629
dentine hypersensitivity
class of disease
orofacial pain
teeth hard tissue disease
Human disease
DOID:698
C07.793.266
denture stomatitis
class of disease
stomatitis
lip disease
DOID:11875
C07.465.864.875
dependent personality disorder
class of disease
personality disorder
dependency
disease
personality disorder that is characterized by a pervasive psychological dependence on other people
DOID:10931
F03.675.200
Dependent personality disorder
depersonalization disorder
class of disease
dissociative disorder
depersonalization
dissociative disorder in which the sufferer is affected by persistent or recurrent feelings of depersonalization and/or derealization
DOID:11038
dermal unilateral segmental cavernous angioma
class of disease
cavernous hemangioma
Human disease
DOID:3148
dermatitis
class of disease
symptom or sign
skin disease
skin and integumentary tissue symptom
disease
inflammation of the skin
DOID:2723
C17.800.174
Dermatitis
dermatitis herpetiformis
class of disease
symptom or sign
autoimmune skin disease
bullous skin disease
pemphigoid
disease
human disease
DOID:8505
C17.800.174.360
C17.800.865.360
C20.111.318
Dermatitis herpetiformis
dermatographia
class of disease
physical urticaria
disease
human skin condition, responsible for "skin writing" effect in those affected
DOID:743
Dermatographic urticaria
dermatomycosis
class of disease
skin disease
fungal infectious disease
skin infection
cutaneous mycosis that results in fungal infection located in skin or of its appendages, has material basis in Ascomycota fungi other than the dermatophytes
DOID:1563
DOID:0050134
C01.150.703.302
C01.800.200
C17.800.838.208
dermatosis papulosa nigra
class of disease
dermatitis
seborrheic keratosis
Human disease
DOID:4400
Dermatosis papulosa nigra
dermis tumor
class of disease
skin benign neoplasm
Human disease
DOID:2438
dermoid cyst
class of disease
cystic teratoma
disease
tissue disease
DOID:2658
C04.182.201
C04.557.465.910.250
Dermoid cysts
dermoid cyst of ovary
class of disease
ovarian cyst
ovarian cancer
dermoid cyst
ovarian benign neoplasm
Human disease
DOID:5117
Ovarian dermoid cysts
dermoid cyst of skin
class of disease
skin cancer
skin benign neoplasm
dermoid cyst
Human disease
DOID:13691
descending colon cancer
class of disease
plump cancer
Human disease
DOID:12190
desmoid disease, hereditary
class of disease
aggressive fibromatosis
syndrome
autosomal genetic disease
desmoid tumor (DT) is a benign, locally invasive soft tissue tumor associated with a high recurrence rate but with no metastatic potential
DOID:0111349
desmoplastic small-round-cell tumor
class of disease
soft-tissue sarcoma
sarcoma
aggressive, rare cancer
DOID:6785
C04.557.450.795.315
Desmoplastic small round cell tumour
detrusor sphincter dyssynergia
class of disease
neurogenic bladder
bladder disease
Human disease
DOID:12145
deuteranopia
class of disease
congenital color blindness
color blindness
red–green color blindness
dichromatopsia
human disease, green color blindness
DOID:13909
Deuteranopia
developmental and epileptic encephalopathy
class of disease
electroclinical syndrome
human disease
DOID:0112202
developmental and epileptic encephalopathy 100
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0070386
developmental and epileptic encephalopathy 101
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0070387
developmental and epileptic encephalopathy 102
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0070388
developmental and epileptic encephalopathy 103
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0070389
developmental and epileptic encephalopathy 104
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0070390
developmental and epileptic encephalopathy 108
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0070394
developmental and epileptic encephalopathy 109
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0070378
developmental and epileptic encephalopathy 110
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0070395
developmental and epileptic encephalopathy 67
class of disease
developmental and epileptic encephalopathy
autosomal dominant disease
human disease
DOID:0112203
developmental and epileptic encephalopathy 68
class of disease
autosomal recessive disease
developmental and epileptic encephalopathy
human disease
DOID:0112204
developmental and epileptic encephalopathy 69
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0112205
developmental and epileptic encephalopathy 70
class of disease
autosomal dominant disease
developmental and epileptic encephalopathy
human disease
DOID:0112206
developmental and epileptic encephalopathy 71
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0112207
developmental and epileptic encephalopathy 72
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0112208
developmental and epileptic encephalopathy 73
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0112209
developmental and epileptic encephalopathy 74
class of disease
developmental and epileptic encephalopathy
autosomal dominant disease
human disease
DOID:0112210
developmental and epileptic encephalopathy 75
class of disease
developmental and epileptic encephalopathy
autosomal recessive disease
human disease
DOID:0112211
developmental and epileptic encephalopathy 78
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0112214
developmental and epileptic encephalopathy 79
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0112215
developmental and epileptic encephalopathy 80
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0112216
developmental and epileptic encephalopathy 81
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0112217
developmental and epileptic encephalopathy 83
class of disease
autosomal recessive disease
developmental and epileptic encephalopathy
human disease
DOID:0112218
developmental and epileptic encephalopathy 84
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0112219
developmental and epileptic encephalopathy 89
class of disease
developmental and epileptic encephalopathy
human disease
DOID:0112223
developmental coordination disorder
class of disease
motor disorder
specific developmental disorder
disease
neurodevelopmental condition
DOID:9923
F03.625.813
Dyspraxia
developmental delay and seizures with or without movement abnormalities
class of disease
syndromic intellectual disability
human disease
DOID:0080473
developmental disorder
class of disease
mental disorder
developmental disability
neurodevelopmental disorder
disease
disease of mental health that occur during a child's developmental period between birth and age 18 resulting in retarding of the child's psychological or physical development
DOID:0060037
dextro-looped transposition of the great arteries 1
class of disease
dextro-transposition of the great arteries
genetic disease
autosomal dominant disease
dextro-looped transposition of the great arteries that has material basis in heterozygous missense mutation in the MED13L gene on chromosome 12q24
DOID:0060771
dextrocardia
class of disease
heart position anomaly
congenital heart disease
disease
rare congenital defect in which the apex of the heart is located on the right side of the body
DOID:9565
C14.240.400.280
C14.280.400.280
C16.131.240.400.280
C16.131.810.250
Dextrocardia
diabetes
class of disease
glucose metabolism disease
disease
group of metabolic disorders characterized by high blood sugar levels over a prolonged period
DOID:9351
C18.452.394.750
C19.246
Diabetes mellitus
diabetes
class of disease
glucose metabolism disease
human disease
DOID:0081062
diabetic angiopathy
class of disease
peripheral vascular disease
complications of diabetes mellitus
human disease
DOID:11713
C14.907.320
C19.246.099.500
Diabetic angiopathy
diabetic autonomic neuropathy
class of disease
autonomic neuropathy
diabetic neuropathy
Autonomic neuropathy that is caused by diabetes mellitus
DOID:11503
diabetic cataract
class of disease
cataract
ocular manifestation of diabetes
Human disease
DOID:13328
diabetic encephalopathy
class of disease
encephalopathy
complications of diabetes mellitus
brain disease that is characterized by functional impairment of cognition, cerebral signal conduction, neurotransmission and synaptic plasticity, and underlying structural pathology associated with diabetes
DOID:0050850
diabetic ketoacidosis
class of disease
complications of diabetes mellitus
type 2 diabetes
ketoacidosis
metabolic acidosis
disease
potentially life-threatening complication in people with diabetes mellitus
DOID:1837
DOID:10626
C18.452.076.176.652.500
C18.452.394.750.535
C19.246.099.812
Diabetic ketoacidosis
diabetic macular edema
class of disease
macular retinal edema
diabetic retinopathy
Human disease
DOID:9191
Diabetic macular edema
diabetic neuropathy
class of disease
complications of diabetes mellitus
peripheral neuropathy
disease
neurological complication of persistently high blood sugar
DOID:9743
C10.668.829.300
C19.246.099.937
Diabetic neuropathy
diabetic polyneuropathy
class of disease
diabetic neuropathy
Human disease
DOID:12785
diabetic retinopathy
class of disease
ocular manifestation of diabetes
diabetic angiopathy
retinal vascular disease
disease
human disease
DOID:8947
C11.768.257
C14.907.320.382
C19.246.099.500.382
Diabetic retinopathy
diaphragm disease
class of disease
muscular disease
respiratory disease
human disease
DOID:10481
Disorders of diaphragm
diaphragmatic eventration
class of disease
diaphragm disease
congenital or acquired abnormality characterized by elevation of the hemidiaphragm
DOID:10480
C06.198.257
C16.131.314.244
diarrhea
class of disease
symptom or sign
gastrointestinal system disease
clinical sign
feces and droppings symptom
disease
loose or liquid bowel movements
DOID:13250
C23.888.821.214
Diarrhea
diclofenac allergy
class of disease
drug allergy
drug allergy that has allergic trigger diclofenac
DOID:0040031
diencephalic astrocytoma
class of disease
diencephalic neoplasm
brain glioma
brain astrocytoma
glioma
Human disease
DOID:4855
diencephalic neoplasm
class of disease
supratentorial cancer
human disease
DOID:3843
differentiated thyroid carcinoma
class of disease
thyroid carcinoma
thyroid gland adenocarcinoma
Differentiated thyroid carcinoma (DTC), also known as papillary or follicular thyroid carcinoma, is a slow-growing malignancy usually presenting in adults as an asymptomatic thyroid mass
DOID:0080525
differentiating neuroblastoma
class of disease
neuroblastoma
Human disease
DOID:4160
diffuse alopecia areata
class of disease
alopecia areata
alopecia areata that involves diffuse loss of hair over the whole scalp
DOID:0060157
diffuse cutaneous mastocytosis
class of disease
cutaneous mastocytosis
Human disease
DOID:3665
diffuse cystic renal dysplasia
class of disease
cystic kidney disease
autosomal dominant disease
human disease
DOID:0111682
diffuse gastric cancer
class of disease
stomach cancer
human disease
DOID:0080763
diffuse glomerulonephritis
class of disease
glomerulonephritis
Human disease
DOID:4781
diffuse infiltrative lymphocytosis syndrome
class of disease
syndrome
lymphocytosis
AIDS related disease
Human disease
DOID:6677
diffuse interstitial keratitis
class of disease
interstitial keratitis
Human disease
DOID:13353
diffuse large B-cell lymphoma
class of disease
B-cell lymphoma
aggressive B-cell non-Hodgkin lymphoma
type of lymphoma (cancer)
DOID:0050745
C04.557.386.480.150.585
C15.604.515.569.480.150.585
C20.683.515.761.480.150.585
Diffuse large B-cell lymphoma
diffuse lipomatosis
class of disease
lipomatosis
Human disease
DOID:3923
diffuse meningeal melanocytosis
class of disease
central nervous system melanocytic neoplasm
Human disease
DOID:6379
diffuse midline glioma, H3 K27M-mutant
class of disease
glioma
juvenile astrocytoma
human disease
DOID:0080684
diffuse peritoneal leiomyomatosis
class of disease
leiomyomatosis
primary peritoneal tumor
leiomyoma
peritoneal benign neoplasm
Human disease
DOID:5728
diffuse pulmonary fibrosis
class of disease
pulmonary fibrosis
human disease
DOID:5641
diffuse scleroderma
class of disease
systemic scleroderma
variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement
DOID:1580
C17.300.799.602
C17.800.784.602
diffuse secondary choroid atrophy
class of disease
choroidal sclerosis
human disease
DOID:981
diffuse uterine leiomyomatosis
class of disease
uterine fibroid
uterine corpus leiomyomatosis
Human disease
DOID:5917
digenic disease
class of disease
polygenic disease
polygenic disease that is characterized by expression of a phenotype that requires the presence of pathogenic variants in two different genes
DOID:0080578
dihydropyrimidinase deficiency
class of disease
pyrimidine metabolic disorder
autosomal recessive disease
human disease
DOID:0111629
dilated cardiomyopathy 1A
class of disease
dilated cardiomyopathy
genetic disease
dilated cardiomyopathy that has material basis in mutation in the LMNA gene on chromosome 1q21
DOID:0110425
dilated cardiomyopathy 1B
class of disease
dilated cardiomyopathy
genetic disease
dilated cardiomyopathy that has material basis in variation in the chromosome region 9q13
DOID:0110443
dilated cardiomyopathy 1H
class of disease
dilated cardiomyopathy
genetic disease
monogenic disease
dilated cardiomyopathy that has material basis in variation in the chromosome region 2q14-q22
DOID:0110429
dilated cardiomyopathy 1K
class of disease
dilated cardiomyopathy
genetic disease
monogenic disease
dilated cardiomyopathy that has material basis in variation in the chromosome region 6q12-q16
DOID:0110437
dilated cardiomyopathy 1KK
class of disease
dilated cardiomyopathy
genetic disease
autosomal dominant disease
dilated cardiomyopathy that has material basis in mutation in the MYPN gene on chromosome 10q21
DOID:0110445
dilated cardiomyopathy 1Q
class of disease
dilated cardiomyopathy
genetic disease
monogenic disease
A dilated cardiomyopathy that has material basis in variation in the chromosome region 7q22.3-q31.1.
DOID:0110442
dioctophymiasis
class of disease
parasitic helminthiasis infectious disease
kidney disease
skin disease
A parasitic helminthiasis infectious disease that involves parasitic infection by the nematode Dioctophyme renale in humans after eating undercooked food. The larvae are found in the subcutaneous nodules and kidneys.
DOID:0050260
diphenylmethane-4,4'-diisocyanate allergic asthma
class of disease
isocyanates allergic asthma
allergic asthma to isocyanates that has allergic trigger diphenylmethane-4,4-diisocyanate
DOID:0040042
diphenylmethane-4,4'-diisocyanate allergic contact dermatitis
class of disease
allergic contact dermatitis
allergic contact dermatitis that has allergic trigger diphenylmethane-4,4-diisocyanate
DOID:0040052
diphtheritic cystitis
class of disease
cystitis
diphtheria
cystitis which involves inflammation and formation of a dense fibrous false membrane on the mucous membrane of the bladder
DOID:13306
diphtheritic peritonitis
class of disease
peritonitis
diphtheria
peritonitis which involves inflammation of peritoneal cavity by Corynebacterium diphtheriae
DOID:13310
diplegia of upper limb
class of disease
neurological disorder
Diplegia
Human disease
DOID:862
discharging ear
class of disease
symptom or sign
ear disease
discharge
human disease
DOID:10261
discoid lupus erythematosus of eyelid
class of disease
discoid lupus erythematosus
noninfectious dermatoses of eyelid
Human disease
DOID:9076
discrete subaortic stenosis
class of disease
subvalvular aortic stenosis
Human disease
DOID:5804
C14.280.484.150.070.210
C14.280.955.249.070.210
disease
class of disease
health problem
biological process
abnormal condition negatively affecting organisms
DOID:4
C23.550.288
Diseases and disorders
disease of anatomical entity
class of disease
disease
disease that manifests in a defined anatomical structure
DOID:7
disease of cellular proliferation
class of disease
disease
disease characterized by abnormally rapid cell division
DOID:14566
C04.697
C23.550.727
dislocation of ear ossicle
class of disease
middle ear disease
conductive hearing loss
ear disease
Human disease
DOID:11129
disodium cromoglycate allergy
class of disease
drug allergy
metal allergy
drug allergy that has allergic trigger disodium cromoglycate
DOID:0040073
displacement of cardia through esophageal hiatus
class of disease
hiatus hernia
Human disease
DOID:12641
disseminated chorioretinitis
class of disease
chorioretinitis
Human disease
DOID:8787
disseminated eosinophilic collagen disease
class of disease
collagen disease
eosinophilia
Human disease
DOID:9499
disseminated intravascular coagulation
class of disease
thrombophilia
disease
pathological process characterized by the widespread activation of the clotting cascade that results in the formation of blood clots in the small blood vessels throughout the body
DOID:11247
C15.378.100.220
C15.378.463.250
C15.378.925.220
Disseminated intravascular coagulation
disseminated superficial actinic porokeratosis
class of disease
keratosis
porokeratosis
Human disease
DOID:3805
dissociated nystagmus
class of disease
pathologic nystagmus
Human disease
DOID:13174
dissociative amnesia
class of disease
dissociative disorder
amnesia
disease
Human disease
DOID:11037
Dissociative amnesia
dissociative disorder
class of disease
mental disorder
dissociation
disease
disease of mental health in which the normally well-integrated functions of memory, identity, perception, or consciousness are separated (dissociated)
DOID:10935
F03.300
distal arthrogryposis type 1
class of disease
distal arthrogryposis
human disease
DOID:0111596
distal arthrogryposis type 10
class of disease
autosomal dominant disease
distal arthrogryposis
human disease
DOID:0111593
distal arthrogryposis type 1A
class of disease
autosomal dominant disease
distal arthrogryposis type 1
human disease
DOID:0111597
distal arthrogryposis type 1B
class of disease
distal arthrogryposis type 1
autosomal dominant disease
human disease
DOID:0111598
distal arthrogryposis type 2A
class of disease
Freeman–Sheldon syndrome
autosomal dominant disease
human disease
DOID:0111605
distal arthrogryposis type 2B1
class of disease
autosomal dominant disease
Sheldon-Hall syndrome
human disease
DOID:0111600
distal arthrogryposis type 2B2
class of disease
Sheldon-Hall syndrome
autosomal dominant disease
human disease
DOID:0111601
distal arthrogryposis type 2B3
class of disease
Sheldon-Hall syndrome
autosomal dominant disease
human disease
DOID:0111602
distal arthrogryposis type 3
class of disease
autosomal dominant disease
distal arthrogryposis
human disease
DOID:0111607
distal arthrogryposis type 4
class of disease
distal arthrogryposis
human disease
DOID:0111610
distal arthrogryposis type 5
class of disease
autosomal dominant disease
distal arthrogryposis
human disease
DOID:0111608
distal arthrogryposis type 5D
class of disease
distal arthrogryposis
autosomal recessive disease
human disease
DOID:0111594
distal arthrogryposis type 6
class of disease
distal arthrogryposis
human disease
DOID:0111609
distal biliary tract carcinoma
class of disease
bile duct carcinoma
extrahepatic bile duct carcinoma
Human disease
DOID:5923
distal hereditary motor neuronopathy type 2
class of disease
autosomal dominant distal hereditary motor neuronopathy characterized by adult onset of slowly progressive distal atrophy and weakness
DOID:0111206
distal hereditary motor neuronopathy type 2A
class of disease
distal hereditary motor neuronopathy type 2
A distal hereditary motor neuropathy type 2 that has material basis in heterozygous mutation in HSPB8 on 12q24.23.
DOID:0111208
distal hereditary motor neuronopathy type 5
class of disease
autosomal dominant distal hereditary motor neuropathy
autosomal dominant distal hereditary motor neuronopathy characterized by muscle weakness and wasting, predominantly confined to the hands, and often exclusively involve thenar and/or interosseus dorsalis I eminences
DOID:0111203
distal hereditary motor neuronopathy type 5A
class of disease
distal hereditary motor neuronopathy type 5
A distal hereditary motor neuronopathy type 5 that has material basis in heterozygous mutation in GARS on 7p14.3 or BSCL2 on 11q12.3.
DOID:0111204
distal hereditary motor neuronopathy type 7
class of disease
autosomal dominant distal hereditary motor neuropathy
autosomal dominant distal hereditary motor neuronopathy characterized by slowly progressive distal atrophy and weakness affecting first the upper limbs and later the lower limbs and vocal cord paresis
DOID:0111199
distal hereditary motor neuronopathy type 7A
class of disease
distal hereditary motor neuronopathy type 7
human disease
DOID:0111201
distal hereditary motor neuronopathy type 7B
class of disease
distal hereditary motor neuronopathy type 7
A distal hereditary motor neuropathy type 7 that has material basis in heterozygous mutation in DCTN1 on 2p13.1.
DOID:0111202
distal hereditary motor neuronopathy type 8
class of disease
autosomal dominant distal hereditary motor neuropathy
human disease
DOID:0111215
distal hereditary motor neuronopathy type 9
class of disease
autosomal dominant distal hereditary motor neuropathy
human disease
DOID:0111212
distal hereditary motor neuropathy type 1
class of disease
nervous system heredodegenerative disease
autosomal dominant distal hereditary motor neuropathy
autosomal dominant neurodegenerative disorder characterized by juvenile onset, distal motor weakness without sensory impairment, and anterior horn cell degeneration
DOID:0111200
distal hereditary motor neuropathy type 2B
class of disease
distal hereditary motor neuronopathy type 2
A distal hereditary motor neuropathy type 2 that has material basis in heterozygous mutation in HSPB1 on 7q11.23.
DOID:0111207
distal muscular dystrophy 3
class of disease
distal muscular dystrophy that has significant linkage to 2 distinct regions on chromosomes 8p22-q11 and 12q13-q22
DOID:0111189
distal myopathy 1
class of disease
distal muscular dystrophy
genetic disease
autosomal dominant disease
distal muscular dystrophy characterized by autosomal dominant inheritance that has material basis in mutation in the MYH7 gene on chromosome 14q11
DOID:0070197
distal spinal muscular atrophy type 3
class of disease
nervous system heredodegenerative disease
autosomal recessive distal hereditary motor neuropathy
autosomal recessive distal hereditary motor neuronopathy
human disease
DOID:0111211
distal spinal muscular atrophy type 4
class of disease
autosomal recessive distal hereditary motor neuronopathy
human disease
DOID:0111213
distal spinal muscular atrophy type 5
class of disease
autosomal recessive distal hereditary motor neuronopathy
human disease
DOID:0111214
disuse amblyopia
class of disease
amblyopia
Human disease
DOID:10378
diversion colitis
class of disease
colitis
colitis caused by diversion of the fecal stream due to complication of ileostomy or colostomy
DOID:0060187
diverticulitis
class of disease
symptom or sign
intestinal disease
diverticular disease
inflammatory disease
sigmoiditis
disease
digestive disease caused by an inflammation of a herniating pouch (diverticulum) within the wall of the intestine, most often colon
DOID:7475
C01.539.463.199.375
C06.405.205.282.500
Diverticulitis
diverticulitis of colon
class of disease
colonic disease
diverticulitis
colonic diverticulosis
colonic disease characterized by the formation and inflammation of diverticula within the colon wall
DOID:13254
C06.405.469.158.587.500
C01.539.463.199.375.250
C06.405.205.282.500.250
dominant beta-thalassemia
class of disease
beta thalassemia
autosomal dominant disease
Dominant beta-thalassemia is a form of beta-thalassemia (see this term) resulting in moderate to severe anemia
DOID:0080770
dominant dystrophic epidermolysis bullosa
class of disease
epidermolysis bullosa dystrophica
autosomal dominant disease
human disease
DOID:0080224
dominant pericentral pigmentary retinopathy
class of disease
retinitis pigmentosa
autosomal dominant disease
retinitis pigmentosa that is characterized pigmentary retinal degeneration with onset in the teens leading to blindness in the sixth ans seventh decades of life
DOID:0110420
dopamine beta-hydroxylase deficiency
class of disease
autonomic nervous system disease
Congenital disorders of amino acid metabolism
inherited metabolic disorder
primary orthostatic hypotension
disorder of catecholamine synthesis
neurometabolic disease
ptosis
neurological disorder
genetic disease
genetic metabolic disorder
DOID:0090145
double pterygium
class of disease
pterygium
Human disease
DOID:10525
drug allergy
class of disease
allergy
drug intolerance
human disease
DOID:0060500
C20.543.206
C25.100.468
drug psychosis
class of disease
drug-induced mental disorder
substance-induced psychosis
psychosis
Psychotic organic mental disorders resulting from the toxic effect of drugs and chemicals or other harmful substance
DOID:1742
C25.723.809
C25.775.746
F03.700.675.600
F03.900.746
drug-induced hearing loss
class of disease
deafness
nonsyndromic deafness that is characterized by cochlear or vestibular dysfunction resulting in loss of hearing caused by drug ototoxicity
DOID:0070310
drug-induced hepatitis
class of disease
hepatitis
hepatotoxicity
disease
Human disease
DOID:2044
C06.552.195.200
C25.100.562.200
C25.723.260.200
drug-induced lupus erythematosus
class of disease
symptom or sign
adverse drug reaction
lupus erythematosus
disease
lupus erythematosus caused by chronic use of certain drugs
DOID:0040093
drug-induced mental disorder
class of disease
substance-related disorder
adverse drug reaction
substance-induced psychosis
Human disease
DOID:1203
dry beriberi
class of disease
beriberi
beriberi that is located in the nervous system and has symptom difficulty walking, numbness in extremities, tingling in extremities, paralysis of lower legs, difficulty speaking, confusion, and vomiting
DOID:0070318
dry eye syndrome
class of disease
lacrimal apparatus disease
corneal and conjunctival dryness due to deficient tear production
DOID:10140
C11.496.260
dumping syndrome
class of disease
postgastrectomy syndrome
disease
Human disease
DOID:14495
C06.405.748.630.310
C23.550.767.812.500
duodenal atresia
class of disease
atresia
duodenal stenosis
atresia of small intestine
gastroduodenal malformation
intestinal atresia
disease
congenital disorder of digestive system
DOID:0080216
Duodenal atresia
duodenal disease
class of disease
intestinal disease
small-intestine disease
Human disease
DOID:4072
C06.405.469.275
duodenal gastrinoma
class of disease
duodenum cancer
gastrinoma
duodenal neuroendocrine tumor, well differentiated, low or intermediate grade
Human disease
DOID:7959
duodenal neoplasm
class of disease
small intestine neoplasm
duodenal disease
Human disease
DOID:1737
C04.588.274.476.411.445
C06.301.371.411.445
C06.405.249.411.445
C06.405.469.275.270
C06.405.469.491.445
Duodenal neoplasms
duodenal obstruction
class of disease
duodenal disease
bowel obstruction
Human disease
DOID:3558
C06.405.469.275.395
C06.405.469.531.311
duodenal somatostatinoma
class of disease
duodenum cancer
duodenal neuroendocrine tumor, well differentiated, low or intermediate grade
Human disease
DOID:7479
duodenal ulcer
class of disease
peptic ulcer disease
Human disease
DOID:1724
C06.405.469.275.800.348
C06.405.748.586.349
Duodenal ulcers
duodenitis
class of disease
intestinal disease
disease
Human disease
DOID:8643
C06.405.205.462.249
C06.405.469.275.600
C06.405.469.326.750
Duodenitis
duodenum adenocarcinoma
class of disease
duodenum cancer
small intestine adenocarcinoma
adenocarcinoma
duodenum cancer that derives from epithelial cells of glandular origin
DOID:10816
Duodenal adenocarcinoma
duodenum adenoma
class of disease
duodenal neoplasm
adenoma of small intestine
duodenal disease
benign neoplasms by histologic type
adenoma
duodenal benign neoplasm that has material basis in epithelial tissue with glandular origin
DOID:0050927
duodenum cancer
class of disease
small intestine cancer
small intestine carcinoma
duodenal disease
duodenal neoplasm
small intestine cancer that is located in the beginning section of the small intestine
DOID:10021
Duodenal cancer
dysembryoplastic neuroepithelial tumour
class of disease
neuronal and mixed glio-neuronal tumor
low grade glioma
central nervous system organ benign neoplasm
epilepsy
type of brain tumour
DOID:2679
Dysembryoplastic neuroepithelial tumour
dysgammaglobulinemia
class of disease
selective immunoglobulin deficiency disease
selective immunoglobulin deficiency disease that is caused by a reduction in some types of gamma globulins
DOID:11702
C15.378.147.333
C20.673.430
dysgerminoma
class of disease
germ cell cancer
ovarian cancer
disease
germ cell cancer that derives from cells that give rise to egg cells
DOID:4441
C04.557.465.330.300
Dysgerminoma
dysgerminoma of ovary
class of disease
dysgerminoma
ovarian primitive germ cell tumor
dysgerminoma that is located in the ovary
DOID:5511
Ovarian dysgerminoma
dysgraphia
class of disease
writing disorder
learning disability
disease
developmental or acquired neurological condition
DOID:4540
Dysgraphia
dyshormonogenic goiter
class of disease
goiter
Human disease
DOID:12175
dyskinesia of esophagus
class of disease
esophageal motility disorder
esophageal disease
human disease
DOID:9192
dyskinetic cerebral palsy
class of disease
cerebral palsy
human disease
DOID:0050672
dysplastic nevus syndrome
class of disease
autosomal dominant disease
syndrome
disease
Human skin disease
DOID:10041
C04.557.665.560.260
C04.700.305
C16.320.700.305
Dysplastic nevus syndrome
dysthymic disorder
class of disease
mood disorder
disease
psychological disorder
DOID:12139
F03.600.300.400
dystonia
class of disease
movement disorders
rare genetic dystonia
disease
human disease
DOID:543
C10.597.350.300
C23.888.592.350.300
Dystonia
dystonia 21
class of disease
dystonia
generalized isolated dystonia
genetic disease
autosomal dominant disease
A dystonia characterized by autosomal dominant inheritance of late onset pure torsion dystonia that has material basis in variation in the chromosome region 2q14.3-q21.3.
DOID:0090046
dystonia 5
class of disease
dystonia
genetic disease
autosomal dominant disease
autosomal recessive disease
human disease
DOID:0090043
dystransthyretinemic hyperthyroxinemia
class of disease
hyperthyroxinemia
autosomal dominant disease
human disease
DOID:0080219
dystrophies primarily involving the retinal pigment epithelium
class of disease
fundus dystrophy
retinitis pigmentosa
Human disease
DOID:14252
ear disease
class of disease
sensory system disease
human disease
DOID:2742
C09.218
Diseases and disorders of the ear and mastoid process
early congenital syphilis
class of disease
congenital syphilis
Human disease
DOID:0050488
early infantile epileptic encephalopathy 1
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy characterized by X-linked recessive inheritance that has material basis in mutation in the ARX gene on chromosome Xp21
DOID:0080468
early infantile epileptic encephalopathy 12
class of disease
Ohtahara syndrome
An early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the PLCB1 gene on chromosome 20p12.3.
DOID:0080459
early infantile epileptic encephalopathy 13
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the SCN8A gene on chromosome 12q13
DOID:0080445
early infantile epileptic encephalopathy 14
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy characterized by refractory focal seizures developing by 6 months of age and arrest of psychomotor development that has material basis in heterozygous mutation in the KCNT1 gene on chromosome 9q34
DOID:0080439
early infantile epileptic encephalopathy 16
class of disease
Ohtahara syndrome
human disease
DOID:0080449
early infantile epileptic encephalopathy 19
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the GABRA1 gene on chromosome 5q34
DOID:0080431
early infantile epileptic encephalopathy 2
class of disease
Ohtahara syndrome
human disease
DOID:0080467
early infantile epileptic encephalopathy 21
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the NECAP1 gene on chromosome 12p13
DOID:0080443
early infantile epileptic encephalopathy 23
class of disease
Ohtahara syndrome
autosomal recessive disease
early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the DOCK7 gene on chromosome 1p31
DOID:0080415
early infantile epileptic encephalopathy 24
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the HCN1 gene on chromosome 5p12
DOID:0080429
early infantile epileptic encephalopathy 25
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the SLC13A5 gene on chromosome 17p13
DOID:0080453
early infantile epileptic encephalopathy 26
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the KCNB1 gene on chromosome 20q13
DOID:0080461
early infantile epileptic encephalopathy 27
class of disease
Ohtahara syndrome
human disease
DOID:0080444
early infantile epileptic encephalopathy 29
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the AARS gene on chromosome 16q22
DOID:0080451
early infantile epileptic encephalopathy 30
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the SIK1 gene on chromosome 21q22
DOID:0080465
early infantile epileptic encephalopathy 31
class of disease
Ohtahara syndrome
developmental and epileptic encephalopathy
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the DNM1 gene on chromosome 9q34
DOID:0080437
early infantile epileptic encephalopathy 32
class of disease
Ohtahara syndrome
human disease
DOID:0080416
early infantile epileptic encephalopathy 33
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the EEF1A2 gene on chromosome 20q13
DOID:0080463
early infantile epileptic encephalopathy 34
class of disease
Ohtahara syndrome
human disease
DOID:0080460
early infantile epileptic encephalopathy 35
class of disease
Ohtahara syndrome
human disease
DOID:0080458
early infantile epileptic encephalopathy 37
class of disease
Ohtahara syndrome
human disease
DOID:0080435
early infantile epileptic encephalopathy 38
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in homozygous mutation in the ARV1 gene on chromosome 1q42
DOID:0080417
early infantile epileptic encephalopathy 39
class of disease
Ohtahara syndrome
infantile epileptic encephalopathy that has material basis in mutation in the SLC25A12 gene on chromosome 2q31
DOID:0080349
DOID:0080423
early infantile epileptic encephalopathy 40
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the GUF1 gene on chromosome 4p12
DOID:0080427
early infantile epileptic encephalopathy 41
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the SLC1A2 gene on chromosome 11p13
DOID:0080442
early infantile epileptic encephalopathy 42
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the CACNA1A gene on chromosome 19p13
DOID:0080454
early infantile epileptic encephalopathy 43
class of disease
Ohtahara syndrome
autosomal dominant disease
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the GABRB3 gene on chromosome 15q11
DOID:0080447
early infantile epileptic encephalopathy 44
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the UBA5 gene on chromosome 3q22
DOID:0080424
early infantile epileptic encephalopathy 45
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the GABRB1 gene on chromosome 4p13
DOID:0080428
early infantile epileptic encephalopathy 46
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the GRIN2D gene on chromosome 19q13
DOID:0080456
early infantile epileptic encephalopathy 47
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the FGF12 gene on chromosome 3q28
DOID:0080425
early infantile epileptic encephalopathy 48
class of disease
Ohtahara syndrome
human disease
DOID:0080448
early infantile epileptic encephalopathy 49
class of disease
Ohtahara syndrome
human disease
DOID:0080441
early infantile epileptic encephalopathy 51
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy characterized by onset of intractable seizures and hypotonia in the first days or weeks of life that has material basis in homozygous or compound heterozygous mutation in the MDH2 gene on chromosome 7q11
DOID:0080433
early infantile epileptic encephalopathy 52
class of disease
Ohtahara syndrome
human disease
DOID:0080455
early infantile epileptic encephalopathy 53
class of disease
Ohtahara syndrome
human disease
DOID:0080464
early infantile epileptic encephalopathy 54
class of disease
Ohtahara syndrome
human disease
DOID:0080418
early infantile epileptic encephalopathy 55
class of disease
Ohtahara syndrome
human disease
DOID:0080283
early infantile epileptic encephalopathy 56
class of disease
Ohtahara syndrome
human disease
DOID:0080282
early infantile epileptic encephalopathy 57
class of disease
Ohtahara syndrome
human disease
DOID:0080284
early infantile epileptic encephalopathy 58
class of disease
Ohtahara syndrome
human disease
DOID:0080285
early infantile epileptic encephalopathy 59
class of disease
Ohtahara syndrome
infantile epileptic encephalopathy
autosomal dominant disease
human disease
DOID:0080291
early infantile epileptic encephalopathy 60
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the CNPY3 gene on chromosome 6p
DOID:0080432
early infantile epileptic encephalopathy 61
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the ADAM22 gene on chromosome 7q21
DOID:0080434
early infantile epileptic encephalopathy 62
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the SCN3A gene on chromosome 2q24
DOID:0080420
early infantile epileptic encephalopathy 63
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the CPLX1 gene on chromosome 4p16
DOID:0080426
early infantile epileptic encephalopathy 65
class of disease
Ohtahara syndrome
human disease
DOID:0080430
early infantile epileptic encephalopathy 66
class of disease
Ohtahara syndrome
early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the PACS2 gene on chromosome 14q32
DOID:0080446
early infantile epileptic encephalopathy 8
class of disease
Ohtahara syndrome
hyperekplexia
human disease
DOID:0080215
early infantile epileptic encephalopathy 82
class of disease
autosomal recessive disease
Ohtahara syndrome
human disease
DOID:0080715
early invasive cervical adenocarcinoma
class of disease
cervical adenocarcinoma
Human disease
DOID:8307
early onset absence epilepsy
class of disease
childhood electroclinical syndrome
childhood electroclinical syndrome characterized by the occurrence of typical absence seizures starting between the age of four and ten years
DOID:0050708
early yaws
class of disease
yaws
A yaws that results in initial papule at the site of entry of bacteria. Without treatment, this is followed by disseminated skin lesions over the body. Bone pain and bone lesions may also occur.
DOID:10568
early-onset vitamin B6-dependent epilepsy
class of disease
autosomal recessive disease
epilepsy
human disease
DOID:0080769
eating disorder
class of disease
specific developmental disorder
nutrition disorder
disease
habit of eating either insufficient or excessive food, to the detriment of health
DOID:8670
F03.400
Eating disorder
eccrine acrospiroma
class of disease
eccrine sweat gland neoplasm
Human disease
DOID:5442
C04.557.470.035.175.588
C04.557.470.550.175.588
eccrine adenocarcinoma
class of disease
eccrine sweat gland cancer
adenocarcinoma
eccrine sweat gland cancer that derives from epithelial cells of glandular origin
DOID:4920
eccrine mixed tumor of skin
class of disease
eccrine sweat gland neoplasm
Human disease
DOID:2079
Chondroid syringoma
eccrine papillary adenocarcinoma
class of disease
eccrine adenocarcinoma
Human disease
DOID:5591
eccrine sweat gland cancer
class of disease
sweat gland cancer
eccrine sweat gland neoplasm
Human disease
DOID:4921
eccrine sweat gland neoplasm
class of disease
sweat gland neoplasm
human disease
DOID:173
eclampsia
class of disease
pre-eclampsia
disease
life emergency
pre-eclampsia characterized by the presence of seizures
DOID:13593
DOID:12269
DOID:12268
C13.703.395.124
Eclampsia
ecthyma
class of disease
impetigo
Human disease
DOID:11907
C01.150.252.410.890.168
C01.150.252.819.210
C01.800.720.210
C17.800.695.210
C17.800.838.765.210
Ecthyma
ectodermal dysplasia 1
class of disease
hypohidrotic ectodermal dysplasia
X-linked recessive disease
human disease
DOID:0111664
ectodermal dysplasia 10A
class of disease
hypohidrotic ectodermal dysplasia
autosomal dominant disease
human disease
DOID:0111663
ectodermal dysplasia 10B
class of disease
hypohidrotic ectodermal dysplasia
autosomal recessive disease
human disease
DOID:0111665
ectodermal dysplasia 11B
class of disease
hypohidrotic ectodermal dysplasia
autosomal recessive disease
human disease
DOID:0111654
ectodermal dysplasia 14
class of disease
autosomal recessive disease
ectodermal dysplasia
human disease
DOID:0111662
ectodermal dysplasia 15
class of disease
ectodermal dysplasia
autosomal recessive disease
human disease
DOID:0111651
ectodermal dysplasia 4
class of disease
autosomal recessive disease
pure hair-nail type ectodermal dysplasia
human disease
DOID:0111658
ectodermal dysplasia 5
class of disease
pure hair-nail type ectodermal dysplasia
autosomal recessive disease
human disease
DOID:0111657
ectodermal dysplasia 6
class of disease
autosomal recessive disease
pure hair-nail type ectodermal dysplasia
human disease
DOID:0111659
ectodermal dysplasia 7
class of disease
autosomal recessive disease
pure hair-nail type ectodermal dysplasia
human disease
DOID:0111660
ectodermal dysplasia 8
class of disease
autosomal recessive disease
ectodermal dysplasia
human disease
DOID:0111661
ectodermal dysplasia 9
class of disease
autosomal recessive disease
pure hair-nail type ectodermal dysplasia
human disease
DOID:0111656
ectomesenchymoma
class of disease
central nervous system mesenchymal non-meningothelial tumor
nervous system cancer
human disease
DOID:4055
ectopic Cushing syndrome
class of disease
hyperaldosteronism
ACTH-dependent Cushing syndrome
human disease
DOID:0060890
C04.730.713.317
ectopic pregnancy
class of disease
female reproductive system disease
human pregnancy
disease
female reproductive system disease characterized by the implantation of the embryo outside the uterine cavity
DOID:0060329
C13.703.733
Ectopic pregnancy
ectopic thymus
class of disease
thymus gland disease
Human disease
DOID:6307
ectothrix infectious disease
class of disease
tinea capitis vale
hair diseases
Human disease
DOID:0050097
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1
class of disease
ectrodactyly–ectodermal dysplasia–cleft syndrome
An EEC syndrome characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 7q11.2-q21.3.
DOID:0060784
ectrodactyly–ectodermal dysplasia–cleft syndrome
class of disease
autosomal dominant disease
ectodermal dysplasia
syndrome
autosomal dominant disease characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip-palate)
DOID:0060782
ectropion
class of disease
eyelid disease
human disease
DOID:1570
C11.338.362
Ectropion
eczematous dermatitis of eyelid
class of disease
noninfectious dermatoses of eyelid
Human disease
DOID:1893
egg allergy
class of disease
food allergy
health effects of eggs
food allergy that is an allergy or hypersensitivity to dietary substances from the yolk or whites of eggs, causing an overreaction of the immune system which may lead to severe physical symptoms
DOID:4377
C20.543.480.370.150
ego-dystonic sexual orientation
class of disease
gender dysphoria
disease
psychiatric diagnosis
DOID:13352
electroclinical syndrome
class of disease
epilepsy
Human disease
DOID:0050701
elephantiasis
class of disease
lymphedema
Human disease
DOID:4976
C15.604.496.320
Elephantiasis
embryoma
class of disease
embryonal cancer
carcinosarcoma and embryonal cancer that is located in embryonic tissue and results in a mass of rapidly growing cells
DOID:4766
Embryonal tumors
embryonal cancer
class of disease
germ cell cancer
germ cell cancer that is associated with an embryo
DOID:688
embryonal carcinoma
class of disease
embryonal cancer
extragonadal germ cell cancer
extragonadal non-dysgerminomatous germ cell tumor
carcinoma
disease
embryonal cancer that is a type of germ cell tumour, located in the ovaries or testes
DOID:3308
C04.557.465.200
Embryonal carcinoma
embryonal extrahepatic bile duct rhabdomyosarcoma
class of disease
bile duct rhabdomyosarcoma
Human disease
DOID:3253
embryonal rhabdomyosarcoma
class of disease
rhabdomyosarcoma
embryonal cancer
rhabdomyosarcoma with mesenchymally-derived malignant cells resembling the developing skeletal muscle of the embryo
DOID:3246
C04.557.450.590.550.660.675
C04.557.450.795.550.660.675
embryonal testis carcinoma
class of disease
embryonal carcinoma
testicular cancer
testicular non-seminomatous germ cell cancer
testicular pure germ cell tumor
embryonal carcinoma that is located in the testis
DOID:5680
emphysematous cholecystitis
class of disease
cystitis
cholecystitis
bacterial infectious disease with inflammation of the gallbladder characterized by air-filled expansions in interstitial or subcutaneous tissues
DOID:9765
C06.130.564.263.500.500
enamel caries
class of disease
dental caries
Human disease
DOID:217
enamel erosion
class of disease
dental erosion
Human disease
DOID:2497
encapsulated thymoma
class of disease
thymoma
Human disease
DOID:3278
encephalitis
class of disease
symptom or sign
brain inflammatory disease
encephalopathy
neurological symptom
disease
acute inflammation of the brain with flu-like symptoms
DOID:9588
C10.228.140.430
C10.586.250
Encephalitis
encephalomalacia
class of disease
encephalopathy
Human disease
DOID:2034
C10.228.140.461
encephalomyelitis
class of disease
central nervous system disease
inflammatory disease
disease
inflammation of the brain and spinal cord
DOID:640
C10.228.228.291
C10.228.440
C01.207.291
Encephalomyelitis
encephalopathy
class of disease
central nervous system disease
disease
central nervous system diseases located in the brain
DOID:936
C10.228.140
Encephalopathy
encephalopathy due to defective mitochondrial and peroxisomal fission 1
class of disease
syndrome
human disease
DOID:0070347
end stage renal failure
class of disease
chronic renal insufficiency
human disease
DOID:783
endemic goiter
class of disease
goiter
nutritional deficiency disease
human disease
DOID:13198
C19.874.283.300
endobronchial leiomyoma
class of disease
lung leiomyoma
bronchial neoplasm
Human disease
DOID:6608
endobronchial lipoma
class of disease
bronchial neoplasm
respiratory system benign neoplasm
lipoma
Human disease
DOID:10183
endocardial fibroelastosis
class of disease
endocardium disease
familial restrictive cardiomyopathy
non-familial restrictive cardiomyopathy
non-familial dilated cardiomyopathy
endocardium disease that is characterized by endocardium becoming massively fibrosed and thickened wih elastic tissue resulting in a restrictive cardiomyopathy.
DOID:12929
C14.280.238.281
endocarditis
class of disease
symptom or sign
endocardium disease
pancarditis
cardiovascular system symptom
disease
endocardium disease characterized by inflammation of the endocardium of the heart chambers and valves
DOID:10314
C14.280.282
Endocarditis
endocardium cancer
class of disease
heart cancer
neoplasm of endocardium
endocardium disease
Human disease
DOID:5877
endocervical adenocarcinoma
class of disease
endocervical carcinoma
adenocarcinoma
endocervical carcinoma that derives from epithelial cells of glandular origin
DOID:0050940
Endocervical adenocarcinoma
endocervical carcinoma
class of disease
cervix carcinoma
malignant neoplasm of endocervix
Human disease
DOID:7519
endocervical type cervical adenomyoma
class of disease
cervical adenomyoma
Human disease
DOID:8177
endocervical type cervical mucinous adenocarcinoma
class of disease
cervical mucinous adenocarcinoma
Human disease
DOID:8340
endocervicitis
class of disease
cervicitis
inflammatory disease
Human disease
DOID:5757
endocrine exophthalmos
class of disease
orbital disease
exophthalmos
Human disease
DOID:12359
endocrine gland cancer
class of disease
organ system cancer
endocrine gland neoplasm
endocrine system disease
organ system cancer located in endocrine system that is characterized by uncontrolled cellular proliferation of the hormone producing glands of the endocrine system
DOID:170
endocrine organ benign neoplasm
class of disease
organ system benign neoplasm
endocrine gland neoplasm
endocrine system disease
organ system benign neoplasm that is located in endocrine glands which secretes a type of hormone directly into the bloodstream to regulate the body
DOID:0060089
endocrine pancreas disease
class of disease
pancreas disease
endocrine system disease
disease involving the endocrine pancreas
DOID:1428
endocrine system disease
class of disease
disease of anatomical entity
disease
type of disease affecting the endocrine system
DOID:28
DOID:1922
C19
Endocrine diseases and disorders
endodermal sinus pattern testicular yolk sac tumor
class of disease
testicular yolk sac tumor
Human disease
DOID:7302
endogenous depression
class of disease
major depressive disorder
endogenous mental disorder
mental depression that is characterized by a dysregulation of the endogenous opioid system and not of the monaminergic system
DOID:1595
endometrial adenocarcinoma
class of disease
endometrial carcinoma
adenocarcinoma
endometrial carcinoma that derives from epithelial cells of glandular origin
DOID:2870
Endometrial adenocarcinoma
endometrial adenosquamous carcinoma
class of disease
adenosquamous carcinoma
endometrial squamous cell carcinoma
squamous cell carcinoma
endometrial cancer
endometrial carcinoma that derives from squamous cells and gland-like cells
DOID:5631
endometrial cancer
class of disease
uterine cancer
uterine corpus cancer
endometriosis
endometrial neoplasm
disease
uterine cancer that is located in tissues lining the uterus
DOID:1380
Endometrial cancer
endometrial carcinoma
class of disease
endometrial cancer
carcinoma
endometrial cancer that is located in the tissue lining the uterus
DOID:2871
C04.557.470.200.025.240
C04.588.945.418.948.585.124
C13.351.500.056.630.705.331
C13.351.937.418.685.331
C13.351.937.418.875.200.124
C19.391.630.705.331
endometrial clear cell adenocarcinoma
class of disease
endometrial adenocarcinoma
clear cell adenocarcinoma
Human disease
DOID:5299
endometrial disease
class of disease
uterine disease
Human disease
DOID:1005
Diseases and disorders of endometrium
endometrial hyperplasia
class of disease
uterine benign neoplasm
endometrial disease
disease
uterine benign neoplasm that is characterized by excessive proliferation of the cells of the endometrium
DOID:0080365
C13.351.500.852.228
endometrial mixed adenocarcinoma
class of disease
endometrial adenocarcinoma
Human disease
DOID:7664
endometrial mucinous adenocarcinoma
class of disease
endometrial adenocarcinoma
mucinous adenocarcinoma
human disease
DOID:3707
endometrial small cell carcinoma
class of disease
uterine cancer
endometrial cancer
carcinoma
Human disease
DOID:7139
endometrial squamous cell carcinoma
class of disease
endometrial carcinoma
squamous cell carcinoma
Human disease
DOID:5533
endometrial stromal nodule
class of disease
uterine benign neoplasm
endometrial stromal tumour
human disease
DOID:1373
endometrial stromal sarcoma
class of disease
endometrial stromal tumour
human disease
DOID:4226
C04.557.435.775
C04.557.450.795.332.500
C13.351.500.852.762.200.500.500
C13.351.937.418.875.200.374.500
Endometrial stromal sarcoma
endometrial stromal tumour
class of disease
endometrial cancer
human disease
DOID:5166
C04.557.450.565.325
C04.557.450.795.332
C13.351.500.852.762.200.500
C13.351.937.418.875.200.374
endometrial transitional cell carcinoma
class of disease
endometrial carcinoma
transitional cell carcinoma
Human disease
DOID:4005
endometrial type cervical adenomyoma
class of disease
cervical adenomyoma
Human disease
DOID:8178
endometrioid ovary carcinoma
class of disease
ovary adenocarcinoma
endometrial adenocarcinoma
uterine cancer
endometrial carcinoma
ovarian endometrial cancer
Human disease
DOID:5828
endometriosis
class of disease
female reproductive system disease
endometrial disease
disease
disease linked to the female reproductive system
DOID:289
C12.050.351.500.163
C12.100.250.163
Endometriosis
endometriosis of intestine
class of disease
endometriosis
intestinal disease
Human disease
DOID:11428
Endometriosis of intestine
endometriosis of ovary
class of disease
endometriosis
ovarian disease
Human disease
DOID:11432
endometriosis of pelvic peritoneum
class of disease
endometriosis
Human disease
DOID:11429
endometriosis of rectovaginal septum and vagina
class of disease
endometriosis
vaginal disease
Human disease
DOID:11431
endometritis
class of disease
endometrial disease
disease
inflammation of inner lining of uterus
DOID:1002
C13.351.500.056.750.249
C13.351.500.852.299
Endometritis
endometrium carcinoma in situ
class of disease
in situ carcinoma
endometriosis
uterus carcinoma in situ
Human disease
DOID:5172
endomyocardial fibrosis
class of disease
restrictive cardiomyopathy
Human disease
DOID:12932
C14.280.238.406
endophthalmitis
class of disease
globe disease
eye inflammation
disease
globe disease that is characterized by inflammation of the inside of the eye
DOID:4692
C01.375.265
C11.294.265
endosalpingiosis
class of disease
endometriosis
Human disease
DOID:11427
Endosalpingiosis
endothrix infectious disease
class of disease
tinea capitis vale
hair diseases
tinea capitis that results in fungal infection located in hair, has material basis in Ascomycota fungi that belong to a group called dermatophytes, which produce arthroconidia within the hair shaft only
DOID:0050105
enhanced S-cone syndrome
class of disease
retinal disease
vitreoretinal degeneration
unclassified primitive or secondary maculopathy
genetic disease
autosomal recessive disease
Goldmann-Favre syndrome (GFS) is a vitreoretinal dystrophy characterized by early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular edema, retinoschisis)
DOID:0090059
enophthalmos
class of disease
orbital disease
enophthalmia
disease
posterior displacement of the eyeball within the orbit due to changes in the volume of the orbit (bone) relative to its contents
DOID:11175
C11.675.319
enteric pattern testicular yolk sac tumor
class of disease
testicular yolk sac tumor
Human disease
DOID:8362
enterocele
class of disease
pelvic organ prolapse
Human disease
DOID:1283
Enterocele
enthesopathy
class of disease
connective tissue disease
disease
human disease: a disorder involving the attachment of a tendon or ligament to a bone
DOID:204
C05.651.869.653
C26.874.800.750
Enthesopathy
entropion
class of disease
eyelid disease
disease
medical condition in which the eyelid (usually the lower lid) folds inward
DOID:12397
C11.338.443
Entropion
environmental induced asthma
class of disease
intrinsic asthma
human disease
DOID:0080819
eosinophilia-myalgia syndrome
class of disease
eosinophilia
Human disease
DOID:998
C05.651.290
C10.668.491.387
C15.378.553.231.335
Eosinophilia–myalgia syndrome
eosinophilic gastritis
class of disease
gastritis
chronic gastritis
Human disease
DOID:4030
eosinophilic meningitis
class of disease
chronic meningitis
Human disease
DOID:10361
eosinophilic pneumonia
class of disease
pneumonia
eosinophilia
disease
disease in which an eosinophil, a type of white blood cell, accumulates in the lung
DOID:9498
DOID:5870
C08.381.750
C15.378.553.231.549.750
eosinophilic variant of chromophobe renal cell carcinoma
class of disease
chromophobe renal cell carcinoma
Human disease
DOID:6606
ependymal tumor
class of disease
ependymal tumor
cerebral ventricle cancer
carcinoma
malignant glioma that is derived from ependymal cells, a type of glial cell, located in ventricle lining within the central part of the brain
DOID:5074
Ependymal tumors
epicardium cancer
class of disease
pericardium cancer
neoplasm of epicardium
Human disease
DOID:4699
epicardium lipoma
class of disease
heart lipoma
lipoma
benign neoplasm of epicardium
Human disease
DOID:6284
epidermal appendage tumor
class of disease
skin benign neoplasm
Adnexal and skin appendage neoplasms
epidermal appendage disease
neoplasms located in skin appendages
DOID:2433
epidermodysplasia verruciformis
class of disease
autosomal recessive disease
viral infectious disease
skin disease
immune deficiency with skin involvement
other immunodeficiency syndromes due to defects in innate immunity
primary immunodeficiency disease
disease
Human disease
DOID:13777
C01.925.256.650.810.345
C01.925.825.810.260
C01.925.928.914.345
C17.800.838.790.810.260
Epidermodysplasia verruciformis
epidermolysis bullosa acquisita
class of disease
epidermolysis bullosa
pemphigoid
bullous skin disease
autoimmune skin disease
chronic subepidermal blistering disease associated with autoimmunity to type VII collagen
DOID:4313
C16.131.831.493.080
C17.800.804.493.080
C17.800.827.275.080
C17.800.865.410.080
epidermolysis bullosa herpetiformis
class of disease
epidermolysis bullosa simplex
basal epidermolysis bullosa simplex
genetic disease
autosomal dominant disease
Human disease
DOID:0060735
epidermolysis bullosa with congenital localized absence of skin and deformity of nails
class of disease
dominant dystrophic epidermolysis bullosa
autosomal dominant disease
human disease
DOID:0111347
epidermolytic acanthoma
class of disease
acanthoma
Human disease
DOID:4323
epidermolytic hyperkeratosis
class of disease
skin disease
congenital ichthyosiform erythroderma
keratinopathic ichthyosis
rare and severe form of ichthyosis
DOID:4603
C16.131.831.512.400.375
C16.320.850.400.375
C16.614.492.400.375
C17.800.428.333.250.375
C17.800.804.512.400.375
C17.800.827.400.375
Epidermolytic ichthyosis
epididymal neoplasm
class of disease
male reproductive system neoplasm
epididymis disease
testicular cancer
Human disease
DOID:512
epididymis adenocarcinoma
class of disease
epididymis cancer
adenocarcinoma
epididymis cancer that derives from epithelial cells of glandular origin
DOID:10368
epididymis adenomatoid tumor
class of disease
male reproductive organ benign neoplasm
adenomatoid tumor
benign neoplasm of epididymis
adenoma
Human disease
DOID:745
epididymis cancer
class of disease
male reproductive organ cancer
epididymal neoplasm
epididymis disease
Human disease
DOID:10366
epididymis disease
class of disease
male reproductive system disease
human disease
DOID:0080373
epidural abscess
class of disease
central nervous system disease
abscess
central nervous system cancer
human disease
DOID:11387
C01.207.300
C10.228.228.300
C10.228.228.709.350
C10.228.854.303
C01.207.709.350
C01.830.025.325
epidural neoplasm
class of disease
Spinal cord cancer
Human disease
DOID:3618
C04.588.614.250.803.342
C10.228.854.765.342
C10.551.240.750.200
epidural spinal canal angiolipoma
class of disease
angiolipoma
epidural neoplasm
cell type cancer
spinal cord disease
central nervous system organ benign neoplasm
Human disease
DOID:3617
epidural spinal canal meningioma
class of disease
spinal canal and spinal cord meningioma
Human disease
DOID:3809
epiglottis neoplasm
class of disease
supraglottis neoplasm
neoplasm of hypopharynx
Human disease
DOID:7105
epilepsy
class of disease
dictionary page in Wikipedia
encephalopathy
disease
human neurological disease causing seizures
DOID:1826
C10.228.140.490
Epilepsy
epilepsy, idiopathic generalized, susceptibility to, 8
class of disease
genetic disease
rare genetic epilepsy
generalized epilepsy
human disease
DOID:0111322
epiphora due to excess lacrimation
class of disease
excessive tearing
Human disease
DOID:14244
epiphora due to insufficient drainage
class of disease
excessive tearing
Human disease
DOID:13756
epiphyseal dysplasia, multiple, 6
class of disease
multiple epiphyseal dysplasia
genetic disease
multiple epiphyseal dysplasia due to collagen 9 anomaly
autosomal dominant disease
human disease
DOID:0070301
epiretinal membrane
class of disease
retinal disease
degeneration of macula and posterior pole
disease of the eye in response to changes in the vitreous humor or more rarely, diabetes
DOID:2006
C11.768.328
Epiretinal membrane
episcleritis periodica fugax
class of disease
scleral disease
episcleritis
Human disease
DOID:12124
episodic kinesigenic dyskinesia 2
class of disease
dystonia
genetic disease
autosomal dominant disease
A dystonia characterized by autosomal dominant inheritance of recurrent brief involuntary hyperkinesias triggered by sudden movements that has material basis in variation in the chromosome region 16q13-q22.1.
