All diseases

OMIM ID
305100
OMIM term:
ECTODERMAL DYSPLASIA, HYPOHIDROTIC, X-LINKED; XHED
Alternative terms:
XLHED
ECTODERMAL DYSPLASIA, ANHIDROTIC, X-LINKED; EDA
EDA1
ECTODERMAL DYSPLASIA, HYPOHIDROTIC, 1; HED1
ECTODERMAL DYSPLASIA 1; ED1
CHRIST-SIEMENS-TOURAINE SYNDROME
CST SYNDROME
(∗) Location:
Xq13.1  
(†) Associated OMIM genes:
EDA  
(‡) Associated MGI genes:
Eda  

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