ORPHA:98041
Visceral malformation of the liver, biliary tract, pancreas or spleen
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Visceral malformation of the liver, biliary tract, pancreas or spleen | |
| fr | Malformation viscérale du foie, des voies biliaires, du pancréas ou de la rate | |
| de | Fehlbildung, viszerale: Leber, Gallengänge, Pankreas, Milz | |
| es | Malformación visceral de hígado, vías biliares, páncreas, bazo | |
| it | Malformazioni degli organi: fegato, tratto biliare, pancreas, milza | |
| nl | Viscerale malformatie van lever, galweg, pancreas of milt | |
| pt | Malformação visceral: fígado, trato biliar, pâncreas, baço | |
| pl | Malformacje wątroby, dróg żółciowych, trzustki lub śledziony | |
| cs | Viscerální malformace jater, žlučových cest, pankreatu nebo sleziny | |
| uk | Вісцеральна вада розвитку печінки, жовчовивідних шляхів, підшлункової залози або селезінки | |
| zh | 肝脏/胆道/胰腺/脾脏引起内脏畸形 | |
| tr | Karaciğer, safra yolları, pankreas veya dalağın viseral malformasyonu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681509 | E | 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 (2):
- ORPHA:165711Rare abdominal surgical disease
rare abdominal surgical diseases - ORPHA:93890Rare developmental defect during embryogenesis
rare developmental anomalies during embryogenesis
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98041
- This record as JSON: /data/d/98041.json