myofibrillar myopathy 4

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Summary

Literature (0)

DOID:0080095 - myofibrillar myopathy 4

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

Synonyms: zaspopathy

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

MIM:

MIM:609452 - myopathy, myofibrillar, 4; mfm4

MIM:609452 - myopathy, myofibrillar, 4; mfm4

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)