ORPHA:717619
Capillary-lymphatic-venous malformation
Synonyms: CLVM
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Capillary-lymphatic-venous malformation | CLVM |
| fr | Malformation capillaire-lymphatique-veineuse | = en |
| de | Kapillär-lymphatisch-venöse Fehlbildung | CLVM · Kapillär-lymphatisch-venöse Malformation |
| es | Malformación capilar-linfático-venosa | MCLV |
| it | Malformazione capillare-linfatica-venosa | = en |
| nl | Capillaire-lymfatische-veneuze malformatie | CLVM · Malformatie van capillair, lymfevat en vene |
| pt | Capillary-lymphatic-venous malformation | |
| pl | Malformacja włośniczkowo-limfatyczno-żylna | = en |
| cs | Capillary-lymphatic-venous malformation | = en |
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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 (2):
- ORPHA:211240Genetic vascular anomaly
rare genetic diseases - ORPHA:723518Isolated combined vascular malformation
rare developmental anomalies during embryogenesis; rare circulatory system diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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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/717619
- This record as JSON: /data/d/717619.json