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DO Term : dilated cardiomyopathy 1E [DOID:0110433] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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

synonyms:
CDCD2,
dilated cardiomyopathy with conduction defect 2,
dilated cardiomyopathy with conduction disorder and arrhythmia,
601154,
OMIM:601154,
CMD1E,
ICD10CM:I42.0

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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