ORPHA:2580
OBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome
inactive · referred to ORPHA:102369Rare syndromic 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 Rare syndromic intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome | |
| fr | OBSOLETE : Syndrome d'anomalie des muscles de la ceinture scapulaire-déficience intellectuelle | |
| de | OBSOLET: Schultergürtelsyndrom mit Intelligenzminderung, familiärer Typ | |
| es | OBSOLETO: Síndrome de defectos de la cintura escapular-discapacidad intelectual familiar | |
| it | OBSOLETO: Anomalie dei muscoli del cingolo scapolare - ritardo mentale familiare | |
| nl | OBSOLEET: Schouder- en gordeldefecten - familiale intellectuele achterstand-syndroom | |
| pt | OBSOLETO: Síndrome de anomalia da cintura escapular-perturbação do desenvolvimento intelectual familiar | |
| pl | NIEAKTUALNE: Zespół wad barku i obręczy barkowej zrodzinną niepełnosprawnością intelektualną | |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující defekty ramene a kloubního pletence a familiární mentální retardaci | |
| uk | ЗАСТАРІЛО: Синдром дефектів плечового та поясного суглобів - сімейної розумової відсталості | |
| zh | 弃用:肩带缺陷-家族性智力障碍综合征 | |
| tr | Eski adı: Omuz kuşağı defektleri-ailesel zihinsel yetersizlik 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/2580
- This record as JSON: /data/d/2580.json