All diseases

OMIM ID
193700
OMIM term:
ARTHROGRYPOSIS, DISTAL, TYPE 2A; DA2A
Alternative terms:
FREEMAN-SHELDON SYNDROME; FSS
WHISTLING FACE-WINDMILL VANE HAND SYNDROME
CRANIOCARPOTARSAL DYSTROPHY
CRANIOCARPOTARSAL DYSPLASIA
(∗) Location:
17p13.1  
(†) Associated OMIM genes:
MYH3  
(‡) Associated MGI genes:

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