DOID:0090054
epithelial and subepithelial dystrophy
class of disease
corneal dystrophy
Human disease
DOID:0060440
epithelial malignant thymoma
class of disease
dendritic cell thymoma
Human disease
DOID:7926
epithelial predominant Wilms' tumor
class of disease
nephroblastoma
Human disease
DOID:5189
epithelial predominant pulmonary blastoma
class of disease
pulmonary blastoma
Human disease
DOID:4768
epithelial-myoepithelial carcinoma
class of disease
malignant epithelial tumor of salivary glands
salivary gland cancer
Human disease
DOID:5309
Epithelial-myoepithelial carcinoma
epithelial-stromal TGFBI dystrophy
class of disease
corneal dystrophy
stromal dystrophy
human disease
DOID:0060441
epithelioid cell melanoma
class of disease
melanoma
Human disease
DOID:4360
epithelioid cell synovial sarcoma
class of disease
synovial sarcoma
monophasic synovial sarcoma
Human disease
DOID:5494
epithelioid inflammatory myofibroblastic sarcoma
class of disease
inflammatory myofibroblastic tumour
human disease
DOID:0080372
epithelioid leiomyosarcoma
class of disease
leiomyosarcoma
Human disease
DOID:5264
epithelioid malignant peripheral nerve sheath tumor
class of disease
malignant peripheral nerve sheath tumor
Human disease
DOID:8353
epithelioid neurofibroma
class of disease
neurofibroma
Human disease
DOID:5149
epithelioid sarcoma
class of disease
soft-tissue sarcoma
connective tissue neoplasm
sarcoma
human disease
DOID:6193
Epithelioid sarcoma
epithelioid trophoblastic tumor
class of disease
cervical uterine cancer
lung cancer
cell type cancer
gestational trophoblastic disease
trophoblastic neoplasm
Human disease
DOID:3593
epithelioid type angiomyolipoma
class of disease
angiomyolipoma
angiomyolipoma composed exclusively or predominantly by polygonal epithelioid cells with eosinophilic cytoplasm, often associated with cytologic atypia
DOID:3318
Epithelioid angiomyolipoma
epithelioma cuniculatum
class of disease
verrucous carcinoma
Foot Dermatoses
cutaneous squamous-cell carcinoma
Human disease
DOID:3751
epulis
class of disease
gingival overgrowth
Human disease
DOID:5337
Epulis
equatorial staphyloma
class of disease
scleral staphyloma
Human disease
DOID:13788
erectile dysfunction
class of disease
symptom or sign
sexual dysfunction
reproductive system symptom
disease
form of sexual dysfunction in males
DOID:1875
C12.100.500.214
F03.835.400
C12.100.875.486
C12.200.294.214
Erectile dysfunction
erythema elevatum diutinum
class of disease
vasculitis
reactive neutrophilic dermatose
immune complex mediated vasculitis
vasculitis characterised by red, purple, brown or yellow papules (raised spot), plaques, or nodules, found on the backs of the hands, other extensor surfaces overlying joints, and on the buttocks
DOID:0060567
Erythema elevatum diutinum
erythema multiforme
class of disease
skin disease
erythema
allergy
disease
skin disease that is a type of allergic reaction located in skin, which occurs in response to medications, infections, or illness
DOID:0050185
C17.800.229.400
C17.800.865.475
Erythema multiforme
erythema nodosum
class of disease
reactive neutrophilic dermatose
clinical sign
panniculitis
disease
skin disease
DOID:0080750
C17.800.174.600.375
C17.800.229.413
C20.543.206.380.375
C25.100.468.380.375
Erythema nodosum
erythematosquamous dermatosis
class of disease
skin disease
Human disease
DOID:9097
erythrasma
class of disease
pyoderma
Corynebacterium infection
disease
Human disease
DOID:4131
C01.150.252.410.040.246.694
C01.150.252.819.320
C01.800.720.320
C17.800.838.765.320
Erythrasma
erythrokeratodermia variabilis et progressiva 1
class of disease
autosomal dominant disease
autosomal recessive disease
erythrokeratodermia variabilis
An erythrokeratodermia variabilis that has material basis in heterozygous, homozygous, or compound heterozygous mutation in GJB3 on 1p34.3.
DOID:0111195
erythrokeratodermia variabilis et progressiva 2
class of disease
erythrokeratodermia variabilis
autosomal dominant disease
human disease
DOID:0080248
erythrokeratodermia variabilis et progressiva 3
class of disease
erythrokeratodermia variabilis
autosomal dominant disease
human disease
DOID:0080249
erythrokeratodermia variabilis et progressiva 4
class of disease
erythrokeratodermia variabilis
human disease
DOID:0080250
erythrokeratodermia variabilis et progressiva 5
class of disease
erythrokeratodermia variabilis
autosomal recessive disease
human disease
DOID:0080251
erythrokeratodermia variabilis et progressiva 6
class of disease
erythrokeratodermia variabilis
autosomal dominant disease
human disease
DOID:0080766
erythropoietin polycythemia
class of disease
acquired polycythemia
Human disease
DOID:2839
esophageal adenoid cystic carcinoma
class of disease
esophageal carcinoma
esophageal carcinoma that derives from epithelial cells of the salivary gland
DOID:4878
esophageal adenosquamous carcinoma
class of disease
adenosquamous carcinoma
squamous cell carcinoma
esophageal cancer
esophageal carcinoma that derives from squamous cells and gland-like cells
DOID:5625
esophageal basaloid squamous cell carcinoma
class of disease
basaloid squamous cell carcinoma
esophageal cancer
squamous cell carcinoma
Human disease
DOID:7051
esophageal cancer
class of disease
esophageal neoplasm
esophageal disease
gastrointestinal system cancer
disease
gastrointestinal system cancer that is located in the esophagus
DOID:5041
Esophageal cancer
esophageal candidiasis
class of disease
candidiasis
fungal esophagitis
esophageal disease
candidiasis that involves fungal infection of the esophagus by Candida albicans in immunocompromised people, resulting in lesions, bleeding, painful swallowing and substernal pain
DOID:13146
Esophageal candidiasis
esophageal carcinoma
class of disease
esophageal cancer
carcinoma
esophageal cancer that has material basis in abnormally proliferating cells derives from epithelial cells
DOID:1107
esophageal disease
class of disease
gastrointestinal system disease
gastrointestinal system disease that is located in the esophagus
DOID:6050
C06.405.117
Diseases and disorders of the esophagus
esophageal diverticulosis
class of disease
esophageal disease
esophageal diverticulum
Human disease
DOID:13185
C06.405.117.136
C06.405.205.282.500.438
esophageal leukoplakia
class of disease
esophageal disease
leukoplakia
Human disease
DOID:9021
esophageal neuroendocrine tumor
class of disease
esophageal cancer
Human disease
DOID:5784
esophageal varix
class of disease
vein disorder
esophageal disease
esophageal and gastric varices
disease
Human disease
DOID:112
Esophageal varices
esophagus adenocarcinoma
class of disease
esophageal carcinoma
adenocarcinoma
esophageal carcinoma that derives from epithelial cells of glandular origin
DOID:4914
Adenocarcinomas of esophagus
esophagus carcinoma in situ
class of disease
in situ carcinoma
esophageal disease
Human disease
DOID:9095
esophagus leiomyoma
class of disease
benign neoplasm of esophagus
esophageal disease
gastrointestinal system benign neoplasm
Human disease
DOID:960
esophagus leiomyosarcoma
class of disease
esophagus sarcoma
Human disease
DOID:5276
esophagus liposarcoma
class of disease
esophagus sarcoma
liposarcoma
esophageal cancer
Human disease
DOID:5694
esophagus small cell carcinoma
class of disease
esophageal carcinoma
esophageal neuroendocrine tumor
inherited neuroendocrine tumor
small cell carcinoma
Human disease
DOID:7134
esophagus squamous cell carcinoma
class of disease
esophageal carcinoma
squamous cell carcinoma
esophageal carcinoma that derives from epithelial squamous cells located in the esophagus
DOID:3748
Squamous-cell carcinoma of esophagus
esophagus squamous cell papilloma
class of disease
benign neoplasm of esophagus
esophageal disease
gastrointestinal system benign neoplasm
Human disease
DOID:959
Esophageal squamous papilloma
esophagus verrucous carcinoma
class of disease
esophagus squamous cell carcinoma
verrucous carcinoma
Human disease
DOID:3747
esotropia
class of disease
strabismus
Esotropia is a strabismus in which the eye turns inward toward the nose
DOID:9840
C10.292.562.887.300
C11.590.810.400
Esotropia
essential hypertension
class of disease
arterial hypertension
disease
hypertension with no known cause, the most common type of hypertension
DOID:10825
C14.907.489.165
essential tremor 1
class of disease
autosomal dominant disease
essential tremor
human disease
DOID:0111428
essential tremor 2
class of disease
autosomal dominant disease
essential tremor
human disease
DOID:0111429
essential tremor 3
class of disease
essential tremor
human disease
DOID:0111430
essential tremor 4
class of disease
essential tremor
autosomal dominant disease
human disease
DOID:0111431
essential tremor 5
class of disease
essential tremor
autosomal dominant disease
human disease
DOID:0111432
esthesioneuroblastoma
class of disease
blastoma
head and neck cancer
olfactory nerve neoplasm
disease
rare cancer of the nasal cavity
DOID:369
C04.557.465.625.600.590.650.550.150
C04.557.470.670.590.650.550.150
C04.557.580.625.600.590.650.550.150
C10.292.650.200
estrogen excess
class of disease
ovarian dysfunction
Human disease
DOID:14336
estrogen-receptor negative breast cancer
class of disease
breast cancer
Human disease
DOID:0060076
estrogen-receptor positive breast cancer
class of disease
breast cancer
Hormone receptor positive breast tumor
Human disease
DOID:0060075
ethmoid sinus adenocarcinoma
class of disease
ethmoid sinus cancer
adenocarcinoma
ethmoid sinus cancer that derives from epithelial cells of glandular origin
DOID:2766
ethmoid sinus cancer
class of disease
paranasal sinus cancer
ethmoidal sinus neoplasm
Human disease
DOID:1363
ethmoid sinus squamous cell carcinoma
class of disease
ethmoid sinus cancer
squamous cell carcinoma
Human disease
DOID:2763
ethmoid sinusitis
class of disease
sinusitis
sinusitis which involves infection of ethmoid sinuses that causes pain or pressure behind and between the eyes, tearing, and headache over the forehead
DOID:9507
C08.460.692.752.267
C08.730.749.267
C09.603.692.752.267
C01.748.749.267
ethmoidal sinus neoplasm
class of disease
paranasal sinus neoplasm
Human disease
DOID:1364
eumycotic mycetoma
class of disease
dermatomycosis
mycetoma
disease
chronic granulomatous fungal disease of humans
DOID:13078
Madura foot
eunuchism
class of disease
hypogonadism, male
hypogonadism
disease
hypogonadism that is characterized by the lack of mature male germ cells and testicular hormones
DOID:5003
C19.391.482.293
Eunuchoidism
euthyroid sick syndrome
class of disease
thyroid gland disease
Secondary allostasis of thyroid function in fetal life, starving and in critical illness
DOID:2856
C19.874.255
eversion of lacrimal punctum
class of disease
lacrimal apparatus disease
Human disease
DOID:13651
exanthem
class of disease
symptom or sign
skin disease
rash
disease
human disease
DOID:0050486
C17.800.257
Exanthem
exanthema subitum
class of disease
viral infectious disease
Roseolovirus infectious disease
disease
Human disease
DOID:0050495
C01.925.256.466.850.290
C01.925.825.290
C17.800.257.335
C17.800.838.790.290
Roseola
excessive tearing
class of disease
symptom or sign
lacrimal apparatus disease
tear secretion
eye symptom
disease
overflow of tears onto the face
DOID:13757
Epiphora (medicine)
excoriation
class of disease
symptom or sign
dermatitis
disease
human disease
DOID:9165
exercise-induced bronchoconstriction
class of disease
asthma
dyspnea on effort
intrinsic asthma
medical condition
DOID:0080821
C08.127.108.110
C08.674.095.110
C20.543.480.680.095.110
exfoliation syndrome
class of disease
iris disease
hereditary glaucoma
phacogenic glaucoma
syndrome that occurs when tiny flakes of dandruff-like material build up in the body and are found in the heart, kidneys, liver, lungs, and eye
DOID:13641
C11.941.375.285
exocervical carcinoma
class of disease
cervix carcinoma
Human disease
DOID:2892
exocrine pancreatic insufficiency
class of disease
pancreas disease
Human disease
DOID:13316
C06.689.276
exophthalmic ophthalmoplegia
class of disease
ophthalmoplegia
Human disease
DOID:13135
exostosis
class of disease
hyperostosis
hyperostosis that involves formation of new bone on the surface of preexisting bone
DOID:203
C05.116.540.310
Exostoses
exotropia
class of disease
strabismus
form of strabismus where the eyes are deviated outward
DOID:1143
C10.292.562.887.650
C11.590.810.440
Exotropia
exposure keratitis
class of disease
keratoconjunctivitis
Human disease
DOID:9461
expressive language disorder
class of disease
language disorder
specific language impairment-5
neurodevelopmental condition
DOID:11385
external auditory meatus lipoma
class of disease
sensory organ benign neoplasm
lipoma
external ear neoplasm
benign neoplasm of ear
Human disease
DOID:10203
external resorption
class of disease
tooth resorption
human disease
DOID:14529
extra-adrenal pheochromocytoma
class of disease
malignant pheochromocytoma
adrenal medulla cancer that originate in the ganglia of the sympathetic nervous system and are named based upon the primary anatomical site of origin
DOID:0050936
extracranial neuroblastoma
class of disease
neuroblastoma
Human disease
DOID:371
extracutaneous mastocytoma
class of disease
systemic mastocytosis
mastocytoma
connective tissue neoplasm
benign mastocytoma
genetic hematologic disease
rare genetic immune disease
inherited tumor
rare genetic bone disease
Human disease
DOID:4659
extragonadal germ cell cancer
class of disease
germ cell cancer
extragonadal germ cell tumor
A germ cell cancer that derives from germ cells that are found in areas of the body other than the ovary or testicle. The tumors originate in the sperm forming cells in the testicles or egg producing cells in the ovary.
DOID:4717
extragonadal nonseminomatous germ cell tumor
class of disease
extragonadal germ cell cancer
brain cancer
mediastinal cancer
extragonadal non-dysgerminomatous germ cell tumor
germ cell cancer
nongerminomatous germ cell tumor
extragonadal germ cell cancer that are located in the pineal gland in the brain, located in the mediastinum or located in the abdomen
DOID:5677
extragonadal seminoma
class of disease
seminoma
Human disease
DOID:5838
extrahepatic bile duct adenocarcinoma
class of disease
extrahepatic bile duct carcinoma
adenocarcinoma
bile duct adenocarcinoma
extrahepatic bile duct carcinoma that derives from epithelial cells of glandular origin
DOID:3495
extrahepatic bile duct adenoma
class of disease
bile duct adenoma
biliary tract neoplasm
bile duct ademona and neoplasm of extrahepatic bile duct that are composed of papillary, tubular, or combined tubulopapillary structures lined by dysplastic epithelium
DOID:5438
extrahepatic bile duct carcinoma
class of disease
bile duct carcinoma
bile duct cancer
Human disease
DOID:4682
extrahepatic bile duct cystadenoma
class of disease
bile duct cystadenoma
extrahepatic bile duct adenoma
Human disease
DOID:8105
extrahepatic bile duct leiomyoma
class of disease
leiomyoma
bile duct disease
biliary tract neoplasm
liver leiomyoma
Human disease
DOID:5125
extrahepatic bile duct leiomyosarcoma
class of disease
bile duct sarcoma
leiomyosarcoma
extrahepatic bile duct carcinoma
liver leiomyosarcoma
leiomyosarcoma and sarcoma of bile duct that is located in the bile duct or located in the outside of the liver
DOID:5293
extrahepatic bile duct lipoma
class of disease
biliary tract neoplasm
lipoma
bile duct disease
liver lipoma
human disease
DOID:10209
extrahepatic bile duct papillary adenoma
class of disease
extrahepatic bile duct adenoma
biliary papillomatosis
Human disease
DOID:7503
extrahepatic bile duct small cell adenocarcinoma
class of disease
extrahepatic bile duct adenocarcinoma
liver neuroendocrine carcinoma
Human disease
DOID:5926
extrahepatic biliary papillomatosis
class of disease
biliary papillomatosis
Human disease
DOID:7752
extrahepatic cholestasis
class of disease
cholestasis
non-neoplastic bile duct disorder
Human disease
DOID:13619
C06.130.120.135.150
extramedullary plasmacytoma
class of disease
plasmacytoma
Human disease
DOID:3720
extranodal NK/T-cell lymphoma, nasal type
class of disease
T-cell lymphoma
mature T-cell and NK-cell lymphoma
nasal cavity cancer
medical condition
DOID:0080797
C04.557.386.480.750.199
extraosseous Ewing's sarcoma
class of disease
Ewing sarcoma
Human disease
DOID:4232
extraosseous Ewings sarcoma-primitive neuroepithelial tumor
class of disease
extraosseous Ewing's sarcoma
Human disease
DOID:4985
extraosseous chondrosarcoma
class of disease
chondrosarcoma
chondrosarcoma that is located in exclusively soft tissue
DOID:4549
extraosseous osteosarcoma
class of disease
osteosarcoma
connective tissue neoplasm
Human disease
DOID:3357
extrapulmonary tuberculosis
class of disease
tuberculosis
respiratory disease
DOID:0050598
C01.150.252.410.040.552.846.617
Extrapulmonary tuberculosis
extrapyramidal and movement disorder
class of disease
movement disorders
neurological disorder
disease of the nervous system
DOID:13839
extraskeletal chondroma
class of disease
connective tissue benign neoplasm
Human disease
DOID:3814
extraskeletal mesenchymal chondrosarcoma
class of disease
extraosseous chondrosarcoma
mesenchymal chondrosarcoma
Human disease
DOID:4548
extraskeletal myxoid chondrosarcoma
class of disease
extraosseous chondrosarcoma
myxoid chondrosarcoma
extraosseous chondrosarcoma that has material basis in cells derived from transformed cells that produce cartilage and is characterized by a marked abundance of extracellular mucoid (myxoid) matrix
DOID:6496
extratemporal epilepsy
class of disease
epilepsy
focal epilepsy
epilepsy syndrome that is located in an area of the brain other than the temporal lobe
DOID:2544
extrinsic allergic alveolitis
class of disease
symptom or sign
occupational disease
interstitial lung disease
allergy
disease
human disease
DOID:841
C08.381.483.125
C08.674.055
C20.543.480.680.075
Hypersensitivity pneumonitis
extrinsic asthma
class of disease
chronic asthma
allergy
human disease
DOID:0080811
exudative glomerulonephritis
class of disease
glomerulonephritis
Human disease
DOID:4777
exudative vitreoretinopathy 1
class of disease
exudative vitreoretinopathy
autosomal dominant disease
human disease
DOID:0111412
exudative vitreoretinopathy 3
class of disease
exudative vitreoretinopathy
autosomal dominant disease
human disease
DOID:0111409
exudative vitreoretinopathy 4
class of disease
exudative vitreoretinopathy
autosomal genetic disease
human disease
DOID:0111411
exudative vitreoretinopathy 5
class of disease
exudative vitreoretinopathy
autosomal dominant disease
human disease
DOID:0111408
exudative vitreoretinopathy 6
class of disease
exudative vitreoretinopathy
autosomal dominant disease
human disease
DOID:0111410
exudative vitreoretinopathy 7
class of disease
exudative vitreoretinopathy
autosomal dominant disease
human disease
DOID:0080264
eye accommodation disease
class of disease
eye disease
refraction or accommodation disorder
Human disease
DOID:10034
eye carcinoma
class of disease
ocular cancer
carcinoma
ocular cancer that has material basis in abnormally proliferating cells, derives from epithelial cells and arises from the tissues that cover structures located in the eye
DOID:295
eye degenerative disease
class of disease
eye disease
degenerative disease
neurodegenerative disease that involves the eye
DOID:9799
eye disease
class of disease
eye and adnexa disease
sensory system disease
organ-specific disease
health condition negatively affecting the eye
DOID:5614
C11
Diseases and disorders of the eye and adnexa
eyelid disease
class of disease
eye adnexa disease
skin disease
adnexa disease that is located in the eyelid
DOID:530
C11.338
eyelid neoplasm
class of disease
skin neoplasm
eyelid disease
facial neoplasm
skin benign neoplasm
human disease
DOID:2173
C04.588.443.392.500
C11.319.421
C11.338.526
facial dermatosis
class of disease
skin disease
head and neck disease
Human disease
DOID:3134
C17.800.271
facial nerve disease
class of disease
cranial nerve disease
human disease
DOID:1756
C07.465.299
C10.292.319
facial nerve neoplasm
class of disease
cranial nerve neoplasm
facial nerve disease
Human disease
DOID:1760
Facial nerve neoplasms
facial neuralgia
class of disease
neuralgia
facial nerve disease
orofacial pain
cranial neuralgia
human disease
DOID:13865
C07.465.299.625
C10.292.319.625
facioscapulohumeral muscular dystrophy
class of disease
muscular dystrophy
disease
Muscular dystrophy that classically weakens the muscles of the face (facio), shoulder girdle (scapulo) and upper arm (humerus). Weakness usually is asymmetrical and develops in other areas of the body as well, such as the abdomen and shin.
DOID:11727
C05.651.534.500.400
C10.668.491.175.500.400
C16.320.577.400
Facioscapulohumeral muscular dystrophy
facioscapulohumeral muscular dystrophy 1
class of disease
facioscapulohumeral muscular dystrophy
facioscapulohumeral muscular dystrophy that has material basis in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35
DOID:0111192
facioscapulohumeral muscular dystrophy 2
class of disease
digenic disease
facioscapulohumeral muscular dystrophy
A facioscapulohumeral muscular dystrophy that has material basis in digenic inheritance of a heterozygous mutation in SMCHDI on 18p11.32 and a haplotype on chromosome 4 that is permissive for DUX4 expression.
DOID:0111193
factitious disorder
class of disease
mental disorder
disease of mental health where symptoms are deliberately produced, feigned or exaggerated in order to falsely demonstrate the presence of an illness
DOID:1766
F03.875.375
Factitious disorders
factor VII deficiency
class of disease
inherited blood coagulation disease
blood coagulation disease
autosomal recessive disease
Human disease
DOID:2215
C15.378.100.100.310
C15.378.100.141.310
C15.378.463.310
C16.320.099.310
factor X deficiency
class of disease
inherited blood coagulation disease
blood coagulation disease
autosomal recessive disease
Human disease
DOID:2222
C15.378.100.100.320
C15.378.100.141.320
C15.378.463.320
C16.320.099.320
fallopian tube adenocarcinoma
class of disease
fallopian tube carcinoma
adenocarcinoma
fallopian tube carcinoma that derives from epithelial cells of glandular origin
DOID:3706
fallopian tube adenofibroma
class of disease
fallopian tube benign neoplasm
adenofibroma
serous adenofibroma
Human disease
DOID:5478
fallopian tube adenomatoid tumor
class of disease
fallopian tube benign neoplasm
adenomatoid tumor
adenoma
Human disease
DOID:5196
Adenomatoid tumor of fallopian tube
fallopian tube adenosarcoma
class of disease
fallopian tube carcinosarcoma
Human disease
DOID:1973
fallopian tube benign neoplasm
class of disease
female reproductive organ benign neoplasm
fallopian tube neoplasm
fallopian tube disease
Human disease
DOID:0060111
fallopian tube cancer
class of disease
female reproductive organ cancer
fallopian tube neoplasm
fallopian tube disease
female reproductive organ cancer that is located in fallopian tube
DOID:1964
Fallopian tube cancer
fallopian tube carcinoma
class of disease
fallopian tube cancer
carcinoma
fallopian tube cancer that is located in the fallopian tube
DOID:1963
fallopian tube carcinosarcoma
class of disease
fallopian tube cancer
fallopian tube cancer that is characterized as a mixture of carcinoma and sarcoma and has material basis in epithelial tissue and has material basis in connective tissue
DOID:1970
fallopian tube clear cell adenocarcinoma
class of disease
fallopian tube adenocarcinoma
clear cell adenocarcinoma
Human disease
DOID:5301
fallopian tube cystadenofibroma
class of disease
fallopian tube adenofibroma
cystadenofibroma
Human disease
DOID:8211
fallopian tube disease
class of disease
female reproductive system disease
adnexal disease
Human disease
DOID:1962
C13.351.500.056.390
Diseases and disorders of fallopian tubes
fallopian tube endometrioid adenocarcinoma
class of disease
fallopian tube adenocarcinoma
Human disease
DOID:5831
fallopian tube endometriosis
class of disease
fallopian tube disease
endometriosis
human disease
DOID:11424
Endometriosis of fallopian tube
fallopian tube germ cell cancer
class of disease
fallopian tube cancer
germ cell cancer
Human disease
DOID:5324
fallopian tube gestational choriocarcinoma
class of disease
fallopian tube carcinoma
gestational choriocarcinoma
fallopian tube germ cell cancer
familiar fallopian tube carcinoma
Human disease
DOID:8186
fallopian tube leiomyoma
class of disease
fallopian tube benign neoplasm
leiomyoma
Human disease
DOID:5124
fallopian tube leiomyosarcoma
class of disease
fallopian tube cancer
leiomyosarcoma
Human disease
DOID:1965
fallopian tube mucinous adenocarcinoma
class of disease
fallopian tube adenocarcinoma
fallopian tube mucinous tumor
mucinous adenocarcinoma
human disease
DOID:3704
fallopian tube mucinous tumor
class of disease
fallopian tube benign neoplasm
mucinous tumor
fallopian tube cancer
Human disease
DOID:3705
fallopian tube papillary adenocarcinoma
class of disease
fallopian tube adenocarcinoma
Human disease
DOID:5597
fallopian tube serous adenocarcinoma
class of disease
fallopian tube adenocarcinoma
serous cystadenocarcinoma
Human disease
DOID:5598
fallopian tube serous papilloma
class of disease
fallopian tube benign neoplasm
Human disease
DOID:3173
fallopian tube squamous cell carcinoma
class of disease
fallopian tube carcinoma
squamous cell carcinoma
Human disease
DOID:5540
fallopian tube teratoma
class of disease
fallopian tube germ cell cancer
fallopian tube cancer
Human disease
DOID:5564
fallopian tube transitional cell carcinoma
class of disease
fallopian tube carcinoma
transitional cell carcinoma
Human disease
DOID:4008
familial GPIHBP1 deficiency
class of disease
autosomal recessive disease
familial chylomicronemia syndrome
hyperlipoproteinemia type I
human disease
DOID:0111420
familial adenomatous polyposis 1
class of disease
familial adenomatous polyposis
autosomal dominant disease
familial adenomatous polyposis that has material basis in heterozygous mutation in the APC gene on chromosome 5q22
DOID:0080409
familial adenomatous polyposis 2
class of disease
familial adenomatous polyposis
autosomal recessive disease
familial adenomatous polyposis that has material basis in homozygous or compound heterozygous mutation in the MUTYH gene on chromosome 1p34
DOID:0080410
familial adenomatous polyposis 3
class of disease
familial adenomatous polyposis
familial adenomatous polyposis that has material basis in homozygous or compound heterozygous mutation in the NTHL1 gene on chromosome 16p13
DOID:0080411
familial adult myoclonic epilepsy 4
class of disease
myoclonic epilepsy
benign adult familial myoclonic epilepsy
autosomal dominant disease
human disease
DOID:0111693
familial adult myoclonic epilepsy 6
class of disease
autosomal dominant disease
benign adult familial myoclonic epilepsy
human disease
DOID:0111696
familial adult myoclonic epilepsy 7
class of disease
benign adult familial myoclonic epilepsy
autosomal dominant disease
human disease
DOID:0111694
familial bicuspid aortic valve
class of disease
bicuspid aortic valve
aortic valve disease
human disease
DOID:0080332
familial chronic myelocytic leukemia-like syndrome
class of disease
chronic myeloid leukemia
chronic myeloid leukemia characterized by chronic myelocytic leukemia in early infancy and absence of the BCR/ABL fusion gene (Philadelphia chromosome)
DOID:0060761
familial chylomicronemia due to inhibition of lipoprotein lipase activity
class of disease
familial chylomicronemia syndrome
hyperlipoproteinemia type I
human disease
DOID:0111419
familial chylomicronemia syndrome
class of disease
hyperlipidemia
familial hyperlipidemia
Primary hyperchylomicronemia
human disease
DOID:0111417
familial cold autoinflammatory syndrome 1
class of disease
familial cold urticaria
genetic disease
familial cold autoinflammatory syndrome characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the NLRP gene on chromosome 1q44
DOID:0090062
familial episodic pain syndrome
class of disease
neuropathic pain
peripheral neuropathy
human disease
DOID:0111728
familial episodic pain syndrome 1
class of disease
familial episodic pain syndrome
autosomal dominant disease
human disease
DOID:0111729
familial episodic pain syndrome 2
class of disease
familial episodic pain syndrome
autosomal dominant disease
human disease
DOID:0111730
familial episodic pain syndrome 3
class of disease
familial episodic pain syndrome
autosomal dominant disease
human disease
DOID:0111731
familial erythrocytosis 1
class of disease
primary polycythemia
autosomal dominant disease
Human disease
DOID:0060652
familial erythrocytosis 3
class of disease
primary polycythemia
autosomal dominant disease
human disease
DOID:0080338
familial erythrocytosis 4
class of disease
primary polycythemia
human disease
DOID:0080339
familial erythrocytosis 5
class of disease
primary polycythemia
autosomal dominant disease
human disease
DOID:0080290
familial erythrocytosis 6
class of disease
primary polycythemia
human disease
DOID:0111632
familial erythrocytosis 7
class of disease
primary polycythemia
human disease
DOID:0111631
familial febrile seizures 1
class of disease
febrile seizures, familial
human disease
DOID:0111307
familial febrile seizures 10
class of disease
febrile seizures, familial
human disease
DOID:0111304
familial febrile seizures 11
class of disease
febrile seizures, familial
human disease
DOID:0111308
familial febrile seizures 2
class of disease
febrile seizures, familial
human disease
DOID:0111310
familial febrile seizures 4
class of disease
febrile seizures, familial
human disease
DOID:0111305
familial febrile seizures 5
class of disease
febrile seizures, familial
human disease
DOID:0111306
familial febrile seizures 6
class of disease
febrile seizures, familial
human disease
DOID:0111309
familial febrile seizures 7
class of disease
febrile seizures, familial
human disease
DOID:0111311
familial febrile seizures 8
class of disease
febrile seizures, familial
human disease
DOID:0111298
familial febrile seizures 9
class of disease
febrile seizures, familial
human disease
DOID:0111303
familial glomangioma
class of disease
glomangioma
rare circulatory system disease
inherited renal tumor
cardiovascular cancer
inherited soft tissue tumor
Human disease
DOID:7996
familial glucocorticoid deficiency
class of disease
adrenal gland disease
human disease
DOID:0080620
familial hemiplegic migraine 1
class of disease
familial hemiplegic migraine
familial hemiplegic migraine that is commonly associated with cerebellar degeneration and has material basis in heterozygous mutation in CACNA1A on 19p13
DOID:0111181
familial hemiplegic migraine 2
class of disease
familial hemiplegic migraine
A familial hemiplegic migraine that has material basis in heterozygous mutation in ATP1A2 on 1q23.2.
DOID:0111182
familial hemiplegic migraine 3
class of disease
familial hemiplegic migraine
A familial hemiplegic migraine that has material basis in heterozygous mutation in SCN1A on 2q24.3.
DOID:0111183
familial hemophagocytic lymphohistiocytosis 1
class of disease
familial hemophagocytic lymphohistiocytosis
genetic disease
hemophagocytic lymphohistiocytosis
autosomal recessive disease
A hemophagocytic lymphohistiocytosis that has material basis in an autosomal recessive mutation of HPLH1 on chromosome 9q21.3-q22.
DOID:0110921
familial hepatic adenoma
class of disease
autosomal recessive disease
hepatocellular adenoma
human disease
DOID:0111366
familial hyperinsulinemic hypoglycemia 1
class of disease
hyperinsulinemic hypoglycemia
genetic disease
hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of hyperinsulinemic hypoglycemia that is resistant to diazoxide treatment that has material basis in mutation in the ABCC8 gene on chromosome 11p15
DOID:0070219
familial hyperinsulinemic hypoglycemia 2
class of disease
hyperinsulinemic hypoglycemia
genetic disease
A hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of severe hyperinsulinemic hypoglycemia that is resistant to diazoxide treatment that has material basis in mutation in the KCNJ11 gene on chromosome 11p15.1.
DOID:0070218
familial hyperinsulinemic hypoglycemia 3
class of disease
hyperinsulinemic hypoglycemia
genetic disease
human disease
DOID:0070216
familial hyperinsulinemic hypoglycemia 4
class of disease
hyperinsulinemic hypoglycemia
genetic disease
hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of hyperinsulinemic hypoglycemia with seizures that has material basis in mutation in the HADH gene on chromosome 4q25
DOID:0070215
familial hyperinsulinemic hypoglycemia 5
class of disease
hyperinsulinemic hypoglycemia
genetic disease
human disease
DOID:0070220
familial hyperinsulinemic hypoglycemia 6
class of disease
hyperinsulinemic hypoglycemia
genetic disease
human disease
DOID:0070217
familial hyperinsulinemic hypoglycemia 7
class of disease
hyperinsulinemic hypoglycemia
genetic disease
A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of postexercise hypoglycemia with marked hyperinsulinism that has material basis in mutation in the SLC16A1 gene on chromosome 1p13.2.
DOID:0070214
familial hyperlipidemia
class of disease
lipid metabolism disorder
hyperlipidemia
Human disease
DOID:1168
familial hypertrophic cardiomyopathy
class of disease
hypertrophic cardiomyopathy
familial cardiomyopathy
Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions
DOID:0080326
C14.280.238.100.500
C14.280.484.150.070.160.500
C16.320.160
familial hypertryptophanemia
class of disease
amino acid metabolic disorder
autosomal recessive disease
hypertryptophanemia
human disease
DOID:0111703
familial hypobetalipoproteinemia 1
class of disease
hypobetalipoproteinemia
hypobetalipoproteinemia that has material basis in mutation in the APOB gene on chromosome 2p24
DOID:0111062
familial hypobetalipoproteinemia 2
class of disease
hypobetalipoproteinemia
hypobetalipoproteinemia that has material basis in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31
DOID:0111061
familial hypocalciuric hypercalcemia 1
class of disease
familial hypocalciuric hypercalcemia
genetic disease
familial hypocalciuric hypercalcemia that has material basis in heterozygous loss-of-function mutations in the CASR gene on chromosome 3q21
DOID:0060700
familial isolated trichomegaly
class of disease
Trichomegaly
eyelid disease
autosomal recessive disease
DOID:0111566
familial lipase maturation factor 1 deficiency
class of disease
familial chylomicronemia syndrome
autosomal recessive disease
human disease
DOID:0111422
familial lipoprotein lipase deficiency
class of disease
hyperlipoproteinemia type I
autosomal recessive disease
familial chylomicronemia syndrome
familial hyperlipemia characterized by a deficiency of the enzyme lipoprotein lipase and the subsequent build up of chylomicrons and increased plasma concentration of triglycerides
DOID:14118
familial melanoma
class of disease
melanoma
Human disease
DOID:6846
familial meningioma
class of disease
meningioma
hereditary neoplastic syndromes
Human disease
DOID:4586
familial multiple nevi flammei
class of disease
capillary disease
port-wine stain
human disease
DOID:0111529
familial nephrotic syndrome
class of disease
nephrotic syndrome
genetic disease
monogenic disease
Human disease
DOID:2590
familial partial lipodystrophy type 1
class of disease
familial partial lipodystrophy
familial partial lipodystrophy characterized by loss of adipose tissue that is confined to the extremities with normal or increased fat in other areas of the body
DOID:0070207
familial partial lipodystrophy type 2
class of disease
familial partial lipodystrophy
genetic disease
autosomal dominant disease
familial partial lipodystrophy characterized by autosomal dominant inheritance of loss of subcutaneous fat from the limbs and trunk that has material basis in mutation in the LMNA gene on chromosome 1q21
DOID:0070202
familial partial lipodystrophy type 3
class of disease
familial partial lipodystrophy
genetic disease
autosomal dominant disease
familial partial lipodystrophy characterized by autosomal dominant inheritance that has material basis in mutation in the PPARG gene on chromosome 3p25
DOID:0070204
familial partial lipodystrophy type 6
class of disease
familial partial lipodystrophy
genetic disease
autosomal recessive disease
familial partial lipodystrophy characterized by autosomal recessive inheritance that has material basis in mutation in the LIPE gene on chromosome 19q13
DOID:0070206
familial progressive hyper- and hypopigmentation
class of disease
autosomal dominant disease
skin disease
familial progressive hyperpigmentation
human disease
DOID:0111373
familial renal oncocytoma
class of disease
renal oncocytoma
inherited renal tumor
Human disease
DOID:6244
familial renal papillary carcinoma
class of disease
hereditary renal cell carcinoma
Human disease
DOID:6163
familial retinoblastoma
class of disease
retinoblastoma
hereditary neoplastic syndromes
Human disease
DOID:4648
familial temporal lobe epilepsy 2
class of disease
temporal lobe epilepsy
genetic disease
autosomal dominant disease
A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex or partial seizures and childhood febrile seizures that has material basis in variation in the chromosome region 12q22-q23.3.
DOID:0060755
familial temporal lobe epilepsy 3
class of disease
temporal lobe epilepsy
genetic disease
autosomal dominant disease
A temporal lobe epilepsy characterized by simple or complex partial seizures often accompanied by intense feelings of deja or altered awareness and that has material basis in variation in the chromosome region 4q13.2-q21.3.
DOID:0060750
familial temporal lobe epilepsy 4
class of disease
temporal lobe epilepsy
genetic disease
autosomal dominant disease
temporal lobe epilepsy characterized by autosomal dominant inheritance of occipitotemporal lobe epilepsy and migraine with visual aura and that has material basis in variation in the chromosome region 9q21-q22
DOID:0060753
familial temporal lobe epilepsy 6
class of disease
temporal lobe epilepsy
genetic disease
autosomal dominant disease
temporal lobe epilepsy that has material basis in variation in the chromosome region 3q25-q26
DOID:0060749
familial temporal lobe epilepsy 7
class of disease
temporal lobe epilepsy
genetic disease
familial partial epilepsy
autosomal dominant disease
temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has material basis in heterozygous mutation in the RELN gene on chromosome 7q22
DOID:0060751
familial temporal lobe epilepsy 8
class of disease
temporal lobe epilepsy
genetic disease
autosomal dominant disease
temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has material basis in heterozygous mutation in the GAL gene on chromosome 11q13
DOID:0060754
familial thyroid dyshormonogenesis
class of disease
congenital hypothyroidism
human disease
DOID:0112183
familiar fallopian tube carcinoma
class of disease
fallopian tube carcinoma
inherited gynecological tumor
Human disease
DOID:7266
familiar ovarian carcinoma
class of disease
surface epithelial-stromal tumor
ovarian cancer
carcinoma
Human disease
DOID:6901
farmer's lung
class of disease
extrinsic allergic alveolitis
disease
hypersensitivity pneumonitis
DOID:14453
C08.381.483.125.365
C08.674.055.365
C20.543.480.680.075.365
C24.080.365
fasciitis
class of disease
connective tissue disease
disease
Inflammation process in fascia
DOID:9598
C05.321
Fasciitis
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 1
class of disease
autosomal recessive disease
fatal infantile encephalocardiomyopathy
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in compound heterozygous mutation in the SCO2 gene on chromosome 22q13
DOID:0080357
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3
class of disease
autosomal recessive disease
fatal infantile encephalocardiomyopathy
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in homozygous mutation in the COA5 gene on chromosome 2q11
DOID:0080359
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 4
class of disease
fatal infantile encephalocardiomyopathy
autosomal recessive disease
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in homozygous or compound heterozygous mutation in the COA6 gene on chromosome 1q42
DOID:0080360
fatal multiple mitochondrial dysfunctions syndrome
class of disease
mitochondrial disease
mitochondrial metabolism disease that is characterized by variants in genes involved in mitochondrial energy production, resulting in impairment of energy production at more than one stage of energy metabolism
DOID:0070330
fatty liver disease
class of disease
lipid storage disease
disease
lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis
DOID:9452
C06.552.241
Fatty liver
favism
class of disease
glucose-6-phosphate dehydrogenase deficiency
glucosephosphate dehydrogenase deficiency characterized by a hemolytic reaction to consumption of broad beans
DOID:13628
C15.378.071.141.150.480.370
C15.378.071.141.370
C16.320.070.480.370
C25.723.415.341
C25.723.756.375
febrile neutrophilic dermatosis
class of disease
reactive neutrophilic dermatose
erythema
rare rheumatologic disease
other acquired skin disease
skin disease
allergy
disease
skin disease
DOID:0080746
C17.800.229.800
Febrile neutrophilic dermatosis
febrile seizures, familial
class of disease
febrile seizure
encephalopathy
human disease
DOID:0111297
feline panleukopenia
class of disease
parvovirus infectious disease
cat disease
cat disease
DOID:3799
C01.925.256.700.363
C22.180.460
female breast axillary tail cancer
class of disease
female breast cancer
Human disease
DOID:1650
female breast cancer
class of disease
breast cancer
Human disease
DOID:0050671
female breast carcinoma
class of disease
breast carcinoma
breast carcinoma that is manifested in the female breast
DOID:7843
female breast central part cancer
class of disease
female breast cancer
human disease
DOID:13799
female breast lower-inner quadrant cancer
class of disease
female breast cancer
Human disease
DOID:1649
female breast lower-outer quadrant cancer
class of disease
female breast cancer
Human disease
DOID:13972
female breast upper-inner quadrant cancer
class of disease
female breast cancer
Human disease
DOID:1647
female breast upper-outer quadrant cancer
class of disease
female breast cancer
Human disease
DOID:9773
female infertility of uterine origin
class of disease
uterine disease
female infertility
Human disease
DOID:13589
female reproductive endometrioid cancer
class of disease
female reproductive organ cancer
Endometrioid tumor
human disease
DOID:3001
female reproductive organ benign neoplasm
class of disease
reproductive organ benign neoplasm
female reproductive system disease
human disease
DOID:0060086
female reproductive organ cancer
class of disease
female reproductive system disease
reproductive organ cancer
female reproductive system neoplasm
human disease
DOID:120
Cancers of female genital organs
female reproductive system disease
class of disease
reproductive system disease
female urogenital disease
reproductive system disease that impairs the ability to reproduce
DOID:229
C13.351.500
Diseases and disorders of the female reproductive system
female stress incontinence
class of disease
bladder disease
stress incontinence
Human disease
DOID:724
female urethral cancer
class of disease
urethral cancer
Human disease
DOID:738
female-restricted syndromic X-linked intellectual disability 99
class of disease
X-linked dominant disease
X-linked intellectual disability
human disease
DOID:0112025
femoral cancer
class of disease
bone cancer
neoplasm of femur
bone cancer that is located in the femur
DOID:5546
femoral neuropathy
class of disease
mononeuropathy
mononeuropathy that is characterized by a loss of movement or sensation in parts of the legs due to damage to the femoral nerve
DOID:4196
C10.668.829.500.200
femoral vein thrombophlebitis
class of disease
thrombophlebitis
Human disease
DOID:12282
fetal adenoma
class of disease
follicular adenoma
Human disease
DOID:8102
fetal akinesia deformation sequence
class of disease
Pena-Shokeir syndrome
monogenic disease
syndrome
human disease
DOID:0111375
fetal akinesia deformation sequence syndrome 1
class of disease
fetal akinesia deformation sequence
autosomal recessive disease
human disease
DOID:0111377
fetal akinesia deformation sequence syndrome 2
class of disease
autosomal recessive disease
fetal akinesia deformation sequence
human disease
DOID:0111378
fetal akinesia deformation sequence syndrome 3
class of disease
fetal akinesia deformation sequence
autosomal recessive disease
human disease
DOID:0111376
fetal akinesia deformation sequence syndrome 4
class of disease
fetal akinesia deformation sequence
autosomal recessive disease
human disease
DOID:0111379
fetal alcohol effects
class of disease
fetal alcohol spectrum disorders
fetal alcohol spectrum disorder that results in most, but not all, of the growth deficiency and/or craniofacial features of fetal alcohol syndrome including central nervous system dysfunction due to prenatal alcohol exposure
DOID:0050666
fetal alcohol spectrum disorders
class of disease
specific developmental disorder
congenital disorder
alcohol and health
disease
group of conditions that can occur in a person whose mother drank alcohol during pregnancy
DOID:0050696
C13.703.277.220
C16.300.070
C25.775.100.087.323
Fetal alcohol syndrome
fetal alcohol syndrome
class of disease
fetal alcohol spectrum disorders
disease
severe form of fetal alcohol spectrum disorder
DOID:0050665
Fetal alcohol syndrome
fetal erythroblastosis
class of disease
neonatal alloimmune disease
microcytic anemia
hematological disease of fetus and newborn
Acquired hemolytic anemia
disease
Human disease
DOID:1098
C13.703.277.060
C15.378.295
C16.300.060
C16.614.304
C20.306
Hemolytic disease of the newborn
fetal nicotine spectrum disorder
class of disease
specific developmental disorder
health effects of tobacco
congenital disorder
drug-induced abnormality
specific developmental disorder that is characterized by physical, behavioral and learning birth defects resulting from maternal ingestion of nicotine during pregnancy
DOID:0060606
Smoking and pregnancy
fetishism
class of disease
paraphilia
fetishism
disease
sexual arousal a person receives from an object or situation
DOID:1235
F03.657.350
Sexual fetishism
fibrillary astrocytoma
class of disease
brain tumor
astrocytoma
diffuse astrocytoma
astrocytoma that is characterized as a low grade astrocytoma and has material basis in neoplastic astrocytes
DOID:6726
Fibrillary astrocytoma
fibroblastic liposarcoma
class of disease
liposarcoma
Human disease
DOID:5698
fibrochondrogenesis 1
class of disease
fibrochondrogenesis
autosomal recessive disease
human disease
DOID:0080672
fibrochondrogenesis 2
class of disease
autosomal dominant disease
autosomal recessive disease
fibrochondrogenesis
human disease
DOID:0080673
fibroepithelial basal cell carcinoma
class of disease
basal-cell carcinoma
Human disease
DOID:4291
fibroepithelial polyp of the anus
class of disease
skin tag
benign neoplasm of anus
polyp of rectum
anal disease
Human disease
DOID:8170
Anal skin tags
fibroepithelial polyp of urethra
class of disease
skin tag
urethral disease
polyp
urethral benign neoplasm
Human disease
DOID:8108
fibrogenesis imperfecta ossium
class of disease
syndrome
A syndrome that involves abnormality of collagen synthesis in lamellar bones, with manifestations limited to the skeleton. The initial symptom is frequently spontaneous fractures.
DOID:0080040
fibrolamellar hepatocellular carcinoma
class of disease
hepatocellular carcinoma
A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers.
DOID:5015
fibroma
class of disease
connective tissue benign neoplasm
disease
human disease
DOID:0050871
C04.557.450.565.590.340
Fibromas
fibromyalgia
class of disease
symptom or sign
myositis
chronic pain
disease
chronic disorder of unknown etiology characterized by pain, stiffness, and tenderness
DOID:631
C05.651.324
C05.799.321
C10.668.491.425
Fibromyalgia
fibroosseous pseudotumor of digits
class of disease
bone benign neoplasm
myositis ossificans
Human disease
DOID:8153
fibrosarcoma
class of disease
connective tissue neoplasm
fibroblastic tumour
sarcoma
disease
connective tissue cancer that has material basis in fibrous connective tissue and characterized by the presence of immature proliferating fibroblasts or undifferentiated anaplastic spindle cells in a storiform pattern
DOID:3355
C04.557.450.565.590.350
C04.557.450.795.350
Fibrosarcoma
fibrosarcoma of bone
class of disease
osteosarcoma
fibrosarcoma
bone sarcoma
Human disease
DOID:3354
fibrosarcomatous osteosarcoma
class of disease
conventional central osteosarcoma
Human disease
DOID:7603
fibrosclerosis of breast
class of disease
non-proliferative fibrocystic change of the breast
benign mammary dysplasia
Human disease
DOID:10353
fibrous dysplasia of bone
class of disease
bone remodeling disease
disease
bone remodeling disease that results in the destruction of normal bone and replacing it with fibrous bone tissue
DOID:0080031
C05.116.099.708.375
Fibrous dysplasia
fibrous histiocytoma
class of disease
histiocytoma
Human disease
DOID:4415
C04.557.450.565.590.425.350
fibrous meningioma
class of disease
meningioma
Human disease
DOID:7211
fibrous synovial sarcoma
class of disease
synovial sarcoma
Human disease
DOID:5484
fibular collateral ligament bursitis
class of disease
knee disorder
enthesopathy
Human disease
DOID:9358
filamentary keratitis
class of disease
keratitis
Human disease
DOID:4664
filarial elephantiasis
class of disease
filariasis
skin disease
neglected tropical disease
disease
human disease caused by parasitic worms
DOID:12211
C15.604.496.490
C01.610.335.508.700.750.361.350
C01.920.750
Lymphatic filariasis
finger agnosia
class of disease
agnosia
autotopagnosia
agnosia that is a loss of the ability to distinguish the fingers on the hand
DOID:0060141
fish allergy
class of disease
food allergy
seafood allergy
food allergy triggered by fish
DOID:0060513
fissured tongue
class of disease
tongue disease
disease
benign condition characterized by deep grooves (fissures) in the dorsum of the tongue
DOID:11514
C07.465.910.708
Fissured tongue
flat ductal epithelial atypia
class of disease
breast intraductal proliferative lesion
Human disease
DOID:6841
flat retinoschisis
class of disease
retinoschisis
Human disease
DOID:8464
flavivirus infectious disease
class of disease
Flaviviridae infectious disease
human disease
DOID:993
C01.925.782.350.250
Flavivirus infections
focal chorioretinitis
class of disease
chorioretinitis
Human disease
DOID:1979
focal dystonia
class of disease
dystonia
movement disorders
disease
dystonia that is localized to a specific part of the body
DOID:0050836
focal embolic glomerulonephritis
class of disease
glomerulonephritis
Human disease
DOID:4779
focal epilepsy
class of disease
seizure
epilepsy
disease
epilepsy syndrome characterised by seizures preceded by isolated disturbances of a cerebral function
DOID:2234
C10.228.140.490.360
focal hand dystonia
class of disease
focal dystonia
occupational disease
focal dystonia that affects a single muscle or small group of muscles in the hand resulting from involuntary muscular contractions
DOID:0050841
focal labyrinthitis
class of disease
labyrinthitis
Human disease
DOID:13867
focal nonepidermolytic palmoplantar keratoderma
class of disease
nonepidermolytic palmoplantar keratoderma
human disease
DOID:0111708
focal nonepidermolytic palmoplantar keratoderma 1
class of disease
focal nonepidermolytic palmoplantar keratoderma
autosomal dominant disease
human disease
DOID:0111709
focal nonepidermolytic palmoplantar keratoderma 2
class of disease
autosomal dominant disease
focal nonepidermolytic palmoplantar keratoderma
human disease
DOID:0111711
focal or diffuse nonepidermolytic palmoplantar keratoderma
class of disease
autosomal dominant disease
nonepidermolytic palmoplantar keratoderma
human disease
DOID:0111710
focal segmental glomerulosclerosis 1
class of disease
focal segmental glomerulosclerosis
genetic disease
A focal segmental glomerulosclerosis that has material basis in an autosomal dominant mutation of ACTN4 on chromosome 19q13.2.
