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DO Term : Brugada syndrome 9 [DOID:0110226] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Brugada syndrome that has_material_basis_in heterozygous mutation in the KCND3 gene on chromosome 1p13.

synonyms:
616399,
ICD10CM:I49.8,
OMIM:616399,
BRGDA9

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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