Gallblader arteriovenous malformation
Synonyms: Arteriovenous malformation of gallbladder
- Type
- Malformation syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult, Elderly
- Status
- active
A rare visceral arteriovenous malformation characterized by dilated and tortuous feeding arteries and veins of the gallblader. Patients present with abdominal pain. Association with hepatocellular carcinoma in some patients have been reported.
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Gallblader arteriovenous malformation | Arteriovenous malformation of gallbladder |
| fr | Malformation artérioveineuse de la vésicule biliaire | |
| de | Arteriovenöse Fehlbildung der Gallenblase | |
| es | Malformación arteriovenosa de la vesícula biliar | |
| it | Malformazione arterovenosa della cistifellea | |
| nl | Arterioveneuze malformatie van galblaas | |
| pt | Malformação arteriovenosa da vesícula biliar | Vesícula biliar com malformação arteriovenosa |
| pl | Malformacja tętniczo-żylna pęcherzyka żółciowego | = en |
| cs | Gallblader arteriovenous malformation | = en |
Definition in:
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.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:108971Non-syndromic visceral malformation of the liver, biliary tract, pancreas or spleen
rare developmental anomalies during embryogenesis; rare abdominal surgical diseases; rare transplant-related disorders - ORPHA:693855Visceral fast-flow vascular malformation
rare developmental anomalies during embryogenesis; rare circulatory system diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 9 cases | Worldwide | Case(s) | Validated | ORPHANET | |
| 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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/693869
- This record as JSON: /data/d/693869.json