dilated cardiomyopathy 1KK

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Echinobase

Summary

Literature (0)

DOID:0110445 - dilated cardiomyopathy 1KK

Disease Ontology Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the MYPN gene on chromosome 10q21.

Synonyms: CMD1KK

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:615248 - cardiomyopathy, dilated, 1kk; cmd1kk cardiomyopathy, familial hypertrophic, 22, included; cmh22, included;; cardiomyopathy, familial restrictive, 4, included; rcm4, included

MIM:615248 - cardiomyopathy, dilated, 1kk; cmd1kk cardiomyopathy, familial hypertrophic, 22, included; cmh22, included;; cardiomyopathy, familial restrictive, 4, included; rcm4, included

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), dilated cardiomyopathy (is_a)