All diseases

OMIM ID
158300
OMIM term:
ARTHROGRYPOSIS, DISTAL, TYPE 7; DA7
Alternative terms:
TRISMUS-PSEUDOCAMPTODACTYLY SYNDROME
MOUTH, INABILITY TO OPEN COMPLETELY, AND SHORT FINGER-FLEXOR TENDONS
HECHT SYNDROME
(∗) Location:
17p13.1  
(†) Associated OMIM genes:
MYH8  
(‡) Associated MGI genes:

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