ORPHA:715923
Intraosseous venous malformation
Synonyms: Low-flow vascular malformation of the bone · IOVM
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Autosomal recessive
- Age of onset
- Antenatal, Neonatal
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Intraosseous venous malformation | Low-flow vascular malformation of the bone · IOVM |
| fr | Malformation veineuse osseuse | IOVM |
| de | Intraossäre venöse Fehlbildung | IOVM · Intraossäre venöse Malformation · Low-flow vaskuläre Malformation des Knochens |
| es | Malformación venosa intraósea | IOVM · Malformación vascular ósea de bajo flujo |
| it | Malformazione venosa intraossea | Malformazione vascolare dell'osso a basso flusso · IOVM · Malformazione vascolare ossea a basso flusso |
| nl | Intraossale veneuze malformatie | Low-flow vasculaire malformatie van bot · IOVM · Vaatmalformatie van bot met trage bloedstroom |
| pt | Intraosseous venous malformation | |
| pl | Śródkostna malformacja żylna | = en |
| cs | Intraosseous venous malformation | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q27.8 | NTBT | attributed | validated |
| ICD-11 | LA90.2Y | 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 (2):
- ORPHA:235832Congenital vascular bone syndrome
rare genetic diseases; rare bone diseases - ORPHA:715334Unifocal peripheral venous 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/715923
- This record as JSON: /data/d/715923.json