DISEASES

Disease-gene associations mined from literature

Human genes for congenital muscular dystrophy

Congenital muscular dystrophy [DOID:0050557]

A muscular dystrophy that is an autosomal recessive disorder present at birth, which may result in contractures, scoliosis, respiratory and swallowing difficulties, and foot deformities.

Synonyms:  congenital muscular dystrophy,  DOID:0050557

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9 #10 #11 #12 #13 #14 #15 #16 #17 #18