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Echinobase
Summary Literature (0)
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, HIBM, Hereditary Inclusion Body Myopathy, IBM-3, IBM2, Nonaka Myopathy, Nonaka myopathy, inclusion body myopathy 2, inclusion body myopathy 3,

Echinobase Genes : gne


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

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

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