Disease-gene associations mined from literature

Human genes for inclusion body myositis

Inclusion body myositis [DOID:3429]

A myositis that is characterized by slowly progressive weakness and wasting of both distal and proximal muscles, most apparent in the muscles of the arms and legs that can occur in a sporadic or hereditary forms.

Synonyms:  inclusion body myositis,  DOID:3429,  Distal Myopathy with Rimmed Vacuoles (DMRV),  Distal myopathy, Nonaka type,  HIBM ...

Linkouts:  OMIM #1 #2 #3