ORPHA:715359
Isolated low resistance capillary malformation
Synonyms: Isolated capillary malformation with fast flow
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Infancy, Neonatal
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated low resistance capillary malformation | Isolated capillary malformation with fast flow |
| fr | Malformation capillaire à faible résistance isolée | |
| de | Isolierte kapilläre schnell-fließende Fehlbildung | Isolierte kapilläre fast-flow Malformation |
| es | Malformación capilar aislada de baja resistencia | Malformación capilar aislada de alto flujo |
| it | Malformazione capillare isolata a bassa resistenza | Malformazione capillare isolata a flusso rapido |
| nl | Geïsoleerde capillaire malformatie met lage weerstand | Geïsoleerde capillaire malformatie met snelle bloedstroom · Geïsoleerde fast-flow capillaire malformatie |
| pt | Isolated Capillary malformation with fast-flow | |
| pl | Izolowana malformacja naczyń włosowatych o niskim oporze | = en |
| cs | Isolated low resistance capillary malformation | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q27.8 | NTBT | attributed | 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:715463Low resistance capillary malformation
rare developmental anomalies during embryogenesis; rare circulatory system diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/715359
- This record as JSON: /data/d/715359.json