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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,
Echinobase Genes :
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),
myopathy (is_a)