ORPHA:101938
Rare vascular liver disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare vascular liver disease | |
| fr | Maladie hépatique vasculaire rare | |
| de | Vaskuläre Leberkrankheit, seltene | |
| es | Enfermedad hepática vascular rara | |
| it | Malattia epatica vascolare rara | |
| nl | Zeldzame vasculaire leverziekte | |
| pt | Doença vascular hepática rara | |
| pl | Rzadkie choroby naczyniowe wątroby | |
| cs | Vzácné vaskulární onemocnění jater | |
| uk | Рідкісні судинні захворювання печінки | |
| zh | 罕见血管性肝病 | |
| tr | Nadir vasküler karaciğer hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15113 | E | validated | |
| UMLS | C5681786 | E | validated | |
| GARD | 19788 | E | 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 (1):
- ORPHA:57146Rare hepatic disease
rare hepatic diseases
Children (12):
- ORPHA:131Budd-Chiari syndrome
- ORPHA:95507Congenital anomaly of hepatic vein
- ORPHA:694228Congenital intrahepatic arterioportal fistula
- ORPHA:480531Congenital portosystemic shunt
- ORPHA:699068Fontan-associated liver disease
- ORPHA:693846Hepatic arteriovenous malformation
- ORPHA:890Hepatic veno-occlusive disease
- ORPHA:79124Hepatic veno-occlusive disease-immunodeficiency syndrome
- ORPHA:774Hereditary hemorrhagic telangiectasia
- ORPHA:480524Idiopathic peliosis hepatis
- ORPHA:854Non-malignant and non-cirrhotic portal vein thrombosis
- ORPHA:596937Portosinusoidal vascular disease
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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/101938
- This record as JSON: /data/d/101938.json