{"orpha":363300,"name":"Genetic intractable diarrhea of infancy","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-363300/","orphanet_url":"https://www.orpha.net/en/disease/detail/363300","names":{"fr":{"name":"Diarrhée intraitable de l'enfant d'origine génétique"},"de":{"name":"Intraktable Diarrhoe im Kindesalter, genetisch bedingte"},"es":{"name":"Diarrea intratable genético de la infancia"},"it":{"name":"Diarrea intrattabile genetica dell'infanzia","synonyms":["IDI"]},"nl":{"name":"Genetische hardnekkige diarree in de zuigelingentijd"},"pt":{"name":"Diarreia intratável genética da infância"},"pl":{"name":"Dziecięca biegunka oporna na leczenie uwarunkowana genetycznie","synonyms":["IDI"]},"cs":{"name":"Geneticky podmíněné nezvladatelné průjmy kojenců","synonyms":["IDI"]},"uk":{"name":"Генетично обумовлена невиліковна діарея немовлят"},"zh":{"name":"婴儿遗传性难治性腹泻"},"tr":{"name":"Süt çocuğu genetik inatçı ishali"}},"xrefs":[{"source":"UMLS","code":"C5680980","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]}],"children":[{"orpha":1670,"name":"Chronic diarrhea with villous atrophy","type":"Disease"},{"orpha":329242,"name":"Congenital chronic diarrhea with protein-losing enteropathy","type":"Disease"},{"orpha":714487,"name":"Congenital diarrhea-chronic gastrointestinal inflammation-ocular dysgenesis syndrome","type":"Disease"},{"orpha":103908,"name":"Congenital sodium diarrhea","type":"Disease"},{"orpha":92050,"name":"Congenital tufting enteropathy","type":"Disease"},{"orpha":137622,"name":"Intractable diarrhea-choanal atresia-eye anomalies syndrome","type":"Malformation syndrome"},{"orpha":2290,"name":"Microvillus inclusion disease","type":"Disease"},{"orpha":714490,"name":"PERCC1-related congenital intractable malabsorptive diarrhea","type":"Disease"},{"orpha":522043,"name":"Syndromic autoimmune enteropathy","type":"Clinical group"},{"orpha":563708,"name":"Syndromic congenital sodium diarrhea","type":"Disease"},{"orpha":84064,"name":"Trichohepatoenteric syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}