ORPHA:1499
OBSOLETE: Cortada-Koussef-Matsumoto syndrome
inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
- 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 Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Cortada-Koussef-Matsumoto syndrome | |
| fr | OBSOLETE : Syndrome de Cortada-Koussef-Matsumoto | |
| de | OBSOLET: Cortada-Koussef-Matsumoto-Syndrom | |
| es | OBSOLETO: Síndrome de Cortada-Koussef-Matsumoto | |
| it | OBSOLETO: Sindrome di Cortada-Koussef-Matsumoto | |
| nl | OBSOLEET: Syndroom van Cortada-Koussef-Matsumoto | |
| pt | OBSOLETO: Síndrome Cortada-Koussef-Matsumoto | |
| pl | NIEAKTUALNE: Zespól Cortada, Koussefa i Matsumoto | |
| cs | NEAKTUÁLNÍ: Cortada-Koussef-Matsumoto syndrom | |
| uk | ЗАСТАРІЛО: Синдром Кортада-Куссеф-Мацумото | |
| zh | 弃用：科-库-松综合征 | |
| tr | Eski adı: Cortada-Koussef-Matsumoto 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/1499
- This record as JSON: /data/d/1499.json