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Familial Long Qt Syndrome (MONDO:0019171)

A hereditary cardiac disease characterized by a prolongation of the QT interval at basal ECG and by a high risk of life-threatening arrhythmias.

Overview

Category

syndromic disease

Ontology ID

MONDO:0019171

Internal:19046

Synonyms

LQTS

Long QT Syndrome

Romano-Ward long QT syndrome

Romano-Ward syndrome

Ward-Romano syndrome

congenital long QT syndrome

familial long QT syndrome

hereditary long QT syndrome

Mapped terms

GARD:0016547

MEDGEN:685787

MedDRA:10057926

NANDO:2200228

NORD:1675

OMIMPS:192500

Orphanet:101016

Orphanet:768

SCTID:442917000

UMLS:C1141890

icd11.foundation:1208831985

Child terms

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