{"orpha":165985,"name":"Diazoxide-sensitive diffuse hyperinsulinism","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":["Hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form"],"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-165985/","orphanet_url":"https://www.orpha.net/en/disease/detail/165985","names":{"fr":{"name":"Hyperinsulinisme diffus sensible au diazoxide","synonyms":["Hypoglycémie hyperinsulinémique, forme diffuse sensible au diazoxide"]},"de":{"name":"Hyperinsulinismus, diffuser, Diazoxid-sensitiver","synonyms":["Hyperinsulinämische Hypoglykämie, Diazoxid-sensitive diffuse Form"]},"es":{"name":"Hiperinsulinismo difuso sensible al diazóxido","synonyms":["Hipoglucemia hiperinsulinémica, forma difusa sensible al diazóxido"]},"it":{"name":"Iperinsulinismo diffuso sensibile al diazossido","synonyms":["Ipoglicemia iperinsulinemica, forma diffusa sensibile al diazossido"]},"nl":{"name":"Diazoxidesensitief diffuus hyperinsulinisme","synonyms":["Hyperinsulinemische hypoglycemie, diazoxidesensitieve diffuse vorm"]},"pt":{"name":"Hiperinsulinismo difuso sensível ao diazóxido"},"pl":{"name":"Rozlany hiperinsulinizm wrażliwy na diazoksyd","synonyms":["Hipoglikemia hiperinsulinemiczna, forma rozlana wrażliwa na diazoksyd"]},"cs":{"name":"Difuzní hyperinzulinismus citlivý na diazoxid","synonyms":["Hyperinzulinemická hypoglykemie, difuzní forma citlivá na diazoxid"]},"uk":{"name":"Дифузний гіперінсулінізм, чутливий до діазоксиду","synonyms":["Гіперінсулінемічна гіпоглікемія, чутлива до діазоксиду дифузна форма"]},"zh":{"name":"二氮嗪敏感型弥漫性高胰岛素血症","synonyms":["二氮嗪敏感型弥漫性高胰岛素低血糖症"]},"tr":{"name":"Diazoksite duyarlı yaygın hiperinsülinizm","synonyms":["Hiperinsülinemik hipoglisemi, diazoksit-duyarlı yaygın form"]}},"xrefs":[{"source":"MONDO","code":"0015624","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"15624","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679570","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":657,"name":"Congenital isolated hyperinsulinism","classifications":[150,156,193]}],"children":[{"orpha":276580,"name":"Autosomal dominant hyperinsulinism due to Kir6.2 deficiency","type":"Disease"},{"orpha":276575,"name":"Autosomal dominant hyperinsulinism due to SUR1 deficiency","type":"Disease"},{"orpha":79299,"name":"Congenital glucokinase-related hyperinsulinism","type":"Disease"},{"orpha":263455,"name":"Congenital hyperinsulinism due to HNF4A deficiency","type":"Disease"},{"orpha":165991,"name":"Exercise-induced hyperinsulinism","type":"Disease"},{"orpha":324575,"name":"Hyperinsulinism due to HNF1A deficiency","type":"Disease"},{"orpha":276556,"name":"Hyperinsulinism due to UCP2 deficiency","type":"Disease"},{"orpha":71212,"name":"Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency","type":"Disease"},{"orpha":35878,"name":"Hyperinsulinism-hyperammonemia syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}