ORPHA:1219
Aurocephalosyndactyly
inactive · moved to ORPHA:794Saethre-Chotzen syndrome
Synonyms: Auralcephalosyndactyly · Kurczynski-Casperson 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 Saethre-Chotzen syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Aurocephalosyndactyly | Auralcephalosyndactyly · Kurczynski-Casperson syndrome |
| fr | Auro-céphalo-syndactylie | Syndrome de Kurczynski-Casperson |
| de | Auro-Zephalo-Syndaktylie | Kurczynski-Casperson-Syndrom |
| es | Aurocefalosindactilia | Síndrome de Kurczynski-Casperson |
| it | Aurocefalosindattilia | Sindrome di Kurczynski-Casperson |
| nl | Aurocefalosyndactylie | Kurczynski-Caspersonsyndroom · Auralcefalosyndactylie |
| pt | Aurocefalossindactilia | Auralcefalossindactilia · Síndrome Kurczynski-Casperson |
| pl | Aurocefalosyndaktylia | Aurocefalosyndaktylia · Zespół Kurczynskiego i Caspersona |
| cs | Aurocefalosyndaktylie | Kurczynského-Caspersonové syndrom · Kurczynski-Caspersonové syndrom |
| uk | Ауроцефалосиндактилія | Ауралцефалосиндактилія · Синдром Курчинського-Касперсона |
| zh | 尖头并趾畸形 | Kurczynski-Casperson综合征 |
| tr | Aurosefalosindaktili | Oralsefalosindaktili · Kurczynski-Casperson sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 109050 | E | validated | |
| MeSH | D000168 | E | validated | |
| UMLS | C1862380 | E | validated | |
| MedDRA | 10000590 | 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.
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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/1219
- This record as JSON: /data/d/1219.json