ORPHA:498470
Non-syndromic complex polydactyly
- Type
- Category
- Group
- Group of disorders
- Status
- active
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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-syndromic complex polydactyly | |
| fr | Polydactylie complexe non syndromique | |
| de | Polydaktylie, komplexe, nicht-syndromale | |
| es | Polidactilia compleja no sindrómica | |
| it | Polidattilia complessa non sindromica | |
| nl | Niet-syndromale complexe polydactylie | |
| pt | Polidactilia não sindromática complexa | |
| pl | Niesyndromiczna polidaktylia złożona | |
| cs | Nesyndromická komplexní polydaktylie | |
| uk | Несиндромальна складна полідактилія | |
| zh | 非综合征性复杂多指症 | |
| tr | Sendromik olmayan kompleks polidaktili |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681241 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:2913Non-syndromic polydactyly
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/498470
- This record as JSON: /data/d/498470.json