DOID:0111128
folic acid deficiency anemia
class of disease
deficiency anemia
megaloblastic anemia
nutritional deficiency disease
Human disease
DOID:14026
follicular adenoma
class of disease
thyroid adenoma
Human disease
DOID:6204
follicular basal cell carcinoma
class of disease
basal-cell carcinoma
human disease
DOID:4295
follicular dendritic cell sarcoma
class of disease
dendritic cell sarcoma
Epstein-Barr virus-associated mesenchymal tumor
dendritic cell sarcoma cancer that effects the follicular dendritic cells
DOID:6262
C04.557.227.190
C15.604.250.390.190
Follicular dendritic cell sarcoma
follicular mucinosis
class of disease
mucinosis
alopecia
sebaceous gland anomaly
baldness
Cutaneous focal mucinosis
sebaceous gland disease
Human disease
DOID:9905
C17.300.550.550
C17.800.329.937.122.550
C17.800.794.550
follicular thyroid cancer
class of disease
thyroid carcinoma
adenocarcinoma
thyroid carcinoma that has material basis in follicular cells
DOID:3962
C04.557.470.200.025.060
Follicular thyroid carcinoma
folliculitis
class of disease
dermatitis
hair diseases
disease
Human disease
DOID:4409
C17.800.329.500
Folliculitis
food allergy
class of disease
food hypersensitivity
gastrointestinal allergy
disease
hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system
DOID:3044
C20.543.480.370
Food allergy
form agnosia
class of disease
agnosia
apperceptive agnosia
visual agnosia
agnosia that is a loss of the ability to perceive a whole object while perceiving only parts of details
DOID:0060142
formaldehyde allergic contact dermatitis
class of disease
allergic contact dermatitis
allergic contact dermatitis that has allergic trigger formaldehyde
DOID:0040074
frontal convexity meningioma
class of disease
cerebral convexity meningioma
Human disease
DOID:8000
frontal lobe epilepsy
class of disease
extratemporal epilepsy
focal epilepsy
common form of epilepsy that may appear to be related to a psychiatric problem or a sleep disorder
DOID:3331
C10.228.140.490.360.270
C10.228.140.490.493.188
frontal lobe neoplasm
class of disease
cerebrum cancer
frontal lobe disorder
Human disease
DOID:12016
frontal sinus cancer
class of disease
paranasal sinus cancer
frontal sinus neoplasm
Human disease
DOID:1360
frontal sinus neoplasm
class of disease
paranasal sinus neoplasm
Human disease
DOID:1361
frontal sinus squamous cell carcinoma
class of disease
frontal sinus cancer
squamous cell carcinoma
Human disease
DOID:2441
frontal sinusitis
class of disease
sinusitis
nose disease
sinusitis which involves infection of the frontal sinuses over the eyes in the brow area. This causes pain or pressure in the frontal sinus cavity and headache over the forehead
DOID:10791
C08.460.692.752.387
C08.730.749.387
C09.603.692.752.387
C01.748.749.387
frontometaphyseal dysplasia 1
class of disease
X-linked recessive disease
frontometaphyseal dysplasia
human disease
DOID:0111786
frozen shoulder
class of disease
connective tissue disease
periarthritis humero-scapularis
capsulitis
disease
painful human disease of uncertain origin affecting the shoulder capsule
DOID:14188
Adhesive capsulitis of the shoulder
fruit allergy
class of disease
food allergy
vegetable allergy
type of food allergy caused by fruit
DOID:0060503
functional diarrhea
class of disease
colonic disease
diarrhea
functional colonic disease
Human disease
DOID:11371
functional gastric disease
class of disease
stomach disease
functional gastrointestinal disorder
Human disease
DOID:1159
fundus dystrophy
class of disease
eye disease
retinal degeneration
genetic vitreous-retinal disease
human disease
DOID:8501
C11.768.585.658
fungal esophagitis
class of disease
esophagitis
fungal infectious disease
Human disease
DOID:13147
fungal folliculitis
class of disease
tinea corporis
fungal infection
DOID:13368
Fungal folliculitis
fungal gastritis
class of disease
gastritis
fungal infectious disease
chronic gastritis
gastrointestinal system infectious disease that involves inflammation of the stomach lining caused by fungal infection in immunocompromised patients
DOID:4034
fungal infectious disease
class of disease
infectious disease
bacterial infection and mycosis
disease
disease caused by fungi to animals or humans
DOID:1564
C01.150.703
Diseases and disorders due to fungi
funisitis
class of disease
connective tissue disease
chorioamnionitis
connective tissue disease that is an inflammation of the connective tissue of the umbilical cord
DOID:0050698
gait apraxia
class of disease
apraxia
Human disease
DOID:4260
C10.597.404.400
C10.597.606.881.350.600
C23.888.592.413.400
C23.888.592.604.882.350.600
F01.700.875.350.600
galactose epimerase deficiency
class of disease
galactosemia
autosomal recessive disease
human disease
DOID:0111458
galactose-1-phosphate uridylyltransferase deficiency
class of disease
galactosemia
autosomal recessive disease
human disease
DOID:0111459
gall bladder carcinoma in situ
class of disease
in situ carcinoma
gallbladder disease
Human disease
DOID:0050612
gallamine allergy
class of disease
drug allergy
drug allergy that has allergic trigger gallamine
DOID:0040078
gallbladder adenocarcinoma
class of disease
gallbladder carcinoma
adenocarcinoma
adenocarcinoma of liver and intrahepatic biliary tract
gallbladder carcinoma that derives from epithelial cells of glandular origin
DOID:3500
Gallbladder adenocarcinoma
gallbladder adenoma
class of disease
biliary tract neoplasm
gastrointestinal adenoma
gallbladder polyp
benign neoplasms by histologic type
gallbladder benign neoplasm
adenoma
biliary tract neoplasm that has material basis in epithelial tissue of glandular origin located in the gallbladder
DOID:0050893
gallbladder angiosarcoma
class of disease
angiosarcoma
gallbladder sarcoma
gallbladder cancer
angiosarcoma and gallbladder sarcoma that is located in the gallbladder
DOID:4513
gallbladder benign neoplasm
class of disease
gallbladder neoplasm
biliary tract neoplasm
human disease
DOID:0080640
gallbladder cancer
class of disease
biliary tract cancer
gallbladder neoplasm
gallbladder disease
disease
biliary tract cancer that is located in the gallbladder
DOID:3121
Gallbladder cancer
gallbladder carcinoma
class of disease
gallbladder cancer
carcinoma
gallbladder cancer that has material basis in abnormally proliferating cells derives from epithelial cells
DOID:4948
gallbladder disease
class of disease
gastrointestinal system disease
biliary disease
disease
gastrointestinal system disease that is located in the gallbladder
DOID:0060262
C06.130.564
Diseases and disorders of gallbladder
gallbladder leiomyoma
class of disease
leiomyoma
gallbladder disease
gastrointestinal system benign neoplasm
benign neoplasm of gallbladder
human disease
DOID:5140
gallbladder leiomyosarcoma
class of disease
gallbladder sarcoma
leiomyosarcoma
liver leiomyosarcoma
gallbladder cancer
gallbladder sarcoma that is located in the gallbladder
DOID:5275
gallbladder lipoma
class of disease
biliary tract neoplasm
gallbladder disease
lipoma
liver lipoma
gallbladder benign neoplasm
human disease
DOID:10201
gallbladder lymphoma
class of disease
gallbladder cancer
lymphoma
liver lymphoma
Human disease
DOID:8135
gallbladder melanoma
class of disease
gallbladder cancer
melanoma
Human disease
DOID:8167
gallbladder mucinous carcinoma
class of disease
gallbladder adenocarcinoma
gallbladder carcinoma
Human disease
DOID:6998
gallbladder papillary carcinoma
class of disease
gallbladder adenocarcinoma
carcinoma
gallbladder cancer
Human disease
DOID:7221
gallbladder papillomatosis
class of disease
biliary tract neoplasm
papilloma
Human disease
DOID:3120
gallbladder pleomorphic giant cell adenocarcinoma
class of disease
gallbladder adenocarcinoma
Human disease
DOID:7222
gallbladder rhabdomyosarcoma
class of disease
gallbladder sarcoma
rhabdomyosarcoma
liver rhabdomyosarcoma
gallbladder cancer
gallbladder sarcoma that is located in the gallbladder
DOID:4057
gallbladder sarcoma
class of disease
gallbladder cancer
sarcoma
sarcoma that is located in the gallbladder
DOID:4058
gallbladder signet ring cell adenocarcinoma
class of disease
gallbladder adenocarcinoma
signet ring cell adenocarcinoma
Human disease
DOID:3499
gallbladder small cell carcinoma
class of disease
gallbladder carcinoma
gallbladder neuroendocrine neoplasm
liver neuroendocrine carcinoma
small cell carcinoma
Human disease
DOID:7133
gallbladder squamous cell carcinoma
class of disease
gallbladder carcinoma
squamous cell carcinoma
squamous cell carcinoma of liver and intrahepatic biliary tract
Human disease
DOID:5535
gamma heavy chain disease
class of disease
heavy chain disease
heavy chain disease that results from an overproduction of gamma antibody (IgG)
DOID:0060127
gamma-amino butyric acid metabolism disorder
class of disease
amino acid metabolic disorder
amino acid metabolic disorder characterized by impairment of the GABA catabolic pathway
DOID:0060176
gangliocytoma
class of disease
central nervous system organ benign neoplasm
nervous system benign neoplasm
Human disease
DOID:2426
ganglioglioma
class of disease
benign neoplasms by histologic type
central nervous system organ benign neoplasm
cell type benign neoplasm that has material basis in glial-type cells
DOID:5078
C04.557.465.625.600.380.350
C04.557.470.670.380.350
C04.557.580.625.600.380.350
Ganglioglioma
ganglioneuroblastoma
class of disease
neuroblastoma
neuroblastic tumor
Human disease
DOID:4163
C04.557.465.625.600.590.650.550.300
C04.557.470.670.590.650.550.300
C04.557.580.625.600.590.650.550.300
Ganglioneuroblastoma
ganglioneuroma
class of disease
autonomic nervous system benign neoplasm
rare and benign tumor of the autonomic nerve fibers arising from neural crest sympathogonia
DOID:4817
C04.557.465.625.600.355
C04.557.470.670.355
C04.557.580.625.600.355
Ganglioneuroma
gangliosidosis
class of disease
sphingolipidosis
rare genetic epilepsy
rare dyslipidemia
sphingolipidosis with epilepsy
autosomal recessive disease
disease
Human disease
DOID:2368
C10.228.140.163.100.435.825.300
C16.320.565.189.435.825.300
C16.320.565.398.641.803.350
C16.320.565.595.554.825.300
C18.452.132.100.435.825.300
C18.452.584.563.641.803.350
C18.452.648.189.435.825.300
C18.452.648.398.641.803.350
C18.452.648.595.554.825.300
gangliosidosis GM3
class of disease
gangliosidosis GM1
gangliosidosis that is characterized by neurodegeneration and mild skeletal changes and has material basis in mutation in the gene encoding beta-galactosidase-1
DOID:0080489
gastric adenocarcinoma
class of disease
stomach carcinoma
adenocarcinoma
stomach carcinoma that derives from epithelial cells of glandular origin
DOID:3717
Adenocarcinomas of stomach
gastric adenosquamous carcinoma
class of disease
adenosquamous carcinoma
gastric squamous cell carcinoma
squamous cell carcinoma
stomach carcinoma
Human disease
DOID:5635
gastric antral vascular ectasia
class of disease
capillary disease
ectasia
vascular ectasia
Human disease
DOID:2493
C06.405.748.280
C14.907.075.280
Gastric antral vascular ectasia
gastric body carcinoma
class of disease
stomach carcinoma
Human disease
DOID:6705
gastric cardia adenocarcinoma
class of disease
gastric adenocarcinoma
gastric cardia carcinoma
cardia cancer
Human disease
DOID:6271
gastric cardia carcinoma
class of disease
stomach carcinoma
cardia cancer
Human disease
DOID:6270
gastric diffuse adenocarcinoma
class of disease
gastric adenocarcinoma
diffuse type adenocarcinoma
Human disease
DOID:6217
gastric dilatation
class of disease
stomach disease
Human disease
DOID:3229
C06.405.748.300
gastric fundus cancer
class of disease
stomach cancer
human disease
DOID:10538
gastric fundus carcinoma
class of disease
gastric fundus cancer
carcinoma
Human disease
DOID:6700
gastric gastrinoma
class of disease
stomach cancer
gastrinoma
gastric neuroendocrine tumor, well differentiated, low or intermediate grade
Human disease
DOID:5579
gastric hemangioma
class of disease
benign neoplasm of stomach
gastrointestinal system benign neoplasm
hemangioma of intra-abdominal structure
hemangioma
stomach disease
human disease
DOID:275
gastric leiomyoma
class of disease
gastrointestinal system benign neoplasm
leiomyoma
benign neoplasm of stomach
Human disease
DOID:10087
gastric leiomyosarcoma
class of disease
stomach cancer
gastrointestinal system disease
gastrointestinal system cancer
Human disease
DOID:5280
gastric liposarcoma
class of disease
stomach cancer
gastrointestinal system disease
gastrointestinal system cancer
Human disease
DOID:5700
gastric lymphoma
class of disease
gastrointestinal lymphoma
stomach cancer
Human disease
DOID:10540
gastric mucosal hypertrophy
class of disease
gastritis
rare gastroesophageal disease
genetic disease
rare genetic gastroenterological disease
chronic gastritis
human disease
DOID:8757
C06.405.205.697.410
C06.405.748.398.410
Ménétrier's disease
gastric neuroendocrine neoplasm
class of disease
gastrointestinal neuroendocrine benign tumor
stomach cancer
Human disease
DOID:4715
gastric outlet obstruction
class of disease
stomach disease
Human disease
DOID:3122
C06.405.748.340
Gastric outlet obstruction
gastric papillary adenocarcinoma
class of disease
gastric adenocarcinoma
Human disease
DOID:5593
gastric pylorus carcinoma
class of disease
stomach carcinoma
pylorus cancer
Human disease
DOID:6703
gastric signet ring cell adenocarcinoma
class of disease
gastric diffuse adenocarcinoma
signet ring cell adenocarcinoma
Human disease
DOID:8025
gastric small cell carcinoma
class of disease
stomach carcinoma
gastric neuroendocrine neoplasm
small cell carcinoma
Human disease
DOID:6552
gastric squamous cell carcinoma
class of disease
stomach carcinoma
squamous cell carcinoma
Human disease
DOID:5516
gastric teratoma
class of disease
stomach cancer
gastrointestinal system disease
gastrointestinal system cancer
human disease
DOID:5561
gastric tubular adenocarcinoma
class of disease
gastric adenocarcinoma
Human disease
DOID:6595
gastric ulcer
class of disease
peptic ulcer disease
An ulcerated lesion in the mucosal surface of the stomach. It may progress to involve the deeper layers of the gastric wall.
DOID:10808
C06.405.469.275.800.849
C06.405.748.586.849
Gastric ulcers
gastrin secretion abnormality
class of disease
endocrine pancreas disease
Human disease
DOID:13656
gastrinoma
class of disease
neuroendocrine tumor
disease
neuroendocrine tumor that results in an overproduction of gastric acid
DOID:5577
C04.557.470.200.025.290.500
C04.588.274.761.500.124
C04.588.322.475.500.124
C06.301.761.500.124
C06.689.667.500.124
C19.344.421.500.124
Gastrinoma
gastritis
class of disease
stomach disease
disease
stomach disease that is an inflammation of the lining of the stomach
DOID:4029
C06.405.205.697
C06.405.748.398
Gastritis
gastroduodenal Crohn's disease
class of disease
Crohn's disease
inflammatory bowel disease characterized by inflammation located in stomach and located in duodenum, has symptom nausea, has symptom vomiting, has symptom weight loss and has symptom loss of appetite
DOID:0060191
gastroduodenitis
class of disease
peptic ulcer disease
hemorrhagic duodenitis
gastritis
disease
Human disease
DOID:8644
gastroenteritis
class of disease
symptom or sign
gastrointestinal system disease
digestive sign
disease
medical condition characterized by inflammation of the stomach and/or small intestine
DOID:2326
C06.405.205
Gastroenteritis
gastroesophageal adenocarcinoma
class of disease
adenocarcinoma
gastroesophageal cancer
gastroesophageal cancer that has material basis in abnormally proliferating cells, derives from epithelial cells, which originate in glandular tissue
DOID:0080375
gastroesophageal cancer
class of disease
gastrointestinal system cancer
gastrointestinal system cancer that is located in the proximal esophagus and the distal stomach
DOID:0080374
gastroesophageal junction adenocarcinoma
class of disease
gastrointestinal carcinoma
gastroesophageal adenocarcinoma
Human disease
DOID:4944
gastroesophageal reflux disease
class of disease
genetic disease
stomach disease
esophagitis
gastrointestinal system disease
esophageal disease
chronic disease caused by stomach acid coming up from the stomach into the esophagus
DOID:8534
C06.405.117.119.500.484
Gastroesophageal reflux disease
gastrointestinal adenoma
class of disease
gastrointestinal system cancer
adenoma
gastrointestinal system benign neoplasm
Human disease
DOID:4147
gastrointestinal allergy
class of disease
allergy
hypersensitivity reaction type I disease located in the gastrointestinal tract
DOID:0060502
gastrointestinal anthrax
class of disease
anthrax
gastrointestinal system disease
human disease
DOID:13386
gastrointestinal carcinoma
class of disease
gastrointestinal system cancer
carcinoma
gastrointestinal system cancer that has material basis in epithelial cells
DOID:0050922
gastrointestinal lymphoma
class of disease
gastrointestinal system cancer
gastrointestinal system disease
non-Hodgkin lymphoma
lymphoma
Human disease
DOID:903
gastrointestinal neuroendocrine benign tumor
class of disease
gastrointestinal system benign neoplasm
gastrointestinal system disease
gastroenteropancreatic neuroendocrine neoplasm
Human disease
DOID:4148
gastrointestinal neuroendocrine tumor
class of disease
gastrointestinal neoplasm
neuroendocrine tumor
gastrointestinal system cancer
gastrointestinal system cancer that has material basis in neuroendocrine cells
DOID:0050626
gastrointestinal stromal tumor
class of disease
Stromal tumor
rare genetic intestinal disease
inherited digestive tract tumor
mesenchymal tumor of small intestine
gastrointestinal system cancer
human disease
DOID:9253
C04.557.450.565.370
C06.301.371.308
C06.405.249.308
Gastrointestinal stromal tumors
gastrointestinal system benign neoplasm
class of disease
organ system benign neoplasm
gastrointestinal neoplasm
gastrointestinal system disease
organ system benign neoplasm located in gastrointestinal tract organs
DOID:0050624
Benign neoplasms of gastrointestinal tract
gastrointestinal system cancer
class of disease
digestive system cancer
gastrointestinal neoplasm
organ system cancer
gastrointestinal system disease
organ system cancer located in gastrointestinal tract that is manifested in organs of the gastrointestinal system
DOID:3119
Gastrointestinal cancers
gastrointestinal system disease
class of disease
disease of anatomical entity
disease
disease involving the gastrointestinal tract
DOID:77
C06
Diseases and disorders of the digestive system
gastrointestinal tularemia
class of disease
tularemia
gastrointestinal system disease
tularemia that results in formation of ulcerative lesions located in gastrointestinal tract
DOID:14239
gastrojejunal ulcer
class of disease
peptic ulcer disease
Human disease
DOID:10927
gastroparesis
class of disease
functional gastric disease
disease
Human disease
DOID:11914
C06.405.748.543
C23.888.592.636.263
Gastroparesis
geleophysic dysplasia 1
class of disease
geleophysic dysplasia
autosomal recessive disease
human disease
DOID:0111725
geleophysic dysplasia 3
class of disease
geleophysic dysplasia
autosomal dominant disease
human disease
DOID:0111727
gemistocytic astrocytoma
class of disease
astrocytoma
human disease
DOID:7005
gender dysphoria
class of disease
mental disorder
dysphoria
disease
mental distress resulting from mismatch between gender identity and biological gender assigned at birth
DOID:1234
F03.835.550
gene duplication disease
class of disease
monogenic disease
human disease
DOID:0080712
generalized anxiety disorder
class of disease
anxiety disorder
disease
anxiety disorder that is characterized by long-lasting anxiety that is not focused on any one object or situation
DOID:14320
Generalized anxiety disorder
generalized atherosclerosis
class of disease
atherosclerosis
Human disease
DOID:2347
generalized dystonia
class of disease
dystonia
human disease
DOID:0050835
C10.228.140.079.357
C10.228.662.300.200
C10.574.500.393
C16.320.400.330
generalized epidermolysis bullosa simplex
class of disease
epidermolysis bullosa simplex
basal epidermolysis bullosa simplex
autosomal dominant disease
epidermolysis bullosa simplex that is characterized by widespread blisters that appear at birth or in early infancy
DOID:0080511
generalized epilepsy
class of disease
epilepsy
seizure
epilepsy syndrome that is characterised by generalised seizures with no apparent cause which arise from independent foci or epileptic circuits that involve the whole brain
DOID:1827
C10.228.140.490.375
generalized epilepsy with febrile seizures plus 1
class of disease
generalized epilepsy with febrile seizures plus
human disease
DOID:0111302
generalized epilepsy with febrile seizures plus 10
class of disease
generalized epilepsy with febrile seizures plus
human disease
DOID:0111296
generalized epilepsy with febrile seizures plus 2
class of disease
generalized epilepsy with febrile seizures plus
human disease
DOID:0111294
generalized epilepsy with febrile seizures plus 4
class of disease
generalized epilepsy with febrile seizures plus
human disease
DOID:0111293
generalized epilepsy with febrile seizures plus 6
class of disease
generalized epilepsy with febrile seizures plus
human disease
DOID:0111300
generalized epilepsy with febrile seizures plus 7
class of disease
generalized epilepsy with febrile seizures plus
human disease
DOID:0111295
generalized epilepsy with febrile seizures plus 8
class of disease
generalized epilepsy with febrile seizures plus
human disease
DOID:0111299
generalized epilepsy with febrile seizures plus 9
class of disease
generalized epilepsy with febrile seizures plus
human disease
DOID:0111301
genetic disease
class of disease
hereditary disorder
disease
health problem caused by one or more abnormalities in the genome
DOID:630
DOID:0050325
C16.320
Genetic diseases and disorders
geniculate ganglionitis
class of disease
facial nerve disease
Human disease
DOID:14075
geniculate herpes zoster
class of disease
herpes zoster
poliomyelitis
facial nerve disease
disorder that is caused by the reactivation of varicella zoster virus in the geniculate ganglion, a nerve cell bundle of the facial nerve
DOID:9210
C01.925.256.466.930.750.733
C07.465.299.750
C09.218.513
C10.292.319.750
Ramsay Hunt syndrome type II
genital leiomyoma
class of disease
reproductive organ benign neoplasm
leiomyoma cutis
human disease
DOID:5147
geographic tongue
class of disease
symptom or sign
inflammation
tongue disease
smooth tongue
disease
atrophic glossitis that is characterized as an inflammatory condition of the mucous membrane of the tongue, usually on the dorsal surface
DOID:1455
C07.465.910.363.447
Geographic tongue
germ cell and embryonal cancer
class of disease
germ cell cancer
sarcoma
germ cell cancer that is derives from a mixture of germs cells and embryonal cells
DOID:3095
germ cell benign neoplasm
class of disease
benign neoplasms by histologic type
germ cell tumor
human disease
DOID:0080601
germ cell cancer
class of disease
cell type cancer
germ cell tumor
A cell type cancer that has_material_basis_in abnormally proliferating cells derived_from germ cells.
DOID:2994
Germ cell cancers
germinoma
class of disease
germ cell cancer
disease
germ cell cancer that lacks histologic differentiation, usually a brain tumor
DOID:3304
C04.557.465.330
Germinoma
gestational choriocarcinoma
class of disease
choriocarcinoma
extragonadal non-dysgerminomatous germ cell tumor
extragonadal germ cell cancer
gestational trophoblastic disease
Human disease
DOID:2025
gestational diabetes
class of disease
diabetes
complication of pregnancy, childbirth and the puerperium
diabetes mellitus and pregnancy
disease
condition in which a woman without diabetes develops high blood sugar levels during pregnancy
DOID:11714
DOID:1550
C12.050.703.170
C18.452.394.750.448
C19.246.200
Gestational diabetes
gestational ovarian choriocarcinoma
class of disease
choriocarcinoma of ovary
malignant non-dysgerminomatous germ cell tumor of ovary
ovarian cancer
gestational choriocarcinoma
Human disease
DOID:7591
gestational uterine corpus choriocarcinoma
class of disease
gestational choriocarcinoma
uterine corpus choriocarcinoma
Human disease
DOID:8187
giant axonal neuropathy
class of disease
axonal neuropathy
genetic disease
autosomal recessive disease
human disease
DOID:0090068
C10.500.300.490
C10.574.500.495.490
C10.668.829.325
C10.668.829.800.300.490
C16.131.666.300.490
C16.320.400.375.490
giant cell glioblastoma
class of disease
glioblastoma
glioblastoma multiforme that is characterized by a prevalence of bizarre, multinucleated giant cells
DOID:3074
giant cell reparative granuloma
class of disease
giant-cell tumor of bone
Human disease
DOID:1866
C05.500.368
C07.320.391
C07.465.714.258.557
C23.550.382.468
giant cell tumor
class of disease
connective tissue neoplasm
bone benign neoplasm
Human disease
DOID:200
C04.557.450.565.380
Giant cell tumors
giant hemangioma
class of disease
cavernous hemangioma
Human disease
DOID:5774
giant papillary conjunctivitis
class of disease
blepharoconjunctivitis
papillary conjunctivitis
allergic conjunctivitis
Human disease
DOID:2457
giant-cell carcinoma of the lung
class of disease
large-cell lung carcinoma
Sarcomatoid carcinoma of the lung
malignant giant cell tumor
lung carcinoma that is located in large undifferentiated cells
DOID:5583
C04.557.470.200.220
giant-cell tumor of bone
class of disease
bone neoplasm
giant cell tumor
disease
giant cell tumor and bone cancer and bone tissue neoplasm that results in the presence of multinucleated giant cells (osteoclast-like cell)
DOID:4305
C04.557.450.565.380.380
C04.557.450.565.575.420
Giant-cell tumor of bone
gingival disease
class of disease
periodontal disease
human disease
DOID:1483
C07.465.714.258
gingival fibromatosis 5
class of disease
gingival fibromatosis
autosomal dominant disease
human disease
DOID:0080280
gingival hypertrophy
class of disease
gingival overgrowth
Human disease
DOID:5338
C07.465.714.258.428.260
gingival overgrowth
class of disease
gingival disease
Human disease
DOID:3086
C07.465.714.258.428
Gingival enlargement
gingival recession
class of disease
gingival disease
periodontal atrophy
human disease
DOID:1134
C07.465.714.258.447
C07.465.714.354.625
Gingival recession
gingivitis
class of disease
symptom or sign
symptom
gingival disease
periodontitis
disease
inflammation of the gums
DOID:3087
C07.465.714.258.480
Gingivitis
glandular cystitis
class of disease
chronic cystitis
A reactive inflammatory disorder affecting the bladder. It is characterized by the development of small cysts in the bladder wall. The cysts are lined by metaplastic glandular cells.
DOID:2392
Cystitis glandularis
glandular pattern ovarian yolk sac tumor
class of disease
ovarian endodermal sinus tumor
Human disease
DOID:6511
glandular tularemia
class of disease
tularemia
tularemia that results in swelling of regional lymph glands
DOID:0050382
glandular-alveolar pattern testicular yolk sac tumor
class of disease
testicular yolk sac tumor
Human disease
DOID:7930
glans penis cancer
class of disease
penile cancer
Human disease
DOID:11839
glassy cell variant cervical adenosquamous carcinoma
class of disease
cervical adenosquamous carcinoma
cervical adenosquamous carcinoma that is a rare form and is composed of cells with a glass-like cytoplasm
DOID:8361
glaucoma
class of disease
eye disease
disease
eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function
DOID:1686
C11.525.381
Glaucoma
glaucomatous atrophy of optic disc
class of disease
optic atrophy
eye degenerative disease
human disease
DOID:10337
glioblastoma
class of disease
astrocytoma
disease
human disease
DOID:3068
C04.557.465.625.600.380.080.335
C04.557.470.670.380.080.335
C04.557.580.625.600.380.080.335
Glioblastoma
glioblastoma classical subtype
class of disease
glioblastoma
glioblastoma multiforme that is characterized by abnormally high levels of epidermal growth factor receptor and the absence of p53 mutations
DOID:0050803
glioblastoma mesenchymal subtype
class of disease
glioblastoma
glioblastoma multiforme that is characterized by the most frequent number of mutation of the Neurofibromin 1 gene
DOID:0050805
glioblastoma neural subtype
class of disease
glioblastoma
glioblastoma multiforme that is characterized by the expression of several gene types that are also typical of the brain's normal, noncancerous nerve cells, or neurons
DOID:0050806
glioblastoma proneural subtype
class of disease
glioblastoma
glioblastoma multiforme that is characterized by IDH1 and p53 mutations and Platelet Derived Growth Factor A amplification
DOID:0050804
glioma
class of disease
cell type cancer
brain tumor
spinal disease
bone cancer
brain cancer
disease
type of tumor that starts in the brain or spine
DOID:3070
C04.557.465.625.600.380
C04.557.470.670.380
C04.557.580.625.600.380
Gliomas
gliomatosis cerebri
class of disease
brain cancer
rare primary brain tumor
DOID:6128
Gliomatosis cerebri
gliosarcoma
class of disease
glioblastoma
Human disease
DOID:3071
C04.557.465.625.600.380.400
C04.557.470.670.380.400
C04.557.580.625.600.380.400
Gliosarcoma
globe disease
class of disease
eye disease
Human disease
DOID:1242
globoszoospermia
class of disease
Teratospermia
male infertility
autosomal recessive disease
spermatogenic failure
male infertility characterized by round-headed spermatozoa lacking an acrosome
DOID:0111156
Globoszoospermia
glomangioma
class of disease
benign perivascular tumor
glomus tumor
Human disease
DOID:2436
glomangiomatosis
class of disease
benign perivascular tumor
glomus tumor
Human disease
DOID:6906
glomangiomyoma
class of disease
benign perivascular tumor
glomus tumor
human disease
DOID:8020
glomangiosarcoma
class of disease
glomus tumor
Human disease
DOID:5233
glomeruloid hemangioma
class of disease
hemangioma
Human disease
DOID:486
glomerulonephritis
class of disease
symptom or sign
nephritis
glomerulopathy
disease
nephritis that causes inflammation of the glomeruli located in kidney
DOID:2921
C12.777.419.570.363
C13.351.968.419.570.363
Glomerulonephritis
glomerulosclerosis
class of disease
glomerulonephritis
glomerulonephritis that is characterized by hardening of the glomerulus in the kidney
DOID:0050851
Glomerulosclerosis
glossitis
class of disease
symptom or sign
tongue disease
inflammatory disease
disease
soreness of the tongue, or more usually inflammation with depapillation of the dorsal surface of the tongue
DOID:1456
C07.465.910.363
Glossitis
glossopharyngeal motor neuropathy
class of disease
motor neuritis
glossopharyngeal nerve disease
Human disease
DOID:7558
glossopharyngeal nerve disease
class of disease
cranial nerve disease
Human disease
DOID:3418
C10.292.450
glossopharyngeal nerve paralysis
class of disease
glossopharyngeal nerve disease
cranial nerve palsy
Human disease
DOID:3816
glossopharyngeal neuralgia
class of disease
glossopharyngeal nerve disease
neuralgia
cranial neuralgia
Human disease
DOID:14423
glottis cancer
class of disease
laryngeal cancer
glottis neoplasm
Human disease
DOID:2595
glottis carcinoma
class of disease
glottis cancer
carcinoma
Human disease
DOID:2599
glottis neoplasm
class of disease
laryngeal neoplasm
Human disease
DOID:2597
glucocorticoid deficiency 1
class of disease
familial glucocorticoid deficiency
autosomal recessive disease
human disease
DOID:0080621
glucocorticoid-induced osteoporosis
class of disease
corticosteroid-induced osteoporosis
osteoporosis
Human disease
DOID:0060343
glucose intolerance
class of disease
hyperglycemia
disease
pre-diabetic state of hyperglycemia that is associated with insulin resistance and increased risk of cardiovascular pathology. IGT may precede type 2 diabetes mellitus by many years
DOID:10603
C18.452.394.952.500
glucose metabolism disease
class of disease
carbohydrate metabolism disease
metabolic disease
metabolic disorder characterized by abnormal blood glucose levels
DOID:4194
C18.452.394
Glucose metabolism disorders
glucose-6-phosphate dehydrogenase deficiency
class of disease
carbohydrate metabolic disorder
disease
carbohydrate metabolic disorder that is characterised by abnormally low levels of glucose-6-phosphate dehydrogenase (abbreviated G6PD or G6PDH)
DOID:2862
C15.378.071.141.150.480
C16.320.070.480
C16.320.565.202.402
C18.452.648.202.402
Glucose-6-phosphate dehydrogenase deficiency
glutathionuria
class of disease
Congenital disorders of amino acid metabolism
inborn disorder of the gamma-glutamyl cycle
amino acid metabolic disorder
autosomal recessive disease
Gamma-glutamyl transpeptidase deficiency is characterized by increased glutathione concentration in the plasma and urine
DOID:0111257
gluten allergy
class of disease
food allergy
gluten-related disorder
allergy involving gluten
DOID:0060057
glycogen metabolism disorder
class of disease
carbohydrate metabolic disorder
carbohydrate metabolism disorder that is characterized by abnormal accumulation or depletion of liver glycogen
DOID:0050728
glycogen storage disease
class of disease
glycogen metabolism disorder
overload disease
carbohydrate metabolic disorder
disease
glycogen metabolism disorder that has material basis in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types
DOID:2747
C16.320.565.202.449
C18.452.648.202.449
Glycogen storage disease
glycogen storage disease IX
class of disease
glycogen storage disease
glycogen storage disease characterized by deficiency of hepatic phosphorylase kinase activity
DOID:0050594
Glycogen storage disease type IX
glycogen-rich clear cell breast carcinoma
class of disease
breast adenocarcinoma
clear cell carcinoma
Human disease
DOID:5310
goat milk allergy
class of disease
milk allergy
milk allergy triggered by Capra hircus milk
DOID:0060522
goiter
class of disease
thyroid gland disease
disease
swelling of the thyroid gland
DOID:12176
C19.874.283
Goiters
gonadal disease
class of disease
endocrine system disease
endocrine system disease that is located in the gonads
DOID:2277
C19.391
Diseases and disorders of gonads
gonadal dysgenesis
class of disease
hypogonadism
sex differentiation disease
disease
congenital disorder of the reproductive system
DOID:14447
C12.706.316.309
C13.351.875.253.309
C16.131.939.316.309
C19.391.119.309
gonadoblastoma
class of disease
benign neoplasms by histologic type
cell type benign neoplasm that is composed of a mixture of gonadal elements
DOID:3301
C04.557.465.420
C04.557.475.395
C12.706.316.096.687.500
C12.706.316.309.388.500
C13.351.875.253.096.687.500
C13.351.875.253.309.388.500
C16.131.939.316.096.687.500
C16.131.939.316.309.388.500
C19.391.119.096.687.500
C19.391.119.309.388.500
Gonadoblastoma
gonococcal bursitis
class of disease
bursitis
gonococcal infectious diseases
Human disease
DOID:13453
gonococcal seminal vesiculitis
class of disease
vesiculitis
gonorrhea
human disease
DOID:10400
gonococcal spondylitis
class of disease
spondylitis
gonorrhea
Human disease
DOID:13127
gonococcal synovitis
class of disease
synovitis
gonococcal infectious diseases
Human disease
DOID:13454
gout
class of disease
symptom or sign
arthritis
genetic disease
crystal arthropathy
metabolic disease
disease
medical condition that results in recurrent pain and swelling of joints
DOID:13189
C05.550.114.423
C05.550.354.500
C05.799.414
C16.320.565.798.368
C18.452.648.798.368
Gout
granular cell carcinoma
class of disease
carcinoma
carcinoma that derives from epithelial cells, with polygonal accumulation of secondary lysosomes in the cytoplasm
DOID:4903
granular cell leiomyosarcoma
class of disease
leiomyosarcoma
rare nervous system tumor
malignant granular cell myoblastoma
Human disease
DOID:5258
granular cell tumor
class of disease
skin benign neoplasm
Human disease
DOID:2411
C04.557.450.590.350
Granular cell tumor
granuloma annulare
class of disease
dermatitis
necrobiotic disorders
Human disease
DOID:3777
C17.300.200.495.380
C17.800.550.380
C23.550.382.375
Granuloma annulare
granulomatous amebic encephalitis
class of disease
Balamuthia infection
acanthamoebiasis
primary amebic meningoencephalitis
encephalopathy
Human disease
DOID:0050246
Granulomatous amoebic encephalitis
granulomatous angiitis
class of disease
vasculitis
central nervous system vasculitis
Human disease
DOID:2555
granulomatous dermatitis
class of disease
dermatitis
Human disease
DOID:4397
granulomatous endometritis
class of disease
endometritis
chronic endometritis
Human disease
DOID:4561
granulomatous gastritis
class of disease
gastritis
chronic gastritis
Human disease
DOID:4038
granulomatous hepatitis
class of disease
hepatitis
hepatic granuloma
Human disease
DOID:2239
granulomatous myositis
class of disease
myositis
Human disease
DOID:3428
granulomatous orchitis
class of disease
testicular disease
Human disease
DOID:3089
granulosa cell tumour
class of disease
ovarian cancer
sex cord-gonadal stromal tumor
Human disease
DOID:2999
C04.557.475.750.656
C04.588.322.455.398
C13.351.500.056.630.705.398
C13.351.937.418.685.398
C19.344.410.398
C19.391.630.705.398
Granulosa cell tumors
gray zone lymphoma
class of disease
lymphoma
lymphoma that is characterized by having cellular features of both classic Hodgkin's lymphomas and large B-cell Lymphomas
DOID:5822
green color blindness
class of disease
dichromatopsia
deuteranopia
human disease
DOID:13909
green mud crab allergy
class of disease
crustacean allergy
crustacean allergy triggered by Scylla paramamosain
DOID:0060526
growth hormone insensitivity syndrome with immune dysregulation 2
class of disease
syndrome
autosomal dominant disease
human disease
DOID:0080837
growth hormone secreting pituitary adenoma 2
class of disease
growth hormone secreting pituitary adenoma
human disease
DOID:0112007
gynatresia
class of disease
female reproductive system disease
atresia
Human disease
DOID:429
C13.351.500.320
gynecomastia
class of disease
sex differentiation disease
human disorder, which causes the appearance of breasts in males
DOID:12698
C17.800.090.875
Gynecomastia
gyrate atrophy of the choroid
class of disease
disease
choroid disease
central gyrate choroidal dystrophy
Human disease
DOID:1415
C11.270.468
C11.941.160.578
C16.320.290.468
haemophilus meningitis
class of disease
bacterial meningitis
Haemophilus influenzae infectious disease
bacterial meningitis that has material basis in Haemophilus influenzae infection
DOID:0080179
C01.150.252.223.500.425
C01.150.252.400.700.433.615
C10.228.228.180.500.425
C10.586.625.280.393
C01.207.180.500.425
hair diseases
class of disease
integumentary system disease
integumentary system disease that is located in hair
DOID:421
C17.800.329
hair follicle neoplasm
class of disease
skin benign neoplasm
hair diseases
skin tumor derived from the hair matrix
DOID:5375
hairy cell leukemia
class of disease
chronic lymphocytic leukemia
B-cell leukemia
disease
chronic lymphocytic leukemia that is characterized by over production of B cells (lymphocytes) by the bone marrow where the B cells appear hairy under a microscope
DOID:285
C04.557.337.415
C15.604.515.553
C20.683.515.517
Hairy cell leukemia
hairy tongue
class of disease
tongue disease
disease
Human disease
DOID:13500
C07.465.910.791
Black hairy tongue
hallucinogen abuse
class of disease
substance abuse
substance abuse that involves the recurring use of hallucinogenic drugs despite negative consequences
DOID:12797
hallucinogen dependence
class of disease
substance dependence
hallucinogen abuse
drug dependence that involves the continued use of hallucinogenic drugs despite problems related to use of the substance
DOID:9977
hand dermatosis
class of disease
skin disease
disease class
DOID:3158
C17.800.338
head and neck cancer
class of disease
organ system cancer
head and neck neoplasms
respiratory system cancer
disease
organ system cancer in the head or neck region
DOID:11934
DOID:3680
Head and neck cancer
head and neck carcinoma
class of disease
head and neck cancer
carcinoma
human disease
DOID:1542
heart cancer
class of disease
cardiovascular cancer
Primary tumors of the heart
heart disease
thoracic cancer
cardiovascular cancer located in the heart
DOID:117
Heart cancer
heart disease
class of disease
cardiovascular disease
cardiovascular system disease that involves the heart
DOID:114
C14.280
Diseases and disorders of the heart
heart fibrosarcoma
class of disease
heart sarcoma
fibrosarcoma
Human disease
DOID:6033
heart leiomyosarcoma
class of disease
heart sarcoma
Human disease
DOID:5261
heart lipoma
class of disease
cardiovascular organ benign neoplasm
Primary tumors of the heart
heart disease
benign neoplasm of heart
lipoma
Human disease
DOID:6285
heart lymphoma
class of disease
heart cancer
lymphoma
Human disease
DOID:6547
heart malignant hemangiopericytoma
class of disease
heart sarcoma
hemangiopericytoma
heart sarcoma that is a soft tissue sarcoma located in the heart
DOID:6034
heart sarcoma
class of disease
heart cancer
sarcoma and malignant neoplasm of heart that is located in the heart
DOID:5262
heart septal defect
class of disease
congenital heart disease
Human disease
DOID:1681
C14.240.400.560
C14.280.400.560
C16.131.240.400.560
Heart septal defects
heart valve disease
class of disease
heart disease
disease
disease in the valves of the heart
DOID:4079
C14.280.484
Diseases and disorders of the heart valves
heavy chain disease
class of disease
type IV hypersensitivity
hypersensitivity reaction type IV disease that results from a proliferation of cells producing immunoglobulin heavy chains
DOID:0060125
C15.378.147.780.490
C15.604.515.435
C20.683.780.490
hemangioblastoma
class of disease
hemangioma
rare nervous system tumor
disease
tumor of the central nervous system that originates from the vascular system
DOID:5241
C04.557.645.375.380.370
Hemangioblastomas
hemangioma
class of disease
angioma
vascular neoplasm
cardiovascular organ benign neoplasm
benign neoplasms by histologic type
vascular disease
disease
cell type benign neoplasm that has physical basis in endothelial cells that line blood vessels
DOID:255
C04.557.645.375
Skin hemangioma
hemangioma of intra-abdominal structure
class of disease
hemangioma
Human disease
DOID:254
hemangioma of lung
class of disease
hemangioma
lung benign neoplasm
human disease
DOID:490
hemangioma of orbit
class of disease
orbital disease
hemangioma
Human disease
DOID:14459
hemangioma of peripheral nerve
class of disease
hemangioma
peripheral nervous system benign neoplasm
peripheral neuropathy
Human disease
DOID:482
hemangioma of spleen
class of disease
splenic disease
hemangioma of intra-abdominal structure
Human disease
DOID:256
hemangioma of subcutaneous tissue
class of disease
skin hemangioma
subcutaneous tissue disease
vascular skin disease
skin benign neoplasm
hemangioma
Human disease
DOID:13081
hemangiopericytic tumor
class of disease
perivascular tumor
Human disease
DOID:3850
hemangiopericytoma
class of disease
connective tissue neoplasm
hemangiopericytic tumor
soft tissue cancer that is a soft tissue sarcoma and originates in the pericytes in the walls of capillaries
DOID:264
C04.557.645.380
Haemangiopericytoma
hematocele of tunica vaginalis testis
class of disease
symptom or sign
testicular disease
hematocele
Human disease
DOID:12332
C12.294.287
C23.550.414.817
Hematocele
hematologic cancer
class of disease
symptom or sign
organ system cancer
hematopoietic system disease
tumor of hematopoietic and lymphoid tissues
immune system cancer located in the hematological system that is characterized by uncontrolled cellular proliferation in blood, bone marrow and lymph nodes
DOID:2531
Cancers of the lymph nodes and haematopoiesis
hematopoietic system disease
class of disease
symptom
disease of anatomical entity
disorder which primarily affects the blood
DOID:74
C15.378
Diseases and disorders of the blood
hemidystonia
class of disease
multifocal dystonia
multifocal dystonia that involves the arm and leg on the same side of the body
DOID:0050846
hemiparesis
class of disease
symptom or sign
paresis
paralysis
central nervous system disease
disease
weakness of one side of the body
DOID:10969
hemochromatosis type 1
class of disease
HFE hereditary haemochromatosis
genetic disease
hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22
DOID:0111029
hemochromatosis type 2
class of disease
iron overload
HFE hereditary haemochromatosis
hemochromatosis characterized by autosomal recessive inheritance of early onset of severe iron loading with symptoms including; hypogonadotropic hypogonadism, cardiomyopathy, arthropathy, and liver fibrosis or cirrhosis
DOID:0111034
hemochromatosis type 2B
class of disease
hemochromatosis type 2
genetic disease
hemochromatosis type 2 that has material basis in homozygous mutation in the HAMP gene on chromosome 19q13
DOID:0111032
hemoglobin C
class of disease
hemoglobinopathy
congenital hemolytic anemia
disease
Human disease
DOID:2859
C15.378.071.141.150.490
C15.378.420.463
C16.320.070.490
C16.320.365.463
hemoglobin D disease
class of disease
hemoglobinopathy
congenital hemolytic anemia
Human disease
DOID:5378
hemoglobin E
class of disease
hemoglobinopathy
congenital hemolytic anemia
variant form of human hemoglobin
DOID:5379
D12.776.124.400.463.375
D12.776.422.316.762.426.375
hemoglobin H disease
class of disease
alpha thalassemia
alpha thalassemia that has material basis in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other
DOID:0110031
hemoglobinopathy
class of disease
congenital hemolytic anemia
genetic disease
hemolytic anemia
hemoglobin variant
disease
genetic defect causing abnormal hemoglobin structure
DOID:2860
C15.378.420
C16.320.365
hemoglobinuria
class of disease
proteinuria
hemolytic anemia
disease
condition in which the oxygen transport protein hemoglobin is found in abnormally high concentrations in the urine
DOID:582
C12.777.934.734.634
C13.351.968.934.734.634
C23.888.942.750.634
hemolytic-uremic syndrome
class of disease
kidney disease
disease
Human disease
DOID:12554
C12.050.351.968.419.936.463
C12.200.777.419.936.463
C15.378.071.141.610
C15.378.140.855.925.500
C12.950.419.936.463
C15.378.243.937.925.500
Hemolytic-uremic syndrome
hemometra
class of disease
uterine disease
menstrual disorder
disease
Human disease
DOID:9958
C13.351.500.852.495
Hematometra
hemopericardium
class of disease
pericardial effusion
pericardial effusion that results from blood in the pericardial sac
DOID:11482
Hemopericardium
hemophagocytic lymphohistiocytosis
class of disease
lymphatic system disease
disease
uncommon hematologic disorder seen more often in children than in adults
DOID:0050120
C15.604.250.410.575
Hemophagocytic lymphohistiocytosis
hemophilia A
class of disease
symptom or sign
hemophilia
coagulation factor deficiency
X-linked recessive disease
blood coagulation disease
disease
X-linked disease that has material basis in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged
DOID:12134
C15.378.100.100.500
C15.378.100.141.500
C15.378.463.500
C16.320.099.500
Hemophilia A
hemophilia B
class of disease
coagulation factor deficiency
inherited blood coagulation disease
X-linked recessive disease
blood coagulation disease
disease
An inherited blood coagulation disease that has material basis in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.
DOID:12259
C15.378.100.100.510
C15.378.100.141.510
C15.378.463.510
C16.320.099.510
C16.320.322.235
Hemophilia B
hemopneumothorax
class of disease
pneumothorax
hemothorax
disease
medical term describing the combination of two conditions: pneumothorax, or air in the chest cavity, and hemothorax (also called hæmothorax), or blood in the chest cavity
DOID:2718
C08.528.338
C23.550.414.904.500
hemorrhagic cystitis
class of disease
cystitis
Inflammation of the bladder resulting in bloody urine
DOID:0050859
C12.050.351.968.829.495.250
C12.200.777.829.495.250
C12.950.829.495.250
hemorrhagic disease
class of disease
blood coagulation disease
disease
human disease
DOID:2213
C15.378.463
hemorrhoid
class of disease
gastrointestinal system disease
pelvic varices
anorectal disorder
anal disease
skin disease
disease
vascular structures in the anal canal
DOID:9746
C06.405.469.860.401
C14.907.449
Hemorrhoids
hemosiderosis
class of disease
iron overload
iron metabolism disease
disease
iron metabolism disease that has material basis in an accumulation of hemosiderin, an iron-storage complex, resulting in iron overload
DOID:12119
C18.452.565.500.500
Hemosiderosis
hepatic angiomyolipoma
class of disease
liver neoplasm
Human disease
DOID:3317
hepatic flexure cancer
class of disease
ascending colon cancer
Human disease
DOID:260
hepatic hemangioma
class of disease
liver neoplasm
hemangioma of intra-abdominal structure
hemangioma
hepatic vascular disease
non-cancerous tumor of the liver
DOID:271
Liver hemangioma
hepatic infarction
class of disease
hepatic vascular disease
infarction
ischemic hepatitis
Human disease
DOID:13738
C06.552.289
C23.550.513.355.500
C23.550.717.489.500
Hepatic infarction
hepatic osteogenic sarcoma
class of disease
extraosseous osteosarcoma
liver cancer
Human disease
DOID:6370
hepatic vascular disease
class of disease
vascular disease
liver disease
vascular disease that is located in the liver
DOID:272
hepatic veno-occlusive disease
class of disease
hepatic vascular disease
vein disorder
hepatic vascular disease that is characterized by obstruction of some of the small veins of the liver
DOID:0080177
C06.552.360
C14.907.460
hepatitis
class of disease
symptom or sign
liver disease
inflammation
liver symptom
disease
inflammation of the liver tissue
DOID:2237
C06.552.380
Hepatitis
hepatobiliary neoplasm
class of disease
gastrointestinal system benign neoplasm
liver and intrahepatic bile duct neoplasm
gastrointestinal system neoplasm located in the hepatobiliary system
DOID:3117
hepatobiliary system cancer
class of disease
gastrointestinal system cancer
liver and intrahepatic bile duct neoplasm
gastrointestinal system cancer that is located in the hepatobiliary system
DOID:0080355
hepatoblastoma
class of disease
liver cancer
disease
uncommon malignant liver cancer occurring in infants and children
DOID:687
C04.557.435.380
Hepatoblastoma
hepatocellular adenoma
class of disease
liver neoplasm
endocrine gland cancer
benign neoplasms by histologic type
adenoma
disease
Hepatocellular adenoma (HA) is a rare benign tumor of the liver
DOID:0050868
C04.557.470.035.120
C04.588.274.623.040
C06.301.623.040
C06.552.697.040
Hepatic adenoma
hepatocellular carcinoma
class of disease
liver carcinoma
disease
liver carcinoma that has material basis in undifferentiated hepatocytes
DOID:684
C04.557.470.200.025.255
C04.588.274.623.160
C06.301.623.160
C06.552.697.160
Hepatocellular carcinoma
hepatocellular clear cell carcinoma
class of disease
hepatocellular carcinoma
clear cell carcinoma
clear cell adenocarcinoma
Human disease
DOID:5016
hepatoid adenocarcinoma
class of disease
adenocarcinoma
adenocarcinoma with morphologic characteristics similar to hepatocellular carcinoma, arising from an anatomic site other than the liver
DOID:0060534
hepatoid pattern ovarian yolk sac tumor
class of disease
ovarian endodermal sinus tumor
Human disease
DOID:6512
hepatoid pattern testicular yolk sac tumor
class of disease
testicular yolk sac tumor
Human disease
DOID:8195
hepatopulmonary syndrome
class of disease
liver disease
Human disease
DOID:900
C06.552.455
C08.381.385
hepatorenal syndrome
class of disease
acute kidney injury
disease
Human disease
DOID:11823
C06.552.465
C12.777.419.291
C13.351.968.419.291
Hepatorenal syndrome
hereditary ataxia
class of disease
neurodegeneration
neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements
DOID:0050951
hereditary Wilms' tumor
class of disease
nephroblastoma
inherited renal tumor
nephroblastoma that results in either bilateral disease or a family history of Wilms' tumour
DOID:5183
hereditary alpha tryptasemia syndrome
class of disease
gene duplication disease
syndrome
DOID:0080714
hereditary angioedema
class of disease
symptom or sign
angioedema
disease
Hereditary angioedema (HAE) is a genetic disease characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain
DOID:14735
C14.907.079.500
C16.320.798.500.500
C17.800.862.945.066.500
C20.543.480.904.066.500
C20.673.795.500.500
Hereditary angioedema
hereditary breast ovarian cancer
class of disease
autosomal dominant disease
hereditary neoplastic syndromes
syndrome
disease
autosomal dominant disease characterized by the higher than normal tendency to develop breast and ovarian cancers in genetically related families
DOID:5683
C04.588.180.483
C04.588.322.455.431
C04.700.517
C13.351.500.056.630.705.431
C13.351.937.418.685.431
C16.320.700.517
C17.800.090.500.483
C19.344.410.431
C19.391.630.705.431
hereditary choroidal atrophy
class of disease
choroidal sclerosis
human disease
DOID:9794
hereditary combined deficiency of vitamin K-dependent clotting factors
class of disease
monogenic disease
blood coagulation disease
human disease
DOID:0112172
hereditary conventional renal cell carcinoma
class of disease
hereditary renal cell carcinoma
renal clear cell carcinoma
Human disease
DOID:7192
hereditary diffuse gastric cancer
class of disease
hereditary gastric cancer
stomach cancer
autosomal dominant disease
diffuse gastric cancer
medical condition
DOID:0080764
hereditary lymphedema
class of disease
lymphedema
Primary lymphedema
disease
lymphedema commonly located in legs, caused by congenital abnormalities in the lymphatic system
DOID:0050580
hereditary lymphedema I
class of disease
hereditary lymphedema
hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood
DOID:0070212
hereditary lymphedema IA
class of disease
hereditary lymphedema
genetic disease
autosomal dominant disease
hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in mutation in the FLT4 gene on chromosome 5q35
DOID:0070210
hereditary lymphedema IB
class of disease
hereditary lymphedema
autosomal dominant disease
A hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in the chromosomal region 6q16.2-q22.1.
DOID:0070211
hereditary lymphedema IC
class of disease
hereditary lymphedema
genetic disease
autosomal dominant disease
hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in mutation in the GJC2 gene on chromosome 1q42
DOID:0070208
hereditary lymphedema ID
class of disease
hereditary lymphedema
genetic disease
autosomal dominant disease
hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in mutation in the VEGFC gene on chromosome 4q34
DOID:0070209
hereditary lymphedema II
class of disease
hereditary lymphedema
autosomal dominant disease
hereditary lymphedema characterized by onset around puberty of chronic lymphedema particularly in the lower limbs with an apparent autosomal dominant pattern of inheritance
DOID:0070213
hereditary mixed polyposis syndrome 1
class of disease
hereditary mixed polyposis syndrome
chromosomal duplication syndrome
human disease
DOID:0111685
hereditary motor and sensory neuropathy
class of disease
congenital disorder
Sensorimotor neuropathy
peripheral neuropathy
hereditary peripheral neuropathy
congenital disorder of nervous system
DOID:2477
C10.500.300
C10.574.500.495
C10.668.829.800.300
C16.131.666.300
C16.320.400.375
Hereditary motor and sensory neuropathies
hereditary neutrophilia
class of disease
leukocyte disease
neutrophilia
rare genetic immune disease
genetic hematologic disease
genetic disease
autosomal dominant disease
human disease
DOID:0090120
hereditary night blindness
class of disease
night blindness
Human disease
DOID:8498
hereditary nonpolyposis colorectal cancer type 2
class of disease
Lynch syndrome
A Lynch syndrome that has material basis in mutations in the MLH1 gene on chromosome 3p22.2.
DOID:0070274
hereditary nonpolyposis colorectal cancer type 4
class of disease
Lynch syndrome
Lynch syndrome that has material basis in heterozygous mutation in the PMS2 gene on chromosome 7p22
DOID:0070275
hereditary nonpolyposis colorectal cancer type 5
class of disease
Lynch syndrome
Lynch syndrome that has material basis in heterozygous mutation in the MSH6 gene on chromosome 2p16
DOID:0070272
hereditary nonpolyposis colorectal cancer type 6
class of disease
Lynch syndrome
Lynch syndrome that has material basis in heterozygous mutation in the TGFBR2 gene on chromosome 3p22
DOID:0070273
hereditary nonpolyposis colorectal cancer type 7
class of disease
Lynch syndrome
A Lynch syndrome that has material basis in mutation in the MLH3 gene on chromosome 14q24.3.
DOID:0070276
hereditary nonpolyposis colorectal cancer type 8
class of disease
Lynch syndrome
chromosomal deletion syndrome
human disease
DOID:0070270
hereditary papulotranslucent acrokeratoderma
class of disease
cholesteatoma
keratosis of the hands and feet characterized by persistent, asymptomatic, yellowish to white papules and plaques associated with fine-textured scalp hair and an atopic diathesis
DOID:0060360
hereditary renal cell carcinoma
class of disease
renal cell carcinoma
inherited renal tumor
human disease
DOID:4455
hereditary retinal dystrophy
class of disease
fundus dystrophy
genetic disease
hereditary eye disease
Human disease
DOID:8500
hereditary sensory and autonomic neuropathy
class of disease
hereditary disorder
peripheral neuropathy
congenital disorder of nervous system
DOID:0050548
C10.500.250
C10.574.500.493
C10.668.829.800.175
C16.131.666.310
C16.320.400.415
hereditary sensory and autonomic neuropathy type 1
class of disease
hereditary sensory and autonomic neuropathy
hereditary sensory neuropathy characterized by slowly progressing, prominent, predominantly distal sensory loss and autonomic disturbances with juvenile or adult onset and autosomal dominant inheritance
DOID:0070162
hereditary sensory and autonomic neuropathy type 1A
class of disease
hereditary sensory and autonomic neuropathy type 1
genetic disease
autosomal dominant disease
hereditary sensory and autonomic neuropathy type 1 characterized by onset of sensorimotor axonal neuropathy in the first or second decades of life that has material basis in heterozygous mutation in the SPTLC1 gene on chromosome 9q22
DOID:0070152
hereditary sensory and autonomic neuropathy type 2
class of disease
hereditary sensory and autonomic neuropathy
hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood
DOID:0070161
hereditary sensory neuropathy X-linked
class of disease
hereditary sensory and autonomic neuropathy
X-linked recessive disease
hereditary sensory neuropathy characterized by X-linked inheritance of slowly progressing neuropathy with onset in the first or second decade of life
DOID:0070159
hereditary sensory neuropathy type 1B
class of disease
hereditary sensory and autonomic neuropathy
genetic disease
autosomal dominant disease
hereditary sensory neuropathy characterized by axonal neuropathy with distal sensory impairment, cough, and gastroesophageal reflux that has material basis in variation in the chromosome region 3p24-p22
DOID:0070148
hereditary spastic paraplegia 14
class of disease
hereditary spastic paraplegia
pure or complex autosomal recessive spastic paraplegia
autosomal recessive disease
hereditary spastic paraplegia that has material basis in variation in the chromosome region 3q27-q28
DOID:0110767
hereditary spastic paraplegia 16
class of disease
hereditary spastic paraplegia
pure or complex X-linked spastic paraplegia
X-linked recessive disease
A hereditary spastic paraplegia that has material basis in variation in the chromosome region Xq11.2.
