Ectodermal dysplasia, anhidrotic, with cleft lip/palate[1]
Rapp–Hodgkin syndrome was formerly thought to be a unique
autosomal dominant disorder due to a P63 gene mutation. However, it was recently shown to the same disease as
Hay–Wells syndrome.[2]
^"Rapp–Hodgkin syndrome". The Genetic and Rare Diseases Information Center. NIH. Retrieved 19 March 2019.
^Clements SE, Techanukul T, Holden ST, et al. (September 2010). "Rapp–Hodgkin and Hay–Wells ectodermal dysplasia syndromes represent a variable spectrum of the same genetic disorder". Br. J. Dermatol. 163 (3): 624–9.
doi:
10.1111/j.1365-2133.2010.09859.x.
PMID20491771.
S2CID44866051.