{"orpha":108973,"name":"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-108973/","orphanet_url":"https://www.orpha.net/en/disease/detail/108973","names":{"fr":{"name":"Malformation viscérale syndromique du foie, des voies biliaires, du pancréas ou de la rate"},"de":{"name":"Syndromale viszerale Fehlbildungen der Leber, der Gallenwege, der Bauchspeicheldrüse oder der Milz"},"es":{"name":"Malformación visceral sindrómica del hígado, vías biliares, páncreas o bazo"},"it":{"name":"Malformazione viscerale sindromica del fegato, delle vie biliari, del pancreas o della milza"},"nl":{"name":"Syndromale viscerale malformatie van lever, galwegen, pancreas of milt"},"pt":{"name":"Malformação visceral do fígado, vias biliares, pâncreas ou baço sindrómica"},"pl":{"name":"Syndromiczna malformacja trzewna wątroby, dróg żółciowych, trzustki lub śledziony"},"cs":{"name":"Syndromické viscerální malformace"},"uk":{"name":"Синдромальна вісцеральна вада розвитку"},"zh":{"name":"综合征性内脏畸形"},"tr":{"name":"Sendromik viseral malformasyon"}},"xrefs":[{"source":"MONDO","code":"15214","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681762","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":98041,"name":"Visceral malformation of the liver, biliary tract, pancreas or spleen","classifications":[147,182]}],"children":[{"orpha":52,"name":"Alagille syndrome","type":"Malformation syndrome"},{"orpha":244283,"name":"Biliary atresia with splenic malformation syndrome","type":"Malformation syndrome"},{"orpha":527468,"name":"Diaphragmatic hernia-short bowel-asplenia syndrome","type":"Malformation syndrome"},{"orpha":293864,"name":"Hypoplastic pancreas-intestinal atresia-hypoplastic gallbladder syndrome","type":"Malformation syndrome"},{"orpha":564,"name":"Meckel syndrome","type":"Malformation syndrome"},{"orpha":689829,"name":"Microphthalmia-motor delay-language delay-brain anomalies-diaphragmatic hernia syndrome","type":"Disease"},{"orpha":556955,"name":"Pancreatic agenesis-holoprosencephaly syndrome","type":"Disease"},{"orpha":294415,"name":"Renal-hepatic-pancreatic dysplasia","type":"Malformation syndrome"},{"orpha":97548,"name":"Right isomerism","type":"Clinical subtype"},{"orpha":2063,"name":"Splenogonadal fusion-limb defects-micrognathia syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}