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| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Lown-Ganong-Levine syndrome | OBSOLETE: Atrial tachyarrhythmia with short PR interval · OBSOLETE: LGL syndrome |
| fr | OBSOLETE : Syndrome de Lown-Ganong-Levine | OBSOLETE : Syndrome LGL · OBSOLETE : Tachyarythmie atriale avec intervalle PR court |
| de | OBSOLET: Lown-Ganong-Levine-Syndrom | |
| es | OBSOLETO: Síndrome de Lown-Ganong-Levine | OBSOLETO: Síndrome LGL · OBSOLETO: Taquiarritmia auricular con intervalo PR corto |
| it | OBSOLETO: Sindrome di Lown-Ganong-Levine | OBSOLETO: Tachiaritmia atriale con intervallo PR corto · OBSOLETO: Sindrome LGL |
| nl | OBSOLEET: Syndroom van Lown-Ganong-Levine | OBSOLEET: Atriale tachyaritmie met kort PR-interval · OBSOLEET: LGL-syndroom |
| pt | OBSOLETO: Síndrome Lown-Ganong-Levine | OBSOLETO: Taquiarritmia auricular com intervalo PR curto |
| pl | NIEAKTUALNE: Częstoskurcz przedsionkowy ze skróconym odstępem PR | NIEAKTUALNE: Zespół Lowna, Ganonga i Levine'a |
| cs | NEAKTUÁLNÍ: Síňová tachyarytmie s krátkým PR intervalem | NEAKTUÁLNÍ: Syndrom krátkého PQ · NEAKTUÁLNÍ: Lownův-Ganongův-Levineův syndrom · NEAKTUÁLNÍ: Lown-Ganong-Levineův syndrom |
| uk | Синдром Лауна-Ганонга-Левіна | Передсердна тахіаритмія з коротким інтервалом PR · Синдром LGL |
| zh | Lown-Ganong-Levine综合征 | 房性快速心律失常伴PR间期缩短 |
| tr | Lown-Ganong-Levine sendromu | LGL sendromu · Kısa PR aralığı ile atriyal taşiaritmi |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/844
- This record as JSON: /data/d/844.json