Rapp–Hodgkin ectodermal dysplasia syndrome

Rapp–Hodgkin syndrome
Classification and external resources
OMIM	129400
[]

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.

It was first characterized in 1968.

...
Wikipedia