Disease-gene associations mined from literature

Human genes for Duchenne muscular dystrophy

Duchenne muscular dystrophy [DOID:11723]

A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy.

Synonyms:  Duchenne muscular dystrophy,  DOID:11723,  Duchenne muscular dystrophies,  Muscular dystrophy, Duchenne,  Muscular dystrophy Duchenne

Linkouts:  OMIM