DISEASES

Disease-gene associations mined from literature

Human genes for inclusion body myositis

Inclusion body myositis [DOID:3429]

A myositis that is characterized by late onset of skeletal muscle inflammation, weakness, and atrophy with cytoplasmic granules and vacuoles in the muscle.

Synonyms:  inclusion body myositis,  DOID:3429,  inclusion body myositises

Linkouts:  OMIM #1 #2 #3