All diseases

OMIM ID
173650
OMIM term:
KINDLER SYNDROME
Alternative terms:
POIKILODERMA, HEREDITARY ACROKERATOTIC
BULLOUS ACROKERATOTIC POIKILODERMA OF KINDLER AND WEARY
POIKILODERMA, CONGENITAL, WITH BULLAE, WEARY TYPE
(∗) Location:
20p12.3  
(†) Associated OMIM genes:
FERMT1  
(‡) Associated MGI genes:
Fermt1  

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