ORPHA:715284
Spinal cord arteriovenous malformation, nidus type
Synonyms: SCAVM
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Spinal cord arteriovenous malformation, nidus type | SCAVM |
| fr | Malformation artério-veineuse de la moelle épinière, type nidus | = en |
| de | Arteriovenöse Fehlbildung des Rückenmarks vom Nidus-Typ | Arteriovenöse Malformation des Rückenmarks · SCAVM |
| es | Malformación arteriovenosa de la médula espinal, tipo nido | MAV de la médula espinal · SCAVM |
| it | Malformazione arterovenosa del midollo spinale a nido | = en |
| nl | Arterioveneuze malformatie van ruggenmerg, nidus-type | = en |
| pt | Spinal cord arteriovenous malformation | |
| pl | Malformacja tętniczo-żylna rdzenia kręgowego | = en |
| cs | Spinal cord arteriovenous malformation, nidus type | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:715025Spinal fast-flow vascular malformation
rare developmental anomalies during embryogenesis; rare neurological diseases; rare circulatory system diseases
No children.
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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.
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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/715284
- This record as JSON: /data/d/715284.json