ORPHA:723264
Syndromic port-wine 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.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Syndromic port-wine capillary malformation | |
| fr | Malformation capillaire syndromique type naevus en tache de vin | |
| de | Syndromale kapilläre Fehlbildung vom Portwein-Typ | Syndromale kapilläre Malformation |
| es | Malformación capilar sindrómica en vino de Oporto | |
| it | Malformazione capillare sindromica a macchia di vino-porto | |
| nl | Syndromale capillaire malformatie, wijnvlek-type | Syndromale capillaire malformatie type naevus flammeus |
| pt | Syndromic port-wine capillary malformation | |
| pl | Syndromic port-wine capillary malformation | |
| cs | Syndromic port-wine capillary malformation |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:211247Rare capillary malformation
rare developmental anomalies during embryogenesis; rare circulatory system diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
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/723264
- This record as JSON: /data/d/723264.json