DISEASES

Disease-gene associations mined from literature

Human genes for nemaline myopathy

Nemaline myopathy [DOID:3191]

A congenital structural myopathy characterized by generally non-progressive muscle weakness of varying severity; certain muscle fibers show the presence of rod-like structures called nemaline bodies.

Synonyms:  nemaline myopathy,  DOID:3191,  Nemaline body disease,  nemaline rod myopathy,  rod myopathy ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7