All diseases

OMIM ID
608328
OMIM term:
WEILL-MARCHESANI SYNDROME 2; WMS2
Alternative terms:
WEILL-MARCHESANI SYNDROME, AUTOSOMAL DOMINANT
SPHEROPHAKIA-BRACHYMORPHIA SYNDROME
MESODERMAL DYSMORPHODYSTROPHY, CONGENITAL
GLAUCOMA-LENS ECTOPIA-MICROSPHEROPHAKIA-STIFFNESS-SHORTNESS SYNDROME; GEMSS
(∗) Location:
15q21.1  
(†) Associated OMIM genes:
FBN1  
(‡) Associated MGI genes:
Fbn1  

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