Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (3)
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, Distal Myopathy with Rimmed Vacuoles (DMRV), Distal myopathy, Nonaka type, HIBM, Hereditary Inclusion Body Myopathy, IBM-3, IBM2, Nonaka Myopathy, Nonaka myopathy, inclusion body myopathy 2, inclusion body myopathy 3,

Xenbase Genes : gne, myh2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007827 - inclusion body myositis

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): myositis (is_a)