DISEASES

Disease-gene associations mined from literature

Human genes for nemaline myopathy

Nemaline myopathy [DOID:3191]

Nemaline myopathy (also called rod myopathy or nemaline rod myopathy) is a congenital, hereditary neuromuscular disorder that causes muscle weakness, generally nonprogressive, of varying severity.

Synonyms:  nemaline myopathy,  DOID:3191,  Nemaline body disease,  Nemaline myopathy (disorder),  Nemaline body disorder ...