DOID:0110769
hereditary spastic paraplegia 19
class of disease
hereditary spastic paraplegia
autosomal dominant pure spastic paraplegia
autosomal dominant disease
hereditary spastic paraplegia that has material basis in variation in the chromosome region 9q
DOID:0110772
hereditary spastic paraplegia 24
class of disease
hereditary spastic paraplegia
autosomal recessive complex spastic paraplegia
autosomal recessive disease
hereditary spastic paraplegia that has material basis in variation in the chromosome region 13q14
DOID:0110775
hereditary spastic paraplegia 25
class of disease
hereditary spastic paraplegia
autosomal recessive complex spastic paraplegia
autosomal recessive disease
A hereditary spastic paraplegia that has material basis in variation in the chromosome region 6q23-q24.1.
DOID:0110776
hereditary spastic paraplegia 27
class of disease
hereditary spastic paraplegia
autosomal recessive complex spastic paraplegia
autosomal recessive disease
A hereditary spastic paraplegia that has material basis in variation in the chromosome region 10q22.1-q24.1.
DOID:0110778
hereditary spastic paraplegia 29
class of disease
hereditary spastic paraplegia
autosomal dominant complex spastic paraplegia
autosomal dominant disease
A hereditary spastic paraplegia that has material basis in variation in the chromosome region 1p31.1-p21.1.
DOID:0110780
hereditary spastic paraplegia 32
class of disease
hereditary spastic paraplegia
autosomal recessive complex spastic paraplegia
autosomal recessive disease
hereditary spastic paraplegia that has material basis in variation in the chromosome region 14q12-q21
DOID:0110783
hereditary spastic paraplegia 34
class of disease
hereditary spastic paraplegia
X-linked pure spastic paraplegia
X-linked recessive disease
hereditary spastic paraplegia that has material basis in variation in the chromosome region Xq24-q25
DOID:0110785
hereditary spastic paraplegia 36
class of disease
hereditary spastic paraplegia
autosomal dominant complex spastic paraplegia
autosomal dominant disease
hereditary spastic paraplegia that has material basis in variation in the chromosome region 12q23-q24
DOID:0110787
hereditary spastic paraplegia 37
class of disease
hereditary spastic paraplegia
autosomal dominant pure spastic paraplegia
autosomal dominant disease
A hereditary spastic paraplegia that has material basis in variation in the chromosome region 8p21.1-q13.3.
DOID:0110788
hereditary spastic paraplegia 38
class of disease
hereditary spastic paraplegia
autosomal dominant complex spastic paraplegia
autosomal dominant disease
hereditary spastic paraplegia that has material basis in variation in the chromosome region 4p16-p15
DOID:0110789
hereditary spastic paraplegia 41
class of disease
hereditary spastic paraplegia
autosomal dominant pure spastic paraplegia
autosomal dominant disease
A hereditary spastic paraplegia that has material basis in variation in the chromosome region 11p14.1-p11.2.
DOID:0110793
hereditary spherocytosis
class of disease
congenital hemolytic anemia
spherocytosis
disease
congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape
DOID:12971
C15.378.071.141.150.785
C16.320.070.785
Hereditary spherocytosis
hereditary spherocytosis type 3
class of disease
hereditary spherocytosis
genetic disease
autosomal recessive disease
A hereditary spherocytosis that has material basis in an autosomal dominant mutation of SPTA1 on chromosome 1q23.1.
DOID:0110918
hernia of ovary and fallopian tube
class of disease
female reproductive system disease
Human disease
DOID:12735
heroin dependence
class of disease
opiate dependence
opiate dependence that involves the continued use of heroin despite problems related to use of the substance
DOID:9976
C25.775.675.400
herpes gestationis
class of disease
vesiculobullous skin disease
dermatosis of pregnancy
pemphigoid
autoimmune skin disease
disease
dermatosis of pregnancy
DOID:14482
DOID:0040098
C13.703.570
C17.800.865.700
Gestational pemphigoid
hexahydrophthalic anhydride allergic asthma
class of disease
allergic asthma
allergic asthma that has allergic trigger hexahydrophthalic anhydride
DOID:0040051
hexamethylene diisocyanate allergic asthma
class of disease
isocyanates allergic asthma
allergic asthma to isocyanates that has allergic trigger hexamethylene diisocyanate
DOID:0040040
hidradenitis
class of disease
sweat gland disease
human disease
DOID:2282
C17.800.946.315
hidradenoma
class of disease
sweat gland neoplasm
epithelial skin neoplasm
benign neoplasms by histologic type
human disease
DOID:3896
C04.557.470.035.175
C04.557.470.550.175
Hidradenoma
hidrocystoma
class of disease
apocrine sweat gland neoplasm
benign neoplasm of sweat gland
Human disease
DOID:3893
C04.557.470.035.175.375
C04.557.470.550.175.375
Hidrocystoma
high pressure neurological syndrome
class of disease
central nervous system disease
diving disorder
neurological and physiological disorder experienced by divers
DOID:3230
C10.228.566
C24.410
hilar lung carcinoma
class of disease
lung carcinoma
lung hilum cancer
Human disease
DOID:8207
hilar lung neoplasm
class of disease
lung benign neoplasm
Human disease
DOID:5767
histidine metabolism disease
class of disease
amino acid metabolic disorder
amino acid metabolic disorder that involves deficiency in histidine
DOID:9265
histidinemia
class of disease
histidine metabolism disease
histidine metabolism disease that involves a deficiency of the enzyme histidase
DOID:0060168
histiocytic and dendritic cell cancer
class of disease
hematologic cancer
lymphoid hemopathy
sarcoma and hematologic cancer that derives from follicular lymphoma
DOID:5621
histiocytoid hemangioma
class of disease
hemangioma
Human disease
DOID:474
histiocytoma
class of disease
connective tissue neoplasm
connective tissue benign neoplasm
Human disease
DOID:4231
C04.557.450.565.590.425
Histiocytoma
histiocytosis
class of disease
lymphatic system disease
disease
lymphatic system disease that is characterized by an excessive number of histiocytes
DOID:3405
C15.604.250
Histiocytoses
histoplasmosis
class of disease
primary systemic mycosis
genetic disease
disease
human disease
DOID:1731
C01.150.703.450
Histoplasmosis
histoplasmosis meningitis
class of disease
fungal meningitis
histoplasmosis
Human disease
DOID:12246
histoplasmosis retinitis
class of disease
retinitis
Human disease
DOID:11316
Presumed ocular histoplasmosis syndrome
histrionic personality disorder
class of disease
personality disorder
disease
personality disorder characterized by excessive emotionality and attention-seeking
DOID:334
F03.675.400
Histrionic personality disorder
hole retinal cyst
class of disease
degeneration of macula and posterior pole
retinoschisis and retinal cysts
retinal perforation
Human disease
DOID:13214
holoprosencephaly
class of disease
symptom or sign
nervous system malformations
syndrome
disease
congenital disorder of the nervous system
DOID:4621
C05.660.207.410
C10.500.034.875
C16.131.077.410
C16.131.260.380
C16.131.621.207.410
C16.131.666.034.875
C16.320.180.380
Holoprosencephaly
holoprosencephaly 1
class of disease
holoprosencephaly
genetic disease
autosomal dominant disease
A holoprosencephaly that has material basis in variation in the chromosome region 21q22.3.
DOID:0110881
holoprosencephaly 2
class of disease
holoprosencephaly
genetic disease
autosomal dominant disease
holoprosencephaly that has material basis in mutation in the homeobox-containing SIX3 gene on chromosome 2p21
DOID:0110872
holoprosencephaly 5
class of disease
holoprosencephaly
genetic disease
autosomal dominant disease
holoprosencephaly that has material basis in heterozygous mutation in the ZIC2 gene on chromosome 13q32
DOID:0110878
holoprosencephaly 6
class of disease
holoprosencephaly
genetic disease
A holoprosencephaly that has material basis in variation in the chromosome region 2q37.1-q37.3.
DOID:0110874
holoprosencephaly 8
class of disease
holoprosencephaly
genetic disease
holoprosencephaly that has material basis in variation in the chromosome region 14q13
DOID:0110879
holoprosencephaly 9
class of disease
holoprosencephaly
genetic disease
autosomal dominant disease
holoprosencephaly that has material basis in heterozygous mutation in the GLI2 gene on chromosome 2q14
DOID:0110873
homocarnosinosis
class of disease
gamma-amino butyric acid metabolism disorder
inborn disorder of peptide metabolism
encephalopathy
gamma-amino butyric acid metabolism disorder that is characterized by an excess of homocarnosine in the brain and has material basis in a deficiency of serum carnosinase in its ability to hydrolyze homocarnosine
DOID:0060177
hordeolum
class of disease
symptom or sign
blepharitis
eyelid disease
disease
bacterial infection of an oil gland in the eyelid
DOID:9909
C01.150.252.289.400
C01.375.354.400
C11.294.354.400
C11.338.648
Stye
hordeolum externum
class of disease
blepharitis
human disease
DOID:13134
horned turban snail allergy
class of disease
snail allergy
snail allergy triggered by Turbo cornutus
DOID:0060531
human cytomegalovirus infection
class of disease
viral infectious disease
cytomegaloviral disease
human disease
DOID:0080827
human immunodeficiency virus infectious disease
class of disease
viral infectious disease
Lentivirus infectious disease
disease affecting the human immune system
DOID:526
C20.673.480
C01.778.640.400
C01.925.782.815.616.400
C01.925.813.400
C01.221.250.875
C01.221.812.640.400
C12.100.937.640.400
human monocytic ehrlichiosis
class of disease
ehrlichiosis
disease
human disease
DOID:0050026
humeroradial synostosis
class of disease
synostosis
Human disease
DOID:0060467
hyaline body myopathy
class of disease
congenital myopathy
human disease
DOID:0111267
hyaline fibromatosis syndrome
class of disease
autosomal recessive disease
connective tissue disease
fibromatosis
human disease
DOID:0111669
hyalinizing trabecular adenoma
class of disease
follicular adenoma
thyroid adenoma
human disease
DOID:6203
hydranencephaly with renal aplasia-dysplasia
class of disease
genetic disease
autosomal recessive disease
syndrome
human disease
DOID:0080327
hydrocele
class of disease
male reproductive system disease
human disease
DOID:9912
C12.294.882
Hydrocele
hydrolethalus syndrome 1
class of disease
hydrolethalus syndrome
human disease
DOID:0111355
hydrolethalus syndrome 2
class of disease
hydrolethalus syndrome
human disease
DOID:0111356
hydronephrosis
class of disease
urinary tract obstruction
kidney disease
disease
human disease
DOID:11111
C12.777.419.307
C13.351.968.419.307
Hydronephrosis
hydrophthalmos
class of disease
primary congenital glaucoma
Human disease
DOID:11212
C11.250.480
C11.525.381.407.480
C16.131.384.480
C16.614.438
hydrops of gallbladder
class of disease
gallbladder disease
Human disease
DOID:9717
hyper IgE recurrent infection syndrome 2
class of disease
autosomal recessive disease
Job's syndrome
human disease
DOID:0080594
hyper IgE recurrent infection syndrome 3
class of disease
Job's syndrome
autosomal recessive disease
human disease
DOID:0080595
hyper IgE recurrent infection syndrome 4
class of disease
autosomal recessive disease
Job's syndrome
human disease
DOID:0080596
hyper-IgM syndrome type 4
class of disease
hyper IgM syndrome
hyperimmunoglobulin syndrome
hyperimmunoglobulin syndrome characterized by normal or increased serum IgM concentrations associated with low or absent serum IgG, IgA, and IgE concentrations, indicating a defect in the class-switch recombination (CSR) process
DOID:0060760
hyperalphalipoproteinemia 1
class of disease
cholesterol-ester transfer protein deficiency
autosomal dominant disease
hyperalphalipoproteinemia
human disease
DOID:0111369
hyperandrogenism
class of disease
gonadal disease
sex differentiation disease
disease
medical condition characterized by excessive levels of androgens in the body
DOID:11613
C12.050.351.875.253.064.500
C12.050.351.875.253.090.750
C16.131.939.316.064.500
C16.131.939.316.129.750
C19.391.119.064.500
C19.391.119.090.750
C12.200.706.316.064.500
C12.200.706.316.090.750
C12.800.316.064.500
C12.800.316.090.750
Hyperandrogenism
hypercalcemia
class of disease
calcium metabolism disease
disease
high calcium (Ca2+) level in the blood serum
DOID:12678
C18.452.174.451
C18.452.950.340
Hypercalcemia
hypercalcemic sarcoidosis
class of disease
sarcoidosis
hypercalcemia
Human disease
DOID:13407
hypercalcemic type ovarian small cell carcinoma
class of disease
ovarian small cell carcinoma
Human disease
DOID:7651
hypercementosis
class of disease
teeth hard tissue disease
Human disease
DOID:12733
C07.793.422
hyperekplexia 1
class of disease
hyperekplexia
genetic disease
autosomal recessive disease
autosomal dominant disease
hyperekplexia that has material basis in heterozygous, homozygous, or compound heterozygous mutation in the GLRA1 gene on chromosome 5q32
DOID:0060696
C10.228.590
hyperekplexia 4
class of disease
hyperekplexia
autosomal recessive disease
hyperekplexia that is characterized by extreme hypertonia, stiff and rigid appeareance and that has material basis in homozygous mutation in the ATAD1 gene on chromosome 10q23
DOID:0080581
hyperglobulinemic purpura
class of disease
purpura
Human disease
DOID:3325
C14.907.454.550
C15.378.100.802.250
C15.378.463.515.550
C23.550.414.950.250
C23.888.885.687.250
hyperglycemia
class of disease
abnormally high value
glucose metabolism disease
disease
human disease
DOID:4195
C18.452.394.952
Hyperglycemia
hyperhomocysteinemia
class of disease
sulfuraminoacidemia
amino acid metabolic disorder
disease
amino acid metabolic disorder that involves an abnormally large level of homocysteine in the blood
DOID:9279
C16.320.565.100.480
C18.452.603.378
C18.452.648.100.480
C18.654.521.500.133.699.418
hyperimmunoglobulin syndrome
class of disease
B cell deficiency
Human disease
DOID:2959
hyperinsulinemia
class of disease
endocrine pancreas disease
glucose metabolism disease
pancreas disease
condition in which there are excess levels of insulin circulating in the blood relative to the level of glucose
DOID:2018
hyperlipoproteinemia type IV
class of disease
hyperlipidemia
familial hyperlipidemia
human disease
DOID:1172
C16.320.565.398.487
C18.452.584.500.500.644.490
C18.452.584.500.500.851.500
C18.452.648.398.487
C18.452.584.563.487
hypermanganesemia with dystonia
class of disease
metal metabolism disorder
metal metabolism disorder that is characterized by involuntary, sustained muscle contractions (dystonia) and other uncontrolled movements resulting from excessive accumulation of manganese
DOID:0080535
hypermanganesemia with dystonia 1
class of disease
hypermanganesemia with dystonia
human disease
DOID:0080536
hypermethioninemia
class of disease
amino acid metabolic disorder
An amino acid metabolic disorder that involves an excess of the amino acid methionine, in the blood. This condition can occur when methionine is not broken down properly in the body.
DOID:0050544
hypermobility of coccyx
class of disease
spondyloarthropathy
Human disease
DOID:12537
hypermobility syndrome
class of disease
arthropathy
joint hypermobility
disease
human disease: joints that stretch farther than normal
DOID:13781
Hypermobility
hyperopia
class of disease
symptom or sign
refractive error
disease
visual defect which causes to see the far objects clearly and near objects unclearly
DOID:9834
C11.744.479
Hyperopia
hyperostosis
class of disease
bone remodeling disease
disease
human disease
DOID:205
C05.116.540
Hyperostosis
hyperphosphatemia
class of disease
phosphorus metabolism disease
genetic disease
disease
electrolyte disorder in which there is an elevated level of phosphate in the blood.
DOID:0050459
C18.452.750.199
Hyperphosphatemia
hyperphosphatemic familial tumoral calcinosis
class of disease
calcinosis
genetic disease
Tumoral calcinosis
autosomal recessive disease
human disease
DOID:0111063
hyperpigmentation of eyelid
class of disease
pigmentation disorder
eyelid disease
Human disease
DOID:10122
hyperpituitarism
class of disease
pituitary gland disease
anterior pituitary gland disease
disease
endocrine disease
DOID:2444
C10.228.140.617.738.250
C19.700.355
hyperprolinemia type 1
class of disease
hyperprolinemia
autosomal recessive disease
hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the proline dehydrogenase gene on chromosome 22q11
DOID:0080542
hyperprolinemia type 2
class of disease
hyperprolinemia
autosomal recessive disease
hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the pyrroline-5-carboxylate dehydrogenase gene on chromosome 1p36
DOID:0080543
hyperprothrombinemia
class of disease
thrombophilia
autosomal dominant disease
human disease
DOID:0080701
hypersecretion glaucoma
class of disease
glaucoma
Human disease
DOID:11148
hypersensitivity vasculitis
class of disease
type III hypersensitivity
Human disease
DOID:9809
C14.907.940.910
C20.543.520.910
hypersomnia
class of disease
symptom or sign
sleep disorder
neurological disorder
sleep disturbance
disease
excessive sleep
DOID:8619
C10.886.425.800.200
F03.870.400.800.200
hypersplenism
class of disease
splenic disease
disease
Human disease
DOID:6376
C15.604.744.293
hypertensive encephalopathy
class of disease
intracranial hypertension
encephalomyelitis
disease
general brain dysfunction due to significantly high blood pressure
DOID:9427
C10.228.140.631.500
hypertensive retinopathy
class of disease
retinal disease
complications of hypertension
disease
Human disease
DOID:11561
C11.768.346
C14.907.489.815
Hypertensive retinopathy
hyperthecosis
class of disease
ovarian disease
hyperplasia of the theca interna of the ovary
DOID:7347
hypertrichosis
class of disease
hair diseases
epidermal disease
genetic hair anomaly
disease
hair disease characterized by hair growth that is abnormal in quantity or location
DOID:420
C17.800.329.875
Hypertrichosis
hypertrichosis of eyelid
class of disease
eyelid degenerative disease
hypertrichosis
nervous system heredodegenerative disease
eyelid disease
hypertrichosis (disease) that involves the eyelid
DOID:11669
hypertrophic cardiomyopathy 1
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYH7 gene on chromosome 14q12
DOID:0110307
hypertrophic cardiomyopathy 10
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in mutation in the MYL2 gene
DOID:0110316
hypertrophic cardiomyopathy 11
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the ACTC1 gene on chromosome 15q14
DOID:0110317
hypertrophic cardiomyopathy 12
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the CSRP3 gene on chromosome 11p15
DOID:0110318
hypertrophic cardiomyopathy 13
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TNNC1 gene on chromosome 3p21
DOID:0110319
hypertrophic cardiomyopathy 14
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in mutation in the MYH6 gene
DOID:0110320
hypertrophic cardiomyopathy 15
class of disease
familial hypertrophic cardiomyopathy
human disease
DOID:0110321
hypertrophic cardiomyopathy 16
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYOZ2 gene on chromosome 4q26
DOID:0110322
hypertrophic cardiomyopathy 17
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12
DOID:0110323
hypertrophic cardiomyopathy 18
class of disease
familial hypertrophic cardiomyopathy
A hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1.
DOID:0110324
hypertrophic cardiomyopathy 2
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2)
DOID:0110308
hypertrophic cardiomyopathy 20
class of disease
familial hypertrophic cardiomyopathy
A hypertrophic cardiomyopathy that hhas material basis in heterozygous mutation in the NEXN gene on chromosome 1p31.1.
DOID:0110326
hypertrophic cardiomyopathy 21
class of disease
familial hypertrophic cardiomyopathy
A hypertrophic cardiomyopathy associated that has material basis in region 7p12.1-q21 variation.
DOID:0110311
hypertrophic cardiomyopathy 25
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TCAP gene on chromosome 17q12
DOID:0110328
hypertrophic cardiomyopathy 3
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22
DOID:0110309
hypertrophic cardiomyopathy 4
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding cardiac myosin-binding protein C (MYBPC3) on chromosome 11p11
DOID:0110310
hypertrophic cardiomyopathy 6
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2)
DOID:0110312
hypertrophic cardiomyopathy 7
class of disease
familial hypertrophic cardiomyopathy
A hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.
DOID:0110313
hypertrophic cardiomyopathy 8
class of disease
familial hypertrophic cardiomyopathy
hypertrophic cardiomyopathy that has material basis in homozygous or heterozygous mutation in the MYL3 gene
DOID:0110314
hypertrophic elongation of cervix
class of disease
cervix disease
Human disease
DOID:2251
hypertrophic pyloric stenosis
class of disease
pyloric stenosis
pyloric stenosis characterized by the enlargement of the muscle surrounding the pylorus, causing severe projectile non-bilious vomiting
DOID:12638
C06.405.748.340.690.500
hypertrophy of tongue papillae
class of disease
tongue disease
Human disease
DOID:13333
hypertropia
class of disease
strabismus
disease
Human disease
DOID:9837
Hypertropia
hyperuricemia
class of disease
acquired metabolic disease
disease
acquired metabolic disease that has material basis in an abnormally high level of uric acid in the blood.
DOID:1920
C23.550.449
Hyperuricemia
hypervitaminosis A
class of disease
overnutrition
hypervitaminosis
disease
Human disease
DOID:9972
C18.654.301
hypervitaminosis D
class of disease
overnutrition
hypervitaminosis
disease
excess of Vitamin D leading to abnormalities
DOID:9971
hypoactive sexual desire disorder
class of disease
psychosexual disorder
sexual dysfunction
disease
sexual dysfunction
DOID:13868
F03.835
hypobetalipoproteinemia
class of disease
hypolipoproteinemia
disease
hypolipoproteinemia characterized by permanently low levels of apolipoprotein B and LDL cholesterol resulting from an impaired ability to absorb and transport fats
DOID:1390
C16.320.565.398.500.440
C18.452.584.500.875.440
C18.452.648.398.500.440
C18.452.584.563.500.440
hypochondriasis
class of disease
somatoform disorder
nosophobia
disease
somatoform disorder that involves an excessive preoccupation or worry about having a serious illness
DOID:12883
F03.875.450
hypochondrogenesis
class of disease
osteochondrodysplasia
achondrogenesis
genetic disease
spinal disease
monogenic disease
human disease
DOID:0080044
hypochromic anemia
class of disease
anemia
generic term for any type of anemia in which the red blood cells (erythrocytes) are paler than normal
DOID:11759
C15.378.071.196
hypoglossal nerve disease
class of disease
glossopharyngeal nerve disease
human disease
DOID:13814
C10.292.525
hypoglossal nerve neoplasm
class of disease
cranial nerve neoplasm
hypoglossal nerve disease
Human disease
DOID:3198
hypoglycemic coma
class of disease
encephalopathy
coma
hypoglycemia
human disease
DOID:1607
hypogonadism
class of disease
gonadal disease
disease
endocrine disease
DOID:1924
C19.391.482
Hypogonadism
hypogonadotropic hypogonadism 12 with or without anosmia
class of disease
hypogonadotropic hypogonadism
genetic disease
hypogonadotropic hypogonadism that has material basis in homozygous mutation in the GNRH1 gene on chromosome 8p21
DOID:0090072
hypogonadotropic hypogonadism 16 with or without anosmia
class of disease
hypogonadotropic hypogonadism
genetic disease
autosomal dominant disease
hypogonadotropic hypogonadism that has material basis in mutation in the SEMA3A gene on chromosome 7, sometimes in association with mutations in other genes
DOID:0090080
hypogonadotropic hypogonadism 2 with or without anosmia
class of disease
hypogonadotropic hypogonadism
genetic disease
hypogonadotropic hypogonadism that has material basis in heterozygous mutation in the FGFR1 gene on chromosome 8p11, sometimes in association with mutation in other genes
DOID:0090083
hypohidrosis
class of disease
sweat gland disease
abnormal sudomotor regulation
Human disease
DOID:11155
C17.800.946.370
hypolipoproteinemia
class of disease
lipid metabolism disorder
disease
Human disease
DOID:1387
C16.320.565.398.500
C18.452.584.500.875
C18.452.648.398.500
C18.452.584.563.500
hypomyelinating leukodystrophy
class of disease
leukodystrophy
Hereditary CNS demyelinating disease
leukodystrophy characterized by T2 hyperintensity and T1 iso- or hyperintensity of affected white matter in the central nervous system
DOID:0060786
hypomyelinating leukodystrophy 14
class of disease
hypomyelinating leukodystrophy
autosomal recessive disease
human disease
DOID:0080296
hypomyelinating leukoencephalopathy
class of disease
spinocerebellar ataxia
Human disease
DOID:0050987
hypoparathyroidism, familial isolated
class of disease
genetic hypoparathyroidism
hypoparathyroidism
human disease
DOID:0111387
hypopharynx cancer
class of disease
carcinoma
pharyngeal cancer
neoplasm of hypopharynx
pharynx cancer that is located in the hypopharynx
DOID:8533
Hypopharyngeal cancer
hypophosphatemic nephrolithiasis/osteoporosis
class of disease
kidney disease
familial hypophosphatemia
human disease
DOID:0080655
hypopigmentation of eyelid
class of disease
eyelid degenerative disease
pigmentation disorder
eyelid disease
human disease
DOID:11668
hypopyon
class of disease
symptom or sign
iridocyclitis
eye symptom
disease
Human disease
DOID:10443
Hypopyon
hypopyon ulcer
class of disease
hypopyon
corneal ulcer
Human disease
DOID:10442
hypospadias
class of disease
non-syndromic urogenital tract malformation of male
penile disease
congenital disorder
disease
condition in which the urethra does not open from the head of the penis
DOID:10892
C12.294.494.400
C12.706.516
C13.351.875.466
C16.131.939.516
Hypospadias
hypothalamic disease
class of disease
thalamic disease
encephalopathy
human disease
DOID:1931
C10.228.140.617
hypothalamic neoplasm
class of disease
diencephalic neoplasm
brain cancer
connective tissue neoplasm
hypothalamic disease
human disease
DOID:3644
C04.588.614.250.195.885.500
C10.228.140.211.885.500
C10.228.140.617.477
C10.551.240.250.700.500
hypothyroidism
class of disease
thyroid gland disease
disease
human disease
DOID:1459
C19.874.482
Hypothyroidism
hypotonia-cystinuria syndrome
class of disease
syndrome
cystinuria
chromosomal deletion syndrome
human disease
DOID:0060858
hypotrichosis 1
class of disease
hypotrichosis
genetic disease
autosomal dominant disease
A hypotrichosis that has material basis in a autosomal dominant mutation of APCDD1 on chromosome 18p11.22.
DOID:0110698
hypotrichosis 10
class of disease
hypotrichosis
genetic disease
autosomal recessive disease
A hypotrichosis that has material basis in an autosomal recessive mutation on chromosome 7p22.3-p21.3.
DOID:0110707
hypotrichosis 14
class of disease
hypotrichosis simplex
hypotrichosis
human disease
DOID:0080582
hypotrichosis 4
class of disease
hypotrichosis
genetic disease
autosomal dominant disease
A hypotrichosis that has material basis in a autosomal dominant mutation of HR on chromosome 8p21.3.
DOID:0110701
hypotrichosis 5
class of disease
hypotrichosis
genetic disease
autosomal dominant disease
A hypotrichosis that has material basis in a mutation on chromosome 1p21.1-q21.3.
DOID:0110702
hypotrichosis 9
class of disease
hypotrichosis
genetic disease
autosomal recessive disease
A hypotrichosis that has material basis in an autosomal recessive mutation on chromosome 10q11.23-q22.3.
DOID:0110706
hypotrichosis of eyelid
class of disease
eyelid degenerative disease
hypotrichosis
eyelid disease
hypotrichosis that involves the eyelid
DOID:11671
hypotropia
class of disease
strabismus
Human disease
DOID:9841
ichthyosis follicularis-alopecia-photophobia syndrome 1
class of disease
X-linked recessive disease
syndrome
Ichthyosis follicularis with alopecia and photophobia syndrome
human disease
DOID:0111821
ideomotor apraxia
class of disease
apraxia
Human disease
DOID:4627
C10.597.606.881.350.200
C23.888.592.604.882.350.200
F01.700.875.350.200
idiopathic corneal edema
class of disease
corneal edema
Human disease
DOID:11033
idiopathic generalized epilepsy 11
class of disease
generalized epilepsy
human disease
DOID:0111312
idiopathic generalized epilepsy 12
class of disease
generalized epilepsy
human disease
DOID:0111313
idiopathic generalized epilepsy 13
class of disease
generalized epilepsy
human disease
DOID:0111314
idiopathic generalized epilepsy 14
class of disease
generalized epilepsy
human disease
DOID:0111315
idiopathic generalized epilepsy 15
class of disease
generalized epilepsy
human disease
DOID:0111316
idiopathic generalized epilepsy 2
class of disease
generalized epilepsy
human disease
DOID:0111317
idiopathic generalized epilepsy 3
class of disease
generalized epilepsy
human disease
DOID:0111318
idiopathic generalized epilepsy 4
class of disease
generalized epilepsy
human disease
DOID:0111319
idiopathic generalized epilepsy 5
class of disease
generalized epilepsy
human disease
DOID:0111320
idiopathic generalized epilepsy 7
class of disease
generalized epilepsy
human disease
DOID:0111321
idiopathic generalized epilepsy 9
class of disease
generalized epilepsy
human disease
DOID:0111323
idiopathic orbital inflammatory disease
class of disease
orbital granuloma
chronic orbital inflammation
Human disease
DOID:9369
C11.675.679
idiopathic peripheral autonomic neuropathy
class of disease
autonomic nervous system disease
autonomic peripheral neuropathy
human disease
DOID:11488
idiopathic progressive polyneuropathy
class of disease
polyneuropathy
human disease
DOID:10593
idiopathic pulmonary fibrosis
class of disease
idiopathic interstitial pneumonia
pulmonary fibrosis
chronic, irreversible and ultimately fatal disease characterized by a progressive decline in lung function
DOID:0050156
C08.381.483.487.500
C08.381.765.500
Idiopathic pulmonary fibrosis
idiopathic scoliosis
class of disease
scoliosis
scoliosis with no known cause
DOID:0060250
ileal neoplasm
class of disease
small intestine neoplasm
ileal disease
human disease
DOID:10156
C04.588.274.476.411.501
C06.301.371.411.501
C06.405.249.411.501
C06.405.469.420.501
C06.405.469.491.501
ileitis
class of disease
Crohn's disease
enteritis
inflammatory bowel disease characterized by inflammation located in ileum, has symptom diarrhea, has symptom abdominal pain, often in the right lower quadrant, has symptom weight loss
DOID:0060189
C06.405.205.462.624
C06.405.469.326.875
C06.405.469.420.520
Ileitis
ileum cancer
class of disease
small intestine cancer
ileal neoplasm
small intestine cancer that is located in the ileum
DOID:10153
ileus
class of disease
bowel obstruction
disease
human disease characterized by impairment of intestinal peristalsis; in modern language usually excludes mechanical bowel obstruction
DOID:8440
C06.405.469.531.492
Ileus
iliac vein thrombophlebitis
class of disease
thrombophlebitis
Human disease
DOID:10880
immature cataract
class of disease
senile cataract
Human disease
DOID:10997
immature teratoma
class of disease
teratoma
Human disease
DOID:5563
immature teratoma of ovary
class of disease
malignant ovarian germ cell neoplasm
malignant non-dysgerminomatous germ cell tumor of ovary
ovarian biphasic or triphasic teratoma
Human disease
DOID:6331
immune disorder
class of disease
disease of anatomical entity
a disease of the immune system
DOID:2914
C20
Diseases and disorders of the immune system
immune system cancer
class of disease
organ system cancer
immune disorder
organ system cancer located in the immune system that is characterized by uncontrolled cellular proliferation in organs of the immune system
DOID:0060083
immune system organ benign neoplasm
class of disease
organ system benign neoplasm
immune disorder
organ system benign neoplasm located in the immune system organs
DOID:0060092
immune-complex glomerulonephritis
class of disease
glomerulonephritis
Human disease
DOID:4784
immunodeficiency 11A
class of disease
autosomal recessive disease
severe combined immunodeficiency
human disease
DOID:0111957
immunodeficiency 11B
class of disease
autosomal dominant disease
T cell deficiency
human disease
DOID:0111958
immunodeficiency 15A
class of disease
autosomal dominant disease
combined immunodeficiency
severe combined immunodeficiency due to IKK2 deficiency
human disease
DOID:0111960
immunodeficiency 15B
class of disease
severe combined immunodeficiency
autosomal recessive disease
severe combined immunodeficiency due to IKK2 deficiency
human disease
DOID:0111959
immunodeficiency 18
class of disease
autosomal recessive disease
primary immunodeficiency disease
human disease
DOID:0111971
immunodeficiency 19
class of disease
autosomal recessive disease
severe combined immunodeficiency
human disease
DOID:0111972
immunodeficiency 28
class of disease
autosomal recessive disease
primary immunodeficiency disease
human disease
DOID:0111995
immunodeficiency 32A
class of disease
autosomal dominant disease
dendritic cell deficiency
human disease
DOID:0111986
immunodeficiency 32B
class of disease
monocyte, dendritic cell, and NK cell deficiency
autosomal recessive disease
human disease
DOID:0111985
immunodeficiency 45
class of disease
autosomal recessive disease
primary immunodeficiency disease
primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection
human disease
DOID:0111994
immunodeficiency 51
class of disease
primary immunodeficiency disease
autosomal recessive disease
human disease
DOID:0111996
immunodeficiency 52
class of disease
T cell deficiency
autosomal recessive disease
human disease
DOID:0111983
immunodeficiency 53
class of disease
autosomal recessive disease
combined immunodeficiency
human disease
DOID:0111992
immunodeficiency 55
class of disease
autosomal recessive disease
combined immunodeficiency
human disease
DOID:0111993
immunodeficiency 57
class of disease
autosomal recessive disease
primary immunodeficiency disease
human disease
DOID:0111952
immunodeficiency 58
class of disease
autosomal recessive disease
combined immunodeficiency
human disease
DOID:0111984
immunodeficiency 59
class of disease
autosomal recessive disease
B cell and dendritic cell deficiency
human disease
DOID:0111974
immunodeficiency 60
class of disease
combined immunodeficiency
autosomal dominant disease
human disease
DOID:0111954
immunodeficiency 62
class of disease
autosomal recessive disease
B cell deficiency
human disease
DOID:0111991
immunodeficiency 63
class of disease
autosomal recessive disease
T cell and NK cell immunodeficiency
human disease
DOID:0111997
immunodeficiency 64
class of disease
T cell, B cell, and NK cell deficiency
autosomal recessive disease
human disease
DOID:0111980
immunodeficiency 65
class of disease
primary immunodeficiency disease
autosomal recessive disease
human disease
DOID:0111978
immunodeficiency 66
class of disease
primary immunodeficiency disease
autosomal recessive disease
human disease
DOID:0111998
immunodeficiency 69
class of disease
autosomal recessive disease
T cell and NK cell immunodeficiency
human disease
DOID:0112006
immunodeficiency 70
class of disease
autosomal dominant disease
combined immunodeficiency
human disease
DOID:0112005
immunodeficiency 71
class of disease
combined immunodeficiency
autosomal recessive disease
human disease
DOID:0112004
immunodeficiency 72
class of disease
autosomal recessive disease
combined immunodeficiency
human disease
DOID:0112015
immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia
class of disease
autosomal dominant disease
combined immunodeficiency
human disease
DOID:0112061
immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
class of disease
combined immunodeficiency
autosomal recessive disease
human disease
DOID:0112062
immunodeficiency-centromeric instability-facial anomalies syndrome
class of disease
autosomal recessive disease
DNA repair defect other than combined T-cell and B-cell immunodeficiencies
syndrome
autosomal recessive disease characterized by immunodeficiency, rearrangements in the vicinity of the centromeres of chromosomes 1, 9, and 16 and facial anomalies in most cases
DOID:0090007
immunoglobulin A deficiency
class of disease
selective immunoglobulin deficiency disease
B cell deficiency
genetic disease
disease
dysgammaglobulinemia characterized by a deficiency of immunoglobulin A
DOID:0060025
C15.378.147.333.500
C20.673.430.500
immunoglobulin beta deficiency
class of disease
B cell deficiency
Human disease
DOID:0060026
imperforate anus
class of disease
congenital disorder
atresia
anorectal anomalies
anal disease
congenital disorder of digestive system
DOID:10488
C06.198.050
C16.131.314.094
Imperforate anus
impulse control disorder
class of disease
mental disorder
disease
disease of mental health that involves a failure to resist an impulsive act or behaviour that may be harmful to self or others
DOID:10937
F03.250
Habit and impulse disorders
in situ carcinoma
class of disease
pre-malignant neoplasm
In situ neoplasm
disease
human disease
DOID:8719
C04.557.470.200.240
Carcinomas in situ
inborn errors of purine–pyrimidine metabolism
class of disease
inherited metabolic disorder
inherited metabolic disorder involving dysfunction of purine and pyrimidine metabolism
DOID:653
C16.320.565.798
C18.452.648.798
inborn errors pyruvate metabolism
class of disease
carbohydrate metabolic disorder
human disease
DOID:3648
C16.320.565.202.810
C18.452.648.202.810
inborn metabolic brain disease
class of disease
metabolic brain disease
Human disease
DOID:889
C10.228.140.163.100
C16.320.565.189
C18.452.132.100
C18.452.648.189
inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
class of disease
inclusion body myopathy with Paget disease of bone and frontotemporal dementia
autosomal dominant disease
human disease
DOID:0111385
inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2
class of disease
inclusion body myopathy with Paget disease of bone and frontotemporal dementia
autosomal dominant disease
human disease
DOID:0111384
inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3
class of disease
inclusion body myopathy with Paget disease of bone and frontotemporal dementia
autosomal dominant disease
human disease
DOID:0111386
incontinentia pigmenti achromians
class of disease
skin disease
disease
Human disease
DOID:3156
indeterminate leprosy
class of disease
leprosy
paucibacillary leprosy
leprosy that is an early form of the disease which causes one to a few hypopigmented or erythematous macules
DOID:11851
indolent myeloma
class of disease
smouldering myeloma
multiple myeloma
Human disease
DOID:9550
indolent systemic mastocytosis
class of disease
mastocytoma
systemic mastocytosis
human disease
DOID:4660
infancy electroclinical syndrome
class of disease
electroclinical syndrome
epilepsy syndrome
Epilepsy in children
electroclinical syndrome with onset in infancy occurring between birth and one year of age
DOID:0050703
infant gynecomastia
class of disease
breast disease
gynecomastia
human disease
DOID:11603
infantile epileptic encephalopathy
class of disease
infancy electroclinical syndrome
childhood onset epileptic encephalopathy
West syndrome
Human disease
DOID:2481
C10.228.140.490.375.760
C10.228.140.490.493.875
infantile hypophosphatasia
class of disease
hypophosphatasia
A hypophosphatasia that has material basis in an autosomal recessive mutation of ALPL on chromosome 1p36.12.
DOID:0110914
infantile or early childhood epileptic encephalopathy 1
class of disease
electroclinical syndrome
infantile epileptic encephalopathy
human disease
DOID:0080472
infantile or early childhood epileptic encephalopathy 2
class of disease
electroclinical syndrome
autosomal dominant disease
electroclinical syndrome characterized by onset of seizures in infancy or early childhood, global developmental delay and variable intellectual disability that has material basis in heterozygous mutation in the GABRB2 gene on chromosome 5q34
DOID:0080471
infantile osteopetrosis with neuroaxonal dysplasia
class of disease
neuroaxonal dystrophy
osteopetrosis
This syndrome is characterized by osteopetrosis, agenesis of the corpus callosum, cerebral atrophy and a small hippocampus
DOID:0070343
infantile-onset distal myopathy
class of disease
distal muscular dystrophy
distal muscular dystrophy characterized by autosomal dominant inheritance, infantile onset and progressive disease development
DOID:0070196
infected hydrocele
class of disease
hydrocele
Human disease
DOID:9911
infectious disease
class of disease
disease
infection associated with diseases
disease caused by infection of pathogenic biological agents in a host organism
DOID:0050117
C01.539.221
Infectious diseases and disorders
infective endocarditis
class of disease
endocarditis
cardiovascular Infection
infectious disease
disease
endocarditis that is characterized by inflammation of the endocardium caused by infectious agents.
DOID:0060000
infective urethral stricture
class of disease
urethral stricture
Human disease
DOID:13658
inferior myocardial infarction
class of disease
myocardial infarction
Human disease
DOID:5850
C14.280.647.500.187
C14.907.585.500.187
C23.550.513.355.750.187
C23.550.717.489.750.187
inferolateral myocardial infarct
class of disease
myocardial infarction
Human disease
DOID:5852
infertility
class of disease
symptom or sign
reproductive system disease
reproductive system symptom
disease
inability of a person, animal or plant to reproduce by natural means that is no intervention of contraceptive techniques
DOID:5223
C12.294.365
C13.351.500.365
Infertility
infertility due to extratesticular cause
class of disease
male infertility
Human disease
DOID:14096
infiltrating angiolipoma
class of disease
angiolipoma
Human disease
DOID:3615
infiltrating bladder lymphoepithelioma-like carcinoma
class of disease
invasive bladder transitional cell carcinoma
human disease
DOID:7600
infiltrating bladder urothelial carcinoma sarcomatoid variant
class of disease
invasive bladder transitional cell carcinoma
sarcomatoid transitional cell carcinoma
Human disease
DOID:7553
infiltrating lipoma
class of disease
lipoma
Human disease
DOID:7014
infiltrating nipple syringomatous adenoma
class of disease
nipple neoplasm
Human disease
DOID:7839
infiltrating renal pelvis transitional cell carcinoma
class of disease
renal pelvis transitional cell carcinoma
Human disease
DOID:0050620
infiltrating ureter transitional cell carcinoma
class of disease
ureter transitional cell carcinoma
Human disease
DOID:6845
infiltrative basal cell carcinoma
class of disease
basal-cell carcinoma
Human disease
DOID:4299
inflamed seborrheic keratosis
class of disease
seborrheic keratosis
Human disease
DOID:11685
inflammatory MFH
class of disease
malignant fibrous histiocytoma
Human disease
DOID:6192
inflammatory and toxic neuropathy
class of disease
peripheral neuropathy
acquired peripheral neuropathy
Human disease
DOID:2537
inflammatory bowel disease 1
class of disease
inflammatory bowel diseases
genetic disease
An inflammatory bowel disease that has material basis in mutations in the NOD2 gene on chromosome 16q12.1.
DOID:0110892
inflammatory bowel disease 11
class of disease
inflammatory bowel diseases
genetic disease
inflammatory bowel disease that has material basis in variation in the chromosome region 7q22
DOID:0110894
inflammatory bowel disease 12
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
An inflammatory bowel disease that has material basis in variation in the chromosome region 3p21.3
DOID:0110887
inflammatory bowel disease 13
class of disease
inflammatory bowel diseases
genetic disease
An inflammatory bowel disease that has material basis in variation in the ABCB1 gene on chromosome 7q21.1.
DOID:0110893
inflammatory bowel disease 15
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
inflammatory bowel disease that has material basis in variation in the chromosome region 10q21
DOID:0110897
inflammatory bowel disease 16
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
inflammatory bowel disease that has material basis in variation in the chromosome region 9q32
DOID:0110896
inflammatory bowel disease 17
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
An inflammatory bowel disease that has material basis in variation in the IL23R gene on chromosome 1p31.3.
DOID:0110883
inflammatory bowel disease 18
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
An inflammatory bowel disease that has material basis in variation in the chromosome region 5p13.1.
DOID:0110888
inflammatory bowel disease 2
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
An inflammatory bowel disease that has material basis in variation in the chromosome region 12p13.2-q24.1.
DOID:0110900
inflammatory bowel disease 20
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
inflammatory bowel disease that has material basis in variation in the chromosome region 10q23-q24
DOID:0110898
inflammatory bowel disease 21
class of disease
inflammatory bowel diseases
genetic disease
autosomal dominant disease
inflammatory bowel disease that has material basis in variation in the chromosome region 18p11
DOID:0110906
inflammatory bowel disease 22
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
An inflammatory bowel disease that has material basis in variation in the chromosome region 17q21.2.
DOID:0110905
inflammatory bowel disease 23
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
An inflammatory bowel disease that has material basis in variation in the chromosome region 1q32.1.
DOID:0110884
inflammatory bowel disease 24
class of disease
inflammatory bowel diseases
genetic disease
inflammatory bowel disease that has material basis in variation in the chromosome 20q13
DOID:0110908
inflammatory bowel disease 26
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
inflammatory bowel disease that has material basis in variation in the chromosome region 12q15
DOID:0110901
inflammatory bowel disease 27
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
An inflammatory bowel disease that has material basis in variation in the chromosome region 13q13.3
DOID:0110902
inflammatory bowel disease 3
class of disease
inflammatory bowel diseases
genetic disease
autosomal dominant disease
An inflammatory bowel disease that has material basis in variation in the chromosome region 6p21.3.
DOID:0110891
inflammatory bowel disease 4
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
inflammatory bowel disease that has material basis in variation in the chromosome region 14q11-q12
DOID:0110903
inflammatory bowel disease 5
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
inflammatory bowel disease that has material basis in variation in the chromosome region 5q31
DOID:0110889
inflammatory bowel disease 6
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
inflammatory bowel disease that has material basis in variation in the chromosome region 19p13
DOID:0110907
inflammatory bowel disease 7
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
inflammatory bowel disease that has material basis in variation in the chromosome region 1p36
DOID:0110882
inflammatory bowel disease 8
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
inflammatory bowel disease that has material basis in variation in the chromosome region 16p
DOID:0110904
inflammatory bowel disease 9
class of disease
inflammatory bowel diseases
genetic disease
monogenic disease
inflammatory bowel disease that has material basis in variation in the chromosome region 3p26
DOID:0110886
inflammatory bowel diseases
class of disease
intestinal disease
immune disorder
disease
intestinal disease characterized by inflammation located in all parts of digestive tract
DOID:0050589
C06.405.205.731
C06.405.469.432
Inflammatory bowel diseases
inflammatory breast carcinoma
class of disease
breast adenocarcinoma
invasive breast carcinoma
Human disease
DOID:6263
inflammatory diarrhea
class of disease
diarrhea
mucositis
Human disease
DOID:0050132
inflammatory leiomyosarcoma
class of disease
leiomyosarcoma
Human disease
DOID:5251
inflammatory liposarcoma
class of disease
atypical lipomatous tumor
Human disease
DOID:8233
inflammatory myofibroblastic tumour
class of disease
mesenchymal cell neoplasm
connective tissue benign neoplasm
mesenchymal cell neoplasm that has material basis in myofibroblastic cells admixed with inflammatory cells
DOID:0050905
Inflammatory myofibroblastic tumour
inflammatory spondylopathy
class of disease
spondylitis
Human disease
DOID:12105
infratentorial cancer
class of disease
brain cancer
infratentorial neoplasm
brain cancer that is located in the infratentorial region
DOID:4706
infundibulocystic basal cell carcinoma
class of disease
basal-cell carcinoma
inherited skin tumor
Human disease
DOID:4279
inguinal hernia
class of disease
intestinal disease
disease
intestinal disease characterized by a protrusion of abdominal cavity contests through the inguinal canal
DOID:0060320
C23.300.707.374.875
Inguinal hernia
inherited metabolic disorder
class of disease
genetic disease
rare disease
metabolic disease
disease
class of disease including endocrine diseases, nutritional diseases and metabolic diseases
DOID:655
C16.320.565
C18.452.648
Inborn errors of metabolism
inhibited female orgasm
class of disease
female reproductive system disease
anorgasmia
female orgasm
Human disease
DOID:7518
DOID:11110
inner ear cancer
class of disease
auricular cancer
inner ear neoplasm
Human disease
DOID:5102
inner ear disease
class of disease
ear disease
human disease
DOID:2952
DOID:4539
C09.218.568
insulinoma
class of disease
pancreatic cystadenoma
benign neoplasms by histologic type
islet cell adenoma
disease
tumor that produces too much insulin
DOID:3892
C04.557.470.035.100.852
C04.588.274.761.249.500
C04.588.322.475.249.500
C06.301.761.249.500
C06.689.667.249.500
C19.344.421.249.500
Insulinoma
integrative agnosia
class of disease
agnosia
apperceptive agnosia
agnosia that is a loss of the ability to integrate these elements together into comprehensible perceptual wholes while recognizing elements of the whole
DOID:0060143
integumentary system benign neoplasm
class of disease
organ system benign neoplasm
integumentary system neoplasm
organ system benign neoplasm located in the integumentary system organs
DOID:0060121
integumentary system cancer
class of disease
organ system cancer
integumentary system neoplasm
integumentary system disease
organ system cancer that is located in the skin, hair and nails
DOID:0060122
integumentary system disease
class of disease
disease of anatomical entity
disease of anatomical entity that is located in the integumentary system comprising the skin and its appendages
DOID:16
intellectual developmental disorder with short stature and behavioral abnormalities
class of disease
syndrome
autosomal recessive disease
syndromic intellectual disability
human disease
DOID:0111674
intellectual disability
class of disease
specific developmental disorder
cognitive deficit
disability
disease
generalized neurodevelopmental disorder
DOID:1059
C23.888.592.604.646
C10.597.606.360
F01.700.687
F03.625.539
Intellectual disabilities
interdigitating dendritic cell sarcoma
class of disease
histiocytic and dendritic cell cancer
dendritic cell sarcoma
histiocytic and dendritic cell cancer that effect dendritic cells
DOID:7848
C04.557.227.199
C15.604.250.390.199
interleukin-7 receptor alpha deficiency
class of disease
severe combined immunodeficiency
human disease
DOID:0060015
intermediate malignant teratoma
class of disease
immature teratoma
Human disease
DOID:7202
intermediate uveitis
class of disease
uveitis
human disease
DOID:12732
C11.941.879.900
Intermediate uveitis
intermittent asthma
class of disease
chronic asthma
human disease
DOID:0080812
intermittent explosive disorder
class of disease
impulse control disorder
disease
Mood disorder identified by frequent episodes of anger and rage
DOID:12401
intermittent proptosis
class of disease
orbital disease
exophthalmos
Human disease
DOID:12363
intermittent squint
class of disease
strabismus
Human disease
DOID:1942
intermixed schwannian stroma-rich ganglioneuroblastoma
class of disease
ganglioneuroblastoma
Human disease
DOID:5194
internal hemorrhoid
class of disease
hemorrhoid
Human disease
DOID:9749
internal resorption
class of disease
tooth resorption
human disease
DOID:13239
internuclear ophthalmoplegia
class of disease
ophthalmoplegia
strabismus
Human disease
DOID:538
interstitial keratitis
class of disease
connective tissue disease
deep keratitis
human disease
DOID:9857
interstitial myocarditis
class of disease
mediastinitis
myocarditis
Inflammation of the heart characterized by infiltration of the interstitial tissues by inflammatory cells, histiocytes, and the formation of granulomas. Giant cells are often present.
