DISEASES

Disease-gene associations mined from literature

Human genes for congenital muscular dystrophy

Congenital muscular dystrophy [DOID:0050557]

A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted.

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