raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:844

OBSOLETE: Lown-Ganong-Levine syndrome

inactive · referred to ORPHA:101934Genetic cardiac rhythm disease

Synonyms: OBSOLETE: Atrial tachyarrhythmia with short PR interval · OBSOLETE: LGL syndrome

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Genetic cardiac rhythm disease

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Lown-Ganong-Levine syndromeOBSOLETE: Atrial tachyarrhythmia with short PR interval · OBSOLETE: LGL syndrome
frOBSOLETE : Syndrome de Lown-Ganong-LevineOBSOLETE : Syndrome LGL · OBSOLETE : Tachyarythmie atriale avec intervalle PR court
deOBSOLET: Lown-Ganong-Levine-Syndrom
esOBSOLETO: Síndrome de Lown-Ganong-LevineOBSOLETO: Síndrome LGL · OBSOLETO: Taquiarritmia auricular con intervalo PR corto
itOBSOLETO: Sindrome di Lown-Ganong-LevineOBSOLETO: Tachiaritmia atriale con intervallo PR corto · OBSOLETO: Sindrome LGL
nlOBSOLEET: Syndroom van Lown-Ganong-LevineOBSOLEET: Atriale tachyaritmie met kort PR-interval · OBSOLEET: LGL-syndroom
ptOBSOLETO: Síndrome Lown-Ganong-LevineOBSOLETO: Taquiarritmia auricular com intervalo PR curto
plNIEAKTUALNE: Częstoskurcz przedsionkowy ze skróconym odstępem PRNIEAKTUALNE: Zespół Lowna, Ganonga i Levine'a
csNEAKTUÁLNÍ: Síňová tachyarytmie s krátkým PR intervalemNEAKTUÁLNÍ: Syndrom krátkého PQ · NEAKTUÁLNÍ: Lownův-Ganongův-Levineův syndrom · NEAKTUÁLNÍ: Lown-Ganong-Levineův syndrom
ukСиндром Лауна-Ганонга-ЛевінаПередсердна тахіаритмія з коротким інтервалом PR · Синдром LGL
zhLown-Ganong-Levine综合征房性快速心律失常伴PR间期缩短
trLown-Ganong-Levine sendromuLGL sendromu · Kısa PR aralığı ile atriyal taşiaritmi

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

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Genes

0 direct

Orphanet records no gene directly on this code.

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Prevalence and incidence

0 records

No prevalence record in this release.

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HPO phenotypes

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

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Sources for this card