ORPHA:183536
Genetic congenital limb malformation
- 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 | Genetic congenital limb malformation | |
| fr | Anomalie congénitale des membres d'origine génétique | |
| de | Extremitätenfehlbildung, kongenitale, genetisch bedingte | |
| es | Malformación congénita de las extremidades de origen genético | |
| it | Malformazione congenita genetica degli arti | |
| nl | Genetische congenitale ledemaatmisvorming | |
| pt | Malformação genética congénita dos membros | |
| pl | Wrodzona wada kończyn uwarunkowana genetycznie | |
| cs | Geneticky podmíněné vrozené malformace končetin | |
| uk | Генетично обумовлена вроджена вада розвитку кінцівок | |
| zh | 遗传性先天性肢体多发畸形 | |
| tr | Genetik doğumsal ekstremite malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680557 | 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:183530Rare genetic developmental defect during embryogenesis
rare genetic 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/183536
- This record as JSON: /data/d/183536.json