ORPHA:108971
Non-syndromic 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 | Non-syndromic visceral malformation of the liver, biliary tract, pancreas or spleen | |
| fr | Malformation viscérale non syndromique du foie, des voies biliaires, du pancréas ou de la rate | |
| de | Nicht-syndromale viszerale Fehlbildungen der Leber, der Gallenwege, der Bauchspeicheldrüse oder der Milz | |
| es | Malformación visceral no sindrómica del hígado, vías biliares, páncreas o bazo | |
| it | Malformazione viscerale non sindromica del fegato, delle vie biliari, del pancreas o della milza | |
| nl | Niet-syndromale viscerale malformatie van lever, galwegen, pancreas of milt | Niet-syndromale viscerale malformatie van lever, galwegen, alvleesklier of milt |
| pt | Malformação visceral do fígado, vias biliares, pâncreas ou baço não sindrómica | |
| pl | Niesyndromiczna malformacja trzewna wątroby, dróg żółciowych, trzustki lub śledziony | |
| cs | Nesyndromické viscerální malformace | |
| uk | Несиндромальна вісцеральна вада розвитку | |
| zh | 非综合征性内脏畸形 | |
| tr | Sendromik olmayan viseral malformasyon |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15213 | E | validated | |
| UMLS | C5681761 | 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 (3):
- ORPHA:183548Genetic visceral malformation of the liver, biliary tract, pancreas or spleen
rare genetic diseases - ORPHA:506216Rare disorder potentially indicated for bowel transplant
rare transplant-related disorders - ORPHA:98041Visceral malformation of the liver, biliary tract, pancreas or spleen
rare developmental anomalies during embryogenesis; rare abdominal surgical diseases
Children (14):
- ORPHA:674Accessory pancreas
- ORPHA:675Annular pancreas
- ORPHA:53035Caroli disease
- ORPHA:2040Congenital respiratory-biliary fistula
- ORPHA:101351Familial isolated congenital asplenia
- ORPHA:693869Gallblader arteriovenous malformation
- ORPHA:30391Isolated biliary atresia
- ORPHA:662388Isolated gallbladder duplication
- ORPHA:457083Isolated splenogonadal fusion
- ORPHA:693826Pancreatic arteriovenous malformation
- ORPHA:2805Partial pancreatic agenesis
- ORPHA:101063Situs inversus totalis
- ORPHA:693863Splenic arteriovenous malformation
- ORPHA:688523Splenic venous malformation
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/108971
- This record as JSON: /data/d/108971.json