DOID:817
interstitial nephritis
class of disease
nephritis
kidney disease
disease
type of nephritis affecting the interstitium of the kidneys surrounding the tubules
DOID:1063
C12.200.777.419.570.643
C12.050.351.968.419.570.643
C12.950.419.570.643
Tubulointerstitial disease
interval angle-closure glaucoma
class of disease
primary angle-closure glaucoma
Human disease
DOID:13549
intestinal atresia
class of disease
intestinal disease
intestinal malformation
congenital disorder of digestive system
DOID:10486
C06.198.719
C06.405.469.445
C16.131.314.466
Intestinal atresia
intestinal benign neoplasm
class of disease
gastrointestinal system benign neoplasm
intestinal neoplasm
intestinal disease
gastrointestinal system benign neoplasm that is located in the intestine
DOID:4610
intestinal cancer
class of disease
gastrointestinal system cancer
intestinal neoplasm
intestinal disease
gastrointestinal system cancer that is located in the intestine
DOID:10155
Intestinal cancers
intestinal disaccharidase deficiency
class of disease
metabolic disease with intestinal involvement
intestinal disease
carbohydrate metabolic disorder
Human disease
DOID:9868
intestinal disease
class of disease
gastrointestinal system disease
gastrointestinal system disease that is located in the intestine
DOID:5295
C06.405.469
Diseases and disorders of intestines
intestinal impaction
class of disease
bowel obstruction
Human disease
DOID:8448
intestinal neuroendocrine benign tumor
class of disease
intestinal benign neoplasm
gastrointestinal neuroendocrine benign tumor
Human disease
DOID:4119
intestinal perforation
class of disease
intestinal disease
gastrointestinal perforation
Human disease
DOID:2074
C06.405.469.557
intestinal tuberculosis
class of disease
gastrointestinal tuberculosis
intestinal disease
human disease
DOID:13282
intestinal variant cervical mucinous adenocarcinoma
class of disease
cervical mucinous adenocarcinoma
intestinal type carcinoma
Human disease
DOID:8339
intestinal volvulus
class of disease
bowel obstruction
disease
Human disease
DOID:8445
C06.405.469.531.568
C23.300.970.500
Volvulus
intestine carcinoma in situ
class of disease
carcinoma in situ of digestive organ
in situ carcinoma
intestinal disease
Human disease
DOID:9024
intra-abdominal lymph node mast cell malignancy
class of disease
lymph node cancer
mast cell malignancy of lymph nodes
mastocytoma
Human disease
DOID:13005
intracerebral cystic meningioma
class of disease
cerebral meningioma
Human disease
DOID:6113
intracortical osteogenic sarcoma
class of disease
conventional central osteosarcoma
Human disease
DOID:7602
intracranial abscess
class of disease
central nervous system disease
abscess
central nervous system disease that is located in the skull and is characterized by a collection of pus (infected material) inside the skull
DOID:10095
intracranial aneurysm
class of disease
aneurysm
cerebrovascular disease
cerebral arterial disease
disease
cerebrovascular disorder
DOID:10941
C10.228.140.300.510.600
C14.907.055.635
C14.907.253.560.300
Cerebral aneurysms
intracranial arterial disease
class of disease
cerebrovascular disease
human disease
DOID:13089
C10.228.140.300.510
C14.907.253.560
intracranial arteriosclerosis
class of disease
arteriosclerosis
human disease
DOID:13097
C10.228.140.300.510.800
C14.907.137.126.372
C14.907.253.560.350
intracranial berry aneurysm
class of disease
intracranial aneurysm
intracranial aneurysm with a characteristic rounded shape; the most common form of cerebral aneurysm
DOID:0060228
intracranial berry aneurysm 11
class of disease
intracranial berry aneurysm
human disease
DOID:0080974
intracranial berry aneurysm 9
class of disease
intracranial berry aneurysm
human disease
DOID:0080972
intracranial cavernous angioma
class of disease
intracranial structure hemangioma
Human disease
DOID:2516
intracranial chondrosarcoma
class of disease
extraosseous chondrosarcoma
extraskeletal myxoid chondrosarcoma
intracranial tumor
Human disease
DOID:7903
intracranial embolism
class of disease
cerebrovascular disease
disease
Human disease
DOID:4372
C10.228.140.300.525.400
C14.907.253.566.300
C14.907.355.590.213.300
Intracranial embolism
intracranial liposarcoma
class of disease
liposarcoma
Human disease
DOID:5714
intracranial primitive neuroectodermal tumor
class of disease
central nervous system primitive neuroectodermal neoplasm
medulloblastoma
Human disease
DOID:4788
intracranial structure hemangioma
class of disease
hemangioma
intracranial tumor
Human disease
DOID:2517
intracranial thrombosis
class of disease
thrombosis
cerebrovascular disease
thromboembolism
Human disease
DOID:4193
C10.228.140.300.525.425
C14.907.253.566.350
C14.907.355.590.213.350
intracranial vasospasm
class of disease
vasospasm
cerebrovascular disease
disease
Human disease
DOID:13100
C10.228.140.300.900
C14.907.253.951
intracystic papillary adenoma
class of disease
adenoma
Human disease
DOID:2682
intraductal breast myoepitheliosis
class of disease
breast myoepitheliosis
Human disease
DOID:8068
intraductal breast neoplasm
class of disease
breast benign neoplasm
Human disease
DOID:3013
intraductal carcinoma
class of disease
breast carcinoma in situ
breast ductal carcinoma
disease
Human disease
DOID:0060074
C04.557.470.200.025.275
C04.557.470.200.240.187.250
C04.557.470.615.275
Ductal carcinoma in situ
intraductal papillary breast neoplasm
class of disease
intraductal breast neoplasm
Human disease
DOID:1628
intraductal papilloma
class of disease
breast benign neoplasm
papilloma
intraductal breast neoplasm
disease
human disease
DOID:1627
C04.557.470.615.670
Intraductal papilloma
intrahepatic bile duct adenoma
class of disease
bile duct adenoma
Human disease
DOID:5437
intrahepatic bile duct cystadenoma
class of disease
bile duct cystadenoma
intrahepatic bile duct adenoma
Human disease
DOID:6733
intrahepatic biliary papillomatosis
class of disease
biliary papillomatosis
Human disease
DOID:8230
intrahepatic cholangiocarcinoma
class of disease
cholangiocarcinoma
Human disease
DOID:4928
intrahepatic cholestasis
class of disease
cholestasis
medical condition
DOID:1852
C06.130.120.135.250
C06.552.150
intrahepatic cholestasis of pregnancy
class of disease
intrahepatic cholestasis
liver disease of pregnancy
disease
intrahepatic cholestasis characterized by reversible cholestasis typically occurring in the second or third trimester of pregnancy, elevated serum aminotransferases and bile acid level and resolution of symptoms by 2 to 3 weeks after delivery
DOID:0070227
intrahepatic gall duct cancer
class of disease
gallbladder cancer
Human disease
DOID:12298
intramuscular hemangioma
class of disease
hemangioma
muscle neoplasm
Human disease
DOID:468
intraneural perineurioma
class of disease
perineurioma
Human disease
DOID:4696
intraocular lymphoma
class of disease
eye lymphoma
human disease
DOID:775
C04.557.386.435
C04.588.364.447
C15.604.515.569.417
C20.683.515.761.417
intraorbital meningioma
class of disease
orbital cancer
meningioma
meningioma by site and orbital neoplasm that is located in the area around the eye sockets of the skull and results in pressure in the eyes, giving a bulging appearance
DOID:4141
intrapelvic lymph node leukemic reticuloendotheliosis
class of disease
lymph node cancer
Human disease
DOID:12972
intratubular embryonal carcinoma
class of disease
embryonal testis carcinoma
embryonal testis carcinoma that is located within a tubule
DOID:8275
intravascular angioleiomyoma
class of disease
angiomyoma
vascular neoplasm
Human disease
DOID:4266
intravascular fasciitis
class of disease
pseudosarcomatous fibromatosis
Human disease
DOID:9603
intravenous leiomyomatosis
class of disease
leiomyomatosis
vascular disease
Human disease
DOID:5729
intraventricular meningioma
class of disease
cerebral ventricle cancer
meningioma
Human disease
DOID:3772
intrinsic asthma
class of disease
asthma
chronic asthma
human disease
DOID:9360
intussusception
class of disease
bowel obstruction
genetic disease
disease
human disease
DOID:8446
C06.405.469.531.577
Intussusception
invasive bladder transitional cell carcinoma
class of disease
bladder urothelial carcinoma
Invasive urothelial carcinoma
Human disease
DOID:6477
invasive lobular carcinoma
class of disease
breast lobular carcinoma
invasive breast carcinoma
carcinoma
breast cancer
disease
Human disease
DOID:3457
Histopathology of invasive lobular carcinoma (ILC)
invasive malignant thymoma
class of disease
thymoma
Human disease
DOID:3283
invasive tubular breast carcinoma
class of disease
breast adenocarcinoma
invasive ductal carcinoma
Human disease
DOID:6587
inverted follicular keratosis
class of disease
seborrheic keratosis
Human disease
DOID:6945
Inverted follicular keratosis
inverted papilloma
class of disease
papilloma
Human disease
DOID:3179
C04.557.470.700.600.610
Inverted papillomas
inverted transitional papilloma
class of disease
transitional papilloma
inverted papilloma
Human disease
DOID:4630
iodine hypothyroidism
class of disease
hypothyroidism
Human disease
DOID:5083
iris cancer
class of disease
iris neoplasm
uveal cancer
iris disease
Human disease
DOID:3478
iris disease
class of disease
uveal disease
Human disease
DOID:240
DOID:4738
C11.941.375
iritis
class of disease
iris disease
anterior uveitis
disease
human disease
DOID:1406
C11.941.375.385
C11.941.879.780.880.448
iron deficiency anemia
class of disease
symptom or sign
deficiency anemia
nutritional deficiency disease
iron deficiency
hypochromic anemia
disease
anemia caused by a lack of iron
DOID:11758
C15.378.071.196.300
C18.452.565.100
Iron-deficiency anemia
iron metabolism disease
class of disease
mineral metabolism disease
Human disease
DOID:2351
C18.452.565
irregular astigmatism
class of disease
astigmatism
Human disease
DOID:13919
irritable bowel syndrome
class of disease
symptom or sign
functional colonic disease
syndrome
intestinal disease
disease
syndrome that is a functional bowel disorder characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause
DOID:9778
C06.405.469.158.272.608
Irritable bowel syndrome
irritant dermatitis
class of disease
contact dermatitis
human disease
DOID:2772
C17.800.174.255.400
C17.800.815.255.400
Irritant contact dermatitis
ischemic bone disease
class of disease
bone disease
ischemia
bone disease that results in an interruption of blood supply located in bone
DOID:0080008
ischemic colitis
class of disease
colitis
colitis caused by inadequate blood supply to the colon
DOID:0060181
C06.405.205.265.115
C06.405.469.158.188.115
C14.907.286
Ischemic colitis
ischemic fasciitis
class of disease
fasciitis
human disease
DOID:9601
Ischemic fasciitis
ischemic neuropathy
class of disease
peripheral neuropathy
Human disease
DOID:1195
islet cell carcinoma
class of disease
islet cell tumor
gastrointestinal carcinoma
disease
islet cell tumor that has material basis in epithelial cells
DOID:1798
C04.557.470.200.025.290
C04.588.274.761.500
C04.588.322.475.500
C06.301.761.500
C06.689.667.500
C19.344.421.500
Pancreatic neuroendocrine tumors
islet cell tumor
class of disease
pancreatic cancer
pancreatic cancer that is located in the pancreatic islet cells
DOID:1799
isocyanates allergic asthma
class of disease
allergic asthma
occupational asthma
allergic asthma that has allergic trigger isocyanates
DOID:0040041
isolated cryptophthalmia
class of disease
cryptophthalmos
human disease
DOID:0111717
isolated ectopia lentis
class of disease
lens disease
ectopia lentis
A lens disease characterized by abnormal stretching of the zonular fibers resulting in dislocation of the lens. This dislocation may be mild to severe and may progress with age.
DOID:0111148
isolated growth hormone deficiency type IA
class of disease
isolated growth hormone deficiency
human disease
DOID:0060873
isolated growth hormone deficiency type IB
class of disease
isolated growth hormone deficiency
human disease
DOID:0060874
isolated growth hormone deficiency type II
class of disease
isolated growth hormone deficiency
human disease
DOID:0060872
isolated growth hormone deficiency type III
class of disease
isolated growth hormone deficiency
X-linked recessive disease
An isolated growth hormone deficiency characterized by dwarfism, variable occurence of hypogammaglobulinemia, and a generally good response to growth hormone therapy that has material basis in mutation in the BTK gene on chromosome Xq22.1.
DOID:0060875
isolated microphthalmia
class of disease
microphthalmia
microphthalmia that is not part of a larger syndrome
DOID:0080637
isolated microphthalmia 1
class of disease
microphthalmia
genetic disease
isolated microphthalmia
autosomal recessive disease
microphthalmia that has material basis in variation in the chromosomal region 14q32
DOID:0060840
isoniazide allergy
class of disease
drug allergy
drug allergy that has allergic trigger isoniazide
DOID:0040008
isthmicoma
class of disease
hair follicle neoplasm
Human disease
DOID:8426
Isthmicoma
isthmus cancer
class of disease
uterine corpus cancer
Human disease
DOID:9459
jaw cancer
class of disease
bone cancer
neoplasm of jaw
bone cancer and jaw disease that is located in the jaw and results in a swollen jaw, results in numbness or a tingling sensation in jaw, and results in an abnormal growth of the jaw bone
DOID:1862
jaw-winking syndrome
class of disease
cranial nerve disease
ptosis
genetic peripheral neuropathy
autosomal dominant condition with incomplete penetrance, in which nursing infants will have rhythmic upward jerking of their upper eyelid
DOID:560
Marcus Gunn phenomenon
jejunal adenocarcinoma
class of disease
jejunal cancer
adenocarcinoma
jejunal cancer that is located in the jejunum and has material basis in epithelial tissue that has glandular origin
DOID:0050926
jejunal cancer
class of disease
small intestine cancer
jejunal neoplasm
human disease
DOID:13499
jejunal neoplasm
class of disease
small intestine neoplasm
jejunal disease
human disease
DOID:3218
C04.588.274.476.411.523
C06.301.371.411.523
C06.405.249.411.523
C06.405.469.491.523
C06.405.469.600.523
jejunal somatostatinoma
class of disease
jejunal cancer
Human disease
DOID:3216
junctional epidermolysis bullosa Herlitz type
class of disease
junctional epidermolysis bullosa
genetic disease
autosomal recessive disease
Human disease
DOID:0060737
juvenile absence epilepsy
class of disease
adolescence-adult electroclinical syndrome
adolescence-adult electroclinical syndrome statring between the age of ten to 17 years characterized by the occurrence of typical absence seizures
DOID:0060172
juvenile absence epilepsy 1
class of disease
juvenile absence epilepsy
human disease
DOID:0111324
juvenile amyotrophic lateral sclerosis with dementia
class of disease
amyotrophic lateral sclerosis
juvenile amyotrophic lateral sclerosis
juvenile amyotrophic lateral sclerosis that is slowly progressive with concomitantly progressive dementia
DOID:0110067
juvenile ankylosing spondylitis
class of disease
autoimmune disease of musculoskeletal system
ankylosing spondylitis
autoimmune disease of musculoskeletal system that is an ankylosing spondylitis with onset during childhood
DOID:0040092
juvenile astrocytoma
class of disease
astrocytoma
childhood cancer
Human disease
DOID:3079
juvenile dermatitis herpetiformis
class of disease
dermatitis herpetiformis
Human disease
DOID:8507
juvenile glaucoma
class of disease
autosomal dominant disease
primary open angle glaucoma
Human disease
DOID:1068
juvenile myelomonocytic leukemia
class of disease
myelodysplastic/myeloproliferative neoplasm
monocytic leukemia
childhood leukemia
Human disease
DOID:0050458
C04.557.337.539.525
C15.378.190.615.520
juvenile myoclonic epilepsy
class of disease
adolescence-adult electroclinical syndrome
Idiopathic generalized epilepsy
myoclonic epilepsy
adolescence-adult electroclinical syndrome that is characterized by brief, involuntary twitching of a muscle or a group of muscles (myoclonus) early in the morning with onset between 12 and 18 years
DOID:4890
C10.228.140.490.493.063.670
C10.228.140.490.375.130.670
juvenile myoclonic epilepsy 10
class of disease
juvenile myoclonic epilepsy
human disease
DOID:0111325
juvenile myoclonic epilepsy 3
class of disease
juvenile myoclonic epilepsy
human disease
DOID:0111326
juvenile myoclonic epilepsy 4
class of disease
juvenile myoclonic epilepsy
human disease
DOID:0111327
juvenile myoclonic epilepsy 9
class of disease
juvenile myoclonic epilepsy
human disease
DOID:0111328
juvenile pilocytic astrocytoma
class of disease
childhood pilocytic astrocytoma
pilocytic astrocytoma
Human disease
DOID:6811
juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome
class of disease
autosomal dominant disease
syndrome
juvenile polyposis syndrome
hereditary hemorrhagic telangiectasia
human disease
DOID:0111543
juvenile type testicular granulosa cell tumor
class of disease
testicular granulosa cell tumor
Human disease
DOID:6032
juvenile xanthogranuloma
class of disease
non-Langerhans-cell histiocytosis
histiocytosis
xanthogranuloma
Human disease
DOID:4424
C15.604.250.410.900
C17.800.973
Juvenile xanthogranuloma
juvenile-onset Parkinson disease
class of disease
Parkinson's disease
young-onset Parkinson disease
human disease
DOID:0060893
juxtacortical chondroma
class of disease
chondroma
Human disease
DOID:2601
juxtacortical chondrosarcoma
class of disease
chondrosarcoma
human disease
DOID:5866
juxtacortical osteosarcoma
class of disease
peripheral osteosarcoma
Human disease
DOID:3373
C04.557.450.565.575.650.655
C04.557.450.795.620.655
keratinizing squamous cell carcinoma
class of disease
squamous cell carcinoma
squamous cell carcinoma that presents as single, isolated cells with bizzare cytoplasmic shapes, intense cytoplasmic eosinophilia, and intensely hyperchromatic, angular nuclei in a background of necrotic and keratinous debris
DOID:5521
keratitis
class of disease
symptom or sign
corneal disease
eye inflammation
inflammatory disease
cornea symptom
disease
corneal disease that is characterized by inflammation of the cornea.
DOID:4677
C11.204.564
Keratitis
keratoacanthoma
class of disease
cutaneous squamous-cell carcinoma
disease
Human disease
DOID:3149
C17.800.417
Keratoacanthoma
keratoconjunctivitis
class of disease
keratitis
conjunctivitis
eye disease
inflammation ("-itis") of the cornea and conjunctiva.
DOID:9368
C11.187.183.394
C11.204.564.585
Keratoconjunctivitis
keratoconjunctivitis sicca
class of disease
dry eye syndrome
keratoconjunctivitis
disease
condition of having dry eyes
DOID:12895
C11.187.183.394.550
C11.204.564.585.630
C11.496.260.394
Dry eye syndrome
keratomalacia
class of disease
corneal degeneration
vitamin A deficiency
keratitis related to vitamin deficiency
disease
Human disease
DOID:11267
keratopathy
class of disease
corneal disease
Human disease
DOID:2283
keratosis
class of disease
skin disease
keratoma
disease
skin disease characterized by growth of keratin on the skin or mucous membranes
DOID:161
C17.800.428
keratosis follicularis spinulosa decalvans, autosomal dominant
class of disease
keratosis follicularis spinulosa decalvans
human disease
DOID:0080755
keratosis pilaris atrophicans faciei
class of disease
keratosis pilaris atropicans
human disease
DOID:0080752
keratosis pilaris atropicans
class of disease
keratosis pilaris
autosomal recessive disease
ichthyosis
human disease
DOID:0080751
kernicterus
class of disease
symptom or sign
encephalopathy
neurometabolic disease
neonatal jaundice
disease
congenital disorder of nervous system
DOID:2382
C10.228.140.163.480
C15.378.295.502
C16.614.304.502
C18.452.132.480
C20.306.502
C23.550.429.750
Kernicterus
kernicterus due to isoimmunization
class of disease
neonatal jaundice
kernicterus
Human disease
DOID:12043
ketoprofen photoallergic dermatitis
class of disease
photodermatitis
drug allergy
photoallergic dermatitis that has allergic trigger ketoprofen
DOID:0040060
kidney angiomyolipoma
class of disease
kidney benign neoplasm
angiomyolipoma
benign perivascular tumor
angiomyolipoma arising from the kidney
DOID:8411
Renal angiomyolipoma
kidney benign neoplasm
class of disease
urinary system benign neoplasm
kidney neoplasm
kidney disease
lipoma
A non-metastasizing neoplasm that arises from the kidney. Representative examples include cystic nephroma, metanephric adenoma, oncocytoma, and urothelial papilloma of the renal pelvis.
DOID:3116
kidney cancer
class of disease
urinary system cancer
kidney neoplasm
kidney disease
disease
urinary system cancer that is located in the kidney
DOID:263
Cancers of kidney
kidney carcinoma in situ
class of disease
kidney disease
in situ carcinoma
Human disease
DOID:9234
kidney clear cell sarcoma
class of disease
kidney cancer
kidney sarcoma
inherited renal tumor
clear-cell sarcoma
kidney sarcoma that has material basis in clear cells that are characterized as cells that look clear when viewed under a microscope
DOID:4880
kidney cortex disease
class of disease
kidney disease
human disease
DOID:0080616
kidney failure
class of disease
symptom or sign
kidney disease
impaired renal function disease
chronic renal disease
urological symptom
disease
disease where the kidneys fail to adequately filter waste products from the blood
DOID:1074
C12.777.419.780
C13.351.968.419.780
kidney fibrosarcoma
class of disease
kidney sarcoma
fibrosarcoma
Human disease
DOID:5982
kidney hemangiopericytoma
class of disease
kidney cancer
kidney cancer which is manifested in the kidney
DOID:262
kidney hypertrophy
class of disease
kidney disease
Global enlargement of the renal parenchyma in one or both kidneys
DOID:9622
kidney infection
class of disease
infection
kidney disease
infectious disease
type of infection that afflicts the kidneys
DOID:782
kidney leiomyosarcoma
class of disease
kidney sarcoma
leiomyosarcoma and sarcoma of kidney that is located in the kidney
DOID:5287
kidney lipoma
class of disease
kidney benign neoplasm
Human disease
DOID:10194
kidney liposarcoma
class of disease
liposarcoma
kidney sarcoma
kidney cancer
liposarcoma that is located in the kidney
DOID:5699
kidney osteogenic sarcoma
class of disease
kidney sarcoma
extraosseous osteosarcoma
kidney sarcoma that starts in the bones and that is located in the kidney
DOID:5983
kidney papillary necrosis
class of disease
kidney disease
disease
Human disease
DOID:2981
C12.777.419.493
C13.351.968.419.493
kidney pelvis papillary carcinoma
class of disease
renal pelvis transitional cell carcinoma
renal pelvis papillary tumor
papillary transitional carcinoma
Human disease
DOID:5973
kidney pelvis sarcomatoid transitional cell carcinoma
class of disease
sarcomatoid transitional cell carcinoma
transitional cell carcinoma
renal pelvis carcinoma
Human disease
DOID:6844
kidney rhabdoid cancer
class of disease
rhabdoid tumor
kidney sarcoma
embryonal cancer that is located in the kidney
DOID:3674
kidney sarcoma
class of disease
kidney cancer
sarcoma
kidney cancer that is located in the kidney's connective tissue
DOID:4242
klebsiellosis
class of disease
bacterial pneumonia
Enterobacteriaceae infectious disease
infection by Klebsiella bacteria
DOID:13272
C01.150.252.400.310.503
kleptomania
class of disease
impulse control disorder
disease
inability to resist the urge to steal
DOID:12400
Kleptomania
kwashiorkor
class of disease
protein-energy malnutrition
disease
dystrophy
protein deficiency
Human disease
DOID:13579
C18.654.521.719.500
Kwashiorkor
kyphoscoliotic heart disease
class of disease
chronic pulmonary heart disease
Human disease
DOID:12325
labia majora carcinoma
class of disease
vulva carcinoma
skin cancer
Human disease
DOID:13389
labia minora cancer
class of disease
vulvar cancer
skin cancer
Human disease
DOID:1243
labia minora carcinoma
class of disease
vulva carcinoma
Human disease
DOID:1293
labium majus cancer
class of disease
vulvar cancer
Human disease
DOID:11905
labyrinthine bilateral reactive loss
class of disease
labyrinthine dysfunction
Human disease
DOID:14413
labyrinthine unilateral reactive loss
class of disease
labyrinthine dysfunction
Human disease
DOID:1776
labyrinthitis
class of disease
otitis interna
inner ear disease
labyrinthosis
disease
inflammation of the labyrinth, fluid-filled channels in the inner ear
DOID:1468
C09.218.568.558
C09.218.705.371
lacrimal apparatus disease
class of disease
eye disease
eye adnexa disease
rare palpebral, lacrimal system and conjunctival disease
rare genetic palpebral, lacrimal system and conjunctival disease
human disease
DOID:1400
C11.496
lacrimal duct cancer
class of disease
lacrimal system cancer
Human disease
DOID:12756
lacrimal duct obstruction
class of disease
lacrimal apparatus disease
stenosis and insufficiency of lacrimal passage
Human disease
DOID:13929
C11.496.456
Nasolacrimal duct obstruction
lacrimal gland adenocarcinoma
class of disease
lacrimal gland carcinoma
adenocarcinoma
human disease
DOID:298
lacrimal gland cancer
class of disease
lacrimal system cancer
lacrimal gland neoplasm
human disease
DOID:294
lacrimal gland carcinoma
class of disease
lacrimal gland cancer
carcinoma
Human disease
DOID:293
lacrimal passage granuloma
class of disease
lacrimal apparatus disease
Human disease
DOID:10174
lacrimal system cancer
class of disease
ocular cancer
lacrimal apparatus disease
human disease
DOID:292
lactic acidosis
class of disease
acidosis
metabolic acidosis
disease
acquired metabolic condition that has material basis in low pH in body tissues and blood accompanied by the buildup of lactate especially D-lactate
DOID:3650
C18.452.076.176.180
Lactic acidosis
lactose intolerance
class of disease
carbohydrate metabolic disorder
malabsorption
food intolerance
disease
condition involving a decreased ability to digest lactose due to a lack of lactase in the small intestines, either genetically or from injury
DOID:10604
C06.405.469.637.506
C16.320.565.202.589
C18.452.603.506
C18.452.648.202.589
Lactose intolerance
lambda 5 deficiency
class of disease
B cell deficiency
genetic disease
monogenic disease
A B cell deficiency that has material basis in mutations in the IGLL1 gene. Lambda 5 mutations an cause a block in B cell development at the transition between the pro-B cell and the pre-B cell stage.
DOID:0060024
language disorder
class of disease
communication disorder
range of neurodevelopmental conditions
DOID:93
C10.597.606.150.500
C23.888.592.604.150.500
large bowel leiomyoma
class of disease
intestinal benign neoplasm
leiomyoma
benign neoplasm of large intestine
Human disease
DOID:5143
large cell carcinoma
class of disease
carcinoma
carcinoma that is composed of large, monotonous rounded or overtly polygonal-shaped cells with abundant cytoplasm
DOID:4552
C04.557.470.200.260
large cell carcinoma with rhabdoid phenotype
class of disease
large-cell lung carcinoma
Human disease
DOID:7480
large cell keratinizing variant squamous cell breast carcinoma
class of disease
breast squamous cell carcinoma
keratinizing squamous cell carcinoma
Human disease
DOID:7461
large cell medulloblastoma
class of disease
medulloblastoma
medulloblastoma that is characterized by cells that are larger than would be normally expected
DOID:3857
large cell neuroendocrine carcinoma
class of disease
large cell carcinoma
neuroendocrine carcinoma
large-cell lung carcinoma
Human disease
DOID:0050872
Large cell neuroendocrine carcinoma
large cell neuroendocrine carcinoma of the lung
class of disease
large cell neuroendocrine carcinoma
large-cell lung carcinoma
pulmonary neuroendocrine tumor
human disease
DOID:6658
large intestine adenocarcinoma
class of disease
large intestine cancer
adenocarcinoma
large intestine cancer that has material basis in epithelial cells of glandular origin
DOID:0050913
large intestine adenoma
class of disease
intestinal benign neoplasm
gastrointestinal adenoma
benign neoplasms by histologic type
intestinal benign neoplasm that has material basis in epithelial tissue with glandular origin and is located in the large intestine
DOID:0050914
large intestine cancer
class of disease
intestinal cancer
colorectal neoplasm
intestinal cancer that effects the long, tube-like organ that is connected to the small intestine at one end and the anus at the other
DOID:5672
large intestine lipoma
class of disease
intestinal benign neoplasm
lipoma
benign neoplasm of large intestine
Human disease
DOID:6460
large-cell acanthoma
class of disease
acanthoma
Human disease
DOID:4321
large-cell lung carcinoma
class of disease
non-small-cell lung carcinoma
large cell carcinoma
disease
Disease
DOID:4556
Large-cell lung carcinoma
large-cell lymphoma
class of disease
lymphatic system cancer
non-Hodgkin lymphoma
Human disease
DOID:8538
laryngeal adenoid cystic carcinoma
class of disease
laryngeal carcinoma
Human disease
DOID:4869
laryngeal cancer
class of disease
head and neck cancer
carcinoma
laryngeal neoplasm
respiratory system cancer
disease
respiratory system cancer that is located in the larynx
DOID:2596
Laryngeal cancer
laryngeal carcinoma
class of disease
laryngeal cancer
carcinoma
larynx cancer that has material basis in epithelial cells
DOID:2600
laryngeal cartilage cancer
class of disease
laryngeal cancer
Human disease
DOID:13348
laryngeal disease
class of disease
upper respiratory tract disease
human disease
DOID:786
C08.360
C09.400
laryngeal mucoepidermoid carcinoma
class of disease
mucoepidermoid carcinoma
laryngeal cancer
Human disease
DOID:4688
laryngeal neoplasm
class of disease
respiratory tract neoplasm
laryngeal disease
neoplasm
respiratory system benign neoplasm
human disease
DOID:2598
C04.588.443.665.481
C08.360.369
C08.785.481
C09.400.369
C09.647.481
Neoplasms of larynx
laryngitis
class of disease
symptom or sign
laryngeal disease
inflammatory disease
throat symptom
disease
inflammation of the larynx
DOID:3437
C08.360.535
C08.730.368
C09.400.535
C01.748.368
Laryngitis
laryngostenosis
class of disease
laryngeal disease
Human disease
DOID:11527
C08.360.591
C09.400.591
C16.131.740.658
laryngotracheitis
class of disease
symptom or sign
upper respiratory tract disease
throat symptom
human disease
DOID:0050148
larynx carcinoma in situ
class of disease
laryngeal disease
in situ carcinoma
Human disease
DOID:9011
larynx leiomyoma
class of disease
laryngeal neoplasm
leiomyoma
Human disease
DOID:10070
larynx leiomyosarcoma
class of disease
leiomyosarcoma
larynx sarcoma that is a smooth muscle connective tissue tymor located in the larynx
DOID:5288
larynx liposarcoma
class of disease
liposarcoma
laryngeal cancer
liposarcoma that is located in the larynx
DOID:5696
larynx sarcoma
class of disease
laryngeal cancer
sarcoma
larynx cancer that has material basis in abnormally proliferating cells derived from embryonic mesoderm
DOID:2877
larynx squamous papilloma
class of disease
laryngeal neoplasm
squamous cell papilloma
laryngeal papillomatosis
Human disease
DOID:10071
late congenital syphilis
class of disease
congenital syphilis
Human disease
DOID:10039
late yaws
class of disease
yaws
yaws that appears after five years of the initial infection and is characterized by disabling consequences of the nose, bones and palmar/plantar hyperkeratosis
DOID:10567
late-adult onset retinitis pigmentosa
class of disease
retinitis pigmentosa
autosomal recessive disease
retinitis pigmentosa that is characterized by onset of symptoms in the fifth or sixth decade of life
DOID:0110421
lateral cystocele
class of disease
pelvic organ prolapse
cystocele
Human disease
DOID:14130
lateral displacement of eye
class of disease
orbital disease
exophthalmos
Human disease
DOID:12360
lateral medullary syndrome
class of disease
brain stem infarction
neurological disorder causing a range of symptoms due to ischemia in the lateral part of the medulla oblongata in the brainstem
DOID:3522
C10.228.140.300.150.477.100.500
C10.228.140.300.775.200.100.500
C14.907.253.092.477.100.500
C14.907.253.855.200.100.500
C23.550.513.355.250.100.500
C23.550.717.489.250.100.500
Lateral medullary syndrome
lateral myocardial infarction
class of disease
myocardial infarction
Human disease
DOID:5853
lateral sinus thrombosis
class of disease
cerebral venous sinus thrombosis
Human disease
DOID:3574
C10.228.140.300.525.425.500.562
C14.907.253.566.350.500.562
C14.907.355.590.213.350.500.562
lateral ventricle meningioma
class of disease
intraventricular meningioma
cerebral meningioma
cerebral ventricle cancer
Human disease
DOID:6115
latex allergy
class of disease
allergy
hazard
disease
hypersensitivity reaction type I disease triggered by latex
DOID:0060532
C20.543.600
learning disability
class of disease
specific developmental disorder
disability
disease
range of neurodevelopmental conditions
DOID:8927
C10.597.606.150.550
C23.888.592.604.150.550
F03.625.562
F03.625.374.188
Learning disabilities
leech infestation
class of disease
ectoparasitism
disease
human disease
DOID:11079
leg dermatosis
class of disease
skin disease
Human disease
DOID:3142
C17.800.446
legionellosis
class of disease
primary bacterial infectious disease
Human disease
DOID:10458
C01.150.252.400.500
C08.730.382
C01.748.382
legume allergy
class of disease
fruit allergy
human disease
DOID:0060904
leiomyoma
class of disease
benign neoplasms by histologic type
smooth muscle tumour
myoma
disease
cell type benign neoplasm that is a benign tumor of smooth muscle cells
DOID:127
C04.557.450.590.450
Leiomyomas
leiomyoma cutis
class of disease
dermis tumor
skin benign neoplasm
leiomyoma
benign tumor that arises from smooth muscle tissue in a hair follicle, forming a papule
DOID:5132
Cutaneous leiomyoma
leiomyomatosis
class of disease
leiomyoma
Human disease
DOID:5138
C04.557.450.590.450.465
leiomyosarcoma
class of disease
smooth muscle cancer
disease
malignant smooth muscle cancer that can arise almost anywhere in the body, but is most common in the uterus, abdomen, or pelvis
DOID:1967
C04.557.450.590.455
C04.557.450.795.455
Leiomyosarcoma
lens disease
class of disease
eye disease
Human disease
DOID:110
C11.510
lens subluxation
class of disease
lens disease
Human disease
DOID:11364
C11.510.598
lens-induced iridocyclitis
class of disease
iridocyclitis
Human disease
DOID:9388
leptomeninges sarcoma
class of disease
malignant leptomeningeal tumor
meninges sarcoma
sarcoma
Human disease
DOID:7689
lesion of sciatic nerve
class of disease
mononeuritis of lower limb
Human disease
DOID:12528
lethal congenital contracture syndrome 1
class of disease
lethal congenital contracture syndrome
genetic disease
lethal congenital contracture syndrome that has material basis in homozygous or compound heterozygous mutation in the mRNA export mediator GLE1 on chromosome 9q34
DOID:0060559
leucine-sensitive hypoglycemia of infancy
class of disease
amino acid metabolic disorder
autosomal dominant disease
human disease
DOID:0112262
leukemia
class of disease
symptom or sign
hematologic cancer
myeloproliferative disorders
disease
group of cancers that usually begin in the bone marrow
DOID:1240
C04.557.337
Leukemias
leukocoria
class of disease
pupil disorder
eye degenerative disease
abnormal white reflection from the retina of the eye
DOID:11772
Leukocoria
leukocyte adhesion deficiency 2
class of disease
leukocyte adhesion deficiency 3
leukocyte adhesion deficiency that is characterized by recurrent bacterial infections, severe growth delay and severe intellectual deficit
DOID:0080492
leukocyte disease
class of disease
symptom or sign
hematopoietic system disease
disease involving the leukocyte
DOID:9500
C15.378.553
Leukocyte disorders
leukodystrophy
class of disease
cerebral degeneration
disease
cerebral degeneration characterized by dysfunction of the white matter of the brain
DOID:10579
Leukodystrophies
leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome
class of disease
nervous system heredodegenerative disease
combined oxidative phosphorylation deficiency
autosomal recessive disease
human disease
DOID:0111493
leukopenia
class of disease
symptom or sign
leukocyte disease
cytopenia
hemic system symptom
disease
decrease in the number of white blood cells
DOID:615
C15.378.553.546
leukoplakia of penis
class of disease
penile disease
leukoplakia
Human disease
DOID:8738
leukoplakia of vagina
class of disease
vaginal disease
leukoplakia
Human disease
DOID:8920
leukorrhea
class of disease
vaginal discharge
disease
type of vaginal discharge
DOID:3766
C13.351.500.894.700.500
leukostasis
class of disease
leukocyte disease
leukocytosis
human disease
DOID:12986
C15.378.553.560
lichen disease
class of disease
skin disease
lichenoid eruption
Human disease
DOID:8574
lichen nitidus
class of disease
lichen disease
Human disease
DOID:8573
C17.800.859.475.545
Lichen nitidus
lichen planus
class of disease
lichen disease
disease
chronic disease of skin, tongue or oral mucosa
DOID:9201
C17.800.859.475.560
Lichen planus
lidocaine allergy
class of disease
drug allergy
drug allergy that has allergic trigger lidocaine
DOID:0040009
limb ischemia
class of disease
ischemia
Human disease
DOID:0050852
Limb ischemia
limb-girdle muscular dystrophy
class of disease
muscular dystrophy
progressive muscular dystrophy
disease
muscular dystrophy characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles
DOID:11724
C05.651.534.500.280
C10.668.491.175.500.149
C16.320.577.280
limbic encephalitis
class of disease
paraneoplastic neurologic syndrome
encephalitis
inflammatory and autoimmune disease with epilepsy
autoimmune disease of the nervous system
Inflammation involving the limbic system in the brain
DOID:0080741
C04.588.614.550.450
C04.730.856.437
C10.228.140.430.525
C10.228.228.245.700
C10.574.781.550
limited scleroderma
class of disease
systemic scleroderma
the least progressive form of systemic scleroderma with skin thickening restricted to the face, neck and areas distal to the elbows and/or knees, sparing the trunk
DOID:1577
C17.300.799.801
C17.800.784.801
linear skin defects with multiple congenital anomalies 1
class of disease
microphthalmia–dermal aplasia–sclerocornea syndrome
X-linked dominant disease
congenital disorder
human disease
DOID:0111808
lingual goiter
class of disease
goiter
Human disease
DOID:13196
C16.131.894.500.500
C19.874.283.802
C19.874.689.500.500
lingual-facial-buccal dyskinesia
class of disease
movement disorders
Human disease
DOID:9854
linitis plastica
class of disease
gastric diffuse adenocarcinoma
stomach carcinoma
disease
Human disease
DOID:4023
C04.557.470.200.025.095.410
Linitis plastica
lip disease
class of disease
mouth disease
human disease
DOID:9297
C07.465.409
Lip disorders
lipid metabolism disorder
class of disease
inherited metabolic disorder
disease
high cholesterol & lipids
DOID:3146
C18.452.584
Dyslipidemia
lipid storage disease
class of disease
lysosomal storage disease
disease
lysosomal storage disease that involves the accumulation of harmful amounts of lipids (fats) in some of the body's cells and tissues
DOID:9455
C16.320.565.398.641
C18.452.584.563.641
C18.452.648.398.641
Lipid storage disorders
lipid-cell variant infiltrating bladder urothelial carcinoma
class of disease
invasive bladder transitional cell carcinoma
Human disease
DOID:7967
lipid-rich breast carcinoma
class of disease
lipid-rich carcinoma
bilateral breast cancer
lipid-rich carcinoma characterized by the presence of cytoplasmic neutral lipids in the vast majority of the malignant cells
DOID:7076
lipid-rich carcinoma
class of disease
breast carcinoma
breast carcinoma characterized by the presence of malignant epithelial cells with clear cytoplasm which contains neutral lipids
DOID:5658
lipoadenoma
class of disease
adenoma
adenoma that is composed of adipose tissue
DOID:5398
lipoatrophic diabetes
class of disease
type 2 diabetes
type 2 diabetes that involves severe lipodystrophy in addition to the traditional signs of diabetes
DOID:11712
C18.452.394.750.149.500
C19.246.300.500
lipoid nephrosis
class of disease
idiopathic nephrotic syndrome
nephrotic syndrome
disease
Human disease
DOID:10966
C12.777.419.630.477
C13.351.968.419.630.477
Minimal change disease
lipoma
class of disease
benign neoplasms by histologic type
adipose tissue neoplasm
disease
benign tumor made of fat tissue
DOID:3315
C04.557.450.550.400
Lipomas
lipoma of colon
class of disease
large intestine lipoma
colonic disease
Human disease
DOID:10655
lipoma of spermatic cord
class of disease
paratesticular lipoma
lipoma
male reproductive organ benign neoplasm
Human disease
DOID:10206
lipoma of the rectum
class of disease
large intestine lipoma
benign neoplasm of rectum
Human disease
DOID:6459
lipomatosis
class of disease
skin disease
Human disease
DOID:3153
C17.800.463
C18.452.584.718
Lipomatosis
liposarcoma
class of disease
lipomatous cancer
sarcoma
disease
lipomatous cancer that arises in fat cells in deep soft tissue retroperitoneum
DOID:3382
C04.557.450.550.420
C04.557.450.795.465
Liposarcoma
liposarcoma of bone
class of disease
osteosarcoma
Human disease
DOID:3381
liposarcoma of the ovary
class of disease
ovary sarcoma
liposarcoma
sarcoma
ovarian cancer
Human disease
DOID:5697
lissencephaly 3
class of disease
autosomal dominant disease
lissencephaly
human disease
DOID:0112232
liver angiosarcoma
class of disease
angiosarcoma
liver cancer
hepatic vascular disease
liver sarcoma
organ type
angiosarcoma and sarcoma of liver and hemangioma of intra-abdominal structure and Ca liver - primary that is located in the liver
DOID:268
Liver angiosarcoma
liver cancer
class of disease
liver tumor
liver disease
rare hepatic and biliary tract tumor
liver neoplasm
hepatobiliary system cancer
endocrine gland cancer
disease
human disease
DOID:3571
Liver cancer
liver carcinoma
class of disease
liver cancer
carcinoma
liver cancer that has material basis in epithelial cells
DOID:686
liver carcinoma in situ
class of disease
in situ carcinoma
liver disease
Human disease
DOID:9132
liver cirrhosis
class of disease
liver disease
cirrosis
disease
chronic disease of the liver, characterized by fibrosis
DOID:5082
C06.552.630
C23.550.355.412
Cirrhosis
liver disease
class of disease
hepatobiliary disease
endocrine system disease
disease
disorder of the human liver
DOID:409
C06.552
Diseases and disorders of liver
liver fibroma
class of disease
liver neoplasm
fibroma
Human disease
DOID:907
liver fibrosarcoma
class of disease
liver sarcoma
fibrosarcoma
fibrosarcoma of soft tissue and sarcoma of liver that is located in the liver
DOID:8022
liver inflammatory pseudotumor
class of disease
Inflammatory pseudotumor
inflammatory myofibroblastic tumour
rare hepatic disease
liver neoplasm
rare hepatic and biliary tract tumor
endocrine gland cancer
liver disease
Human disease
DOID:918
liver leiomyoma
class of disease
liver neoplasm
Human disease
DOID:917
liver leiomyosarcoma
class of disease
liver sarcoma
leiomyosarcoma and sarcoma of liver that is located in the liver
DOID:5296
liver lipoma
class of disease
liver neoplasm
gastrointestinal system benign neoplasm
endocrine organ benign neoplasm
human disease
DOID:10190
liver lymphoma
class of disease
liver cancer
endocrine gland cancer
gastrointestinal lymphoma
rare hepatic disease
lymphoma
Human disease
DOID:901
liver neoplasm
class of disease
liver tumor
hepatobiliary neoplasm
liver disease
endocrine organ benign neoplasm
human disease
DOID:916
C04.588.274.623
C06.301.623
C06.552.697
Benign neoplasms of liver
liver rhabdomyosarcoma
class of disease
liver sarcoma
rhabdomyosarcoma and sarcoma of liver that are located in the liver
DOID:4047
liver sarcoma
class of disease
liver cancer
sarcoma and malignant non-epithelial hepatic and intrahepatic bile duct neoplasm sthat is located in the liver
DOID:270
lobomycosis
class of disease
dermatomycosis
disease
dermatomycosis that results in infection located in skin or located in subcutaneous tissue, has material basis in Lacazia loboi and has symptom crusty plaques, has symptom tumors and results in formation of nodular lesions
DOID:13026
C01.800.200.475
C01.150.703.302.475
C17.800.838.208.475
Lobomycosis
lobular neoplasia
class of disease
breast carcinoma in situ
breast neoplasm
Human disease
DOID:3010
localized anterior staphyloma
class of disease
scleral staphyloma
Human disease
DOID:13787
localized chondrosarcoma
class of disease
chondrosarcoma
Human disease
DOID:5862
localized osteosarcoma
class of disease
osteosarcoma
Human disease
DOID:3356
localized pulmonary fibrosis
class of disease
pulmonary fibrosis
Human disease
DOID:5642
localized scleroderma
class of disease
scleroderma
human disease
DOID:8472
C17.300.787
C17.800.767
Morphea
locked-in syndrome
class of disease
neurological disorder
disease
condition in which a patient is aware but cannot move or communicate verbally due to complete paralysis of nearly all voluntary muscles in the body except for vertical eye movements and blinking
DOID:12697
C10.597.622.760.500
C10.668.416
C23.888.592.636.786.500
long QT syndrome 1
class of disease
long QT syndrome
genetic disease
autosomal dominant disease
A long QT syndrome that has material basis in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4.
DOID:0110644
long QT syndrome 10
class of disease
long QT syndrome
genetic disease
autosomal dominant disease
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3.
DOID:0110651
long QT syndrome 4
class of disease
long QT syndrome
autosomal dominant disease
human disease
DOID:0111701
long bone adamantinoma
class of disease
adamantinoma
adamantinoma that is located in the long bones and results in focal epithelial differentiation
DOID:2775
long bones of lower limb cancer
class of disease
bone cancer
lower limb cancer
bone cancer that is manifested in the long bones of the lower limb
DOID:10149
loose anagen syndrome
class of disease
alopecia
baldness
human disease
DOID:0111702
low compliance bladder
class of disease
bladder disease
disease
human disease
DOID:12144
C12.777.829.866
C13.351.968.829.813
C23.888.942.343.780
low grade glioma
class of disease
glioma
A grade I or grade II glioma arising from the central nervous system. This category includes pilocytic astrocytoma, diffuse astrocytoma, subependymal giant cell astrocytoma, ependymoma, oligodendroglioma, oligoastrocytoma, and angiocentric glioma.
DOID:0080829
low implantation of placenta
class of disease
placenta praevia
Human disease
DOID:1677
low tension glaucoma
class of disease
open-angle glaucoma
Human disease
DOID:13544
C11.640.225
lower respiratory tract disease
class of disease
respiratory disease
respiratory system disease which involves the lower respiratory tract
DOID:0050161
lumbar plexus neoplasm
class of disease
nerve plexus neoplasm
Human disease
DOID:8389
lumbar spinal canal and spinal cord meningioma
class of disease
spinal canal and spinal cord meningioma
Human disease
DOID:7515
lumbosacral lipoma
class of disease
bone benign neoplasm
lipoma
Human disease
DOID:7017
lumbosacral plexus lesion
class of disease
peripheral neuropathy
Human disease
DOID:13913
luminal breast carcinoma
class of disease
breast carcinoma
breast carcinoma by gene expression profile
Human disease
DOID:0060548
luminal breast carcinoma B
class of disease
breast carcinoma
luminal breast carcinoma
human disease
DOID:0080674
lung acinar adenocarcinoma
class of disease
adenocarcinoma of the lung
Human disease
DOID:6482
lung adenoid cystic carcinoma
class of disease
lung carcinoma
adenoid cystic carcinoma
Human disease
DOID:4872
lung adenoma
class of disease
lung benign neoplasm
benign epithelial neoplasm
benign neoplasms by histologic type
adenoma
Human disease
DOID:5386
lung benign neoplasm
class of disease
respiratory system benign neoplasm
lung disease
lung neoplasm
thoracic cancer
human disease
DOID:3683
Benign neoplasms of bronchus and lung
lung carcinoma
class of disease
lung cancer
carcinoma
lung cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the lungs and has symptom cough and has symptom chest discomfort or pain and has symptom weight loss and has symptom hemoptysis
DOID:3905
lung carcinoma in situ
class of disease
in situ carcinoma
lung disease
lung neoplasm
Human disease
DOID:8800
lung clear cell carcinoma
class of disease
clear cell carcinoma
lung carcinoma
Human disease
DOID:7267
lung clear cell-sugar-tumor
class of disease
lung benign neoplasm
perivascular epithelioid cell neoplasm
benign perivascular tumor
Human disease
DOID:5763
lung combined large cell neuroendocrine carcinoma
class of disease
large cell neuroendocrine carcinoma of the lung
combined carcinoma of lung
Human disease
DOID:7207
lung combined type small cell carcinoma
class of disease
lung small cell carcinoma
combined carcinoma of lung
lung small cell carcinoma that is characterized as a multiphasic lung cancer comprised of a mixture of small cell and non-small cell lung carcinoma cells
DOID:5421
lung disease
class of disease
lower respiratory tract disease
disease
respiratory disease
DOID:850
C08.381
lung hilum cancer
class of disease
lung cancer
hilar lung neoplasm
Human disease
DOID:7696
lung leiomyoma
class of disease
lung benign neoplasm
leiomyoma
Human disease
DOID:5136
lung leiomyosarcoma
class of disease
leiomyosarcoma
leiomyosarcoma and sarcoma of lung that is located in the lung
DOID:5265
lung lymphoma
class of disease
lung cancer
lymphoma
Human disease
DOID:6760
lung meningioma
class of disease
lung cancer
malignant neoplasm of meninges
rare genetic respiratory disease
genetic nervous system disorder
ectopic meningioma
Human disease
DOID:5764
lung mixed small cell and squamous cell carcinoma
class of disease
pulmonary neuroendocrine tumor
lung combined type small cell carcinoma
Human disease
DOID:7081
lung mucoepidermoid carcinoma
class of disease
lung carcinoma
mucoepidermoid carcinoma
lung carcinoma that has material basis in a combination of squamous cells, mucus secreting cells and intermediate cells
DOID:0050932
Mucoepidermoid lung carcinoma
lung non-squamous non-small cell carcinoma
class of disease
non-small-cell lung carcinoma
lung non-small cell carcinoma that is characterized by the lack of evidence of squamous differentiation
DOID:0080521
lung oat cell carcinoma
class of disease
lung small cell carcinoma
Human disease
DOID:5411
lung occult adenocarcinoma
class of disease
adenocarcinoma of the lung
Human disease
DOID:7168
lung occult large cell carcinoma
class of disease
large-cell lung carcinoma
lung occult non-small cell carcinoma
Human disease
DOID:7169
lung occult small cell carcinoma
class of disease
lung small cell carcinoma
lung occult carcinoma
Human disease
DOID:5414
lung occult squamous cell carcinoma
class of disease
squamous cell carcinoma of the lung
lung occult carcinoma
Human disease
DOID:6510
lung papillary adenocarcinoma
class of disease
adenocarcinoma of the lung
Human disease
DOID:5588
lung sarcoma
class of disease
lung cancer
sarcoma
lung cancer that is located in the lung and that arises from transformed cells of mesenchymal origin
DOID:2784
lung small cell carcinoma
class of disease
lung carcinoma
small cell carcinoma
lung carcinoma that has material basis in primitive-appearing cells that are smaller than normal cells
DOID:5409
C04.588.894.797.520.109.220.624
C08.381.540.140.750
C08.785.520.100.220.750
lung superior sulcus carcinoma
class of disease
Pancoast tumor
human disease
DOID:8208
lupus erythematosus
class of disease
autoimmune disease
autoimmune disease of musculoskeletal system
disease
human disease
DOID:8857
lupus nephritis
class of disease
glomerulonephritis
disease
inflammation of the kidneys
DOID:0080162
C12.200.777.419.570.363.680
C12.050.351.968.419.570.363.680
C17.300.480.680
C20.111.590.560
C12.950.419.570.363.680
Lupus nephritis
luteoma
class of disease
ovarian benign neoplasm
ovarian disease
disease
ovarian benign neoplasm characterized by solid proliferations of luteinized cells, resulting in a tumor-like ovarian enlargement that regresses during the puerperium
DOID:7880
C04.557.475.750.751
C04.588.322.455.464
C13.351.500.056.630.705.464
C13.351.937.418.685.464
C19.344.410.464
C19.391.630.705.464
Luteoma of pregnancy
luxation of globe
class of disease
globe disease
Human disease
DOID:1241
lymph node adenoid cystic carcinoma
class of disease
lymph node metastasis
carcinoma
lymph node cancer
lymph node carcinoma
Human disease
DOID:0060219
lymph node cancer
class of disease
lymphatic system cancer
lymph node neoplasm
lymph node disease
lymphatic system cancer that is located in the lymph node
DOID:10619
Lymph node cancers
lymph node carcinoma
class of disease
carcinoma
lymph node cancer
human disease
DOID:0080618
lymph node disease
class of disease
lymphatic system disease
Human disease
DOID:9942
Diseases and disorders of lymph nodes
lymph node palisaded myofibroblastoma
class of disease
lymph node cancer
benign neoplasm of lymph node
human disease
DOID:8304
lymphadenitis
class of disease
symptom or sign
lymph node disease
clinical sign
lymphatic system symptom
adenitis
lymph node and lymph vessels inflammation
DOID:1602
C15.604.315
lymphangioma
class of disease
lymphatic system malformation
benign blood vessel neoplasm
disease
malformations of the lymphatic system characterized by lesions that are thin-walled cysts
DOID:1475
C04.557.375.450
Lymphangiomas
lymphangiosarcoma
class of disease
lymphatic system cancer
angiosarcoma associated with lymphedema
skin carcinoma
skin sarcoma
disease
lymphatic system cancer that has material basis in endothelial cells located in lymphatic vessels
DOID:2689
C04.557.375.480
C04.557.450.795.480
lymphatic system cancer
class of disease
immune system cancer
lymphatic system disease
immune system cancer that is located in the lymphatic system and is characterized by uncontrolled cellular proliferation of lymphoid tissue
DOID:0060073
lymphatic system disease
class of disease
immune disorder
immune system disease that is located in the lymphatic system
DOID:75
C15.604
lymphoblastic leukemia
class of disease
leukemia
leukemia that has material basis in lymphoblasts (immature white blood cells)
DOID:1037
lymphoblastic lymphoma
class of disease
symptom or sign
non-Hodgkin lymphoma
lymphoma
lymphatic system symptom
lymphoma that has material basis in immature malignant lymphocytes (lymphoblasts) committed to the B-cell or T-cell lineage and located in primarily lymph nodes or located in extranodal sites
DOID:0080147
lymphocele
class of disease
lymphatic system disease
Human disease
DOID:4347
C04.182.430
C15.604.510
lymphocytic gastritis
class of disease
gastritis
chronic gastritis
Human disease
DOID:4035
lymphoepithelioma-like acinar prostate adenocarcinoma
class of disease
prostate adenocarcinoma
prostatic acinar adenocarcinoma
Human disease
DOID:7246
lymphoepithelioma-like carcinoma
class of disease
carcinoma
large cell carcinoma
carcinoma that is a malignant epithelial neoplasm densely infiltrated by lymphoid cells
DOID:5660
Lymphoepithelioma-like carcinoma
lymphoepithelioma-like thymic carcinoma
class of disease
thymic carcinoma
Human disease
DOID:7599
lymphohistiocytoid mesothelioma
class of disease
malignant pleural mesothelioma
sarcomatoid mesothelioma
Human disease
DOID:7381
lymphoid interstitial pneumonia
class of disease
idiopathic interstitial pneumonia
lymphoproliferative disorders
Human disease
DOID:0050159
lymphoma
class of disease
symptom or sign
hematologic cancer
lymphatic system cancer
lymphoma and pseudolymphoma
lymphoid neoplasm
disease
hematologic cancer that affects lymphocytes
DOID:0060058
C04.557.386
C15.604.515.569
C20.683.515.761
Lymphomas
lymphoma-like variant infiltrating bladder urothelial carcinoma
class of disease
invasive bladder transitional cell carcinoma
Human disease
DOID:7972
lymphopenia
class of disease
symptom or sign
leukopenia
lymphatic system symptom
disease
leukopenia that is the condition of having an abnormally low level of lymphocytes in the blood
DOID:614
C15.378.553.546.605
C20.673.627
C15.378.243.750.605
lymphoplasmacyte-rich meningioma
class of disease
meningioma
Human disease
DOID:4591
lysosomal and lipase deficiency
class of disease
lipid storage disease
lipid storage disease characterized by lysosomal and lipase deficiency
DOID:0080217
macrocystic neurilemmoma
class of disease
neurilemmoma
Human disease
DOID:3203
macrocystic pattern testicular yolk sac tumor
class of disease
testicular yolk sac tumor
Human disease
DOID:7097
macrocytic anemia
class of disease
symptom or sign
anemia
Human disease
DOID:2361
C15.378.071.252
macroglobulinemia
class of disease
plasma protein metabolism disease
Human disease
DOID:9080
macrotrabecular hepatoblastoma
class of disease
hepatoblastoma
Human disease
DOID:5798
macular degeneration
class of disease
retinal degeneration
maculopathy
blindness
retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye
DOID:4448
C11.768.585.439
Macular degeneration
macular hole
class of disease
retinal disease
retinal perforation
maculopathy
small break in the macula, located in the center of the eye's light-sensitive tissue called the retina
DOID:7633
Macular hole
macular keratitis
class of disease
keratitis
human disease
DOID:11871
macular retinal edema
class of disease
retinal edema
maculopathy
disease
Human disease
DOID:4449
C11.768.585.439.245
Macular edema
main bronchus cancer
class of disease
lung cancer
Human disease
DOID:3924
major depressive disorder
class of disease
depressive disorder
mental depression
disease
all-encompassing low mood accompanied by low self-esteem, and by loss of interest or pleasure in normally enjoyable activities
DOID:1470
F03.600.300.375
Major depressive disorder
male breast cancer
class of disease
breast cancer
male breast neoplasm
Human disease
DOID:1614
male genital organ stricture
class of disease
male reproductive system disease
Human disease
DOID:12333
male genital organ vascular disease
class of disease
male reproductive system disease
vascular disease
Human disease
DOID:12335
male infertility
class of disease
symptom or sign
male reproductive system disease
infertility
sexual impotence
disease
inability to father a child
DOID:12336
C12.294.365.700
Male infertility
male reproductive organ benign neoplasm
class of disease
reproductive organ benign neoplasm
male reproductive system neoplasm
male reproductive system disease
human disease
DOID:0060087
male reproductive organ cancer
class of disease
reproductive organ cancer
male reproductive system neoplasm
male reproductive system disease
cancer that is manifested in the male genital system
DOID:3856
male reproductive system disease
class of disease
reproductive system disease
male urogenital disease
reproductive system disease that affects male reproductive organs
DOID:48
C12.294
Diseases and disorders of the male reproductive system
male urethral cancer
class of disease
urethral cancer
Human disease
DOID:736
maleic anhydride allergic asthma
class of disease
allergic asthma
maleic anhydride exposure
allergic asthma that has allergic trigger maleic anhydride
DOID:0040049
malignant acrospiroma
class of disease
acrospiroma
sweat gland cancer
Human disease
DOID:5570
Malignant acrospiroma
malignant adenofibroma
class of disease
carcinosarcoma
Human disease
DOID:4422
malignant adult ependymoma
class of disease
ependymal tumor
anaplastic ependymoma
Human disease
DOID:5890
malignant anus melanoma
class of disease
anal cancer
mucosal melanoma
melanoma
Human disease
DOID:14145
malignant biphasic mesothelioma
class of disease
mesothelioma
Human disease
DOID:4486
malignant breast melanoma
class of disease
breast cancer
Human disease
DOID:4364
malignant cardiac germ cell tumor
class of disease
heart cancer
Human disease
DOID:14535
malignant cardiac peripheral nerve sheath neoplasm
class of disease
malignant peripheral nerve sheath tumor
Human disease
DOID:14534
malignant childhood germ cell neoplasm
class of disease
pediatric germ cell tumor
germ cell cancer
childhood cancer
Human disease
DOID:8149
malignant ciliary body melanoma
class of disease
ciliary body cancer
Human disease
DOID:6524
malignant conjunctival melanoma
class of disease
conjunctival cancer
ocular melanoma
Human disease
DOID:1751
malignant cystadenoma
class of disease
adenocarcinoma
cystadenoma
human disease
DOID:60004
malignant cystic nephroma
class of disease
kidney cancer
nephroblastoma
childhood multilocular cystic kidney neoplasm
kidney cortex disease
Human disease
DOID:7571
malignant dermis tumor
class of disease
skin cancer
Human disease
DOID:5274
malignant epithelial mesothelioma
class of disease
mesothelioma
Human disease
DOID:4489
malignant epithelioid hemangioendothelioma
class of disease
malignant hemangioma
epithelioid hemangioendothelioma
A malignant hemangioma characterized by the presence of epithelioid endothelial cells. The neoplastic cells are arranged in cords and nests, which are embedded in a myxoid to hyalinized stroma.
