All diseases

OMIM ID
305600
OMIM term:
FOCAL DERMAL HYPOPLASIA; FDH
Alternative terms:
FODH; DHOF
GOLTZ SYNDROME
GOLTZ-GORLIN SYNDROME
(∗) Location:
Xp11.23  
(†) Associated OMIM genes:
PORCN  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/cht34hq7