ORPHA:3122
OBSOLETE: Sinus node disease-myopia syndrome
inactive · referred to ORPHA:166282Hereditary sick sinus syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Familial sick sinus syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Sinus node disease-myopia syndrome | |
| fr | OBSOLETE : Syndrome de troubles du rythme-myopie | |
| de | OBSOLET: Sinusknoten-Syndrom und Myopie | |
| es | OBSOLETO: Síndrome de enfermedad del nodo sinusal-miopía | OBSOLETO: Alteraciones del ritmo cardíaco-miopía |
| it | OBSOLETO: Disturbi del ritmo - miopia | |
| nl | OBSOLEET: Sinusknoopziekte - myopie-syndroom | |
| pt | OBSOLETO: Doença do nó sinusal-miopia | |
| pl | NIEAKTUALNE: Choroba wezla zatokowego - miopia | |
| cs | NEAKTUÁLNÍ: Syndrom sinusového uzlu a myopie | |
| uk | ЗАСТАРІЛО: Синдром захворювання синусового вузла-міопії | |
| zh | 弃用:窦房结病-近视综合征 | |
| tr | Eski adı: Roussy-Lévy sendromu: Sinüs düğümü hastalığı-miyopi sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo 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
- Orphanet page: orpha.net/en/disease/detail/3122
- This record as JSON: /data/d/3122.json