All diseases

OMIM ID
277600
OMIM term:
WEILL-MARCHESANI SYNDROME 1; WMS1
Alternative terms:
WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE
SPHEROPHAKIA-BRACHYMORPHIA SYNDROME
MESODERMAL DYSMORPHODYSTROPHY, CONGENITAL
(∗) Location:
19p13.2  
(†) Associated OMIM genes:
ADAMTS10  
(‡) Associated MGI genes:

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