ORPHA:693832
Gastrointestinal tract arteriovenous malformation
Synonyms: Angiodysplasia of the GI tract · GI arteriovenous malformation
- Type
- Malformation syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Childhood, Infancy, Neonatal
- 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 | Gastrointestinal tract arteriovenous malformation | Angiodysplasia of the GI tract · GI arteriovenous malformation |
| fr | Malformation artérioveineuse gastro-intestinale | |
| de | Arteriovenöse Fehlbildung des Gastrointestinaltrakts | Angiodysplasie des Magen-Darm-Trakts |
| es | Malformación arteriovenosa del tracto gastrointestinal | Angiodisplasia del tracto gastrointestinal · Malformación arteriovenosa gastrointestinal |
| it | Malformazione arterovenosa del tratto gastrointestinale | Angiodisplasia del tratto GI · Malformazione arterovenosa GI |
| nl | Arterioveneuze malformatie van maag-darmkanaal | Angiodysplasie van maag-darmkanaal · Arterioveneuze malformatie van tractus gastrointestinalis |
| pt | Malformação arteriovenosa do tracto gastrointestinal | Angiodisplasia do tracto GI · Malformação arteriovenosa GI |
| pl | Malformacja tętniczo-żylna przewodu pokarmowego | = en |
| cs | Gastrointestinal tract arteriovenous malformation | = en |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q27.3 | NTBT | attributed | validated |
| ICD-11 | LA90.3Y | 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 (3):
- ORPHA:165711Rare abdominal surgical disease
rare abdominal surgical diseases - ORPHA:117569Rare intestinal disease
rare gastroenterological diseases - ORPHA:693855Visceral 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.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | <1 / 1 000 000 | — | 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/693832
- This record as JSON: /data/d/693832.json