ORPHA:2474
OBSOLETE: McLain-Dekaban syndrome
inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Synonyms: OBSOLETE: Intellectual disability-coloboma-slimness 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 Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: McLain-Dekaban syndrome | OBSOLETE: Intellectual disability-coloboma-slimness syndrome |
| fr | OBSOLETE : Syndrome de McLain-Dekaban | OBSOLETE : Déficience intellectuelle-minceur-colobome |
| de | OBSOLET: Mclain-Debakian-Syndrom | |
| es | OBSOLETO: Síndrome de McLain-Dekaban | OBSOLETO: Síndrome de discapacidad intelectual-coloboma-delgadez |
| it | OBSOLETO: Sindrome di McLain-Debakian | OBSOLETO: Sindrome disabilità intellettiva-coloboma-magrezza |
| nl | OBSOLEET: Syndroom van McLain-Dekaban | OBSOLEET: Intellectuele achterstand - coloboom - slankheid-syndroom |
| pt | OBSOLETO: Síndrome Mclain-Debakian | OBSOLETO: Síndrome de perturbação do desenvolvimento intelectual-coloboma-magreza |
| pl | NIEAKTUALNE: Zespól McLaina i Dekabana | NIEAKTUALNE: Niepełnosprawność intelektualna - coloboma - wątłość |
| cs | NEAKTUÁLNÍ: McLain-Dekabanův syndrom | = en |
| uk | ЗАСТАРІЛО: Синдром Маклайна-Декабана | ЗАСТАРІЛО: Синдром інтелектуальної недостатності - колобоми - худорлявості |
| zh | 弃用：McLain-Dekaban 综合征 | 智力障碍-缺损-苗条综合征 |
| tr | Eski adı: McLain-Dekaban sendromu | Zihinsel yetersizlik-kolobom-zayıflık 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/2474
- This record as JSON: /data/d/2474.json