DOID:0080190
malignant essential hypertension
class of disease
essential hypertension
Human disease
DOID:10823
malignant eyelid melanoma
class of disease
skin melanoma
Human disease
DOID:10040
malignant fibrous histiocytoma
class of disease
histiocytoma
fibrous histiocytoma
sarcoma
human disease
DOID:1907
malignant fibrous histiocytoma of bone
class of disease
connective tissue neoplasm
osteosarcoma
Human disease
DOID:3352
malignant gastric germ cell tumor
class of disease
stomach cancer
extragonadal germ cell cancer
gastrointestinal system disease
gastrointestinal system cancer
Human disease
DOID:6949
DOID:4716
malignant gastric granular cell tumor
class of disease
stomach cancer
Human disease
DOID:10536
malignant gastric teratoma
class of disease
malignant gastric germ cell tumor
gastric teratoma
extragonadal non-dysgerminomatous germ cell tumor
Human disease
DOID:6948
malignant giant cell tumor
class of disease
giant cell tumor
connective tissue neoplasm
Human disease
DOID:2705
malignant giant cell tumor of soft parts
class of disease
malignant fibrous histiocytoma
malignant giant cell tumor
Human disease
DOID:5638
malignant giant cell tumor of the tendon sheath
class of disease
synovium cancer
Human disease
DOID:2704
malignant glandular tumor of peripheral nerve sheath
class of disease
malignant peripheral nerve sheath tumor
Human disease
DOID:8420
malignant granular cell esophageal tumor
class of disease
esophageal cancer
granular cell tumor
Human disease
DOID:5040
malignant granular cell myoblastoma
class of disease
skin cancer
malignant peripheral nerve neoplasm
granular cell tumor
Human disease
DOID:5042
malignant granular cell skin tumor
class of disease
malignant dermis tumor
malignant granular cell myoblastoma
Human disease
DOID:7639
malignant hemangioma
class of disease
sarcoma
vascular cancer
malignant mixed tumor
cell type cancer of vascular origin, characterized by proliferation of endothelial cells in and about the vascular lumen
DOID:0080189
malignant hypertension
class of disease
symptom or sign
arterial hypertension
hypertensive crisis
disease
condition of markedly elevated blood pressure with diastolic pressure typically greater than 120 mm Hg
DOID:10824
C14.907.489.330
malignant hypertensive renal disease
class of disease
renal hypertension
Human disease
DOID:10177
malignant leptomeningeal tumor
class of disease
meningioma
malignant neoplasm of meninges
meningeal carcinomatosis
Human disease
DOID:6086
malignant mediastinal neurogenic neoplasm
class of disease
mediastinal cancer
mediastinal cancer that has material basis in neural cells
DOID:4691
malignant mediastinum hemangiopericytoma
class of disease
hemangiopericytoma
hemangiopericytoma, malignant
mediastinal cancer
hemangiopericytoma and sarcoma of the mediastinum that is located in the mediastinum
DOID:6209
malignant melanocytic neoplasm of the peripheral nerve sheath
class of disease
malignant peripheral nerve sheath tumor
Human disease
DOID:6345
malignant melanocytic peripheral nerve sheath tumor of mediastinum
class of disease
mediastinal cancer
peripheral neuropathy
malignant melanocytic neoplasm of the peripheral nerve sheath
mediastinum sarcoma
nervous system cancer
Human disease
DOID:7077
malignant mesenchymoma
class of disease
mesenchymoma
Human disease
DOID:5758
malignant mixed tumor
class of disease
Mixed tumor
cell type cancer
cell type cancer that has material basis in cells from two tissues
DOID:154
C04.557.435.525
malignant neoplasm of acoustic nerve
class of disease
cranial nerve malignant neoplasm
vestibulocochlear nerve neoplasm
inner ear cancer
vestibulocochlear nerve disease
ear neoplasms
Human disease
DOID:2814
malignant neoplasm of short bones of lower limb
class of disease
long bones of lower limb cancer
Human disease
DOID:10151
malignant oculomotor nerve tumor
class of disease
cranial nerve III tumor
cranial nerve malignant neoplasm
Human disease
DOID:2816
malignant otitis externa
class of disease
otitis externa
complications of diabetes mellitus
Human disease
DOID:10516
malignant ovarian Brenner tumor
class of disease
ovarian cancer
ovarian Brenner tumor
malignant ovarian surface epithelial-stromal neoplasm
malignant ovarian surface epithelial-stromal neoplasm that has material basis in the surface epithelium of the ovary
DOID:4217
malignant ovarian cyst
class of disease
ovarian cancer
ovarian cyst
Human disease
DOID:2145
malignant ovarian germ cell neoplasm
class of disease
ovarian germ cell neoplasm
rare gynecological tumor
germ cell cancer
ovarian cancer
Human disease
DOID:2155
malignant ovarian surface epithelial-stromal neoplasm
class of disease
surface epithelial-stromal tumor
ovarian cancer
Human disease
DOID:2151
malignant parietal pleura tumor
class of disease
pleural cancer
Human disease
DOID:14032
malignant pediatric adrenal gland pheochromocytoma
class of disease
adrenal gland pheochromocytoma
adrenal gland pheochromocytoma that is characterized by rare chromaffin cell tumors which secrete catecholamines, and has a higher prevalence of hereditary factors and metastatis in children than adults
DOID:0070325
malignant peripheral nerve sheath tumor
class of disease
nerve sheath neoplasms
malignant peripheral nerve neoplasm
Human disease
DOID:5940
Malignant peripheral nerve sheath tumor
malignant peritoneal solitary fibrous tumor
class of disease
peritoneum cancer
peritoneal solitary fibrous tumor
Human disease
DOID:4490
malignant pheochromocytoma
class of disease
adrenal medulla cancer
adrenal medulla cancer that arises within the adrenal medulla, releasing epinephrines and norepinephrines hormones
DOID:0080347
malignant pineal area germ cell neoplasm
class of disease
pinealoma
Human disease
DOID:1660
malignant pleural mesothelioma
class of disease
pleural cancer
benign pleural mesothelioma
mesothelioma
squamous cell carcinoma
respiratory system cancer
pleural disease
pleural cancer that has material basis in mesothelium cells
DOID:7474
Pleural mesothelioma
malignant renovascular hypertension
class of disease
malignant secondary hypertension
renovascular hypertension
renal hypertension
Human disease
DOID:13730
malignant secondary hypertension
class of disease
secondary hypertension
Human disease
DOID:13731
malignant skin fibrous histiocytoma
class of disease
malignant dermis tumor
malignant fibrous histiocytoma
Human disease
DOID:1906
malignant spindle cell melanoma
class of disease
melanoma
hemangiopericytoma
spindle cell cancer
melanoma that is most commonly located in sun-exposed skin and results in formation of spindle-like shaped cells that have a high recurrence rate even with treatment
DOID:3162
malignant spiradenoma
class of disease
eccrine sweat gland cancer
apocrine sweat gland cancer
spiradenoma
Human disease
DOID:7960
malignant struma ovarii
class of disease
struma ovarii
immature teratoma of ovary
Human disease
DOID:5208
malignant syringoma
class of disease
eccrine sweat gland cancer
Human disease
DOID:5569
malignant triton tumor
class of disease
malignant peripheral nerve sheath tumor
human disease
DOID:6707
malignant tumor of undescended testis
class of disease
testicular cancer
cryptorchidism
Human disease
DOID:12276
malignant type A thymoma
class of disease
spindle cell thymoma
Human disease
DOID:7927
malignant type AB thymoma
class of disease
mixed type thymoma
Human disease
DOID:6723
malignant visceral pleura tumor
class of disease
pleural cancer
Human disease
DOID:14033
malt worker's lung
class of disease
extrinsic allergic alveolitis
extrinsic allergic alveolitis which is caused by inhalation of fungal spores of Aspergillus clavatus and Aspergillus fumigatus from moldy barley
DOID:2314
mammary Paget's disease
class of disease
breast adenocarcinoma
disease
type of cancer that may have the appearance of eczema, involving the nipple
DOID:3443
C04.557.470.200.240.187.500
C04.557.470.615.275.625
Paget's disease of the breast
mammary analogue secretory carcinoma
class of disease
salivary gland cancer
carcinoma
salivary gland carcinoma
secretory carcinoma
salivary gland neoplasm
DOID:0080808
C04.557.470.200.588
mammary myofibroblastoma
class of disease
benign neoplasm
muscle tissue neoplasm
breast benign neoplasm
rare, benign tumor of the breast
DOID:1629
mantle cell lymphoma
class of disease
B-cell lymphoma
aggressive B-cell non-Hodgkin lymphoma
disease
B-cell lymphocytic neoplasm due to CD5 positive antigen-naive pregerminal center B-cell within the mantle zone that surrounds normal germinal center follicles
DOID:0050746
C04.557.386.480.525
C15.604.515.569.480.525
C20.683.515.761.480.525
Mantle cell lymphoma
marasmus
class of disease
protein-energy malnutrition
disease
form of severe malnutrition characterized by energy deficiency
DOID:12328
Marasmus
marginal corneal ulcer
class of disease
corneal ulcer
Human disease
DOID:10441
marginal zone B-cell lymphoma
class of disease
B-cell lymphoma
leukocyte disease
group of lymphomas
DOID:0050748
mast cell leukemia
class of disease
leukemia
rare bone disease
mastocytoma
rare leukemia (blood cancer) involving mast cells
DOID:9254
C04.557.337.440
C04.557.337.539.275.440
C20.762.750.750.500
Mast cell leukemia
mast cell sarcoma
class of disease
sarcoma
mastocytoma
human disease
DOID:355
C04.557.450.565.465.124
C20.762.750.375
mastitis
class of disease
symptom or sign
breast disease
breastfeeding difficulties
inflammatory disease
reproductive system disease
skin and integumentary tissue symptom
disease
inflammation of the breast
DOID:10690
C13.703.844.603
C17.800.090.968
Mastitis
mastocytoma
class of disease
tumor of hematopoietic and lymphoid tissues
myeloid neoplasm
solid tumor consisting of mast cells, generally benign
DOID:3664
C04.557.450.565.465.249
C20.762.750.469
Mastocytoma
mastoiditis
class of disease
bone inflammation disease
middle ear disease
disease
middle ear disease characterized by an inflammation of the mucosal lining of the mastoid antrum and the mastoid air cell system inside the mastoid process
DOID:0060322
C01.539.160.495.500
C05.116.165.495.249
C09.218.705.663.652
Mastoiditis
mature B-cell neoplasm
class of disease
B-cell lymphoma
Human disease
DOID:706
mature T-cell and NK-cell lymphoma
class of disease
non-Hodgkin lymphoma
mature T-cell neoplasm
non-Hodgkin lymphoma that has material basis in mature T lymphocytes and natural killer cells
DOID:0050743
mature cataract
class of disease
senile cataract
Human disease
DOID:13717
mature gastric teratoma
class of disease
gastric teratoma
mature teratoma
Human disease
DOID:8118
mature teratoma
class of disease
teratoma
Human disease
DOID:5566
mature teratoma of the ovary
class of disease
mature teratoma
ovarian biphasic or triphasic teratoma
ovarian germ cell teratoma
Human disease
DOID:6231
Mature teratoma of ovary
maturity-onset diabetes of the young
class of disease
diabetes
autosomal dominant disease
disease
genetic disease that has material basis in mutations in the MODY genes disrupting insulin production
DOID:0050524
maturity-onset diabetes of the young type 14
class of disease
maturity-onset diabetes of the young
maturity-onset diabetes of the young that has material basis in heterozygous mutation in the APPL1 gene on chromosome 3p14
DOID:0111111
maturity-onset diabetes of the young type 2
class of disease
maturity-onset diabetes of the young
maturity-onset diabetes of the young that has material basis in heterozygous mutation in the GCK gene on chromosome 7p13
DOID:0111100
maturity-onset diabetes of the young type 3
class of disease
maturity-onset diabetes of the young
A maturity-onset diabetes of the young that has material basis in mutation in the HNF1A gene on chromosome 12q24.31.
DOID:0111102
maturity-onset diabetes of the young type 4
class of disease
maturity-onset diabetes of the young
A maturity-onset diabetes of the young that has material basis in mutation in the PDX1 gene on chromosome 13q12.2.
DOID:0111103
maturity-onset diabetes of the young type 5
class of disease
maturity-onset diabetes of the young
maturity-onset diabetes of the young characterized by abnormal renal development resuting in non-diabetic kidney disease and diabetes that has material basis in mutation in the HNF1B gene on chromosome 17q12
DOID:0111101
maturity-onset diabetes of the young type 6
class of disease
maturity-onset diabetes of the young
maturity-onset diabetes of the young that has material basis in heterozygous mutation in the NEUROD1 gene on chromosome 2q31
DOID:0111104
maxillary sinus cancer
class of disease
paranasal sinus cancer
maxillary sinus neoplasm
Human disease
DOID:1357
maxillary sinus cholesteatoma
class of disease
paranasal sinus disease
cholesteatoma
mouth disease
cholesteatoma located in paranasal sinus
DOID:867
maxillary sinusitis
class of disease
nose disease
sinusitis
mouth disease
sinusitis which involves infection of maxillary sinuses that causes pain or pressure over the cheeks just below the eyes, tooth ache, and headache
DOID:2051
C08.460.692.752.578
C08.730.749.578
C09.603.692.752.578
C01.748.749.578
mechanical ectropion
class of disease
ectropion
Human disease
DOID:1569
mechanical entropion
class of disease
entropion
Human disease
DOID:13112
mechanical lagophthalmos
class of disease
lagophthalmos
Human disease
DOID:13037
mechanical strabismus
class of disease
strabismus
Human disease
DOID:9306
meconium aspiration syndrome
class of disease
lung disease
perinatal respiratory disorder
disease
Human disease
DOID:11049
C08.381.520.687
C08.618.580
C13.703.277.785
C16.300.580
C16.614.580
Meconium aspiration syndrome
medial epicondylitis
class of disease
bone inflammation disease
arm injuries
disease
bone inflammation disease that results in inflammation located in epicondyle
DOID:14087
Golfer's elbow
median arcuate ligament syndrome
class of disease
vascular surgery
rare abdominal surgical disease
syndrome
Human disease
DOID:9892
C06.198.929C14.240.850.922
C14.907.137.527
C16.131.240.850.898
Median arcuate ligament syndrome
median nerve neuropathy
class of disease
mononeuritis of upper limb and mononeuritis multiplex
brachial plexus neuritis
Human disease
DOID:571
C10.668.829.500.500
mediastinal cancer
class of disease
thoracic cancer
mediastinal neoplasm
thoracic cancer that is located in the mediastinum
DOID:5559
Mediastinal cancers
mediastinal granular cell myoblastoma
class of disease
malignant mediastinal neurogenic neoplasm
granular cell tumor
mediastinal neurilemmoma
Human disease
DOID:5046
mediastinal gray zone lymphoma
class of disease
gray zone lymphoma
mediastinal malignant lymphoma
Human disease
DOID:6867
mediastinal lipomatosis
class of disease
lipomatosis
Human disease
DOID:3926
mediastinal malignant lymphoma
class of disease
mediastinal cancer
lymphoma
Human disease
DOID:6868
mediastinal melanocytic neurilemmoma
class of disease
melanotic neurilemmoma
Human disease
DOID:6484
mediastinal mesenchymal tumor
class of disease
mediastinal neoplasm
mesenchymal cell neoplasm
Human disease
DOID:5560
mediastinal neurilemmoma
class of disease
peripheral nerve schwannoma
mediastinal neoplasm
Human disease
DOID:6175
mediastinal osteogenic sarcoma
class of disease
extraosseous osteosarcoma
mediastinum sarcoma
Human disease
DOID:6208
mediastinitis
class of disease
connective tissue disease
mediastinal disease
inflammatory disease
disease
inflammatory process affecting the mediastinum
DOID:819
C08.846.187.790
mediastinum angiosarcoma
class of disease
angiosarcoma
mediastinum sarcoma
angiosarcoma and sarcoma of the mediastinum that is located in the mediastinum
DOID:4525
mediastinum leiomyoma
class of disease
leiomyoma
benign neoplasm of mediastinum
thoracic benign neoplasm
mediastinal neurilemmoma
Human disease
DOID:5123
mediastinum leiomyosarcoma
class of disease
mediastinum sarcoma
leiomyosarcoma
leiomyosarcoma and sarcoma of the mediastinum that derive from smooth muscle and are usually located in the esophagus or located in the main vessels
DOID:5292
mediastinum liposarcoma
class of disease
liposarcoma
mediastinum sarcoma
liposarcoma and mediastinum sarcoma that is located in the mediastinum
DOID:5713
mediastinum neurofibroma
class of disease
malignant mediastinal neurogenic neoplasm
neurofibroma
Human disease
DOID:12064
mediastinum rhabdomyosarcoma
class of disease
mediastinum sarcoma
rhabdomyosarcoma
rhabdomyosarcoma and sarcoma of the mediastinum that is located in the mediastinum and affects children and adolescents
DOID:4049
mediastinum sarcoma
class of disease
mediastinal cancer
sarcoma
mediastinal soft tissue cancer
sarcoma and malignant mediastinal mesenchymnal tumor that is located in the mediastinum
DOID:4050
mediastinum seminoma
class of disease
mediastinal cancer
extragonadal seminoma
mediastinal malignant germ cell tumor
germ cell cancer
Human disease
DOID:6249
mediastinum synovial sarcoma
class of disease
mediastinum sarcoma
synovial sarcoma
sarcoma of the mediastinum and synovial sarcoma that is located in the mediastinum
DOID:5488
mediastinum teratoma
class of disease
mediastinal cancer
mediastinal germ cell tumor
teratoma
Human disease
DOID:5568
medullary colon carcinoma
class of disease
colon carcinoma
colon carcinoma that is characterized by a solid growth pattern
DOID:0080183
medulloadrenal hyperfunction
class of disease
adrenal gland disease
Human disease
DOID:12257
medulloblastoma SHH activated
class of disease
medulloblastoma
human disease
DOID:0080703
medulloblastoma SHH activated and TP53 mutant
class of disease
medulloblastoma SHH activated
human disease
DOID:0080704
medulloblastoma SHH activated and TP53 wild-type
class of disease
medulloblastoma SHH activated
human disease
DOID:0080705
medulloblastoma WNT activated
class of disease
medulloblastoma
human disease
DOID:0080702
medulloblastoma non-WNT/non-SHH
class of disease
medulloblastoma
human disease
DOID:0080706
medulloblastoma non-WNT/non-SHH group 3
class of disease
medulloblastoma non-WNT/non-SHH
human disease
DOID:0080707
medulloblastoma non-WNT/non-SHH group 4
class of disease
medulloblastoma non-WNT/non-SHH
human disease
DOID:0080708
medulloepithelioma
class of disease
central nervous system primitive neuroectodermal neoplasm
Human disease
DOID:4790
Medulloepithelioma
medullomyoblastoma
class of disease
medulloblastoma
Human disease
DOID:3861
mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
class of disease
syndromic intellectual disability
autosomal dominant disease
human disease
DOID:0111403
megacolon
class of disease
colonic disease
disease
colonic disease that is characterized by an abnormal dilation of the colon
DOID:11372
C06.405.469.158.701
Megacolon
megaesophagus
class of disease
esophageal disease
disease
abnormal dilation of the esophagus not due to obstruction
DOID:13186
megalencephalic leukoencephalopathy with subcortical cysts 1
class of disease
megalencephalic leukoencephalopathy with subcortical cysts
genetic disease
autosomal recessive disease
human disease
DOID:0080316
meibomian cyst
class of disease
symptom or sign
internal hordeolum
blepharitis
disease
Cyst in the eyelid caused by chronic granulomatous inflammation of Meibomian gland
DOID:9903
C04.182.197
C11.338.300
Chalazion
melancholia
class of disease
symptom or sign
major depressive disorder
mental depression
disease
DSM-IV subtype of clinical depression
DOID:2848
melanoacanthoma
class of disease
seborrheic keratosis
Human disease
DOID:11684
melanocytic psammomatous MPNST
class of disease
malignant melanocytic neoplasm of the peripheral nerve sheath
Human disease
DOID:6344
melanoma and neural system tumor syndrome
class of disease
hereditary neoplastic syndromes
rare nervous system tumor
rare genetic developmental defect during embryogenesis
inherited nervous system cancer-predisposing syndrome
nervous system cancer
genetic nervous system disorder
inherited tumor
autosomal dominant disease
syndrome
Melanoma and neural system tumor syndrome is an extremely rare tumor association characterized by dual predisposition to melanoma and neural system tumors (typically astrocytoma; see this term)
DOID:0111511
melanoma in congenital melanocytic nevus
class of disease
skin melanoma
congenital melanocytic nevus
skin melanoma that arises from a congenital melanocytic nevus
DOID:0070327
melanoma with features of a Spitz nevus
class of disease
Spitzoid lesion
melanoma
skin melanoma
skin melanoma that is characterized by asymmetric shape, diameter greater than 1 cm, a lesion with a deep invasive component, and a high degree of cytologic atypia
DOID:0070326
Spitzoid melanoma
melanomatosis
class of disease
melanoma
Human disease
DOID:7206
melanotic medulloblastoma
class of disease
medulloblastoma
Human disease
DOID:3868
melanotic neurilemmoma
class of disease
neurilemmoma
Human disease
DOID:3205
melanotic neuroectodermal tumor
class of disease
bone benign neoplasm
neuroectodermal tumor
Human disease
DOID:166
C04.557.465.625.630
C04.557.580.625.630
Melanotic neuroectodermal tumor of infancy
melon allergy
class of disease
fruit allergy
fruit allergy triggered by Cucumis melo plant fruit food product.
DOID:0060509
melphalan allergy
class of disease
drug allergy
drug allergy that has allergic trigger melphalan
DOID:0040066
membranous glomerulonephritis
class of disease
glomerulonephritis
lupus nephritis
disease
human disease
DOID:10976
C12.777.419.570.363.625
C13.351.968.419.570.363.625
C20.111.535
Membranous glomerulonephritis
meningeal melanocytoma
class of disease
central nervous system melanocytic neoplasm
primary melanocytic tumor of central nervous system
malignant neoplasm of meninges
Human disease
DOID:5900
meningeal melanoma
class of disease
malignant leptomeningeal tumor
central nervous system melanocytic neoplasm
Human disease
DOID:6085
meningeal melanomatosis
class of disease
central nervous system melanocytic neoplasm
melanomatosis
malignant neoplasm of meninges
Human disease
DOID:8243
meninges hemangiopericytoma
class of disease
meningioma
hemangiopericytoma
malignant neoplasm of meninges
Human disease
DOID:4957
meninges sarcoma
class of disease
meningioma
malignant neoplasm of meninges
sarcoma
Human disease
DOID:7614
meningioma
class of disease
meningeal neoplasm
central nervous system cancer
disease
Tumor forms from meninges
DOID:3565
C04.557.580.520
C04.557.645.520
C04.588.614.250.580.500
C10.551.240.500.500
Meningioma
meningitis
class of disease
symptom or sign
encephalomyelitis
central nervous system disease
disease
inflammation of the membranes around the brain and spinal cord
DOID:9471
C10.228.614
Meningitis
meningocele
class of disease
spina bifida
cephalocele
Human disease
DOID:1088
C10.500.680.598
C16.131.666.680.598
C23.300.707.968
meningococcal meningitis
class of disease
bacterial meningitis
meningococcal disease
bacterial meningitis that has material basis in Neisseria meningitidis infection
DOID:0080176
DOID:9929
C01.150.252.223.500.750
C01.150.252.400.625.549.449
C10.228.228.180.500.750
C10.586.625.280.505
C01.207.180.500.750
meningoencephalitis
class of disease
symptom or sign
central nervous system disease
meningitis
encephalitis
neurological symptom
disease
central nervous system disease that involves encephalitis which occurs along with meningitis
DOID:10554
C10.228.140.430.550
C10.228.228.245.550
C10.228.228.570
C01.207.245.550
C01.207.570
C10.586.250.550
C10.586.625.500
meningothelial meningioma
class of disease
meningioma
Human disease
DOID:7212
meningovascular neurosyphilis
class of disease
tertiary neurosyphilis
syphilitic meningitis
Human disease
DOID:0050491
mental depression
class of disease
symptom or sign
mood disorder
neurological and physiological symptom
disease
state of low mood and aversion to activity, which can affect a person's thoughts, behavior, motivation, feelings, and sense of well-being
DOID:1596
F01.145.126.350
Depression (mood)
mental disorder
class of disease
disease
distressing thought or behavior pattern
DOID:150
F03
Mental and behavioural diseases and disorders
mepivacaine allergy
class of disease
drug allergy
drug allergy that has allergic trigger mepivacaine
DOID:0040010
meropenem allergy
class of disease
beta-lactam allergy
allergic asthma
beta-lactam allergy that has allergic trigger meropenem
DOID:0040038
mesangial proliferative glomerulonephritis
class of disease
glomerulonephritis
proliferative glomerulonephritis
lupus nephritis
glomerulonephritis associated primarily with the mesangium
DOID:4783
mesenchymal cell neoplasm
class of disease
cell type cancer
Human disease
DOID:3350
mesenchymal chondrosarcoma
class of disease
chondrosarcoma
mesenchymal cell neoplasm
small cell sarcoma
Human disease
DOID:4545
C04.557.450.565.280.280
C04.557.450.795.300.280
mesenchymoma
class of disease
connective tissue neoplasm
Human disease
DOID:2668
C04.557.435.500
mesenteric adenitis
class of disease
lymphadenitis
adenitis
lymphadenitis
DOID:10782
C06.844.520
C15.604.315.618
Mesenteric adenitis
mesenteric vascular occlusion
class of disease
peripheral vascular disease
mesenteric ischemia
Human disease
DOID:13252
C06.405.469.675
C06.844.550
C14.907.137.534
mesocestoidiasis
class of disease
parasitic helminthiasis infectious disease
parasitic helminthiasis infectious disease that involves parasitic cestode infection caused by Mesocestoides lineatus resulting in nausea, diarrhea, abdominal discomfort and vomiting
DOID:0050253
metabolic acidosis
class of disease
acidosis
acquired metabolic disease
disease
lactic acidosis that has material basis in high levels of acid
DOID:0050758
Metabolic acidosis
metabolic disease
class of disease
disease
nutritional and metabolic diseases
disease that involving errors in metabolic processes of building or degradation of molecules
DOID:0014667
C18.452
Metabolic diseases and disorders
metachronous kidney Wilms' tumor
class of disease
nephroblastoma
Human disease
DOID:5178
metachronous osteosarcoma of the bone
class of disease
osteosarcoma
Human disease
DOID:3379
metal allergy
class of disease
allergy
hypersensitivity reaction type I disease triggered by a metal
DOID:0060501
Metal allergies
metal metabolism disorder
class of disease
mineral metabolism disease
inherited metabolic disorder
inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals
DOID:896
C16.320.565.618
C18.452.648.618
metanephric adenoma
class of disease
renal adenoma
Human disease
DOID:6404
Metanephric adenoma
metaphyseal dysplasia
class of disease
osteochondrodysplasia
osteochondrodysplasia that results in thinning and the tendency to fracture located in bone
DOID:0080019
metatypical basal cell carcinoma
class of disease
basal-cell carcinoma
Human disease
DOID:4281
methemoglobinemia
class of disease
hemoglobinopathy
disease
a form of toxic anemia characterized by the presence of methemoglobin in the blood
DOID:10783
C15.378.619
Methemoglobinemia
methotrexate-associated lymphoproliferation
class of disease
lymphoma
Human disease
DOID:5821
methyl isocyanate allergic asthma
class of disease
isocyanates allergic asthma
allergic asthma to isocyanates that has allergic trigger methyl isocyanate
DOID:0040044
methylmalonic acidemia cblB type
class of disease
methylmalonic acidemia
genetic disease
vitamin B12-responsive methylmalonic acidemia
Human disease
DOID:0060743
methylmalonic aciduria and homocystinuria type cblE
class of disease
methylmalonic acidemia
methylmalonic acidemia with homocystinuria
Human disease
DOID:0050732
methylmalonic aciduria and homocystinuria type cblG
class of disease
methylmalonic acidemia
methylmalonic acidemia with homocystinuria
Human disease
DOID:0050733
microcystic adenoma
class of disease
pancreatic cystadenoma
benign neoplasms by histologic type
Human disease
DOID:5403
microcystic meningioma
class of disease
meningioma
Human disease
DOID:4594
microcystic variant infiltrating bladder urothelial carcinoma
class of disease
invasive bladder transitional cell carcinoma
Human disease
DOID:7971
microglandular adenosis
class of disease
breast disease
Human disease
DOID:5998
microglandular adenosis of breast
class of disease
microglandular adenosis
Human disease
DOID:8335
microinvasive cervical squamous cell carcinoma
class of disease
cervical squamous cell carcinoma
Human disease
DOID:8409
microinvasive gastric cancer
class of disease
gastric adenocarcinoma
Human disease
DOID:10541
microlissencephaly
class of disease
lissencephaly
human disease
DOID:0112234
micronodular basal cell carcinoma
class of disease
basal-cell carcinoma
Human disease
DOID:4289
microorchidism
class of disease
testicular disease
hypogonadism, male
congenital human disease
DOID:11994
Microorchidism
micropapillary variant infiltrating bladder urothelial carcinoma
class of disease
invasive bladder transitional cell carcinoma
Human disease
DOID:6976
micropapillomatosis labialis
class of disease
vulvar squamous papilloma
Vestibular papillomatosis
Human disease
DOID:6569
microphthalmia with brain and digit anomalies
class of disease
syndromic microphthalmia
autosomal dominant disease
human disease
DOID:0111805
microphthalmia–dermal aplasia–sclerocornea syndrome
class of disease
syndromic microphthalmia
syndrome
human disease
DOID:0111875
microscopic breast papilloma
class of disease
breast duct papilloma
Human disease
DOID:8225
microscopic colitis
class of disease
colitis
disease
colitis that can only be diagnosed by the examination of colon tissue under a microscope
DOID:0060182
C06.405.205.265.173
C06.405.469.158.188.173
Microscopic colitis
middle cerebral artery infarction
class of disease
cerebral arterial disease
cerebral infarction
cerebral artery occlusion
human disease
DOID:3525
C10.228.140.300.150.477.200.450
C10.228.140.300.510.200.387
C10.228.140.300.775.200.200.450
C14.907.253.092.477.200.450
C14.907.253.560.200.387
C14.907.253.855.200.200.450
middle ear adenoma
class of disease
sensory organ benign neoplasm
middle ear disease
neoplasm of middle ear
benign neoplasms by histologic type
benign neoplasm of ear
Human disease
DOID:5387
middle ear cancer
class of disease
neoplasm of middle ear
auricular cancer
middle ear disease
auditory system cancer that is located in the middle ear
DOID:5099
middle ear cholesterol granuloma
class of disease
otitis media
cholesteatoma
Human disease
DOID:10852
middle lobe syndrome
class of disease
lung disease
atelectasis
human disease
DOID:2810
C08.381.730.542
midface dysplasia
class of disease
osteochondrodysplasia
disease
Human disease
DOID:0050767
midline cystocele
class of disease
pelvic organ prolapse
cystocele
Human disease
DOID:14131
migraine
class of disease
encephalopathy
disease
disorder resulting in recurrent moderate-severe headaches
DOID:6364
C10.228.140.546.399.750
Migraine
migraine with aura
class of disease
migraine
migraine characterized by migraine headache which is preceded or accompanied by a transient focal neurological phenomenon
DOID:10024
C10.228.140.546.399.750.250
migraine without aura
class of disease
migraine
rare genetic headache disorder
migraine that is characterized by migraine headaches that are not accompanied by an aura
DOID:12783
C10.228.140.546.399.750.450
mild pre-eclampsia
class of disease
pre-eclampsia
pre-eclampsia characterized by the presence of hypertension without evidence of end-organ damage, in a woman who was normotensive before 20 weeks' gestation
DOID:10590
miliaria
class of disease
sweat gland disease
disease
Human disease
DOID:1382
C17.800.946.492
Miliaria (disease)
miliaria profunda
class of disease
miliaria
miliaria that is characterized by ductal occlusion of the papillary dermis causing the gland's secretions to leak between the superficial and deep layers of the skin resulting in a rapidly-spreading flesh-colored rash
DOID:0070320
miliaria pustulosa
class of disease
miliaria
miliaria that is characterized by pustules resulting from inflammation and bacterial infection
DOID:0070319
miliaria rubra
class of disease
miliaria
Human disease
DOID:11153
Miliaria rubra
milk allergy
class of disease
food allergy
disease
type of food allergy caused by milk
DOID:4376
C20.543.480.370.500
Milk allergy
mineral metabolism disease
class of disease
acquired metabolic disease
disorder of metabolite absorption and transport
acquired metabolic disease that is characterized by abnormal mineral metabolism
DOID:0050032
Disorders of mineral metabolism
minor vestibular glands adenoma
class of disease
vestibular gland benign neoplasm
adenoma
Human disease
DOID:2075
mirror agnosia
class of disease
agnosia
visual agnosia
agnosia that is a loss of the ability to acknowledge objects in the neglected field that are visible when a mirror reflects the object visible in the non-neglected field
DOID:0060144
mirror movement disorder
class of disease
synkinesis
movement disorders
movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs
DOID:0111153
mitochondrial DNA depletion syndrome 12b
class of disease
autosomal recessive disease
mitochondrial DNA depletion syndrome
mitochondrial DNA depletion syndrome 12
human disease
DOID:0080335
mitochondrial DNA depletion syndrome 14
class of disease
mitochondrial DNA depletion syndrome
human disease
DOID:0080336
mitochondrial DNA depletion syndrome 15
class of disease
autosomal recessive disease
mitochondrial DNA depletion syndrome
human disease
DOID:0080337
mitochondrial DNA depletion syndrome 17
class of disease
mitochondrial DNA depletion syndrome
human disease
DOID:0070448
mitochondrial DNA depletion syndrome 8b
class of disease
mitochondrial DNA depletion syndrome
autosomal recessive disease
human disease
DOID:0070331
mitochondrial complex III deficiency
class of disease
mitochondrial disease
mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial respiratory chain complex III
DOID:0111139
mitochondrial complex V (ATP synthase) deficiency
class of disease
mitochondrial disease
mitochondrial complex deficiency
mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial proton-transporting ATP synthase complex
DOID:0111143
mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1
class of disease
mitochondrial complex V (ATP synthase) deficiency
human disease
DOID:0111748
mitochondrial complex V (ATP synthase) deficiency nuclear type 6
class of disease
mitochondrial complex V (ATP synthase) deficiency
human disease
DOID:0111749
mitochondrial nonsyndromic sensorineural deafness
class of disease
sensorineural hearing loss
mitochondrial deafness
human disease
DOID:0111751
mitochondrial type mitochondrial complex I deficiency
class of disease
mitochondrial complex I deficiency
human disease
DOID:0112100
mitochondrial type mitochondrial complex I deficiency 1
class of disease
mitochondrial type mitochondrial complex I deficiency
human disease
DOID:0112101
mitral valve disease
class of disease
heart valve disease
Human disease
DOID:61
Mitral valve diseases
mitral valve insufficiency
class of disease
mitral valve disease
valve insufficiency
disease
disorder of the heart in which the mitral valve does not close properly when the heart pumps out blood
DOID:11502
C14.280.484.461
Mitral valve insufficiency
mitral valve stenosis
class of disease
mitral valve disease
heart valve stenosis
disease
mitral valve disease that is characterized by the narrowing of the orifice of the mitral valve of the heart
DOID:1754
C14.280.484.517
Mitral valve stenosis
mixed astrocytoma-ependymoma
class of disease
mixed glioma
Human disease
DOID:7907
mixed astrocytoma-ependymoma-oligodendroglioma
class of disease
mixed glioma
Human disease
DOID:7817
mixed cell adenoma
class of disease
adenoma
Human disease
DOID:5385
mixed cell type adenoma of parathyroid
class of disease
parathyroid adenoma
mixed cell adenoma
Human disease
DOID:7610
mixed cell type kidney Wilms' tumor
class of disease
nephroblastoma
Human disease
DOID:5179
mixed cerebral palsy
class of disease
cerebral palsy
subtype of cerebral palsy characterized by both the tight muscle tone of spastic cerebral palsy and the writhing, involuntary muscle movements of athetoid cerebral palsy
DOID:0050673
mixed ductal-endocrine carcinoma
class of disease
pancreatic ductal adenocarcinoma
Human disease
DOID:7716
mixed endometrial stromal and smooth muscle tumor
class of disease
uterine corpus cancer
Human disease
DOID:8302
mixed epithelial stromal tumour
class of disease
malignant mixed tumor
Human disease
DOID:5088
mixed epithelial tumor of ovary
class of disease
ovarian benign neoplasm
Human disease
DOID:6211
mixed epithelial/mesenchymal metaplastic breast carcinoma
class of disease
breast metaplastic carcinoma
Human disease
DOID:7541
mixed extragonadal germ cell cancer
class of disease
mixed germ cell cancer
mixed germ cell cancer that is located in areas of the body other than the ovary or testicle
DOID:0050907
mixed fibrolamellar hepatocellular carcinoma
class of disease
fibrolamellar hepatocellular carcinoma
fibrolamellar carcinoma that is characteirzed by the presence of both pure fibrolamellar hepatocellular carcinoma and conventional hepatocellular carcinoma components
DOID:0080182
mixed germ cell cancer
class of disease
germ cell cancer
germ cell cancer that occurs in many forms
DOID:3306
Mixed germ cell neoplasia
mixed germ cell-sex cord neoplasm
class of disease
malignant mixed tumor
sex cord-gonadal stromal tumor
Human disease
DOID:2996
mixed glioma
class of disease
glioma
Human disease
DOID:5076
mixed gonadal dysgenesis X0/XY
class of disease
Turner syndrome
gonadal dysgenesis
disease
intersex variation
DOID:14449
DOID:0080656
C12.706.316.309.391
C12.706.316.795.249
C13.351.875.253.309.391
C13.351.875.253.795.249
C16.131.260.830.835.249
C16.131.939.316.309.391
C16.131.939.316.795.249
C16.320.180.830.835.249
C19.391.119.309.391
C19.391.119.795.249
mixed hepatoblastoma
class of disease
hepatoblastoma
Human disease
DOID:5789
mixed lacrimal gland cancer
class of disease
lacrimal gland cancer
Human disease
DOID:296
mixed liposarcoma
class of disease
liposarcoma
Human disease
DOID:5703
mixed malaria
class of disease
malaria
malaria that involves infection with more than one species of Plasmodium at the same time
DOID:14325
mixed oligodendroglioma-astrocytoma
class of disease
mixed glioma
Human disease
DOID:7912
mixed phenotype acute leukemia with MLL rearranged
class of disease
acute biphenotypic leukaemia
human disease
DOID:0081037
mixed phenotype acute leukemia, B/myeloid
class of disease
acute biphenotypic leukaemia
human disease
DOID:0081038
mixed receptive-expressive language disorder
class of disease
communication disorder
neurodevelopmental condition
DOID:12685
mixed sleep apnea
class of disease
sleep apnea
human disease
DOID:0080302
mixed testicular germ cell tumor
class of disease
testicular malignant germ cell cancer
mixed germ cell cancer
mixed germ cell cancer that is located in the testis
DOID:4743
mixed type rhabdomyosarcoma
class of disease
rhabdomyosarcoma
Human disease
DOID:4065
mixed type thymoma
class of disease
thymoma
Human disease
DOID:3280
mixed-type liposarcoma
class of disease
liposarcoma
Human disease
DOID:5709
mollusc allergy
class of disease
shellfish allergy
shellfish allergy triggered by Mollusca
DOID:0060523
molybdenum cofactor deficiency type A
class of disease
molybdenum cofactor deficiency
genetic disease
human disease
DOID:0111164
monoclonal gammopathy of uncertain significance
class of disease
monoclonal gammopathy
blood protein disease
human disease
DOID:7442
C15.378.147.542.640
C15.378.147.780.570
C20.683.460.640
C20.683.780.640
monoclonal paraproteinemia
class of disease
plasma protein metabolism disease
paraproteinemia
monoclonal gammopathy
Human disease
DOID:2346
monocular esotropia
class of disease
esotropia
Human disease
DOID:10293
monocular exotropia
class of disease
exotropia
Human disease
DOID:11853
monocyte, dendritic cell, and NK cell deficiency
class of disease
combined immunodeficiency
human disease
DOID:0111966
monocytic leukemia
class of disease
myeloid leukemia
type of myeloid leukemia characterized by a dominance of monocytes in the marrow
DOID:8527
monodermal teratoma
class of disease
ovarian germ cell teratoma
Human disease
DOID:5207
monofixation syndrome
class of disease
strabismus
Human disease
DOID:9843
Monofixation syndrome
monogenic disease
class of disease
genetic disease
Human disease
DOID:0050177
mononeuritis
class of disease
mononeuropathy
Human disease
DOID:1802
mononeuritis multiplex
class of disease
mononeuritis of upper limb and mononeuritis multiplex
Human disease
DOID:1835
mononeuritis of lower limb
class of disease
mononeuritis
Human disease
DOID:9473
mononeuritis of upper limb
class of disease
mononeuritis of upper limb and mononeuritis multiplex
Human disease
DOID:1844
mononeuritis of upper limb and mononeuritis multiplex
class of disease
mononeuritis
Human disease
DOID:572
mononeuropathy
class of disease
peripheral neuropathy
disease
neuropathy that is characterized by damage to a single nerve, which results in loss of movement, sensation, or other function of that nerve
DOID:1188
C10.668.829.500
monophasic synovial sarcoma
class of disease
synovial sarcoma
Human disease
DOID:5495
mood disorder
class of disease
mental disorder
any of various disorders characterised primarily by disturbance in an individual's mood
DOID:3324
F03.600
Mood disorders
morbid obesity
class of disease
obesity
human disease
DOID:11981
C18.654.726.500.700
C23.888.144.699.500.500
E01.370.600.115.100.160.120.699.500.500
G07.100.100.160.120.699.500.500
Obesity
morpheaform basal cell carcinoma
class of disease
basal-cell carcinoma
Human disease
DOID:4292
morphine dependence
class of disease
opiate dependence
opiate dependence that involves the continued use of morphine despite despite problems related to use of the substance
DOID:2560
C25.775.675.600
mosaic variegated aneuploidy syndrome
class of disease
syndrome
aneuploidy
human disease
DOID:0080688
mosaic variegated aneuploidy syndrome 3
class of disease
autosomal recessive disease
mosaic variegated aneuploidy syndrome
human disease
DOID:0080689
motility-related diarrhea
class of disease
diarrhea
Human disease
DOID:0050131
motor neuritis
class of disease
motor neuron disease
Human disease
DOID:683
motor neuron disease
class of disease
neurological disorder
neurodegeneration
disease
group of neurological disorders affecting motor neurons
DOID:231
C10.574.562
C10.668.467
Motor neuron diseases
mouth cancer
class of disease
gastrointestinal system cancer
mouth disease
oral cavity neoplasm
head and neck cancer
disease
gastrointestinal system cancer that is located in the oral cavity
DOID:8618
Oral cancer
mouth disease
class of disease
gastrointestinal system disease
stomatognathic disease
disease of anatomical entity
disease
gastrointestinal system disease that is located in the mouth
DOID:403
C07.465
Diseases and disorders of oral cavity, salivary glands and jaws
movement disorders
class of disease
encephalopathy
motor dysfunction
disease
clinical syndromes with either an excess of movement or a paucity of voluntary and involuntary movements
DOID:480
C10.228.662
Movement disorders
mpox
class of disease
symptom or sign
notifiable disease
viral infectious disease
Poxviridae infectious disease
zoonosis
disease
viral disease
DOID:3292
C01.925.256.743.615
C22.735.750
C22.795.600
Monkeypox
mu chain disease
class of disease
heavy chain disease
heavy chain disease that results from an overproduction of mu antibody (IgM)
DOID:0060128
mucin-rich endometrial endometrioid adenocarcinoma
class of disease
endometrial adenocarcinoma
Human disease
DOID:7293
mucinosis
class of disease
connective tissue disease
metabolic disease
human disease
DOID:3141
C17.300.550
Mucinoses
mucinous adenocarcinoma
class of disease
adenocarcinoma
adenocarcinoma that derives from epithelial cells originating in glandular tissue, which produce mucin
DOID:3030
C04.557.470.200.025.075
C04.557.470.590.075
Pseudomyxoma peritonei
mucinous adenofibroma
class of disease
adenofibroma
Human disease
DOID:2700
mucinous cystadenocarcinoma
class of disease
cystadenocarcinoma
mucinous tumor
cystadenocarcinoma that derives from epithelial cells originating in glandular tissue, with a capsulated structure and mucus-producing cells
DOID:3603
C04.557.470.200.025.480.225
C04.557.470.590.480.225
mucinous cystadenocarcinoma of the lung
class of disease
adenocarcinoma of the lung
mucinous cystadenocarcinoma
lung adenocarcinoma that is a very rare malignant mucus-producing neoplasm arising from the uncontrolled growth of transformed epithelial cells originating in lung tissue
DOID:0080304
mucinous cystadenofibroma
class of disease
cystadenofibroma
benign neoplasm characterized by the presence of cystic structures lined by mucinous columnar epithelial cells in a fibrotic stroma
DOID:6468
mucinous intrahepatic cholangiocarcinoma
class of disease
intrahepatic cholangiocarcinoma
bile duct mucinous adenocarcinoma
Human disease
DOID:7024
mucinous lung adenocarcinoma
class of disease
adenocarcinoma of the lung
mucinous adenocarcinoma
lung adenocarcinoma with tumor cells floating in pools of mucin that distend alveolar spaces
DOID:0080303
mucinous ovarian cystadenoma
class of disease
ovarian cystadenoma
mucinous cystadenoma
Human disease
DOID:3267
Mucinous cystoadenoma of the ovary
mucinous pancreas adenocarcinoma
class of disease
pancreatic adenocarcinoma
mucinous adenocarcinoma
human disease
DOID:0080782
mucinous stomach adenocarcinoma
class of disease
gastric diffuse adenocarcinoma
mucinous adenocarcinoma
Human disease
DOID:3716
mucinous tubular and spindle cell carcinoma
class of disease
renal cell carcinoma
tubulopathy
spindle cell carcinoma
human disease
DOID:4472
Mucinous tubular and spindle cell carcinoma
mucocele of appendix
class of disease
intestinal disease
mucocele
Human disease
DOID:13248
mucoepidermoid esophageal carcinoma
class of disease
esophageal carcinoma
mucoepidermoid carcinoma
Human disease
DOID:4686
mucoepidermoid thyroid carcinoma
class of disease
thyroid carcinoma
mucoepidermoid carcinoma
thyroid gland adenocarcinoma
Human disease
DOID:4687
mucolipidosis type III gamma
class of disease
pseudo-Hurler polydystrophy
mucolipidosis
autosomal recessive disease
human disease
DOID:0080678
mucopolysaccharidosis IV
class of disease
human disease
DOID:0050808
mucopolysaccharidosis Ih
class of disease
autosomal recessive disease
mucopolysaccharidosis I
human disease
DOID:0111390
mucopolysaccharidosis Ih/s
class of disease
autosomal recessive disease
mucopolysaccharidosis I
human disease
DOID:0111389
mucopolysaccharidosis type IIIA
class of disease
Sanfilippo syndrome
autosomal recessive disease
human disease
DOID:0111395
mucopolysaccharidosis type IIIB
class of disease
Sanfilippo syndrome
autosomal recessive disease
human disease
DOID:0111394
mucopolysaccharidosis type IIIC
class of disease
autosomal recessive disease
Sanfilippo syndrome
human disease
DOID:0111393
mucopolysaccharidosis type IIID
class of disease
autosomal recessive disease
Sanfilippo syndrome
human disease
DOID:0111402
mucopolysaccharidosis type IVA
class of disease
Morquio syndrome
autosomal recessive disease
human disease
DOID:0111391
mucopolysaccharidosis type IVB
class of disease
autosomal recessive disease
Morquio syndrome
human disease
DOID:0111392
mucormycosis
class of disease
symptom or sign
zygomycosis
opportunistic mycosis
disease
fungal infection by the order Mucorales
DOID:8485
DOID:0050595
C01.150.703.980.600
mucosal melanoma
class of disease
melanoma
extracutaneous melanoma
melanoma that has material basis in melanocytes located in mucosal membranes lining the respiratory, gastrointestinal and urogenital tract
DOID:0050929
mucositis
class of disease
skin disease
gastrointestinal system disease
gastrointestinal system disease that is characterized by painful inflammation and ulceration of the mucous membranes lining the digestive tract
DOID:0080178
C06.405.205.798
C07.465.584
Mucositis
multicentric papillary thyroid carcinoma
class of disease
papillary thyroid cancer
Human disease
DOID:7086
multicentric reticulohistiocytosis
class of disease
Reticulohistiocytosis
syndrome
syndrome that is characterized by papulonodular skin lesions containing a proliferation of true macrophages associated with arthritis
DOID:11824
multifocal dystonia
class of disease
dystonia
dystonia that involves two or more unrelated body parts
DOID:0050837
multifocal osteogenic sarcoma
class of disease
osteosarcoma
bone sarcoma
Human disease
DOID:3360
multilocular cystic clear cell renal cell carcinoma
class of disease
renal cell carcinoma
renal clear cell carcinoma
human disease
DOID:4463
multiminicore disease
class of disease
human disease
DOID:0080991
multinodular goiter
class of disease
goiter
nodular goiter
goiter characterized by a multinodular enlargement of the thyroid gland
DOID:0050489
multiple benign circumferential skin creases on limbs
class of disease
skin disease
human disease
DOID:0112241
multiple chemical sensitivity
class of disease
syndrome
chronic medical condition of disputed but probably multifactorial etiology (genetic and non-genetic)
DOID:4661
C20.543.312.500
C21.223.500
Multiple chemical sensitivity
multiple congenital anomalies-hypotonia-seizures syndrome
class of disease
lipid metabolism disorder
lipid metabolism disorder that is characterized by phosphatidylinositol glycan anchor biosynthesis class A (PIGA) deficiency
DOID:0080503
multiple cranial nerve palsy
class of disease
glossopharyngeal nerve disease
cranial nerve disease
Human disease
DOID:13866
multiple endocrine neoplasia
class of disease
endocrine gland neoplasm
multiple polyglandular tumor
human disease
DOID:3125
C04.588.322.400
C04.651.600
C04.700.630
C16.320.700.630
C19.344.400
Multiple endocrine neoplasia
multiple epiphyseal dysplasia 2
class of disease
multiple epiphyseal dysplasia
genetic disease
autosomal dominant disease
multiple epiphyseal dysplasia due to collagen 9 anomaly
multiple epiphyseal dysplasia due to collagen 9 anomaly that has material basis in heterozygous mutation in the COL9A2 gene on chromosome 1p34
DOID:0070298
multiple epiphyseal dysplasia 3
class of disease
multiple epiphyseal dysplasia
genetic disease
multiple epiphyseal dysplasia due to collagen 9 anomaly
autosomal dominant disease
multiple epiphyseal dysplasia due to collagen 9 anomaly that has material basis in heterozygous mutation in the COL9A3 gene on chromosome 20q13
DOID:0070304
multiple epiphyseal dysplasia 7
class of disease
multiple epiphyseal dysplasia
genetic disease
autosomal recessive disease
multiple epiphyseal dysplasia that has material basis in homozygous mutation in the CANT1 gene on chromosome 17q25
DOID:0070302
multiple epiphyseal dysplasia due to collagen 9 anomaly
class of disease
multiple epiphyseal dysplasia
genetic disease
monogenic disease
multiple epiphyseal dysplasia that has material basis in mutation in any of the members of the COL9A gene family (COL9A1, COL9A2, COL9A3)
DOID:0070305
multiple epiphyseal dysplasia with myopia and deafness
class of disease
syndrome
autosomal dominant disease
human disease
DOID:0111348
multiple mitochondrial dysfunctions syndrome 6
class of disease
fatal multiple mitochondrial dysfunctions syndrome
autosomal recessive disease
human disease
DOID:0070332
multiple mucosal neuroma
class of disease
neuroma
Human disease
DOID:5155
multiple myeloma
class of disease
leukocyte disease
myeloid neoplasm
immunoproliferative disorder
disease
cancer of plasma cells
DOID:9538
C04.557.595.500
C14.907.454.460
C15.378.147.780.650
C15.378.463.515.460
C20.683.515.845
C20.683.780.650
Multiple myeloma
multiple spinal canal and spinal cord meningioma
class of disease
spinal canal and spinal cord meningioma
Human disease
DOID:7646
multisystem proteinopathy
class of disease
motor neuron disease
human disease
DOID:070355
mumps
class of disease
symptom or sign
parotitis
mumps virus infectious disease
herpangina
salivary gland disease
disease
Human disease caused by paramyxovirus
DOID:10264
C01.925.782.580.600.680.500
C07.465.815.470.800.630
Mumps
muscle neoplasm
class of disease
soft tissue neoplasm
muscular disease
tumors or cancer located in muscle tissue or specific muscles
DOID:461
C04.588.839.500
C05.651.494
muscle tissue disease
class of disease
muscular disease
disease involving the muscle tissue
DOID:66
muscular atrophy
class of disease
muscular disease
atrophic muscular disease
clinical sign
human disease
DOID:767
C10.597.613.612
C23.300.070.500
C23.888.592.608.612
Muscle wasting
musculoskeletal disorder
class of disease
disease of anatomical entity
disease of anatomical entity that occurs in the muscular and/or skeletal system
DOID:17
C05
Diseases and disorders of the musculoskeletal system
musculoskeletal system benign neoplasm
class of disease
organ system benign neoplasm
musculoskeletal neoplasm
organ system benign neoplasm that is located in the muscular and skeletal organs
DOID:0060099
musculoskeletal system cancer
class of disease
organ system cancer
musculoskeletal disorder
musculoskeletal neoplasm
organ system cancer located in the muscular and skeletal organs and characterized by uncontrolled cellular proliferation of the musculoskeletal organs
DOID:0060100
mushroom workers' lung
class of disease
extrinsic allergic alveolitis
Human disease
DOID:2708
mycoplasma infection
class of disease
bacterial infectious disease
primary Mycoplasmataceae infectious disease
disease
bacterial infection with a species of the genus Mycoplasma
DOID:0050407
DOID:5461
C01.150.252.400.610.610
mycosis fungoides
class of disease
cutaneous T cell lymphoma
rare disease
mycosis fungoides and variants
disease
Human disease
DOID:8691
C04.557.386.480.750.800.550
C15.604.515.569.480.750.800.550
C20.683.515.761.480.750.800.550
Mycosis fungoides
mycotic corneal ulcer
class of disease
corneal ulcer
Human disease
DOID:10440
myelitis
class of disease
spinal cord disease
spinal cord disease that is characterized by inflammation of the white matter or gray matter of the spinal cord
DOID:322
C10.228.228.618
C10.228.854.525
Myelitis
myelodysplastic syndrome
class of disease
myeloproliferative disorders
neoplastic syndrome
disease
diverse collection of blood-related medical conditions with ineffective production of the myeloid class of blood cells
DOID:0050908
C15.378.190.625
Myelodysplastic syndrome
myelodysplastic/myeloproliferative neoplasm
class of disease
myeloid neoplasm
myeloid neoplasm that results in the overproduction of white blood cells
DOID:4972
myelofibrosis
class of disease
myeloid neoplasm
acquired aplastic anemia
rare genetic immune disease
disease
myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue
DOID:4971
C15.378.190.636.765
myeloid and lymphoid neoplasms associated with FGFR1 abnormalities
class of disease
myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the FGFR1 gene, resulting in translocations with an 8p11 breakpoint
DOID:0080167
myeloid and lymphoid neoplasms associated with PDGFRA rearrangement
class of disease
myeloid neoplasm associated with PDGFRA rearrangement
myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the PDGFRA gene, most often resulting in the formation of FIP1L1-PDGFRA fusion transcripts
DOID:0080165
myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
class of disease
myeloid neoplasm
myeloid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR1
human disease
DOID:0080164
myeloid leukemia
class of disease
leukemia
disease
leukemia that is located in myeloid tissue
DOID:8692
C04.557.337.539
Myeloid leukemias
myeloid leukemia associated with Down Syndrome
class of disease
acute megakaryoblastic leukemia
human disease
DOID:0080798
myeloid neoplasm
class of disease
myeloproliferative disorders
a bone marrow cancer that is formed of any one of the bone marrow cells belonging to the granulocytic (neutrophil, eosinophil, basophil), monocytic/macrophage, erythroid, megakaryocytic and mast cell lineages.
DOID:0070004
myeloid neoplasms associated with PDGFRB rearrangement
class of disease
myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the PDGFRB gene, most often resulting in the formation of ETV6-PDGFRB fusion transcripts
DOID:0080166
myeloid sarcoma
class of disease
hematologic cancer
solid tumor composed of immature white blood cells[2] called myeloblasts.
