raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:727126

Isolated congenital long QT syndrome without known causative genetic defect

Synonyms: Isolated congenital LQTS without known causative genetic defect

Type
Etiological subtype
Group
Subtype of disorder
Inheritance
Unknown
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

9 of 12 languages
LangNameSynonyms
enIsolated congenital long QT syndrome without known causative genetic defectIsolated congenital LQTS without known causative genetic defect
frSyndrome du QT long congénital isolé sans anomalie génétique causale connueLQTS congénital isolé sans anomalie génétique causale connue
deIsoliertes kongenitales Long-QT-Syndrom ohne bekannten ursächlichen Gendefekt
esSíndrome de QT largo congénito aislado sin defecto genético causal identificadoSQTL congénito aislado sin defecto genético causal identificado
itSindrome del QT lungo congenita isolata senza difetto genetico notoLQTS congenita isolata senza difetto genetico noto
nlGeïsoleerd congenitaal lang-QT-syndroom zonder gekend causaal genetisch defectGeïsoleerd congenitaal LQTS zonder gekend causaal genetisch defect
ptIsolated congenital Long QT syndrome without known causative genetic defect
plIsolated congenital long QT syndrome without known causative genetic defect= en
csIsolated congenital long QT syndrome without known causative genetic defect= en
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card