All diseases

OMIM ID
129400
OMIM term:
RAPP-HODGKIN SYNDROME; RHS
Alternative terms:
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATE OROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED
CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED
(∗) Location:
3q28  
(†) Associated OMIM genes:
TP63  
(‡) Associated MGI genes:

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