ORPHA:2829
Partington-Anderson syndrome
inactive · moved to ORPHA:193Cohen syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Cohen syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Partington-Anderson syndrome | |
| fr | Syndrome de Partington-Anderson | |
| de | Partington-Anderson-Syndrom | |
| es | Síndrome de Partington Anderson | |
| it | Sindrome di Partington-Anderson | |
| nl | Syndroom van Partington-Anderson | |
| pt | Síndrome Partington-Anderson | |
| pl | Zespół Partingtona i Andersona | |
| cs | Partingtonův-Andersonův syndrom | Partington-Andersonův syndrom |
| uk | Синдром Партингтона-Андерсона | |
| zh | Partington-Anderson综合征 | |
| tr | Partington-Anderson sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 260555 | E | validated | |
| MeSH | C536299 | E | validated | |
| UMLS | C1850075 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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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.
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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/2829
- This record as JSON: /data/d/2829.json