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Summary Literature (0)
DOID:0080097 - myofibrillar myopathy 6

Disease Ontology Definition:A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the BAG3 gene on chromosome 10q26.

Synonyms: BAG3-related myofibrillar myopathy

Xenbase Genes : bag3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013061 - myofibrillar myopathy 6

MIM:
MIM:612954 - MYOPATHY, MYOFIBRILLAR, 6; MFM6

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), myofibrillar myopathy (is_a), myopathy (is_a)