{"orpha":108965,"name":"Syndromic gastroduodenal malformation","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-108965/","orphanet_url":"https://www.orpha.net/en/disease/detail/108965","names":{"fr":{"name":"Malformation gastroduodénale syndromique"},"de":{"name":"Gastroduodenale Fehlbildung, syndromale"},"es":{"name":"Malformación gastroduodenal sindrómica"},"it":{"name":"Malformazione gastroduodenale sindromica"},"nl":{"name":"Syndromale gastroduodenale malformatie"},"pt":{"name":"Malformação gastroduodenal sindromática"},"pl":{"name":"Syndromiczna malformacja żołądkowo-dwunastnicza"},"cs":{"name":"Syndromické gastroduodenální malformace"},"uk":{"name":"Синдромальна гастродуоденальна мальформація"},"zh":{"name":"综合征性胃十二指肠畸形"},"tr":{"name":"Sendromik gastroduodenal malformasyon"}},"xrefs":[{"source":"MONDO","code":"15210","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681765","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19858","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":97944,"name":"Gastroduodenal malformation","classifications":[147,156,182]}],"children":[{"orpha":1305,"name":"Feingold syndrome","type":"Malformation syndrome"},{"orpha":2538,"name":"Microgastria-limb reduction defect syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}