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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, Nonaka type, Distal Myopathy with Rimmed Vacuoles, Distal Myopathy with Rimmed Vacuoles (DMRV), Hereditary Inclusion Body Myopathy, HIBM, IBM2, IBM-3, inclusion body myopathy 2, inclusion body myopathy 3, Nonaka myopathy, Nonaka Myopathy
Xenbase Genes
:
gne,
myh2
| MONDO:0007827 - external nose |
| MIM:147421 - INCLUSION BODY MYOSITIS |
| MIM:605637 - CONGENITAL MYOPATHY 6 WITH OPHTHALMOPLEGIA; CMYO6 |
| 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)