dilated cardiomyopathy 1E

Summary

DOID:0110433 - dilated cardiomyopathy 1E

Disease Ontology Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the SCN5A gene on chromosome 3p22.2.

Synonyms: CDCD2, CMD1E, dilated cardiomyopathy with conduction defect 2, dilated cardiomyopathy with conduction disorder and arrhythmia

Xenbase 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

: scn5a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011003 - dilated cardiomyopathy 1E

MONDO:0011003 - dilated cardiomyopathy 1E

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)