{"orpha":108971,"name":"Non-syndromic visceral malformation of the liver, biliary tract, pancreas or spleen","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"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.","url":"https://raremap.alftech.space/d/ORPHA-108971/","orphanet_url":"https://www.orpha.net/en/disease/detail/108971","names":{"fr":{"name":"Malformation viscérale non syndromique du foie, des voies biliaires, du pancréas ou de la rate"},"de":{"name":"Nicht-syndromale viszerale Fehlbildungen der Leber, der Gallenwege, der Bauchspeicheldrüse oder der Milz"},"es":{"name":"Malformación visceral no sindrómica del hígado, vías biliares, páncreas o bazo"},"it":{"name":"Malformazione viscerale non sindromica del fegato, delle vie biliari, del pancreas o della milza"},"nl":{"name":"Niet-syndromale viscerale malformatie van lever, galwegen, pancreas of milt","synonyms":["Niet-syndromale viscerale malformatie van lever, galwegen, alvleesklier of milt"]},"pt":{"name":"Malformação visceral do fígado, vias biliares, pâncreas ou baço não sindrómica"},"pl":{"name":"Niesyndromiczna malformacja trzewna wątroby, dróg żółciowych, trzustki lub śledziony"},"cs":{"name":"Nesyndromické viscerální malformace"},"uk":{"name":"Несиндромальна вісцеральна вада розвитку"},"zh":{"name":"非综合征性内脏畸形"},"tr":{"name":"Sendromik olmayan viseral malformasyon"}},"xrefs":[{"source":"MONDO","code":"15213","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681761","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":183548,"name":"Genetic visceral malformation of the liver, biliary tract, pancreas or spleen","classifications":[156]},{"orpha":506216,"name":"Rare disorder potentially indicated for bowel transplant","classifications":[233]},{"orpha":98041,"name":"Visceral malformation of the liver, biliary tract, pancreas or spleen","classifications":[147,182]}],"children":[{"orpha":674,"name":"Accessory pancreas","type":"Morphological anomaly"},{"orpha":675,"name":"Annular pancreas","type":"Morphological anomaly"},{"orpha":53035,"name":"Caroli disease","type":"Malformation syndrome"},{"orpha":2040,"name":"Congenital respiratory-biliary fistula","type":"Morphological anomaly"},{"orpha":101351,"name":"Familial isolated congenital asplenia","type":"Morphological anomaly"},{"orpha":693869,"name":"Gallblader arteriovenous malformation","type":"Malformation syndrome"},{"orpha":30391,"name":"Isolated biliary atresia","type":"Morphological anomaly"},{"orpha":662388,"name":"Isolated gallbladder duplication","type":"Morphological anomaly"},{"orpha":457083,"name":"Isolated splenogonadal fusion","type":"Morphological anomaly"},{"orpha":693826,"name":"Pancreatic arteriovenous malformation","type":"Malformation syndrome"},{"orpha":2805,"name":"Partial pancreatic agenesis","type":"Morphological anomaly"},{"orpha":101063,"name":"Situs inversus totalis","type":"Morphological anomaly"},{"orpha":693863,"name":"Splenic arteriovenous malformation","type":"Malformation syndrome"},{"orpha":688523,"name":"Splenic venous malformation","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}