inclusion body myositis

Summary

DOID:3429 - inclusion body myositis

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

Synonyms: Distal Myopathy with Rimmed Vacuoles (DMRV), Distal myopathy, Nonaka type, Hereditary Inclusion Body Myopathy, HIBM, IBM-3, IBM2, inclusion body myopathy 2, inclusion body myopathy 3, Nonaka Myopathy, Nonaka myopathy

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: gne

MIM:

MIM:605637 - inclusion body myopathy 3, autosomal dominant; ibm3
MIM:605820 - nonaka myopathy; nm

MIM:605637 - inclusion body myopathy 3, autosomal dominant; ibm3

MIM:605820 - nonaka myopathy; nm

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): myositis (is_a)