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Summary Literature (0)
DOID:0080096 - myofibrillar myopathy 5

Disease Ontology Definition:A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the FLNC gene on chromosome 7q32.

Synonyms: filaminopathy

Xenbase Genes : flnc

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012289 - myofibrillar myopathy 5


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)