ORPHA:459526
Rare genetic capillary 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 | Rare genetic capillary malformation | |
| fr | Malformation capillaire génétique rare | |
| de | Seltene genetische kapilläre Fehlbildung | |
| es | Malformación capilar genética rara | |
| it | Malformazione capillare genetica rara | |
| nl | Zeldzame genetische capillaire malformatie | |
| pt | Malformação capilar genética rara | |
| pl | Rzadka genetycznie uwarunkowana malformacja naczyniowa | |
| cs | Vzácné geneticky podmíněné kapilární malformace | |
| uk | Рідкісна генетично обумовлена капілярна вада розвитку | |
| zh | 遗传性罕见毛细血管畸形 | |
| tr | Nadir genetik kılcal damar malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18728 | E | validated | |
| UMLS | C5681109 | 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:211240Genetic vascular anomaly
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/459526
- This record as JSON: /data/d/459526.json