ORPHA:2913
Non-syndromic 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-syndromic polydactyly | |
| fr | Polydactylie non syndromique | |
| de | Polydaktylie, nicht-syndromale | |
| es | Polidactilia no sindrómica | |
| it | Polidattilia | |
| nl | Polydactylie | |
| pt | Polidactilia não-sindromática | |
| pl | Polidaktylia | |
| cs | Polydaktylie | |
| uk | Несиндромна полідактилія | |
| zh | 非综合征型多指畸形 | |
| tr | Sendromik olmayan polidaktili |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 603596 | E | validated | |
| ICD-11 | LB78 | E | specific | validated |
| MONDO | 0011348 | E | validated | |
| MONDO | 11348 | E | validated | |
| MeSH | D017689 | E | validated | |
| UMLS | C0152427 | E | validated | |
| GARD | 4410 | E | validated | |
| MedDRA | 10036063 | 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:93458Non-syndromic polydactyly, syndactyly and/or hyperphalangy
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases
4
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/2913
- This record as JSON: /data/d/2913.json