ORPHA:708007
Intramuscular fast-flow vascular anomaly
- Type
- Malformation syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Childhood, Infancy, Neonatal
- Status
- active
A rare fast-flow vascular anomaly located within a muscle characterized by the lesions that are usually well-defined and contain smaller vessels without or with only little obvious arteriovenous shunting on imaging. This anomaly is usually associated with pain.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Intramuscular fast-flow vascular anomaly | |
| fr | Anomalie vasculaire intramusculaire à flux rapide | |
| de | Intramuskuläre schnellfließende Gefäßanomalie | Intramuskuläre fast-flow vaskuläre Malformation |
| es | Anomalía vascular intramuscular de alto flujo | |
| it | Anomalia vascolare intramuscolare a flusso rapido | |
| nl | Intramusculaire fast-flow vasculaire anomalie | Intramusculaire vaatafwijking met snelle bloedstroom |
| pt | Intramuscular fast-flow vascular anomaly | |
| pl | Śródmięśniowa anomalia naczyniowa o szybkim przepływie | |
| cs | Intramuscular fast-flow vascular anomaly |
Definition in:
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.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:707944Peripheral fast-flow 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
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.
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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/708007
- This record as JSON: /data/d/708007.json