All diseases

OMIM ID
121050
OMIM term:
ARTHROGRYPOSIS, DISTAL, TYPE 9; DA9
Alternative terms:
BEALS SYNDROME
CONTRACTURAL ARACHNODACTYLY, CONGENITAL; CCA
(∗) Location:
5q23.3  
(†) Associated OMIM genes:
FBN2  
(‡) Associated MGI genes:
Fbn2  

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* quick link - http://q.sanger.ac.uk/g114255c