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DO Term : long QT syndrome 3 [DOID:0110646] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2.

synonyms:
GARD:3286,
OMIM:603830,
603830,
LQT3,
ICD10CM:I45.8,
MESH:C565840

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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