{"orpha":104007,"name":"Congenital enteropathy involving intestinal mucosa development","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-104007/","orphanet_url":"https://www.orpha.net/en/disease/detail/104007","names":{"fr":{"name":"Entéropathie congénitale liée au développement de la muqueuse intestinale"},"de":{"name":"Enteropathie mit Entwicklungsdefekt der intestinalen Mukosa, kongenitale"},"es":{"name":"Enteropatía congénita asociada al desarrollo de la mucosa intestinal"},"it":{"name":"Enteropatia congenita che interessa lo sviluppo delle mucose intestinali"},"nl":{"name":"Congenitale enteropathie met intestinale slijmvliesontwikkeling"},"pt":{"name":"Enteropatia congénita envolvendo o desenvolvimento da mucosa intestinal"},"pl":{"name":"Wrodzona enteropatia obejmująca rozwój błony śluzowej jelita"},"cs":{"name":"Vrozené enteropatie postihující vývoj střevní mukózy"},"uk":{"name":"Вроджена ентеропатія, повязана з розвитком слизової оболонки кишечника"},"zh":{"name":"累及肠粘膜发育的先天性肠病"},"tr":{"name":"Bağırsak mukozası gelişimini içeren doğumsal enteropati"}},"xrefs":[{"source":"MONDO","code":"15182","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681743","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97935,"name":"Rare gastroenterologic disease"},"parents":[{"orpha":165655,"name":"Genetic intestinal disease","classifications":[156]},{"orpha":506216,"name":"Rare disorder potentially indicated for bowel transplant","classifications":[233]},{"orpha":117569,"name":"Rare intestinal disease","classifications":[152]}],"children":[{"orpha":103910,"name":"Congenital enterocyte heparan sulfate deficiency","type":"Disease"},{"orpha":92050,"name":"Congenital tufting enteropathy","type":"Disease"},{"orpha":83620,"name":"Enteric anendocrinosis","type":"Disease"},{"orpha":2290,"name":"Microvillus inclusion disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}