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DO Term : long QT syndrome 2 [DOID:0110645] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1.

synonyms:
OMIM:613688,
LQT2,
MESH:C563614,
ICD10CM:I45.8,
GARD:3285,
613688

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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