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DO Term : long QT syndrome 1 [DOID:0110644] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4.

synonyms:
192500,
OMIM:192500,
ventricular fibrillation with prolonged QT interval,
LQT1,
GARD:3284,
ICD10CM:I45.8

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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