ORPHA:946
OBSOLETE: Acrocephalosyndactyly
inactive · referred to ORPHA:139393Syndromic craniosynostosis
Synonyms: OBSOLETE: Acrocephalosyndactylia
- Type
- Clinical group
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Syndromic craniosynostosis
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Acrocephalosyndactyly | OBSOLETE: Acrocephalosyndactylia |
| fr | OBSOLETE : Acro-céphalo-syndactylie | |
| de | OBSOLET: Akrozephalosyndaktylie | |
| es | OBSOLETO: Acrocefalosindactilia | |
| it | OBSOLETO: Acrocefalosindattilia | OBSOLETO: Acrocefalosindattilia |
| nl | OBSOLEET: Acrocefalosyndactylie | OBSOLEET: ACS · OBSOLEET: Acrocephalosyndactylia |
| pt | OBSOLETO: Acrocefalossindactilia | |
| pl | NIEAKTUALNE: Akrocefalosyndaktylia | NIEAKTUALNE: ACS |
| cs | NEAKTUÁLNÍ: Akrocefalosyndaktylie | NEAKTUÁLNÍ: ACS |
| uk | ЗАСТАРІЛО: Акроцефалосиндактилія | ЗАСТАРІЛО: Акроцефалосиндактилія |
| zh | 尖头并指（趾）畸形 | 尖头并指(趾)畸形 |
| tr | Akrosefalosindaktili | ACS · Akrosefalosindaktili |
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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/946
- This record as JSON: /data/d/946.json