DOID:8683
C04.557.337.539.775
C04.557.450.795.853
Myeloid sarcoma
myelophthisic anemia
class of disease
aplastic anemia
aplastic anemia that is characterized by displacement of hemopoietic bone-marrow tissue either by fibrosis, tumors or granulomas
DOID:2354
C15.378.071.307
C15.378.190.636.085
myeloproliferative disorder, chronic, with eosinophilia
class of disease
myeloproliferative disorders
eosinophilia
myeloproliferative neoplasm
human disease
DOID:0111344
myeloproliferative disorders
class of disease
bone marrow disease
tumor of hematopoietic and lymphoid tissues
connective tissue neoplasm
hematologic cancer
disease
hematopoietic disorders that derive from the blood-forming stem cells of the bone marrow
DOID:4960
C15.378.190.636
Myeloid neoplasms
myeloproliferative neoplasm
class of disease
myeloid neoplasm
myeloproliferative disorders
myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood
DOID:2226
myoblastoma
class of disease
muscle neoplasm
human disease
DOID:5039
myocardial stunning
class of disease
myocardial infarction
state when some section of the myocardium (corresponding to area of a major coronary occlusion) shows a form of contractile abnormality
DOID:9767
C14.280.671
C23.888.582
myocarditis
class of disease
symptom or sign
extrinsic cardiomyopathy
myocardial disorder
pancarditis
cardiovascular system symptom
disease
extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle
DOID:820
C14.280.238.625
Myocarditis
myocardium cancer
class of disease
neoplasm of myocardium
heart cancer
human disease
DOID:9299
myoclonic cerebellar dyssynergia
class of disease
neurodegeneration
nervous system heredodegenerative disease
Ramsay Hunt syndrome
degenerative, neurological disorder characterized by myoclonus epilepsy, intention tremor, progressive ataxia and occasionally cognitive impairment
DOID:12707
C10.228.140.252.700.250
C10.228.854.787.500
C10.574.500.825.250
C16.320.400.780.500
myoclonic dystonia 11
class of disease
myoclonic dystonia
genetic disease
autosomal dominant disease
myoclonic dystonia characterized by autosomal dominant inheritance and association with psychiatric disorder that has material basis in heterozygous mutation in the SGCE gene on chromosome 7q21
DOID:0090034
myoclonic dystonia 15
class of disease
myoclonic dystonia
genetic disease
autosomal dominant disease
myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11
DOID:0090035
myoepithelial carcinoma
class of disease
carcinoma
carcinoma that derives from myoepithelial cells
DOID:4838
myoepithelioma of the head and neck
class of disease
sweat gland neoplasm
neoplasm composed of outgrowths of myoepithelial cells from a sweat gland
DOID:2661
C04.557.435.585
Myoepithelioma of the head and neck
myofascial pain syndrome
class of disease
muscular disease
medically unexplained physical symptom
myalgia
disease
human disease
DOID:431
C05.651.550
myofibrillar myopathy
class of disease
muscular disease
myopathy that is characterized by slowly progressive muscle weakness that can involve both proximal muscles and distal muscles
DOID:0080307
myofibrillar myopathy 10
class of disease
autosomal recessive disease
myofibrillar myopathy
human disease
DOID:0112108
myofibrillar myopathy 3
class of disease
myofibrillar myopathy
autosomal dominant disease
Human disease
DOID:0080094
myofibroma
class of disease
connective tissue neoplasm
benign perivascular tumor
connective tissue benign neoplasm
Human disease
DOID:4386
C04.557.450.565.540
C17.300.680.540
myoma
class of disease
muscle neoplasm
uterine benign neoplasm
disease
human disease
DOID:2691
C04.557.450.590.540
Uterine fibroids
myopathy of extraocular muscle
class of disease
peripheral neuropathy
rare eye disease
muscular disease
myopathy that involves the extra-ocular muscle
DOID:929
myopathy, lactic acidosis, and sideroblastic anemia 1
class of disease
myopathy, lactic acidosis, and sideroblastic anemia
human disease
DOID:0111185
myopathy, lactic acidosis, and sideroblastic anemia 2
class of disease
myopathy, lactic acidosis, and sideroblastic anemia
A myopathy, lactic acidosis, and sideroblastic anemia characterized by marked phenotypic variablity in time of onset and severity of symptoms that has material basis in homozyous or compound heterozygous mutation in YARS2 on 12p11.21.
DOID:0111186
myopathy, lactic acidosis, and sideroblastic anemia 3
class of disease
myopathy, lactic acidosis, and sideroblastic anemia
human disease
DOID:0111184
myopathy, myofibrillar, 11
class of disease
myofibrillar myopathy
human disease
DOID:0081338
myopia
class of disease
symptom or sign
refractive error
visual impairment
disease
visual defect which causes to see the near objects clearly and far objects unclearly
DOID:11830
C11.744.636
Myopia
myosarcoma
class of disease
musculoskeletal system cancer
muscle tissue neoplasm
muscular disease
musculoskeletal system cancer that is located in muscle
DOID:4045
C04.557.450.590.550
C04.557.450.795.550
myositis
class of disease
muscular disease
inflammation
disease
myopathy characterized by muscle inflammation
DOID:633
C05.651.594
C10.668.491.562
myositis fibrosa
class of disease
myositis
Human disease
DOID:9788
myositis ossificans
class of disease
myositis
heterotopic ossification
myositis that is accompanied by ossification of muscle tissue or bony deposits in the muscles
DOID:668
C05.651.594.638
myotonic cataract
class of disease
cataract
Human disease
DOID:82
myotonic disease
class of disease
muscular dystrophy
muscular dystrophy characterized by progressive muscle wasting and weakness
DOID:450
C05.651.662
C10.668.491.606
myringitis bullosa hemorrhagica
class of disease
tympanic membrane disease
disease
tympanic membrane disease that is characterized by blisters on the eardrum resulting from infection
DOID:13791
myxedema
class of disease
hypothyroidism
mucinosis
disease
Human disease
DOID:11634
C17.300.550.590
C19.874.482.638
Myxedema
myxofibrosarcoma
class of disease
fibrous histiocytoma
skeletal muscle cancer
rare nervous system tumor
peripheral neuropathy
fibrosarcoma
fibromyxoid tumor
sarcoma
A malignant fibroblastic neoplasm arising from the soft tissue. It is characterized by the presence of spindle-shaped cells, cellular pleomorphism, thin-walled blood vessels, fibrous septa, and myxoid stroma.
DOID:0080534
myxoid chondrosarcoma
class of disease
chondrosarcoma
myxoid tumor
human disease
DOID:5861
myxoid leiomyosarcoma
class of disease
leiomyosarcoma
Human disease
DOID:5268
myxoid liposarcoma of the ovary
class of disease
liposarcoma of the ovary
myxoid liposarcoma
Human disease
DOID:8023
myxomatous pattern testicular yolk sac tumor
class of disease
testicular yolk sac tumor
Human disease
DOID:8081
myxopapillary ependymoma
class of disease
benign ependymoma
human disease
DOID:5075
myxosarcoma
class of disease
sarcoma
connective tissue neoplasm
human disease
DOID:4136
C04.557.450.565.560
C04.557.450.795.560
nail disease
class of disease
integumentary system disease
integumentary system disease that is located in nail
DOID:4123
C17.800.529
Diseases and disorders of the nails
nanophthalmos
class of disease
microphthalmia
human disease
DOID:0080634
narcissistic personality disorder
class of disease
personality disorder
narcissism
disease
personality disorder that involves an excessive preoccupation with issues of personal adequacy, power, prestige and vanity
DOID:2745
F03.675.500
Narcissistic personality disorder
narcolepsy
class of disease
disease
sleep disorder
excessive daytime sleepiness
Human sleep disorder that involves an excessive urge to sleep and other neurological features
DOID:8986
C10.886.425.800.200.750
F03.870.400.800.200.750
Narcolepsy
nasal cavity cancer
class of disease
sensory system cancer
nasal cancer
nasal cavity neoplasm
nasal cavity disease
respiratory system cancer
respiratory system cancer that is located in the nasal cavity
DOID:10811
nasal cavity disease
class of disease
nose disease
respiratory disease
DOID:2163
nasal cavity lymphoma
class of disease
nasal cavity cancer
lymphoma
human disease
DOID:10813
nasal cavity olfactory neuroblastoma
class of disease
nasal cavity cancer
esthesioneuroblastoma
Human disease
DOID:10812
nasopharyngeal disease
class of disease
upper respiratory tract disease
pharyngeal diseases
respiratory disease
DOID:9561
C07.550.350
C09.775.350
nasopharyngitis
class of disease
nasopharyngeal disease
respiratory disease
DOID:10460
C07.550.350.700
C07.550.781.500
C08.730.561.500
C09.775.350.700
C09.775.649.500
natural killer cell leukemia
class of disease
lymphoblastic leukemia
leukocyte disease
rare bone disease
immune disorder
disease
Human disease
DOID:1035
near-fatal asthma
class of disease
acute asthma
human disease
DOID:0080823
necrobiosis lipoidica
class of disease
skin disease
diabetic dermadrome
necrobiotic disorders
human disease
DOID:3486
C17.300.200.495.545
C17.800.550.545
C17.800.849.495
C18.452.880.495
Necrobiosis lipoidica
necrosis of ear ossicle
class of disease
middle ear disease
ear disease
Human disease
DOID:11783
necrosis of pituitary
class of disease
pituitary gland disease
endocrine disease
DOID:3646
necrotizing enterocolitis
class of disease
gastrointestinal system disease
disease
human disease
DOID:8677
C06.405.205.596.700
C06.405.469.363.700
Neonatal necrotizing enterocolitis
necrotizing fasciitis
class of disease
symptom or sign
fasciitis
necrotizing soft tissue infection
disease
infection that results in the death of the body's soft tissue
DOID:9602
C01.252.825.340
C05.321.550
Necrotizing fasciitis
File:Necrotizing fasciitis left leg.JPEG
necrotizing gastritis
class of disease
gastritis
necrosis
chronic gastritis
Human disease
DOID:4037
necrotizing sialometaplasia
class of disease
salivary gland disease
disease
Human disease
DOID:12901
C07.465.815.802
Necrotizing sialometaplasia
nemaline myopathy 2
class of disease
nemaline myopathy
genetic disease
autosomal recessive disease
nemaline myopathy that has material basis in homozygous or compound heterozygous mutation in the NEB gene on chromosome 2q23
DOID:0110928
nemaline myopathy 3
class of disease
nemaline myopathy
genetic disease
autosomal recessive disease
nemaline myopathy that has material basis in homozygous, compound heterozygous, or heterozygous mutation in the ACTA1 gene on chromosome 1q42
DOID:0110927
neomycin sulfate allergic contact dermatitis
class of disease
allergic contact dermatitis
drug allergy
allergic contact dermatitis that has allergic trigger neomycin sulfate
DOID:0040067
neonatal anemia
class of disease
anemia
Human disease
DOID:11244
C15.378.071.363
C16.614.053
neonatal diabetes mellitus
class of disease
diabetes
neonatal metabolic disturbances
rare genetic diabetes mellitus
It is a congenital form of diabetes
DOID:11717
neonatal infective mastitis
class of disease
mastitis
perinatal infectious disease
Human disease
DOID:13520
neonatal jaundice
class of disease
pigmentation disorder
jaundice
neonatal hyperbilirubinemia
disease
pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant
DOID:2383
C16.614.451.500
C23.550.429.249.500
Neonatal jaundice
neonatal leukemia
class of disease
childhood leukemia
perinatal disease
Human disease
DOID:7756
neonatal myasthenia gravis
class of disease
myasthenia gravis
Human disease
DOID:14043
C10.114.656.650
C10.668.758.725.650
C20.111.258.500.650
neonatal period electroclinical syndrome
class of disease
electroclinical syndrome
perinatal disease
electroclinical syndrome with onset in the neonatal period less than 44 weeks of gestational age
DOID:0050702
neonatal thyrotoxicosis
class of disease
thyrotoxicosis
endocrine disease
DOID:12573
neonatal urinary tract infectious disease
class of disease
urinary system disease
urinary tract infection in children
perinatal infectious disease
Human disease
DOID:1375
neonatal-onset type II citrullinemia
class of disease
citrullinemia
autosomal recessive disease
citrullinemia type II
human disease
DOID:0070341
neovascular glaucoma
class of disease
glaucoma
glaucoma associated with vascular disorder
rare acquired eye disease
Human disease
DOID:1687
C11.525.381.348
nephritis
class of disease
symptom or sign
urological symptom
disease
inflammation of the kidneys
DOID:10952
C12.777.419.570
C13.351.968.419.570
Nephritis
nephrocalcinosis
class of disease
kidney disease
calcinosis
Human disease
DOID:12679
C12.050.351.968.419.590
C12.200.777.419.590
C18.452.174.130.560
C12.950.419.590
Nephrocalcinosis
nephrogenic adenofibroma
class of disease
kidney benign neoplasm
Human disease
DOID:2698
nephrogenic adenoma of the urethra
class of disease
urethral benign neoplasm
nephrogenic adenoma
adenoma
Human disease
DOID:8109
nephrogenic adenoma of urinary bladder
class of disease
bladder benign neoplasm
nephrogenic adenoma
adenoma
Human disease
DOID:7333
nephrogenic diabetes insipidus type 2
class of disease
autosomal dominant disease
nephrogenic diabetes insipidus
autosomal recessive disease
human disease
DOID:0081061
nephrolithiasis
class of disease
kidney disease
kidney stone disease
Human disease
DOID:585
C12.200.777.419.600
C12.200.777.967.249
C12.050.351.968.419.600
C12.050.351.968.967.249
C12.950.419.600
C12.950.967.249
nephroma
class of disease
kidney benign neoplasm
kidney cortex disease
human disease
DOID:0080615
nephronophthisis
class of disease
autosomal recessive disease
medullary cystic kidney disease
kidney disease
congenital disorder of urinary system
DOID:12712
Nephronophthisis
nephronophthisis 1
class of disease
nephronophthisis
nephronophthisis that has material basis in homozygous or compound heterozygous mutation in or deletion of the NPHP1 gene on chromosome 2q13
DOID:0111112
nephropathia epidemica
class of disease
hemorrhagic fever with renal syndrome
human disease
DOID:0050201
nephrosclerosis
class of disease
renal hypertension
disease
medical condition referring to damage to the kidney due to chronic high blood pressure
DOID:11664
C12.777.419.610
C13.351.968.419.610
nephrosis
class of disease
proteinuria
kidney disease
non-inflammatory kidney disease
DOID:2527
C12.777.419.630
C13.351.968.419.630
Nephrosis
nephrotic syndrome 14
class of disease
familial nephrotic syndrome
autosomal recessive disease
human disease
DOID:0080265
nephrotic syndrome 15
class of disease
familial nephrotic syndrome
autosomal recessive disease
human disease
DOID:0080271
nephrotic syndrome 16
class of disease
familial nephrotic syndrome
autosomal recessive disease
human disease
DOID:0080272
nephrotic syndrome type 1
class of disease
familial nephrotic syndrome
autosomal recessive disease
familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13
DOID:0080390
nephrotic syndrome type 17
class of disease
familial nephrotic syndrome
autosomal recessive disease
familial nephrotic syndrome that has material basis in by homozygous or compound heterozygous mutation in the NUP85 gene on chromosome 17q25
DOID:0080392
nephrotic syndrome type 18
class of disease
familial nephrotic syndrome
autosomal recessive disease
familial nephrotic syndrome that has material basis in by homozygous or compound heterozygous mutation in the NUP133 gene on chromosome 1q42
DOID:0080393
nephrotic syndrome type 19
class of disease
familial nephrotic syndrome
autosomal recessive disease
familial nephrotic syndrome that has material basis in compound heterozygous mutation in the NUP160 gene on chromosome 11p11
DOID:0080394
nephrotic syndrome type 2
class of disease
familial nephrotic syndrome
autosomal recessive disease
nephrotic syndrome
human disease
DOID:0080379
nephrotic syndrome type 20
class of disease
familial nephrotic syndrome
human disease
DOID:0070357
nephrotic syndrome type 22
class of disease
familial nephrotic syndrome
autosomal recessive disease
human disease
DOID:0112268
nephrotic syndrome type 3
class of disease
familial nephrotic syndrome
autosomal recessive disease
familial nephrotic syndrome characterized by early childhood onset, steroid restance and diffuse mesangial sclerosis in most patients that has material basis in homozygous or compound heterozygous mutation in the PLCE1 gene on chromosome 10q23
DOID:0080382
nephrotic syndrome type 5
class of disease
familial nephrotic syndrome
autosomal recessive disease
familial nephrotic syndrome characterized by prenatal or neonatal onset of progressive renal failure with proteinurea and edema that has material basis in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p
DOID:0080380
nephrotic syndrome type 7
class of disease
familial nephrotic syndrome
autosomal recessive disease
human disease
DOID:0080388
nephrotic syndrome type 8
class of disease
familial nephrotic syndrome
autosomal recessive disease
familial nephrotic syndrome characterized by neonatal or early childhood onset steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the ARHGDIA gene on chromosome 17q25
DOID:0080389
nephrotic syndrome, type 10
class of disease
familial nephrotic syndrome
autosomal recessive disease
human disease
DOID:0080386
nephrotic syndrome, type 4
class of disease
nephrotic syndrome
familial nephrotic syndrome
autosomal dominant disease
human disease
DOID:0080383
nephrotic syndrome, type 6
class of disease
familial nephrotic syndrome
autosomal recessive disease
human disease
DOID:0080384
nephrotic syndrome, type 9
class of disease
familial nephrotic syndrome
human disease
DOID:0080391
nerve compression syndrome
class of disease
peripheral neuropathy
Human disease
DOID:573
C10.668.829.550
Nerve compression syndromes
nerve fibre bundle defect
class of disease
visual pathway disease
retinal disease
Human disease
DOID:5678
nerve plexus neoplasm
class of disease
peripheral nervous system neoplasm
plexopathy
Human disease
DOID:4693
nerve root neoplasm
class of disease
peripheral nervous system neoplasm
radiculopathy
Human disease
DOID:4698
nerve sheath neoplasms
class of disease
peripheral nervous system neoplasm
neoplasm
peripheral nervous system neoplasm that is located in the connective tissue surrounding nerves
DOID:3193
C04.557.580.600
C10.551.775.500
C10.668.829.725.500
nervous system benign neoplasm
class of disease
organ system benign neoplasm
neurological disorder
nervous system neoplasm
organ system benign neoplasm that is located in the central nervous system or located in the peripheral nervous system
DOID:0060115
nervous system cancer
class of disease
organ system cancer
nervous system neoplasm
neurological disorder
organ system cancer located in the nervous system that affects the central or peripheral nervous system
DOID:3093
Nervous system neoplasms
nervous system hibernoma
class of disease
nervous system cancer
hibernoma
central nervous system lipoma
Human disease
DOID:6607
nervous system malformations
class of disease
congenital disorder
central nervous system disease
neurological disorder
disease
congenital conditions that stem from damage to, or abnormal development of, the budding nervous system
DOID:2490
C10.500
C16.131.666
Congenital diseases and disorders of the nervous system
nested variant infiltrating bladder urothelial carcinoma
class of disease
invasive bladder transitional cell carcinoma
human disease
DOID:7969
neurilemmoma
class of disease
neuroma
disease
benign tumor of the nerve sheat composed of Schwann cells
DOID:3192
C04.557.465.625.650.595
C04.557.580.600.610.595
C04.557.580.625.650.595
Schwannoma
neurilemmoma of the fifth cranial nerve
class of disease
trigeminal nerve neoplasm
neurilemmoma
Human disease
DOID:3202
neurilemmoma of the pleura
class of disease
peripheral nerve schwannoma
pleural disease
respiratory system benign neoplasm
rare respiratory disease
benign neoplasm of pleura
Human disease
DOID:6564
neuritis
class of disease
symptom or sign
peripheral neuropathy
inflammation
disease
inflammation of a nerve or the general inflammation of the peripheral nervous system
DOID:1803
C10.668.829.650
Neuritis
neuroaxonal dystrophy
class of disease
cerebral degeneration
Human disease
DOID:2367
C10.228.140.744
neurobehavioral disorder with prenatal alcohol exposure
class of disease
fetal alcohol spectrum disorders
human disease
DOID:0081052
neuroblastoma
class of disease
cancer
autonomic nervous system neoplasm
neuroblastic tumor
disease
childhood cancer
autonomic nervous system neoplasm derived from immature nerve cells
DOID:769
C04.557.465.625.600.590.650.550
C04.557.470.670.590.650.550
C04.557.580.625.600.590.650.550
Neuroblastoma
neurocirculatory asthenia
class of disease
somatoform disorder
somatoform disorder that involves heart disease symptoms without any identifiable physiological abnormatlities.
DOID:11569
F03.080.500
neurodegeneration
class of disease
central nervous system disease
degenerative disease
disease
central nervous system disease
DOID:1289
C10.574
Neurodegenerative diseases and disorders
neurodegeneration with brain iron accumulation
class of disease
iron metabolism disease
neurodegeneration
genetic neurodegenerative disease with dementia
neuroaxonal dystrophy
neurometabolic disease
metabolic disease with dementia
miscellaneous movement disorder due to genetic neurodegenerative disease
neurodegenerative disease characterized by progressive iron accumulation in the basal ganglia and other regions of the brain, resulting in extrapyramidal movements, such as parkinsonism and dystonia
DOID:0110734
neurodegeneration with brain iron accumulation 2A
class of disease
neurodegeneration with brain iron accumulation
genetic disease
autosomal recessive disease
human disease
DOID:0110735
neurodegeneration with brain iron accumulation 2B
class of disease
neurodegeneration with brain iron accumulation
Infantile neuroaxonal dystrophy
genetic disease
autosomal recessive disease
human disease
DOID:0110736
neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures
class of disease
nervous system heredodegenerative disease
neurodegeneration
autosomal recessive disease
hereditary disease in humans
DOID:0070352
neurodermatitis
class of disease
symptom or sign
dermatitis
lichen disease
Human disease
DOID:3309
C17.800.174.660
C17.800.815.660
Lichen simplex chronicus
neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies
class of disease
syndrome
neurodevelopmental disorder
human disease
DOID:0070346
neurodevelopmental disorder with midbrain and hindbrain malformations
class of disease
syndromic intellectual disability
genetic disease
autosomal recessive disease
human disease
DOID:0080312
neuroectodermal tumor
class of disease
tumor
nervous system cancer
Human disease
DOID:171
C04.557.465.625
C04.557.580.625
neuroendocrine carcinoma
class of disease
carcinoma
neuroendocrine tumor
carcinoma that derives from neuroendocrine cells
DOID:1800
C04.557.465.625.650.240
C04.557.470.200.025.370
C04.557.580.625.650.240
neuroendocrine tumor
class of disease
endocrine gland cancer
rare disease
disease
endocrine gland cancer that has material basis in neuroendocrine cells
DOID:169
C04.557.465.625.650
C04.557.580.625.650
Neuroendocrine tumors
neurofibroma
class of disease
nerve sheath neoplasms
Human disease
DOID:962
C04.557.580.600.580
C10.551.775.500.750
C10.668.829.725.500.600
Neurofibroma
neurofibroma of gallbladder
class of disease
neurofibroma
gallbladder cancer
malignant peripheral nerve neoplasm
liver cancer
endocrine gland cancer
Human disease
DOID:5150
neurofibroma of spinal cord
class of disease
neurofibroma
Spinal cord cancer
human disease
DOID:13742
neurofibroma of the esophagus
class of disease
gastrointestinal system disease
gastrointestinal system cancer
esophageal cancer
neurofibroma
Human disease
DOID:961
neurofibroma of the heart
class of disease
malignant peripheral nerve neoplasm
neurofibroma
Human disease
DOID:9300
neurofibromatosis type I
class of disease
neurofibromatoses
neuro-cardio-facial-cutaneous syndromes
disease
type of neurofibromatosis disease
DOID:0111253
C04.557.580.600.580.590.650
C04.700.645.650
C10.562.600.500
C10.574.500.549.400
C10.668.829.675
C16.320.400.560.400
C16.320.700.645.650
Neurofibromatosis type 1
neurofibromatosis-Noonan syndrome
class of disease
syndrome
autosomal dominant disease
Noonan syndrome and Noonan-related syndrome
neurofibromatosis type I
human disease
DOID:0111683
neurofibrosarcoma
class of disease
neurofibroma
Human disease
DOID:3512
C04.557.450.565.590.350.590
C04.557.450.795.350.590
C04.557.580.600.580.795
C10.551.775.500.750.750
C10.668.829.725.500.600.600
neurogenic arthropathy
class of disease
arthropathy
disease
Human disease
DOID:14286
C05.550.186
Neuropathic arthropathy
neurogenic bladder
class of disease
bladder disease
urination disorder
disease
Human disease
DOID:12143
C10.597.900
C12.200.777.829.839
C12.050.351.968.829.760
C23.888.592.900
C12.950.829.760C
Neurogenic bladder dysfunction
neurogenic bowel
class of disease
intestinal disease
Human disease
DOID:13419
C06.405.469.158.272.804
neurological disorder
class of disease
disease of anatomical entity
disease
disease of an anatomical entity located in the central or peripheral nervous system
DOID:0060052
DOID:863
C10
Diseases and disorders of the nervous system
neuroma
class of disease
nervous system benign neoplasm
peripheral nervous system neoplasm
tumor
nervous system benign neoplasm that is characterized as a nerve tissue tumor
DOID:2001
C04.557.580.600.610
Neuroma
neuromuscular disease
class of disease
peripheral neuropathy
musculoskeletal disorder
disease
neuropathy that affect the nerves that control the voluntary muscles
DOID:440
C10.668
Neuromuscular diseases
neuromuscular junction disease
class of disease
neuromuscular disease
neuromuscular disease that is characterized by the disfunction of conduction through the neuromuscular junction
DOID:439
C10.668.758
neuronal ceroid lipofuscinosis
class of disease
lipid storage disease
eye degenerative disease
nervous system heredodegenerative disease
Human disease
DOID:14503
C10.574.500.550
C16.320.400.600
C16.320.565.398.641.509
C18.452.584.563.641.509
C18.452.648.398.641.509
neuronal ceroid lipofuscinosis 1
class of disease
neuronal ceroid lipofuscinosis
Infantile neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
juvenile neuronal ceroid lipofuscinosis
adult neuronal ceroid lipofuscinosis
genetic disease
human disease
DOID:0110721
neuronal ceroid lipofuscinosis 10
class of disease
neuronal ceroid lipofuscinosis
juvenile neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
adult neuronal ceroid lipofuscinosis
congenital neuronal ceroid lipofuscinosis
genetic disease
neuronal ceroid lipofuscinosis that has material basis in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15
DOID:0110725
neuronal ceroid lipofuscinosis 2
class of disease
neuronal ceroid lipofuscinosis
juvenile neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
genetic disease
A condition associated with mutation(s) in the TPP1 gene, encoding tripeptidyl-peptidase- 1. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments.
DOID:0110726
neuronal ceroid lipofuscinosis 3
class of disease
neuronal ceroid lipofuscinosis
juvenile neuronal ceroid lipofuscinosis
genetic disease
A condition associated with mutation(s) in the CLN3 gene, encoding battenin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments.
DOID:0110731
neuronal ceroid lipofuscinosis 4A
class of disease
neuronal ceroid lipofuscinosis
adult neuronal ceroid lipofuscinosis
genetic disease
Kufs disease
human disease
DOID:0110730
neuronal ceroid lipofuscinosis 5
class of disease
neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
genetic disease
human disease
DOID:0110728
neuronal ceroid lipofuscinosis 6
class of disease
neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
adult neuronal ceroid lipofuscinosis
genetic disease
human disease
DOID:0110729
neuronal ceroid lipofuscinosis 7
class of disease
neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
genetic disease
human disease
DOID:0110722
neuronal ceroid lipofuscinosis 8
class of disease
neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
juvenile neuronal ceroid lipofuscinosis
genetic disease
human disease
DOID:0110723
neuronal ceroid lipofuscinosis 9
class of disease
neuronal ceroid lipofuscinosis
juvenile neuronal ceroid lipofuscinosis
neuronal ceroid lipofuscinosis that is characterized by juvenile-onset of progressive vision loss, progressive ataxia and seziures
DOID:0110733
neuronal intestinal dysplasia
class of disease
colonic disease
intestinal pseudo-obstruction
intestinal dysganglionosis
Human disease
DOID:0080072
neuronal intestinal dysplasia type A
class of disease
neuronal intestinal dysplasia
human disease
DOID:0080679
neuronal intestinal dysplasia type B
class of disease
neuronal intestinal dysplasia
human disease
DOID:0080680
neuronitis
class of disease
central nervous system disease
neurological disorder
inflammatory disease
disease
central nervous system disease that is characterized by neuron inflammation
DOID:8117
neuronopathy, distal hereditary motor, type 5B
class of disease
nervous system heredodegenerative disease
distal hereditary motor neuronopathy type 5
human disease
DOID:0111205
neurooculocardiogenitourinary syndrome
class of disease
syndrome
autosomal dominant disease
human disease
DOID:0111675
neuropathy
class of disease
neurological disorder
disease of or damage to the nerves
DOID:870
Neuropathies
neuroretinitis
class of disease
optic papillitis
focal chorioretinitis
eye disease
Human disease
DOID:10176
neurosarcoidosis
class of disease
sarcoidosis
central nervous system disease
disease with granulomas invoving nervous tissue
DOID:13403
Neurosarcoidosis
neurotrophic keratoconjunctivitis
class of disease
keratoconjunctivitis
Human disease
DOID:12125
neutropenia
class of disease
agranulocytosis
disease
abnormally low concentration of neutrophils in the blood
DOID:1227
C15.378.553.546.184.564
C15.378.243.750.184.564
Neutropenia
nevoid basal cell carcinoma syndrome
class of disease
symptom or sign
autosomal dominant disease
syndrome
an autosomal dominant condition that can cause unusual facial appearances and a predisposition for basal-cell carcinoma
DOID:2512
C04.182.089.530.690.150
C04.557.470.200.165.150
C04.557.470.565.165.150
C04.700.175
C05.116.099.105
C05.500.470.690.150
C07.320.450.670.130
C16.131.077.130
C16.320.700.175
nickel allergic asthma
class of disease
allergic asthma
nickel sensitivity
metal allergy
allergic asthma that has allergic trigger nickel atom
DOID:0040045
night blindness
class of disease
eye disease
retinal disease
vision disorder
disease
condition making it difficult or impossible to see in relatively low light
DOID:8499
C11.966.671
Nyctalopia
nipple carcinoma
class of disease
breast carcinoma
malignant neoplasm of nipple
breast carcinoma that is located in the nipple
DOID:6629
nipple duct carcinoma
class of disease
nipple carcinoma
nipple carcinoma that is located in the nipple duct
DOID:7953
nipple neoplasm
class of disease
breast benign neoplasm
Human disease
DOID:3003
nocturnal asthma
class of disease
chronic asthma
human disease
DOID:0080826
nodal marginal zone B cell lymphoma
class of disease
marginal zone B-cell lymphoma
marginal zone B-cell lymphoma which morphologically resembles lymph nodes involved by marginal zone lymphomas of extranodal or splenic types, but without evidence of extranodal or splenic disease
DOID:0080211
nodular basal cell carcinoma
class of disease
basal-cell carcinoma
Human disease
DOID:4280
nodular degeneration of cornea
class of disease
corneal degeneration
Human disease
DOID:2879
nodular episcleritis
class of disease
scleral disease
episcleritis
Human disease
DOID:728
nodular ganglioneuroblastoma
class of disease
ganglioneuroblastoma
Human disease
DOID:5193
nodular goiter
class of disease
goiter
Human disease
DOID:13197
C19.874.283.501
nodular hidradenoma
class of disease
hidradenoma
Human disease
DOID:2061
nodular medulloblastoma
class of disease
medulloblastoma
Human disease
DOID:3873
nodular melanoma
class of disease
skin melanoma
melanoma that is characterized as highly aggressive and manifests as a uniform blue-black, blue-red, or amelanotic nodule
DOID:10047
Nodular melanoma
nodular nonsuppurative panniculitis
class of disease
panniculitis
subcutaneous tissue disease
cutaneous condition characterized by recurrent subcutaneous nodules that heal with depression of the overlying skin
DOID:1525
C17.300.710.500
C17.800.566.500
nodular prostate
class of disease
prostatic hypertrophy
Human disease
DOID:13206
nodular tenosynovitis
class of disease
connective tissue benign neoplasm
Human disease
DOID:2701
non specific chronic endometritis
class of disease
endometritis
chronic endometritis
Human disease
DOID:4560
non-Hodgkin lymphoma
class of disease
lymphoma
neoplasm
hematopoietic system disease
disease
type of cancer of lymph nodes
DOID:0060060
C04.557.386.480
C15.604.515.569.480
C20.683.515.761.480
Non-Hodgkin lymphomas
non-Langerhans-cell histiocytosis
class of disease
histiocytosis
Human disease
DOID:4330
C15.604.250.410
non-alcoholic fatty liver
class of disease
non-alcoholic fatty liver disease
nonalcoholic fatty liver disease that is characterized by the presence of at least 5% of hepatic steatosis with no evidence of hepatocellular injury in the form of hepatocyte ballooning
DOID:0080546
non-alcoholic fatty liver disease
class of disease
fatty liver disease
disease
storing of excess fat in liver cells, not caused by heavy alcohol use
DOID:0080208
C06.552.241.519
non-alcoholic steatohepatitis
class of disease
non-alcoholic fatty liver disease
Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure.
DOID:0080547
non-arteritic anterior ischemic optic neuropathy
class of disease
anterior ischemic optic neuropathy
Human disease
DOID:0050864
non-congenital cyst of kidney
class of disease
cystic kidney disease
Human disease
DOID:9621
non-controlled substance abuse
class of disease
addiction
substance use disorder
social issue
abuse of chemical substances and/or abuse of any licit substances
DOID:9973
Substance dependence
non-functioning pancreatic endocrine tumor
class of disease
islet cell tumor
non-functioning endocrine neoplasm
Human disease
DOID:7698
non-gestational choriocarcinoma
class of disease
choriocarcinoma
Human disease
DOID:4320
C04.557.465.955.207.438
C04.557.470.200.025.455.750
C04.850.908.208.438
C13.703.720.949.208.438
non-gestational ovarian choriocarcinoma
class of disease
ovarian primitive germ cell tumor
choriocarcinoma of ovary
Human disease
DOID:7665
non-invasive bladder urothelial carcinoma
class of disease
bladder urothelial carcinoma
human disease
DOID:6571
non-proliferative fibrocystic change of the breast
class of disease
breast fibrocystic disease
Human disease
DOID:5997
non-renal secondary hyperparathyroidism
class of disease
hyperparathyroidism
secondary hyperparathyroidism
Human disease
DOID:13575
non-secretory myeloma
class of disease
multiple myeloma
non-functioning endocrine neoplasm
Human disease
DOID:9547
non-small-cell lung carcinoma
class of disease
lung carcinoma
lung cancer
disease
any type of epithelial lung cancer other than small-cell lung carcinoma
DOID:3908
C04.588.894.797.520.109.220.249
C08.381.540.140.500
C08.785.520.100.220.500
Non-small cell lung cancer
non-suppurative otitis media
class of disease
otitis media
otitis media which involves transudation of fluid in the middle ear without pus formation
DOID:11180
non-syndromic X-linked intellectual disability 1
class of disease
X-linked dominant disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112038
non-syndromic X-linked intellectual disability 100
class of disease
non-syndromic X-linked intellectual disability
X-linked recessive disease
human disease
DOID:0112040
non-syndromic X-linked intellectual disability 101
class of disease
non-syndromic X-linked intellectual disability
X-linked recessive disease
human disease
DOID:0112048
non-syndromic X-linked intellectual disability 103
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112020
non-syndromic X-linked intellectual disability 104
class of disease
non-syndromic X-linked intellectual disability
X-linked recessive disease
human disease
DOID:0112018
non-syndromic X-linked intellectual disability 105
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112036
non-syndromic X-linked intellectual disability 107
class of disease
X-linked dominant disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112054
non-syndromic X-linked intellectual disability 14
class of disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112027
non-syndromic X-linked intellectual disability 19
class of disease
non-syndromic X-linked intellectual disability
X-linked dominant disease
human disease
DOID:0112019
non-syndromic X-linked intellectual disability 2
class of disease
X-linked dominant disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112016
non-syndromic X-linked intellectual disability 20
class of disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112023
non-syndromic X-linked intellectual disability 21
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112022
non-syndromic X-linked intellectual disability 23
class of disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112049
non-syndromic X-linked intellectual disability 30
class of disease
non-syndromic X-linked intellectual disability
X-linked recessive disease
human disease
DOID:0112051
non-syndromic X-linked intellectual disability 41
class of disease
X-linked dominant disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112058
non-syndromic X-linked intellectual disability 42
class of disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112057
non-syndromic X-linked intellectual disability 45
class of disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112028
non-syndromic X-linked intellectual disability 46
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112055
non-syndromic X-linked intellectual disability 50
class of disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112029
non-syndromic X-linked intellectual disability 53
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112047
non-syndromic X-linked intellectual disability 58
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112024
non-syndromic X-linked intellectual disability 63
class of disease
non-syndromic X-linked intellectual disability
X-linked dominant disease
human disease
DOID:0112050
non-syndromic X-linked intellectual disability 72
class of disease
non-syndromic X-linked intellectual disability
X-linked recessive disease
human disease
DOID:0112059
non-syndromic X-linked intellectual disability 73
class of disease
non-syndromic X-linked intellectual disability
X-linked recessive disease
human disease
DOID:0112017
non-syndromic X-linked intellectual disability 77
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112039
non-syndromic X-linked intellectual disability 81
class of disease
non-syndromic X-linked intellectual disability
X-linked recessive disease
human disease
DOID:0112033
non-syndromic X-linked intellectual disability 82
class of disease
non-syndromic X-linked intellectual disability
X-linked recessive disease
human disease
DOID:0112052
non-syndromic X-linked intellectual disability 84
class of disease
non-syndromic X-linked intellectual disability
X-linked recessive disease
human disease
DOID:0112030
non-syndromic X-linked intellectual disability 88
class of disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112053
non-syndromic X-linked intellectual disability 89
class of disease
X-linked dominant disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112031
non-syndromic X-linked intellectual disability 9
class of disease
non-syndromic X-linked intellectual disability
X-linked recessive disease
human disease
DOID:0112034
non-syndromic X-linked intellectual disability 90
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112041
non-syndromic X-linked intellectual disability 91
class of disease
non-syndromic X-linked intellectual disability
X-linked dominant disease
human disease
DOID:0112043
non-syndromic X-linked intellectual disability 92
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112032
non-syndromic X-linked intellectual disability 93
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112045
non-syndromic X-linked intellectual disability 96
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112035
non-syndromic X-linked intellectual disability 97
class of disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112046
non-syndromic X-linked intellectual disability 98
class of disease
non-syndromic X-linked intellectual disability
X-linked dominant disease
human disease
DOID:0112044
non-syndromic X-linked intellectual disability 99
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112026
non-syndromic X-linked intellectual disability ARX-related
class of disease
X-linked recessive disease
non-syndromic X-linked intellectual disability
human disease
DOID:0112021
nonencapsulated sclerosing carcinoma
class of disease
papillary thyroid cancer
Human disease
DOID:5914
noninfectious dermatoses of eyelid
class of disease
blepharitis
Human disease
DOID:1894
noninvasive malignant thymoma
class of disease
thymoma
Human disease
DOID:7214
nonossifying fibromyxoid tumor
class of disease
mesenchymal cell neoplasm
fibromyxoid tumor
Human disease
DOID:8305
nonphotosensitive trichothiodystrophy
class of disease
trichothiodystrophy
human disease
DOID:0111867
nonsyndromic aplasia cutis congenita
class of disease
skin disease
aplasia cutis congenita
human disease
DOID:0080661
nonsyndromic congenital nail disorder
class of disease
nail disease
human disease
DOID:0080683
nonsyndromic congenital nail disorder 1
class of disease
nail disease
Twenty-nail dystrophy
inherited isolated nail anomaly
epidermal disease
nonsyndromic congenital nail disorder
autosomal dominant disease
Human disease
DOID:0080079
nonsyndromic congenital nail disorder 2
class of disease
nail disease
inherited isolated nail anomaly
nonsyndromic congenital nail disorder
autosomal dominant disease
Human disease
DOID:0080080
nonsyndromic congenital nail disorder 5
class of disease
nail disease
inherited isolated nail anomaly
nonsyndromic congenital nail disorder
autosomal dominant disease
Human disease
DOID:0080083
nonsyndromic congenital nail disorder 6
class of disease
nail disease
autosomal dominant disease
nonsyndromic congenital nail disorder
Human disease
DOID:0080084
nonsyndromic congenital nail disorder 7
class of disease
nail disease
epidermal disease
inherited isolated nail anomaly
nonsyndromic congenital nail disorder
autosomal dominant disease
Human disease
DOID:0080085
nonsyndromic congenital nail disorder 9
class of disease
nail disease
inherited isolated nail anomaly
autosomal recessive disease
nonsyndromic congenital nail disorder
Human disease
DOID:0080087
nontoxic goiter
class of disease
goiter
Human disease
DOID:13195
normal pressure hydrocephalus
class of disease
communicating hydrocephalus
nervous system heredodegenerative disease
genetic dementia
disease
condition in which there is excess cerebrospinal fluid in the ventricles, and with normal or slightly elevated cerebrospinal fluid pressure
DOID:1572
C10.228.140.602.750
Normal pressure hydrocephalus
normocytic anemia
class of disease
anemia
Human disease
DOID:720
norwegian scabies
class of disease
scabies
Human disease
DOID:14374
Crusted scabies
nose disease
class of disease
upper respiratory tract disease
disease
respiratory disease
DOID:2825
C08.460
C09.603
Diseases and disorders of the nose and paranasal sinuses
notochordal cancer
class of disease
bone cancer
embryonal cancer and bone cancer and mesenchymal cell neoplasm that is located in the notochord
DOID:3303
nuclear senile cataract
class of disease
senile cataract
nuclear sclerosis
Human disease
DOID:13963
nuclear type mitochondrial complex I deficiency
class of disease
mitochondrial complex I deficiency
human disease
DOID:0112065
nuclear type mitochondrial complex I deficiency 1
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112074
nuclear type mitochondrial complex I deficiency 10
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112075
nuclear type mitochondrial complex I deficiency 11
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112089
nuclear type mitochondrial complex I deficiency 12
class of disease
nuclear type mitochondrial complex I deficiency
X-linked recessive disease
human disease
DOID:0112099
nuclear type mitochondrial complex I deficiency 13
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112076
nuclear type mitochondrial complex I deficiency 14
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112094
nuclear type mitochondrial complex I deficiency 15
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112077
nuclear type mitochondrial complex I deficiency 16
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112096
nuclear type mitochondrial complex I deficiency 17
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112078
nuclear type mitochondrial complex I deficiency 18
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112070
nuclear type mitochondrial complex I deficiency 19
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112085
nuclear type mitochondrial complex I deficiency 2
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112083
nuclear type mitochondrial complex I deficiency 20
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112072
nuclear type mitochondrial complex I deficiency 21
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112088
nuclear type mitochondrial complex I deficiency 22
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112069
nuclear type mitochondrial complex I deficiency 23
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112087
nuclear type mitochondrial complex I deficiency 24
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112079
nuclear type mitochondrial complex I deficiency 25
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112067
nuclear type mitochondrial complex I deficiency 26
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112086
nuclear type mitochondrial complex I deficiency 27
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112090
nuclear type mitochondrial complex I deficiency 28
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112095
nuclear type mitochondrial complex I deficiency 29
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112084
nuclear type mitochondrial complex I deficiency 3
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112093
nuclear type mitochondrial complex I deficiency 30
class of disease
nuclear type mitochondrial complex I deficiency
X-linked recessive disease
human disease
DOID:0112098
nuclear type mitochondrial complex I deficiency 31
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112071
nuclear type mitochondrial complex I deficiency 32
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112080
nuclear type mitochondrial complex I deficiency 33
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112097
nuclear type mitochondrial complex I deficiency 34
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112091
nuclear type mitochondrial complex I deficiency 35
class of disease
autosomal recessive disease
mitochondrial complex I deficiency
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112139
nuclear type mitochondrial complex I deficiency 4
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112082
nuclear type mitochondrial complex I deficiency 5
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112068
nuclear type mitochondrial complex I deficiency 6
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112066
nuclear type mitochondrial complex I deficiency 7
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112092
nuclear type mitochondrial complex I deficiency 8
class of disease
nuclear type mitochondrial complex I deficiency
autosomal recessive disease
human disease
DOID:0112081
nuclear type mitochondrial complex I deficiency 9
class of disease
autosomal recessive disease
nuclear type mitochondrial complex I deficiency
human disease
DOID:0112073
null-cell leukemia
class of disease
acute lymphocytic leukemia
Human disease
DOID:9954
nutmeg liver
class of disease
hepatic vascular disease
human disease
DOID:13739
Congestive hepatopathy
nutrition disorder
class of disease
acquired metabolic disease
nutritional and metabolic diseases
food-related disease
disease that results from excessive or inadequate intake of food and nutrients
DOID:374
C18.654
Nutritional diseases and disorders
nutritional deficiency disease
class of disease
nutrition disorder
deficiency
human disease
DOID:5113
C18.654.521.500
Diseases and disorders due to nutritional deficiencies
nutritional optic neuropathy
class of disease
optic nerve disease
optic neuritis
Human disease
DOID:1209
nystagmus, congenital, autosomal recessive
class of disease
congenital nystagmus
autosomal recessive disease
human disease
DOID:0111797
obsessive-compulsive disorder
class of disease
anxiety disorder
impulse control disorder
genetic nervous system disorder
genetic disease
disease
anxiety disorder that involves unwanted and repeated thoughts, feelings, ideas, sensations (obsessions), or behaviors that make them feel driven to do something (compulsions)
DOID:10933
F03.080.600
Obsessive–compulsive disorder
obsessive-compulsive personality disorder
class of disease
personality disorder
disease
personal perfectionism at the cost of flexibility, openness, efficiency & effect on others
DOID:10932
F03.675.150
Obsessive compulsive personality disorder
obstructive hydrocephalus
class of disease
hydrocephalus
abnormal accumulation of cerebrospinal fluid within the ventricles of the brain that occurs as a consequence of an obstruction at any location within the ventricular system that prevents cerebrospinal fluid flowing into the subarachnoid space
DOID:14159
obstructive jaundice
class of disease
cholestasis
jaundice
non-neoplastic bile duct disorder
Human disease
DOID:13603
C23.550.429.500.755
C23.888.885.375.500
Obstructive jaundice
obstructive lung disease
class of disease
lung disease
disease
category of respiratory disease characterized by airway obstruction
DOID:2320
C08.381.495
obstructive nephropathy
class of disease
kidney disease
kidney disease characterized by kidney damage and dysfunction resulting from urinary tract obstruction
DOID:0070314
obstructive sleep apnea
class of disease
sleep apnea
obstruction of the upper airway during sleep
DOID:0050848
C08.618.085.852.850
C10.886.425.800.750.850
occipital lobe neoplasm
class of disease
cerebrum cancer
Human disease
DOID:910
occlusion of gallbladder
class of disease
gallbladder disease
Human disease
DOID:9714
occlusion precerebral artery
class of disease
cerebrovascular disease
human disease
DOID:5976
occupational asthma
class of disease
occupational disease
asthma
environmental induced asthma
medical condition caused or exacerbated by the workplace
DOID:0080820
C08.127.108.495
C08.674.095.495
C20.543.480.680.095.495
C24.102
occupational dermatitis
class of disease
contact dermatitis
occupational disease
disease
Human disease
DOID:4404
C17.800.174.255.700
C17.800.815.255.700
C24.270
ochronosis
class of disease
connective tissue disease
clinical sign
disease
syndrome caused by the accumulation of homogentisic acid in connective tissues
DOID:14223
C23.550.744
Ochronosis
ocular albinism
class of disease
eye disease
albinism
disease
human disease
DOID:0050633
C11.270.040.090
C16.320.290.040.090
C16.320.565.100.102.090
C16.320.850.080.090
C17.800.621.440.102.090
C17.800.827.080.090
C18.452.648.100.102.090
ocular albinism type 2
class of disease
ocular albinism
eye disease
X-linked recessive disease
Human disease
DOID:0050630
ocular albinism with sensorineural deafness
class of disease
ocular albinism
Waardenburg's syndrome
autosomal dominant disease
digenic disease
human disease
DOID:0090100
ocular cancer
class of disease
sensory system cancer
eye tumor
eye disease
disease
type of cancer un the eye
DOID:2174
ocular hyperemia
class of disease
conjunctival disease
Human disease
DOID:1248
ocular hypertension
class of disease
eye disease
hypertension
disease
eye disease that is characterized by elevated intraocular pressure in the absence of optic nerve damage or visual field loss
DOID:9282
C11.525
ocular hypotension
class of disease
eye disease
hypotension
Human disease
DOID:790
C11.540
ocular motility disease
class of disease
cranial nerve disease
eye adnexa disease
eye disease
human disease
DOID:1279
C10.228.758
C10.292.562
C11.590
ocular tuberculosis
class of disease
extrapulmonary tuberculosis
eye disease
tuberculosis
Human disease
DOID:233
DOID:0070344
C01.150.252.289.800
C01.375.354.800
C11.294.354.800
oculocutaneous albinism type 2
class of disease
oculocutaneous albinism
oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13
DOID:0070096
oculocutaneous albinism type 3
class of disease
oculocutaneous albinism
oculocutaneous albinism that has material basis in an autosomal recessive mutation of TYRP1 on chromosome 9p23
DOID:0070097
oculocutaneous albinism type 4
class of disease
oculocutaneous albinism
An oculocutaneous albinism that has material basis in an autosomal recessive mutation of SLC45A2 on chromosome 5p13.2.
DOID:0070098
oculocutaneous albinism type IA
class of disease
oculocutaneous albinism
An oculocutaneous albinism that has material basis in an autosomal recessive null mutation of TYR on chromosome 11q14.3 with no residual protein activity.
DOID:0070094
oculocutaneous albinism type IB
class of disease
oculocutaneous albinism
An oculocutaneous albinism that has material basis in an autosomal recessive hypomorphic mutation of TYR on chromosome 11q14.3 with retention of some residual protein activity.
DOID:0070095
oculocutaneous albinism type V
class of disease
oculocutaneous albinism
oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA5 on chromosome 4q24
DOID:0070099
oculoglandular tularemia
class of disease
tularemia
tularemia that results in inflammation of eye and swelling of lymph glands in front of the ear
DOID:13226
oculogyric crisis
class of disease
focal dystonia
disease
focal dystonia that is characterized by a prolonged involuntary upward deviation of the eyes
DOID:0050842
oculomotor nerve paralysis
class of disease
third cranial nerve disease
paralytic squint
Human disease
DOID:11550
C10.292.562.700
C11.590.436
Oculomotor nerve palsy
oculopharyngodistal myopathy 4
class of disease
Oculopharyngodistal myopathy
human disease
DOID:0081300
odontoclasia
class of disease
dental caries
Human disease
DOID:11736
olecranon bursitis
class of disease
enthesopathy
bursitis
disease
Human disease
DOID:12581
Olecranon bursitis
olfactory groove meningioma
class of disease
anterior cranial fossa meningioma
Human disease
DOID:8057
olfactory nerve disease
class of disease
glossopharyngeal nerve disease
encephalopathy
Human disease
DOID:367
C10.292.650
oligoasthenoteratospermia
class of disease
oligospermia
Teratospermia
asthenozoospermia
male infertility
A form of male infertility that is characterized by a combination of low number or oligozoospermia, poor motility or asthenozoospermia, and abnormal shape or teratozoospermia of sperms. OAT is the most common cause of male subfertility.
DOID:0070311
oligodendroglioma
class of disease
glioma
disease
type of glioma that are believed to originate from the oligodendrocytes of the brain or from a glial precursor cell
DOID:3181
C04.557.465.625.600.380.590
C04.557.470.670.380.590
C04.557.580.625.600.380.590
Oligodendrogliomas
oligohydramnios
class of disease
placenta disease
disease
placenta disease that is characterized by a deficiency of amniotic fluid sometimes resulting in an embryonic defect through adherence between embryo and amnion
DOID:12215
C13.703.560
Oligohydramnios
oligospermia
class of disease
male infertility
disease
semen with abnormally low concentration of sperm
DOID:14228
C12.294.365.700.508
Oligospermia
olivopontocerebellar atrophy
class of disease
neurodegeneration
group of sporadic and inherited neurodegenerative disorders affecting the cerebellum, pons, and inferior olives
DOID:14784
C10.177.575.550.375
C10.228.140.079.612.600
C10.228.140.252.700.650
C10.228.662.550.600
C10.228.854.787.750
C10.574.500.825.650
C10.574.625.600
C16.320.400.780.750
omphalocele
class of disease
congenital disorder
abdominal wall defect
disease
physical disorder characterized by a defect in the development of the abdominal wall muscles, resulting in the intestines, liver and other organs to remain outside of the abdomen in a sac
DOID:0060327
Omphalocele
oncocytic breast carcinoma
class of disease
breast adenocarcinoma
invasive breast carcinoma
Human disease
DOID:6585
oophoritis
class of disease
symptom or sign
ovarian disease
inflammatory disease
disease
human disease
DOID:10974
C13.351.500.056.630.450
C13.351.500.056.750.500
C19.391.630.450
open-angle glaucoma
class of disease
glaucoma
glaucoma characterized by optic nerve damage resulting in progressive loss of visual field and increased pressure in the eye due to trabecular blockage
DOID:1067
C11.525.381.407
ophthalmia neonatorum
class of disease
gonococcal eye infectious disease
bacterial conjunctivitis
Human disease
DOID:9699
ophthalmia nodosa
class of disease
eye disease
Human disease
DOID:9722
ophthalmomyiasis
class of disease
myiasis
eye disease
parasitic eye infection
myiasis that involves parasitic infestation of Oestrus ovis larvae in the eye causing severe irritation, edema, and pain
DOID:0050268
ophthalmoplegia
class of disease
symptom or sign
ocular motility disease
paralysis
disease
Human disease
DOID:539
C10.292.562.750
C10.597.622.447
C11.590.472
C23.888.592.636.447
Ophthalmoparesis
opiate dependence
class of disease
substance dependence
opioid use disorder
drug dependence that involves the continued use of opiate drugs despite despite problems related to use of the substance
DOID:2559
opioid use disorder
class of disease
addiction
substance abuse
opioid-related disorders
disease
substance abuse disorder that involves the recurring use of opioid drugs despite negative consequences
DOID:11206
Opioid use disorder
opportunistic bacterial infectious disease
class of disease
bacterial infectious disease
opportunistic infection
bacterial infectious disease that results in infection by bacteria in individuals whose host defense mechanisms have been compromised
DOID:0050340
opportunistic mycosis
class of disease
systemic mycosis
opportunistic infection
A systemic mycosis that results in fungal infection located in human body of immunocompromised individuals, has material basis in Fungi. The organisms invade via the respiratory tract, alimentary tract, or intravascular devices.
