ORPHA:108973
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 | Syndromic visceral malformation of the liver, biliary tract, pancreas or spleen | |
| fr | Malformation viscérale syndromique du foie, des voies biliaires, du pancréas ou de la rate | |
| de | Syndromale viszerale Fehlbildungen der Leber, der Gallenwege, der Bauchspeicheldrüse oder der Milz | |
| es | Malformación visceral sindrómica del hígado, vías biliares, páncreas o bazo | |
| it | Malformazione viscerale sindromica del fegato, delle vie biliari, del pancreas o della milza | |
| nl | Syndromale viscerale malformatie van lever, galwegen, pancreas of milt | |
| pt | Malformação visceral do fígado, vias biliares, pâncreas ou baço sindrómica | |
| pl | Syndromiczna malformacja trzewna wątroby, dróg żółciowych, trzustki lub śledziony | |
| cs | Syndromické viscerální malformace | |
| uk | Синдромальна вісцеральна вада розвитку | |
| zh | 综合征性内脏畸形 | |
| tr | Sendromik viseral malformasyon |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15214 | E | validated | |
| UMLS | C5681762 | 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:183548Genetic visceral malformation of the liver, biliary tract, pancreas or spleen
rare genetic diseases - ORPHA:98041Visceral malformation of the liver, biliary tract, pancreas or spleen
rare developmental anomalies during embryogenesis; rare abdominal surgical diseases
Children (10):
- ORPHA:52Alagille syndrome
- ORPHA:244283Biliary atresia with splenic malformation syndrome
- ORPHA:527468Diaphragmatic hernia-short bowel-asplenia syndrome
- ORPHA:293864Hypoplastic pancreas-intestinal atresia-hypoplastic gallbladder syndrome
- ORPHA:564Meckel syndrome
- ORPHA:689829Microphthalmia-motor delay-language delay-brain anomalies-diaphragmatic hernia syndrome
- ORPHA:556955Pancreatic agenesis-holoprosencephaly syndrome
- ORPHA:294415Renal-hepatic-pancreatic dysplasia
- ORPHA:97548Right isomerism
- ORPHA:2063Splenogonadal fusion-limb defects-micrognathia syndrome
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/108973
- This record as JSON: /data/d/108973.json