DOID:2473
oppositional defiant disorder
class of disease
specific developmental disorder
emotional and behavioral disorders
disease
human disorder involving hostility and defiance
DOID:0050856
F03.625.094.475
Oppositional defiant disorder
optic atrophy 10
class of disease
autosomal dominant disease
optic atrophy
human disease
DOID:0111434
optic atrophy 11
class of disease
autosomal recessive isolated optic atrophy
autosomal recessive disease
optic atrophy
human disease
DOID:0111436
optic atrophy 2
class of disease
optic atrophy
human disease
DOID:0111443
optic atrophy 4
class of disease
Kjer's optic neuropathy
optic atrophy
autosomal dominant disease
human disease
DOID:0111440
optic atrophy 5
class of disease
Kjer's optic neuropathy
optic atrophy
autosomal dominant disease
human disease
DOID:0111438
optic atrophy 6
class of disease
autosomal recessive isolated optic atrophy
optic atrophy
autosomal recessive disease
human disease
DOID:0111435
optic atrophy 9
class of disease
autosomal recessive disease
optic atrophy
human disease
DOID:0111442
optic disk drusen
class of disease
optic nerve disease
Human disease
DOID:13561
C10.292.700.450
C11.640.513
optic nerve astrocytoma
class of disease
optic nerve glioma
optic nerve disease
astrocytoma
neuromuscular disease
human disease
DOID:4991
optic nerve disease
class of disease
cranial nerve disease
vision disorder
peripheral neuropathy
visual pathway disease
neuro-ophthalmological disease
disease
cranial nerve disease that is located in the optic nerve
DOID:1891
C10.292.700
C11.640
Optic neuropathy
optic nerve glioma
class of disease
optic nerve tumor
glioma
visual pathway glioma
brain glioma
human disease
DOID:4992
C04.557.465.625.600.380.795
C04.557.470.670.380.795
C04.557.580.625.600.380.795
C04.588.614.300.600.600
C04.588.614.596.240.240.500
C10.292.225.800.500
C10.292.700.500.500
C10.551.360.500.500
C10.551.775.250.500.500
C11.640.544.500
optic neuritis
class of disease
optic nerve disease
eye disease
encephalomyelitis
disease
optic nerve disease that results in inflammation located in optic nerve which may cause a complete or partial loss of vision
DOID:1210
C10.292.700.550
C11.640.576
Optic neuritis
optic papillitis
class of disease
optic neuritis
human disease
DOID:10175
oral cavity carcinoma in situ
class of disease
in situ carcinoma
mouth cancer
mouth disease
carcinoma in situ of digestive organ
Human disease
DOID:0050610
oral hairy leukoplakia
class of disease
mouth disease
oral mucosa leukoplakia
disease
mouth disease characterized by a white patch on the lateral sides of the tongue with a corrugated or hairy appearance; caused by Epstein-Barr virus
DOID:0060315
C01.925.256.466.313.500
C04.588.443.591.545.500
C04.834.512.513.500
C07.465.565.545.500
C23.300.816.513.500
oral leukoedema
class of disease
mouth disease
Leukoedema
Human disease
DOID:4557
C07.465.385
oral mucosa leukoplakia
class of disease
mouth disease
leukoplakia
Human disease
DOID:9655
C04.588.443.591.545
C04.834.512.513
C07.465.565.545
C23.300.816.513
Oral leukoplakia
oral submucous fibrosis
class of disease
mouth disease
rare maxillo-facial surgical disease
human disease
DOID:5773
C07.465.654
oral-facial-digital syndrome
class of disease
syndrome
genetic disease that is characterized by malformations of the face, oral cavity, and digits with polycystic kidney disease and variable involvement of the central nervous system and has material basis in X-linked inheritance of an OFD gene
DOID:4501
C05.116.099.370.652
C05.660.207.700
C16.131.077.676
C16.131.260.830.670
C16.131.621.207.700
C16.320.180.830.670
C16.320.714
orange allergy
class of disease
fruit allergy
fruit allergy triggered by Citrus sinensis plant fruit food product.
DOID:0060508
orbit embryonal rhabdomyosarcoma
class of disease
orbit rhabdomyosarcoma
embryonal rhabdomyosarcoma
Human disease
DOID:3258
orbit rhabdomyosarcoma
class of disease
orbit sarcoma
Human disease
DOID:3259
orbital cancer
class of disease
bone cancer
orbit neoplasm
orbital disease
Human disease
DOID:4143
orbital cyst
class of disease
orbital disease
Human disease
DOID:14233
orbital disease
class of disease
eye adnexa disease
bone disease
adnexa disease that is located in the eye socket
DOID:930
C11.675
orbital granuloma
class of disease
chronic orbital inflammation
Human disease
DOID:10499
orbital osteomyelitis
class of disease
acute orbital inflammation
osteomyelitis
Human disease
DOID:11232
orbital periostitis
class of disease
acute orbital inflammation
human disease
DOID:11231
orbital tenonitis
class of disease
acute orbital inflammation
Human disease
DOID:11233
orchitis
class of disease
testicular disease
inflammatory disease
disease
inflammation of the testes
DOID:2518
C12.294.829.493
C19.391.829.493
Orchitis
organ system benign neoplasm
class of disease
benign neoplasm
disease of anatomical entity
benign neoplasm that is classified by the organ system from which it is arising from
DOID:0060085
organ system cancer
class of disease
cancer
cancer by anatomical entity
cancer that is classified based on the organ it starts in
DOID:0050686
C04.588
organic acidemia
class of disease
amino acid metabolic disorder
amino acid metabolic disorder that disrupts normal amino acid metabolism causing a building up of branched-chain amino acids
DOID:0060159
orofacial cleft 1
class of disease
cleft lip and cleft palate
autosomal dominant disease
An orofacial cleft characterized by autosomal dominant inheritance that has material basis in variation in chromosome region 6p24.3.
DOID:0080395
orofacial cleft 10
class of disease
cleft lip and cleft palate
orofacial cleft that has material basis in mutation in the SUMO1 gene on chromosome 2q33
DOID:0080403
orofacial cleft 11
class of disease
cleft lip and cleft palate
human disease
DOID:0080404
orofacial cleft 12
class of disease
cleft lip and cleft palate
An orofacial cleft that has material basis in variation in the chromosome region 8q24.3.
DOID:0080405
orofacial cleft 13
class of disease
cleft lip and cleft palate
autosomal dominant disease
orofacial cleft characterized by autosomal doninant inhertitance that has material basis in variation in chromosome region 1p33 associated with enrichment of the T allele of SNP rs3827730
DOID:0080406
orofacial cleft 14
class of disease
cleft lip and cleft palate
autosomal recessive disease
human disease
DOID:0080407
orofacial cleft 15
class of disease
cleft lip and cleft palate
orofacial cleft that has material basis in mutation in the DLX4 gene on chromosome 17q21
DOID:0080408
orofacial cleft 2
class of disease
cleft lip and cleft palate
orofacial cleft that has material basis in variation in the chromosome region 2p13
DOID:0080396
orofacial cleft 3
class of disease
cleft lip and cleft palate
orofacial cleft that has material basis in variation in the chromosomal region 19q13
DOID:0080397
orofacial cleft 4
class of disease
cleft lip and cleft palate
orofacial cleft that has material basis in variation in the 4q21-q31 chromosomal region
DOID:0080398
orofacial cleft 5
class of disease
cleft lip and cleft palate
human disease
DOID:0080399
orofacial cleft 6
class of disease
autosomal dominant disease
cleft lip and cleft palate
human disease
DOID:0080593
orofacial cleft 7
class of disease
cleft lip and cleft palate
autosomal recessive disease
orofacial cleft that has material basis in by homozygous mutation in the PVRL1 gene on chromosome 11q23
DOID:0080400
orofacial cleft 8
class of disease
cleft lip and cleft palate
orofacial cleft that has material basis in heterozygous mutation in the TP63 gene on chromosome 3q28
DOID:0080401
orofacial cleft 9
class of disease
cleft lip and cleft palate
An orofacial cleft that has material basis in variation in the chromosome region 13q33.1-q34.
DOID:0080402
orofaciodigital syndrome VIII
class of disease
oral-facial-digital syndrome
X-linked recessive disease
human disease
DOID:0060378
oromandibular dystonia
class of disease
focal dystonia
lingual-facial-buccal dyskinesia
focal, segmental or multifocal dystonia
focal dystonia that is characterized by distortions of the mouth and tongue.
DOID:0050843
oropharyngeal anthrax
class of disease
gastrointestinal anthrax
human disease
DOID:0050059
orthostatic proteinuria
class of disease
symptom or sign
kidney disease
proteinuria
Human disease
DOID:9617
osmotic diarrhea
class of disease
diarrhea
chronic diarrhea
Human disease
DOID:0050130
ossifying fibroma
class of disease
bone benign neoplasm
bone benign neoplasm that is located in the mouth and results in an overgrowth of gingival tissue due to irritation or trauma
DOID:180
C04.557.450.565.575.400
C04.557.450.565.590.340.360
ossifying fibromyxoid tumour
class of disease
fibromyxoid tumor
mesenchymal cell neoplasm
human disease
DOID:2685
osteoarticular tuberculosis
class of disease
extrapulmonary tuberculosis
bone disease
extrapulmonary tuberculosis that results in formation of lesions located in bone
DOID:1639
C01.150.252.410.040.552.846.617.525
C01.160.886
C05.116.165.886
osteoblastoma
class of disease
bone benign neoplasm
osteogenic neoplasm
disease
Human disease
DOID:0060098
C04.557.450.565.575.600
Osteoblastoma
osteochondrodysplasia
class of disease
bone development disease
bone development disease that results in defective development of cartilage or bone
DOID:2256
C05.116.099.708
C16.320.728
Osteochondrodysplasias
osteochondrosis
class of disease
symptom or sign
ischemic bone disease
disease
ischemic bone disease that results in necrosis followed by regrowth in children and teens located in bone
DOID:8125
C05.116.821
Osteochondrosis
osteoclast-like giant cell neoplasm of the pancreas
class of disease
pancreatic ductal adenocarcinoma
undifferentiated pancreatic carcinoma
Human disease
DOID:7718
osteogenesis imperfecta 21
class of disease
osteogenesis imperfecta
human disease
DOID:0112201
osteogenesis imperfecta type 1
class of disease
osteogenesis imperfecta
genetic disease
autosomal dominant disease
An osteogenesis imperfecta that is characterized by bone fragility and blue sclerae and has material basis in dominantly inherited mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.
DOID:0110334
osteogenesis imperfecta type 16
class of disease
osteogenesis imperfecta
osteogenesis imperfecta that has material basis in contiguous gene deletion on chromosome 11p11
DOID:0110345
osteogenesis imperfecta type 18
class of disease
autosomal recessive disease
osteogenesis imperfecta
human disease
DOID:0111848
osteogenesis imperfecta type 20
class of disease
autosomal recessive disease
osteogenesis imperfecta
human disease
DOID:0111849
osteogenesis imperfecta type 3
class of disease
osteogenesis imperfecta
genetic disease
autosomal dominant disease
An osteogenesis imperfecta that is characterized by progressive limb and spinal deformity and normal sclerae and has material basis in mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.
DOID:0110339
osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
class of disease
osteogenesis imperfecta
dentinogenesis imperfecta
blue sclera
osteogenesis imperfecta found in a single South African family
DOID:0110335
osteomalacia
class of disease
bone remodeling disease
disease
bone remodeling disease that has material basis in a vitamin D deficiency which results in softening located in bone
DOID:10573
C05.116.198.816.640
C18.452.104.816.640
C18.452.174.845.640
C18.654.521.500.133.770.734.640
osteomyelitis
class of disease
bone inflammation disease
infectious disease
disease
bone inflammation disease that has material basis in infection located in bone or located in bone marrow
DOID:1019
C01.160.495
C05.116.165.495
Osteomyelitis
osteonecrosis
class of disease
symptom or sign
necrosis
ischemic bone disease
disease
bone death caused when the bone no longer receives blood supply
DOID:10159
C05.116.852
C23.550.717.732
Aseptic osteonecrosis
osteopoikilosis
class of disease
osteosclerosis
osteosclerosis that results in numerous bone islands located in skeleton
DOID:11991
C05.116.099.708.702.685
C17.300.705
Osteopoikilosis
osteoporosis
class of disease
bone resorption disease
disease
bone resorption disease characterized by the thinning of bone tissue and decreased mechanical strength
DOID:11476
C05.116.198.579
C18.452.104.579
Osteoporosis
osteosarcoma
class of disease
bone cancer
cell type cancer
bone sarcoma
osteogenic neoplasm
disease
childhood cancer
bone cancer that is located in bone that has material basis in cells of mesenchymal origin
DOID:3347
C04.557.450.565.575.650
C04.557.450.795.620
Osteosarcoma
osteosarcoma arising in bone Paget's disease
class of disease
bone osteosarcoma
mammary Paget's disease
Human disease
DOID:7542
osteosclerosis
class of disease
bone remodeling disease
disease
bone remodeling disease that results in abnormal elevated bone density or mass
DOID:4254
C05.116.099.708.702
otomycosis
class of disease
symptom or sign
otitis externa
dermatomycosis
disease
human disease
DOID:0050147
C01.150.703.658
C09.218.736
Otomycosis
otopalatodigital syndrome spectrum disorder
class of disease
bone development disease
DOID:0111782
otosclerosis
class of disease
inner ear disease
disease
otitis interna characterized by an abnormal bone growth in the middle ear
DOID:12185
C09.218.768
Otosclerosis
otospondylomegaepiphyseal dysplasia, autosomal dominant
class of disease
osteochondrodysplasia
autosomal dominant disease
human disease
DOID:0080677
outlet dysfunction constipation
class of disease
constipation
Human disease
DOID:2088
ovarian Brenner tumor
class of disease
ovarian benign neoplasm
ovarian benign neoplasm that has material basis in the surface epithelium of the ovary
DOID:2636
Brenner tumour
ovarian Wilms' cancer
class of disease
ovarian cancer
malignant neoplasm of ovary and nephroblastoma that is located in the ovaries
DOID:2153
ovarian angiosarcoma
class of disease
angiosarcoma
ovary sarcoma
sarcoma
ovarian cancer
human disease
DOID:4527
ovarian benign neoplasm
class of disease
female reproductive organ benign neoplasm
ovarian neoplasm
endocrine organ benign neoplasm
ovarian disease
human disease
DOID:0060112
Benign neoplasms of the ovary
ovarian biphasic or triphasic teratoma
class of disease
ovarian germ cell teratoma
Human disease
DOID:6232
ovarian cancer
class of disease
female reproductive organ cancer
ovarian neoplasm
ovarian disease
endocrine gland cancer
rare genetic endocrine disease
inherited gynecological tumor
disease
female reproductive organ cancer that is located in the ovary
DOID:2394
Ovarian cancer
ovarian carcinoma
class of disease
malignant ovarian surface epithelial-stromal neoplasm
carcinoma
human disease
DOID:4001
ovarian carcinosarcoma
class of disease
malignant ovarian surface epithelial-stromal neoplasm
carcinosarcoma
mixed Müllerian tumor
Human disease
DOID:6170
ovarian clear cell adenocarcinoma
class of disease
ovary adenocarcinoma
clear cell adenocarcinoma
Human disease
DOID:5304
ovarian clear cell adenofibroma
class of disease
ovarian benign neoplasm
Human disease
DOID:5897
ovarian clear cell cystadenocarcinoma
class of disease
ovarian cystadenocarcinoma
ovarian clear cell adenocarcinoma
Human disease
DOID:7438
ovarian clear cell cystadenofibroma
class of disease
ovarian clear cell adenofibroma
clear cell cystadenofibroma
Human disease
DOID:5896
ovarian clear cell malignant adenofibroma
class of disease
ovarian cancer
Human disease
DOID:6554
ovarian cyst
class of disease
ovarian disease
ovarian neoplasm
disease
fluid-filled sac in the ovary
DOID:5119
C04.182.612
C13.351.500.056.630.580
C19.391.630.580
Ovarian cysts
ovarian cystadenocarcinoma
class of disease
ovary adenocarcinoma
cystadenocarcinoma
ovarian cystadenoma
human disease
DOID:3605
ovarian cystadenoma
class of disease
ovarian benign neoplasm
benign epithelial neoplasm
human disease
DOID:3269
ovarian cystic teratoma
class of disease
mature teratoma of the ovary
Human disease
DOID:5118
Mature cystic teratoma of ovary
ovarian disease
class of disease
female reproductive system disease
gonadal disease
adnexal disease
Human disease
DOID:1100
C13.351.500.056.630
C19.391.630
Diseases and disorders of ovaries
ovarian dysfunction
class of disease
ovarian disease
Human disease
DOID:1414
ovarian dysgenesis 1
class of disease
autosomal recessive disease
46 XX gonadal dysgenesis
46 XX gonadal dysgenesis that has material basis in homozygous or compound heterozygous mutation in the gene encoding follicle-stimulating hormone receptor on chromosome 2p16
DOID:0080493
ovarian dysgenesis 4
class of disease
autosomal recessive disease
46 XX gonadal dysgenesis
46 XX gonadal dysgenesis that has material basis in homozygous mutation in the MCM9 gene on chromosome 6q22
DOID:0080496
ovarian dysgenesis 5
class of disease
autosomal recessive disease
46 XX gonadal dysgenesis
46 XX gonadal dysgenesis that has material basis in homozygous mutation in the SOHLH1 gene on chromosome 9q34
DOID:0080497
ovarian dysgenesis 6
class of disease
autosomal recessive disease
46 XX gonadal dysgenesis
46 XX gonadal dysgenesis that has material basis in homozygous mutation in the NUP107 gene on chromosome 12q15
DOID:0080498
ovarian dysgenesis 7
class of disease
autosomal recessive disease
46 XX gonadal dysgenesis
46 XX gonadal dysgenesis that has material basis in homozygous mutation in the MRPS22 gene on chromosome 3q23
DOID:0080499
ovarian dysgenesis 8
class of disease
46 XX gonadal dysgenesis
autosomal dominant disease
46 XX gonadal dysgenesis that has material basis in heterozygous mutation in the ESR2 gene on chromosome 14q23
DOID:0080500
ovarian embryonal carcinoma
class of disease
embryonal carcinoma
malignant non-dysgerminomatous germ cell tumor of ovary
ovarian cancer
embryonal carcinoma that is located in the ovary
DOID:5681
ovarian endodermal sinus tumor
class of disease
ovarian primitive germ cell tumor
malignant non-dysgerminomatous germ cell tumor of ovary
endodermal sinus tumor
Human disease
DOID:5350
ovarian endometrial cancer
class of disease
surface epithelial-stromal tumor
Endometrioid tumor
female reproductive endometrioid cancer
ovary epithelial cancer that has material basis in the endometrium and is located in the ovary
DOID:6212
ovarian endometrioid adenofibroma
class of disease
ovarian benign neoplasm
Human disease
DOID:5480
ovarian endometrioid cystadenofibroma
class of disease
ovarian endometrioid adenofibroma
cystadenofibroma
Human disease
DOID:7411
ovarian endometrioid cystadenoma
class of disease
ovarian cystadenoma
Human disease
DOID:7191
ovarian endometrioid malignant adenofibroma
class of disease
ovarian carcinosarcoma
malignant adenofibroma
Human disease
DOID:6445
ovarian endometrioid stromal sarcoma
class of disease
ovary sarcoma
Human disease
DOID:5169
ovarian fetiform teratoma
class of disease
mature teratoma of the ovary
Human disease
DOID:6314
ovarian germ cell monodermal and highly specialized teratoma
class of disease
monodermal teratoma
Human disease
DOID:2641
ovarian germ cell neoplasm
class of disease
ovarian neoplasm
germ cell tumor
germ cell and embryonal neoplasms
ovarian cancer
benign or malignant ovarian tumor that originates in the germ (egg) cells of the ovary
DOID:2156
Germ cell neoplasms
ovarian germ cell teratoma
class of disease
ovarian germ cell neoplasm
teratoma
gonadal teratoma
female reproductive organ cancer
Human disease
DOID:5567
Ovarian teratomas
ovarian gonadoblastoma
class of disease
ovarian benign neoplasm
gonadoblastoma
Human disease
DOID:3578
ovarian large-cell neuroendocrine carcinoma
class of disease
ovarian carcinoma
familiar ovarian carcinoma
inherited neuroendocrine tumor
large cell neuroendocrine carcinoma
Human disease
DOID:4555
ovarian lymphoma
class of disease
ovarian cancer
lymphoma
Human disease
DOID:2150
ovarian malignant mesothelioma
class of disease
ovarian cancer
Human disease
DOID:2143
ovarian melanoma
class of disease
ovarian cancer
ovarian cancer that has material basis in melanoctyes
DOID:0050928
ovarian mesodermal adenosarcoma
class of disease
ovarian carcinosarcoma
adenosarcoma
adenosarcoma and malignant ovarian endometroid tumorthat is located in the ovary
DOID:4115
ovarian mixed germ cell neoplasm
class of disease
ovarian primitive germ cell tumor
mixed germ cell cancer
Human disease
DOID:5936
ovarian mucinous adenocarcinoma
class of disease
ovary adenocarcinoma
malignant ovarian mucinous tumor
mucinous adenocarcinoma
human disease
DOID:3606
ovarian mucinous adenofibroma
class of disease
ovarian benign neoplasm
human disease
DOID:6469
ovarian mucinous cystadenocarcinoma
class of disease
ovarian cystadenocarcinoma
mucinous cystadenocarcinoma
ovarian mucinous adenocarcinoma
Human disease
DOID:3604
ovarian mucinous cystadenofibroma
class of disease
ovarian mucinous adenofibroma
mucinous cystadenofibroma
Human disease
DOID:7013
ovarian mucinous malignant adenofibroma
class of disease
malignant ovarian mucinous tumor
malignant adenofibroma
ovarian mucinous neoplasm
Human disease
DOID:6278
ovarian mucinous neoplasm
class of disease
surface epithelial-stromal tumor
mucinous tumor
Human disease
DOID:6067
Ovarian mucinous tumors
ovarian papillary cystadenoma
class of disease
ovarian papillary neoplasm
papillary adenoma
ovarian cystadenoma
Human disease
DOID:6405
ovarian papillary neoplasm
class of disease
surface epithelial-stromal tumor
Human disease
DOID:6214
ovarian primitive germ cell tumor
class of disease
malignant ovarian germ cell neoplasm
Human disease
DOID:5351
ovarian serous adenofibroma
class of disease
ovarian benign neoplasm
serous adenofibroma
Human disease
DOID:5474
ovarian serous carcinoma
class of disease
ovarian carcinoma
serous carcinoma
ovarian serous tumor
ovarian carcinoma that has material basis in the lining of the ovary and produces a serum-like fluid
DOID:0050933
Ovarian serous carcinoma
ovarian serous cystadenofibroma
class of disease
ovarian serous adenofibroma
cystadenofibroma
Human disease
DOID:7320
ovarian serous cystadenoma
class of disease
serous cystadenoma
ovarian benign neoplasm
ovarian cystadenocarcinoma
serous cystadenocarcinoma
ovarian cystadenoma
ovarian serous tumor
ovary serous adenoma that has material basis in glandular epithelium, in which cystic accumulations of retained secretions are formed
DOID:5746
DOID:3914
C04.557.470.035.320.240
C04.557.470.590.485.240
Ovarian serous cystadenoma
ovarian sex cord-stromal tumor
class of disease
sex cord-gonadal stromal tumor
A benign or malignant neoplasm that arises from the ovary and is composed of granulosa cells, Sertoli cells, Leydig cells, theca cells, and fibroblasts. Representative examples include thecoma, fibroma, Sertoli cell tumor, and granulosa cell tumor.
DOID:0080369
ovarian small cell carcinoma
class of disease
ovarian carcinoma
small cell carcinoma
Human disease
DOID:6179
ovarian solid teratoma
class of disease
mature teratoma of the ovary
Human disease
DOID:6315
ovarian squamous cell carcinoma
class of disease
ovarian squamous cell neoplasm
squamous cell carcinoma
ovarian cancer
Human disease
DOID:5531
ovarian squamous cell neoplasm
class of disease
surface epithelial-stromal tumor
Human disease
DOID:5532
ovarian surface papilloma
class of disease
ovarian papillary neoplasm
Human disease
DOID:6407
ovary adenocarcinoma
class of disease
ovarian carcinoma
adenocarcinoma
ovarian carcinoma that derives from epithelial cells of glandular origin
DOID:3713
Adenocarcinomas of the ovary
ovary leiomyosarcoma
class of disease
leiomyosarcoma
Human disease
DOID:5263
ovary mixed epithelial carcinoma
class of disease
ovarian carcinoma
Human disease
DOID:6898
DOID:6899
ovary neuroendocrine neoplasm
class of disease
ovarian cancer
neuroendocrine tumor
Human disease
DOID:3002
ovary papillary carcinoma
class of disease
ovarian papillary neoplasm
ovarian carcinoma
Human disease
DOID:6408
ovary rhabdomyosarcoma
class of disease
ovary sarcoma
rhabdomyosarcoma
Human disease
DOID:4059
ovary sarcoma
class of disease
ovarian cancer
sarcoma
human disease
DOID:2146
ovary serous adenocarcinoma
class of disease
ovary adenocarcinoma
ovarian serous carcinoma
ovary adenocarcinoma that derives from the lining of a cavity that produces a serum-like fluid (a serous cavity)
DOID:5744
Serous adenocarcinoma of the ovary
overhydrated hereditary stomatocytosis
class of disease
macrocytic anemia
autosomal dominant disease
hereditary stomatocytosis
human disease
DOID:0111562
overnutrition
class of disease
nutrition disorder
malnutrition
form of malnutrition in which the intake of nutrients is oversupplied
DOID:654
C18.654.726
ovine and caprine brucellosis
class of disease
brucellosis
A brucellosis that involves an infection caused by Brucella melitensis [NCBITaxon:29459] in cattle, goats, sheep and humans. The disease has symptom fever, has symptom malaise, has symptom anorexia, has symptom limb pain and has symptom back pain.
DOID:14456
oxirane allergy
class of disease
drug allergy
drug allergy that has allergic trigger oxirane
DOID:0040082
oxyphilic adenoma
class of disease
endocrine organ benign neoplasm
oncocytic neoplasm
benign epithelial neoplasm
disease
Human disease
DOID:5389
C04.557.470.035.140
Oncocytoma
oxyphilic endometrial endometrioid adenocarcinoma
class of disease
endometrial adenocarcinoma
Human disease
DOID:6865
pain agnosia
class of disease
agnosia
absence of pain sensation
agnosia that is a loss of the ability to perceive and process pain
DOID:0060145
pain disorder
class of disease
somatoform disorder
disease
pain
somatoform disorder that involves chronic pain in one or more areas, and is thought to be caused by psychological stress.
DOID:0060164
palindromic rheumatism
class of disease
syndrome
arthritis
human disease
DOID:1166
palladium allergic contact dermatitis
class of disease
allergic contact dermatitis
metal allergy
allergic contact dermatitis that has allergic trigger palladium
DOID:0040055
palmoplantar keratosis
class of disease
keratosis
foot diseases
epidermal disease
disease
keratosis characterized by abnormal thickening of the palms and the soles
DOID:3390
C16.320.850.475
C17.800.428.435
C17.800.827.475
Palmoplantar keratodermas
pancreas disease
class of disease
endocrine system disease
endocrine system disease that is located in the pancreas
DOID:26
C06.689
Diseases and disorders of pancreas
pancreas lymphoma
class of disease
pancreatic cancer
lymphoma
human disease
DOID:1792
pancreas sarcoma
class of disease
pancreatic cancer
sarcoma
pancreatic cancer that is located in the pancreas and that arises from transformed cells of mesenchymal origin
DOID:1796
pancreatic ACTH hormone producing tumor
class of disease
islet cell tumor
Human disease
DOID:7697
pancreatic acinar cell adenocarcinoma
class of disease
pancreatic adenocarcinoma
Acinar cell carcinoma of the pancreas
acinar adenocarcinoma
pancreatic adenocarcinoma that has material basis in cells with morphological resemblance to acinar cells and is associated with increased serum lipase
DOID:5742
pancreatic adenocarcinoma
class of disease
pancreatic carcinoma
adenocarcinoma
pancreatic carcinoma that derives from epithelial cells of glandular origin
DOID:4074
Adenocarcinomas of the pancreas
pancreatic cancer
class of disease
endocrine gland cancer
pancreas disease
pancreatic neoplasm
gastrointestinal system cancer
disease
endocrine gland cancer located in the pancreas
DOID:1793
Pancreatic cancer
pancreatic carcinoma
class of disease
pancreatic cancer
carcinoma
gastrointestinal carcinoma
pancreas cancer that derives from epithelial cells located in the pancreas
DOID:4905
pancreatic cholera
class of disease
endocrine pancreas disease
Human disease
DOID:6977
pancreatic colloid cystadenocarcinoma
class of disease
pancreatic cystadenocarcinoma
mucinous cystadenocarcinoma
Human disease
DOID:7234
pancreatic cystadenocarcinoma
class of disease
pancreatic adenocarcinoma
cystadenocarcinoma
Human disease
DOID:4073
pancreatic cystadenoma
class of disease
benign neoplasm of exocrine pancreas
endocrine organ benign neoplasm
benign neoplasm of pancreas
gastrointestinal system benign neoplasm
pancreas disease
human disease
DOID:3918
pancreatic delta cell neoplasm
class of disease
islet cell tumor
Human disease
DOID:4433
pancreatic ductal adenocarcinoma
class of disease
pancreatic adenocarcinoma
pancreatic adenocarcinoma that derives from pancreatic duct cells
DOID:3498
pancreatic ductal carcinoma
class of disease
pancreatic cancer
ductal carcinoma
pancreatic carcinoma
most common cancer of the pancreas
DOID:3587
C04.557.470.200.025.232.750
C04.557.470.615.132.750
C04.588.274.761.750
C04.588.322.475.750
C06.301.761.750
C06.689.667.625
C19.344.421.750
pancreatic foamy gland adenocarcinoma
class of disease
pancreatic adenocarcinoma
Human disease
DOID:7577
pancreatic gastrinoma
class of disease
islet cell tumor
functional pancreatic neuroendocrine tumor
Human disease
DOID:5580
pancreatic intraductal papillary-colloid carcinoma
class of disease
pancreatic adenocarcinoma
pancreatic intraductal papillary-mucinous neoplasm
Human disease
DOID:7574
pancreatic intraductal papillary-mucinous adenoma
class of disease
pancreatic intraductal papillary-mucinous neoplasm
adenoma of pancreas
gastrointestinal system benign neoplasm
adenoma
Human disease
DOID:7851
pancreatic intraductal papillary-mucinous neoplasm
class of disease
cancer of exocrine pancreas
Human disease
DOID:7575
pancreatic invasive intraductal papillary-mucinous carcinoma
class of disease
pancreatic intraductal papillary-colloid carcinoma
Human disease
DOID:8150
pancreatic invasive mucinous cystadenocarcinoma
class of disease
pancreatic colloid cystadenocarcinoma
Human disease
DOID:7236
pancreatic mucinous cystadenoma
class of disease
mucinous cystadenoma
pancreatic cystadenoma
human disease
DOID:7235
pancreatic mucinous ductal ectasia
class of disease
pancreas disease
Human disease
DOID:13313
pancreatic non-functioning delta cell tumor
class of disease
pancreatic delta cell neoplasm
non-functioning pancreatic endocrine tumor
Human disease
DOID:7840
pancreatic non-invasive intraductal papillary-mucinous carcinoma
class of disease
pancreatic intraductal papillary-colloid carcinoma
pancreatic intraductal papillary-mucinous neoplasm
Human disease
DOID:7685
pancreatic non-invasive mucinous cystadenocarcinoma
class of disease
pancreatic colloid cystadenocarcinoma
human disease
DOID:7237
pancreatic serous cystadenocarcinoma
class of disease
pancreatic cystadenocarcinoma
serous cystadenocarcinoma
pancreatic serous cystic neoplasm
Human disease
DOID:5751
pancreatic serous cystadenoma
class of disease
serous cystadenoma
pancreatic cystadenoma
disease
human disease
DOID:3917
Serous cystadenoma pancreas
pancreatic serous cystic neoplasm
class of disease
pancreatic exocrine neoplasm
Serous tumour
cystic lesions of the pancreas
cancer of exocrine pancreas
Human disease
DOID:3919
Serous cystic neoplasms of the pancreas
pancreatic signet ring cell adenocarcinoma
class of disease
pancreatic ductal adenocarcinoma
signet ring cell adenocarcinoma
Human disease
DOID:3497
pancreatic solid pseudopapillary carcinoma
class of disease
pancreatic carcinoma
pancreatic carcinoma that is characterized by its papillary architecture
DOID:6827
pancreatic somatostatinoma
class of disease
islet cell tumor
pancreatic delta cell neoplasm
somatostatinoma
Human disease
DOID:4432
pancreatic squamous cell carcinoma
class of disease
pancreatic cancer
squamous cell carcinoma
squamous cell carcinoma located in the pancreas
DOID:0080323
pancreatic steatorrhea
class of disease
pancreas disease
steatorrhea
Human disease
DOID:10610
pancreatic vasoactive intestinal peptide producing tumor
class of disease
islet cell tumor
Human disease
DOID:5741
pancreatoblastoma
class of disease
pancreatic carcinoma
rare epithelial tumor of pancreas
disease
Human disease
DOID:6823
pancytopenia
class of disease
anemia
cytopenia
disease
medical condition in which there is a reduction in the number of red and white blood cells, as well as platelets
DOID:12450
C15.378.243.875
panhypopituitarism, X-linked
class of disease
panhypopituitarism
X-linked disease
human disease
DOID:0111779
panic disorder
class of disease
anxiety disorder
disease
anxiety disorder characterized by reoccurring unexpected panic attacks
DOID:594
F03.080.700
Panic disorder
panniculitis
class of disease
fibromyalgia
connective tissue disease
skin disease
disease
Inflammation of the subcutaneous adipose tissue
DOID:1526
C17.300.710
C17.800.566
Panniculitis
panuveitis
class of disease
uveitis
Human disease
DOID:12030
C11.941.879.780
papillary adenocarcinoma
class of disease
adenocarcinoma
adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue
DOID:3112
C04.557.470.200.025.085
papillary adenofibroma
class of disease
adenofibroma
biphasic polypoid neoplasm characterized by the presence of papillary projections that are lined by epithelial cells and fibrotic stroma
DOID:5479
papillary adenoma
class of disease
glandular cell epithelial neoplasm
adenoma
Human disease
DOID:3172
papillary carcinoma
class of disease
carcinoma
carcinoma derived from epithelial cells with finger-like projections
DOID:3113
C04.557.470.200.360
C04.557.470.700.360
papillary conjunctivitis
class of disease
conjunctivitis
Human disease
DOID:2458
papillary craniopharyngioma
class of disease
craniopharyngioma
Human disease
DOID:3847
papillary cystadenocarcinoma
class of disease
cystadenocarcinoma
papillary cystic tumor
cystadenocarcinoma that derives from epithelial cells originating in glandular tissue, with cysts and papillary endophytic projections
DOID:3110
C04.557.470.200.025.480.230
C04.557.470.590.480.230
papillary eccrine adenoma
class of disease
eccrine sweat gland neoplasm
papillary adenoma
Human disease
DOID:5446
papillary ependymoma
class of disease
benign ependymoma
human disease
DOID:5505
papillary extrahepatic bile duct adenocarcinoma
class of disease
extrahepatic bile duct adenocarcinoma
Human disease
DOID:6931
papillary follicular thyroid adenocarcinoma
class of disease
papillary thyroid cancer
Human disease
DOID:3968
C04.557.470.200.025.060.225
C04.557.470.200.025.085.225
papillary hidradenoma
class of disease
hidradenoma
Human disease
DOID:5439
Papillary hidradenoma
papillary meningioma of the cerebellum
class of disease
cerebellum cancer
rhabdoid meningioma
papillary meningioma
brain meningioma
Human disease
DOID:5057
papillary pattern testicular yolk sac tumor
class of disease
testicular yolk sac tumor
Human disease
DOID:8193
papillary renal cell carcinomas
class of disease
renal cell carcinoma
renal cell carcinoma that is characterized by the development of multiple, bilateral papillary renal tumors
DOID:4465
papillary serous adenocarcinoma
class of disease
papillary adenocarcinoma
papillary adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures with psammoma bodies
DOID:2632
papillary squamous carcinoma
class of disease
squamous cell carcinoma
papillary carcinoma
Human disease
DOID:4385
papillary thymic adenocarcinoma
class of disease
thymus adenocarcinoma
Human disease
DOID:5595
papillary thyroid cancer
class of disease
thyroid carcinoma
papillary carcinoma
differentiated thyroid carcinoma
thyroid carcinoma that is characterized by the small mushroom shape of the tumor which has a stem attached to the epithelial layer
DOID:3969
C04.557.470.200.025.085.612
C04.588.322.894.400
C04.588.443.915.400
C19.344.894.400
C19.874.788.400
Thyroid papillary carcinoma
papillary transitional carcinoma
class of disease
transitional cell carcinoma
transitional cell carcinoma that has several papillary fronds with central fibrovascular core lined by transitional type epithelium
DOID:4012
Urothelial papillary carcinoma
papillary urothelial neoplasm of low malignant potential
class of disease
bladder papillary transitional cell neoplasm
urinary tract non-invasive transitional cell neoplasm
papillary urothelial lesion
human disease
DOID:6239
papilledema
class of disease
optic nerve disease
disease
Human disease
DOID:146
C10.292.700.900
C11.640.710
Papilledema
papilloma
class of disease
benign neoplasms by histologic type
papillary tumor
disease
cell type benign neoplasm that is composed of epithelial tissue on papillae of vascularized connective tissue
DOID:2615
C04.557.470.700.600
Papillomas
parachordoma
class of disease
mesenchymal cell neoplasm
Human disease
DOID:2647
paralytic ileus
class of disease
bowel obstruction
ileus
Human disease
DOID:8442
Paralytic ileus
paralytic lagophthalmos
class of disease
lagophthalmos
Human disease
DOID:12958
paralytic poliomyelitis
class of disease
poliomyelitis
central nervous system disease
Human disease
DOID:0050515
paralytic squint
class of disease
strabismus
cranial nerve palsy
Human disease
DOID:10863
parameningeal embryonal rhabdomyosarcoma
class of disease
embryonal rhabdomyosarcoma
embryonal rhabdomyosarcoma located in the parameningeal region
DOID:0060338
parametritis
class of disease
pelvic inflammatory diseases
inflammatory disease
uterine disease
Human disease
DOID:1260
C13.351.500.056.750.750
parametrium malignant neoplasm
class of disease
uterine adnexa cancer
broad ligament malignant neoplasm
Human disease
DOID:11746
paramyotonia congenita of Von Eulenburg
class of disease
neuromuscular disease
autosomal dominant disease
paramyotonia congenita
human disease
DOID:0111538
paranasal sinus disease
class of disease
nose disease
respiratory disease
DOID:1352
C08.460.692
C09.603.692
paranasal sinus lymphoma
class of disease
paranasal sinus cancer
lymphoma
human disease
DOID:1355
paranasal sinus neoplasm
class of disease
respiratory tract neoplasm
paranasal sinus disease
respiratory system benign neoplasm
human disease
DOID:1350
C04.588.443.665.650.693
C08.460.669.693
C08.460.692.503
C08.785.600.693
C09.603.669.693
C09.603.692.503
C09.647.685.693
Neoplasms of paranasal sinuses
paranasal sinus sarcoma
class of disease
paranasal sinus cancer
sarcoma
sarcoma and malignant tumor of nasal sinuses that is located in the paranasal sinus
DOID:1362
paraneoplastic pemphigus
class of disease
pemphigus
human disease
DOID:0080852
paraneoplastic polyneuropathy
class of disease
inflammatory and toxic neuropathy
peripheral neuropathy
paraneoplastic neurologic syndrome
Human disease
DOID:8681
C04.588.614.550.700
C04.730.856.700
C10.574.781.850
C10.668.829.800.662
paranoid personality disorder
class of disease
personality disorder
disease
mental disorder characterized by paranoia and a pervasive, long-standing suspiciousness and generalized mistrust of others
DOID:10938
F03.675.600
Paranoid personality disorder
parapharyngeal meningioma
class of disease
meningioma
Human disease
DOID:8216
paraphilia
class of disease
psychosexual disorder
sexual and gender disorder
disease
experience of intense sexual arousal to atypical objects, situations, or individuals
DOID:0060044
F03.657
Paraphilias
paraphimosis
class of disease
phimosis
disease
medical condition in which the foreskin of a penis becomes trapped behind the glans penis
DOID:5334
C12.294.494.684.587
Paraphimosis
paraplegia
class of disease
symptom or sign
central nervous system disease
paralysis
disease
impairment in motor or sensory function of the lower extremities
DOID:607
C10.597.622.669
C23.888.592.636.637
Paraplegia
parapsoriasis
class of disease
psoriasis
disease
Human disease
DOID:9088
C17.800.859.575
parasagittal meningioma
class of disease
cerebral convexity meningioma
Human disease
DOID:6869
parasitic Ichthyosporea infectious disease
class of disease
parasitic infectious diseases
parasitic infectious disease that involves parasitic infection by the members of the class Ichthyosporea, which are parasites of fish and other animals
DOID:0050291
C03.600
parasitic conjunctivitis
class of disease
chronic conjunctivitis
parasitic eye infection
Human disease
DOID:13341
parasitic eyelid infestation
class of disease
blepharitis
parasitic eye infection
Human disease
DOID:13823
parasitic protozoa infectious disease
class of disease
parasitic infectious diseases
disease
parasitic disease caused by a protozoan
DOID:2789
C01.610.752
paratesticular lipoma
class of disease
reproductive organ benign neoplasm
lipoma
Human disease
DOID:10207
parathyroid adenoma
class of disease
parathyroid neoplasm
benign parathyroid gland neoplasm
benign neoplasms by histologic type
adenoma
disease
Human disease
DOID:7608
Parathyroid adenoma
parathyroid gland disease
class of disease
endocrine system disease
endocrine disease
DOID:11201
C19.642
parathyroid oncocytic adenoma
class of disease
parathyroid adenoma
oxyphilic adenoma
Human disease
DOID:7611
parathyroid transitional clear cell adenoma
class of disease
parathyroid adenoma
Human disease
DOID:7609
paraurethral gland cancer
class of disease
female reproductive organ cancer
paraurethral gland neoplasm
Human disease
DOID:14059
paraurethral gland neoplasm
class of disease
urethral benign neoplasm
Human disease
DOID:2139
parenchymatous neurosyphilis
class of disease
tertiary neurosyphilis
Human disease
DOID:0050490
parietal lobe ependymoma
class of disease
parietal lobe malignant neoplasm
ependymoma
parietal lobe neoplasm that has material basis in cells lining the ventricles of the brain
DOID:0050903
paronychia
class of disease
nail disease
disease
bacterial or fungal nail infection of the hand or foot
DOID:13117
C01.539.800.460
C17.800.529.639
C17.800.838.486
Paronychia (disease)
parotid disease
class of disease
salivary gland disease
Human disease
DOID:10302
C07.465.815.470
Diseases and disorders of parotid glands
parotitis
class of disease
parotid disease
inflammatory disease
sialadenitis
disease
parotid disease characterized by the inflammation of one or both parotid glands
DOID:10301
C07.465.815.470.800
C07.465.815.793.500
parovarian cyst
class of disease
female reproductive system disease
embryonic cyst of fallopian tube
Human disease
DOID:4333
C04.182.668
C23.300.306.500
paroxysmal nonkinesigenic dyskinesia 2
class of disease
Paroxysmal dyskinesia
dystonia
genetic disease
human disease
DOID:0090047
pars planitis
class of disease
intermediate uveitis
chorioretinitis
ciliary body disease
rare genetic eye disease
disease
Human disease
DOID:12731
C11.941.160.478.700
C11.941.879.780.900.300.659
C11.941.879.900.500
parthenolide allergic contact dermatitis
class of disease
allergic contact dermatitis
allergic contact dermatitis that has allergic trigger parthenolide
DOID:0040072
partial androgen insensitivity syndrome
class of disease
X-linked recessive disease
androgen insensitivity syndrome
medical condition
DOID:0080776
partial arterial retinal occlusion
class of disease
retinal artery occlusion
Human disease
DOID:14522
partial circumpapillary choroid dystrophy
class of disease
hereditary choroidal atrophy
human disease
DOID:9811
partial lipodystrophy
class of disease
lipodystrophy
lipodystrophy that is characterized by partial loss of adipose tissue
DOID:0080299
partial motor epilepsy
class of disease
focal epilepsy
Human disease
DOID:3327
C10.228.140.490.360.272
partial optic atrophy
class of disease
optic atrophy
human disease
DOID:10631
partial pancreatic agenesis
class of disease
pancreas disease
agenesis
pancreatic agenesis
pancreas disease that is characterized by the failure of the pancreas to develop prior to birth
DOID:0050877
partial retinal vein occlusion
class of disease
retinal vein occlusion
Human disease
DOID:1726
partial sensory epilepsy
class of disease
focal epilepsy
Human disease
DOID:3330
C10.228.140.490.360.275
partial third-nerve palsy
class of disease
paralytic squint
oculomotor nerve paralysis
Human disease
DOID:10864
patellar tendinitis
class of disease
tendinitis
knee disorder
knee extensor tendonitis
Human disease
DOID:10471
Patellar tendinitis
patent blue V allergy
class of disease
drug allergy
drug allergy that has allergic trigger patent blue V
DOID:0040080
paternal uniparental disomy of chromosome 14
class of disease
uniparental disomy of paternal origin
uniparental disomy 14
syndrome
human disease
DOID:0111712
pathologic nystagmus
class of disease
nystagmus
ocular motility disease
abnormal eye movements
Human disease
DOID:9650
C10.292.562.675
C11.590.400
patterned macular dystrophy 1
class of disease
patterned macular dystrophy
human disease
DOID:0060866
patulous eustachian tube
class of disease
physiological condition
eustachian tube disease
eustachian tube disorder
DOID:12358
peach allergy
class of disease
fruit allergy
fruit allergy triggered by Prunus persica plant fruit food product.
DOID:0060510
peanut allergy
class of disease
tree nut allergy
legume allergy
vegetable allergy
type of food allergy caused by peanuts
DOID:4378
C20.543.480.370.572.750
pediatric CNS choriocarcinoma
class of disease
malignant childhood germ cell neoplasm
central nervous system choriocarcinoma
rare childhood malignant neoplasm
choriocarcinoma
Human disease
DOID:6639
pediatric CNS embryonal cell carcinoma
class of disease
central nervous system childhood germ cell tumor
central nervous system embryonal carcinoma
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
brain cancer
Human disease
DOID:7231
pediatric angiosarcoma
class of disease
angiosarcoma
rare childhood malignant neoplasm
angiosarcoma that affects children
DOID:4505
pediatric cerebral ependymoblastoma
class of disease
ependymoblastoma
Human disease
DOID:7841
pediatric ependymoma
class of disease
ependymoma
childhood cancer
ependymal tumor
childhood neoplasm
human disease
DOID:5509
pediatric epithelioid sarcoma
class of disease
epithelioid sarcoma
rare childhood malignant neoplasm
Human disease
DOID:7095
pediatric fibrosarcoma
class of disease
fibrosarcoma
rare childhood malignant neoplasm
Human disease
DOID:3520
pediatric germ cell tumor
class of disease
germ cell tumor
childhood neoplasm
Human disease
DOID:6053
pediatric hepatocellular carcinoma
class of disease
hepatocellular carcinoma
childhood cancer of liver
Pediatric hepatocellular carcinoma (pediatric HCC) is a rare, aggressive, malignant hepatic tumor that develops mainly in children over 10 years of age
DOID:0070322
pediatric infratentorial ependymoblastoma
class of disease
childhood infratentorial neoplasm
ependymoblastoma
infratentorial cancer
childhood central nervous system primitive neuroectodermal neoplasm
rare childhood malignant neoplasm
Human disease
DOID:7522
pediatric infratentorial ependymoma
class of disease
infratentorial cancer
pediatric ependymoma
brain ependymoma
childhood infratentorial neoplasm
childhood cancer
Human disease
DOID:7501
pediatric leptomeningeal melanoma
class of disease
meningeal melanoma
Human disease
DOID:6089
pediatric liposarcoma
class of disease
liposarcoma
rare childhood malignant neoplasm
Human disease
DOID:5695
pediatric low-grade glioma
class of disease
low grade glioma
human disease
DOID:0080830
pediatric lymphoma
class of disease
lymphoma
rare childhood malignant neoplasm
Human disease
DOID:5823
pediatric meningioma
class of disease
meningioma
pediatric central nervous system tumor
Human disease
DOID:4593
pediatric mesenchymal chondrosarcoma
class of disease
mesenchymal chondrosarcoma
childhood cancer
Human disease
DOID:4546
pediatric myxoid chondrosarcoma
class of disease
myxoid chondrosarcoma
childhood cancer
Human disease
DOID:6494
pediatric osteosarcoma
class of disease
osteosarcoma
rare childhood malignant neoplasm
Human disease
DOID:3361
pediatric ovarian dysgerminoma
class of disease
pediatric ovarian germ cell tumor
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
dysgerminoma of ovary
dysgerminoma of ovary that occurs in children
DOID:7340
pediatric ovarian germ cell tumor
class of disease
ovarian germ cell neoplasm
pediatric germ cell tumor
Human disease
DOID:6084
pediatric supratentorial ependymoma
class of disease
supratentorial cancer
pediatric ependymoma
brain ependymoma
Human disease
DOID:7502
pediatric testicular germ cell tumor
class of disease
testicular germ cell tumor
pediatric germ cell tumor
Human disease
DOID:6082
peliosis hepatis
class of disease
hepatic vascular disease
Human disease
DOID:914
C06.552.802
Peliosis hepatis
pellagra
class of disease
nutritional deficiency disease
other acquired skin disease
skin disease
disease
Human disease
DOID:8457
C18.654.521.500.133.699.529
Pellagra
pelvic inflammatory diseases
class of disease
female reproductive system disease
adnexal disease
infectious disease
disease
infection of uterus, fallopian tubes, ovaries or the inner surface of pelvis
DOID:1003
C01.635.500
C12.050.351.500.056.750
C12.100.250.056.750
Pelvic inflammatory disease
pelvic lipomatosis
class of disease
lipomatosis
Human disease
DOID:3927
pelvic muscle wasting
class of disease
pelvic organ prolapse
pelvic floor dysfunction
Human disease
DOID:11629
pelvic organ prolapse
class of disease
female reproductive system disease
prolapse
pelvic organs protruding from the opening of the vagina
DOID:1284
C23.300.842.624
Female genital prolapse
pelvic varices
class of disease
varicose veins
Human disease
DOID:9742
pemphigoid
class of disease
autoimmune skin disease
bullous skin disease
human disease
DOID:0080841
penicillin drug reaction
class of disease
adverse drug reaction
beta-lactam allergy
Side effects of penicillin
beta-lactam allergy triggered by penicillin
DOID:0060520
penicilliosis
class of disease
opportunistic mycosis
disease
Human disease
DOID:0050288
penile cancer
class of disease
penile neoplasm
male reproductive organ cancer
penile disease
disease
cancer of the penis
DOID:11615
Penile cancer
penile disease
class of disease
male reproductive system disease
Human disease
DOID:1529
C12.294.494
penile neoplasm
class of disease
male reproductive system neoplasm
penile disease
male reproductive organ benign neoplasm
human disease
DOID:11624
C04.588.945.440.715
C12.294.260.500
C12.294.494.591
C12.758.409.500
Penile neoplasms
penile urethral cancer
class of disease
male urethral cancer
Human disease
DOID:8223
penis Paget's disease
class of disease
penis carcinoma
extramammary Paget's disease
adenocarcinoma of penis
genetic urogenital tumor
Human disease
DOID:3448
Penile Paget's disease
penis basal cell carcinoma
class of disease
penis carcinoma
basal-cell carcinoma
rare skin disease
human disease
DOID:4277
penis basaloid carcinoma
class of disease
penis squamous cell carcinoma
basaloid squamous cell carcinoma
Human disease
DOID:7047
penis carcinoma
class of disease
penile cancer
carcinoma
penile cancer that is located in the skin or tissues of the penis
DOID:3449
penis carcinoma in situ
class of disease
in situ carcinoma
penile disease
penis squamous cell carcinoma
carcinoma in situ of male genital organs
Human disease
DOID:8872
penis mixed squamous cell carcinoma
class of disease
penis squamous cell carcinoma
Human disease
DOID:8009
penis non-invasive verrucous carcinoma
class of disease
penis verrucous carcinoma
penis carcinoma in situ
cervical verrucous carcinoma
Human disease
DOID:5907
penis papillary carcinoma
class of disease
penis squamous cell carcinoma
papillary squamous carcinoma
Human disease
DOID:8013
penis sarcoma
class of disease
penile cancer
sarcoma
sarcoma and malignant neoplasm of penis that is located in the penis
DOID:11838
penis squamous cell carcinoma
class of disease
penis carcinoma
squamous cell carcinoma
penis carcinoma that has material basis in squamous cells
DOID:5518
Squamous-cell carcinoma of the penis
penis verrucous carcinoma
class of disease
penis squamous cell carcinoma
verrucous carcinoma
penis papillary carcinoma
Human disease
DOID:5908
peptic esophagitis
class of disease
peptic ulcer disease
esophagitis
gastroesophageal reflux disease
human disease
DOID:13976
C06.405.117.620.420
C06.405.205.663.420
C06.405.469.275.800.523
C06.405.748.586.524
peptic ulcer disease
class of disease
gastrointestinal system disease
duodenal disease
disease
ulcer of an area of the gastrointestinal tract
DOID:750
C06.405.469.275.800
C06.405.748.586
Peptic ulcers
perforated corneal ulcer
class of disease
corneal ulcer
Human disease
DOID:10445
perforated ulcer
class of disease
peptic ulcer disease
gastric perforation
medical condition of the gastrointestinal tract wall
DOID:752
C06.405.469.275.800.698
C06.405.748.586.698
perforation of bile duct
class of disease
biliary tract disease
Human disease
DOID:13409
periampullary adenocarcinoma
class of disease
ampulla of Vater adenocarcinoma
Human disease
DOID:8110
periampullary adenoma
class of disease
ampulla of Vater neoplasm
adenoma
Human disease
DOID:0050849
perianal gland tumor
class of disease
cancer in dogs
anus neoplasm
dog disease
DOID:4550
C04.588.083
C04.588.274.476.411.307.790.040.040
C06.301.371.411.307.790.040.040
C06.405.249.411.307.790.040.040
C06.405.469.491.307.790.040.040
C06.405.469.860.101.163.083
C06.405.469.860.180.500.040.040
C22.073
perianal hematoma
class of disease
hemorrhoid
Human disease
DOID:9745
Perianal hematoma
perianal skin Paget's disease
class of disease
anal margin carcinoma
extramammary Paget's disease
anal Paget's disease
Human disease
DOID:7708
periapical abscess
class of disease
periapical periodontitis
dental abscess
localized collection of pus associated with a tooth
DOID:2562
C01.539.830.025.650
C07.320.830.700.700
C07.465.714.306.700.700
C07.465.714.533.487.700
periapical periodontitis
class of disease
inflammation
periodontitis
dental pulp disease
periapical disease
tooth pathology
Human disease
DOID:823
C07.320.830.700
C07.465.714.306.700
C07.465.714.533.487
pericardial effusion
class of disease
symptom or sign
pericardium disease
cardiovascular system symptom
disease
pericardium disease that is characterized by an abnormal accumulation of fluid in the pericardial cavity
DOID:118
C14.280.695
Pericardial effusion
pericardial mesothelioma
class of disease
pericardium cancer
mesothelioma
Human disease
DOID:6201
pericarditis
class of disease
pericardium disease
inflammation
inflammatory disease
heart disease
disease
pericardium disease that is characterized by an inflammation of the pericardium and has symptom chest pain
DOID:1787
C14.280.720
Pericarditis
pericardium cancer
class of disease
heart cancer
neoplasm of pericardium
pericardium disease
Human disease
DOID:116
pericardium leiomyoma
class of disease
leiomyoma
benign neoplasm of pericardium
pericardium disease
cardiovascular organ benign neoplasm
Human disease
DOID:5137
pericholangitis
class of disease
ascending cholangitis
primary sclerosing cholangitis
Human disease
DOID:14272
perichondritis of auricle
class of disease
otitis externa
acquired deformities of the ear
Human disease
DOID:222
Perichondritis
pericoronitis
class of disease
gingival disease
human disease
DOID:3671
C07.465.714.258.771
Pericoronitis
periductal breast myoepitheliosis
class of disease
breast myoepitheliosis
Human disease
DOID:7520
perinatal intestinal perforation
class of disease
intestinal perforation
perinatal digestive system disorder
Human disease
DOID:2073
perinatal jaundice due to hepatocellular damage
class of disease
neonatal jaundice
Neonatal hepatitis
Human disease
DOID:11452
perineocele
class of disease
pelvic organ prolapse
human disease
DOID:12637
perinephritis
class of disease
kidney disease
inflammatory disease
connective tissue disease
human disease
DOID:2982
C12.777.419.685
C13.351.968.419.685
perineural angioma
class of disease
deep angioma
hemangioma
central nervous system organ benign neoplasm
Human disease
DOID:8331
perineurioma
class of disease
nerve sheath neoplasms
Human disease
DOID:4697
Perineuroma
periocular meningioma
class of disease
meningioma
intraorbital meningioma
Human disease
DOID:8030
periodic limb movement disorder
class of disease
symptom or sign
sleep disorder
disease
sleep disorder that involves involuntary limb movement during sleep
DOID:9207
C10.886.425.800.600
C10.886.659.618
periodontal disease
class of disease
tooth pathology
jaw disease
disease
human disease
DOID:3388
C07.465.714
periodontitis
class of disease
periodontal disease
disease
gum disease
DOID:824
C07.465.714.533
Periodontitis
periodontosis
class of disease
periodontal disease
tooth pathology
human disease
DOID:9893
periosteal chondrosarcoma
class of disease
chondrosarcoma
Human disease
DOID:5859
periosteal osteogenic sarcoma
class of disease
peripheral osteosarcoma
Human disease
DOID:6489
periostitis
[[:d:Q112193867|class of disea