{"orpha":276525,"name":"Familial hyperinsulinism","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["FHI","Familial hyperinsulinemic hypoglycemia"],"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-276525/","orphanet_url":"https://www.orpha.net/en/disease/detail/276525","names":{"fr":{"name":"Hyperinsulinisme familial","synonyms":["FHI","Hypoglycémie hyperinsulinémique familiale"]},"de":{"name":"Hyperinsulinismus, familiärer","synonyms":["FHI","Hypoglykämie, hyperinsulinämische, familiäre"]},"es":{"name":"Hiperinsulinismo familiar","synonyms":["Hipoglucemia hiperinsulinémica familiar"]},"it":{"name":"Iperinsulinismo familiare","synonyms":["FHI","Ipoglicemia iperinsulinemica familiare"]},"nl":{"name":"Familiaal hyperinsulinisme","synonyms":["FHI","Familiale hyperinsulinemische hypoglycemie"]},"pt":{"name":"Hiperinsulinismo familiar"},"pl":{"name":"Hiperinsulinizm rodzinny","synonyms":["FHI","Rodzinna hipoglikemia hiperinsulinemiczna"]},"cs":{"name":"Familiární hyperinzulinismus","synonyms":["FHI","Familiární hyperinzulinemická hypoglykémie"]},"uk":{"name":"Сімейний гіперінсулінізм","synonyms":["Сімейна гіперінсулінемічна гіпоглікемія","FHI"]},"zh":{"name":"家族性高胰岛素血症","synonyms":["家族性高胰岛素低血糖"]},"tr":{"name":"Ailesel hiperinsülinizm","synonyms":["FHI","Ailesel hiperinsülinemik hipoglisemi"]}},"xrefs":[{"source":"MONDO","code":"0017182","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17182","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5848294","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":443095,"name":"Hyperinsulinemic hypoglycaemia","classifications":[193]},{"orpha":156638,"name":"Rare genetic endocrine disease","classifications":[156]}],"children":[{"orpha":544628,"name":"Atypical Fanconi syndrome-neonatal hyperinsulinism syndrome","type":"Disease"},{"orpha":657,"name":"Congenital isolated hyperinsulinism","type":"Clinical group"},{"orpha":263458,"name":"Hyperinsulinism due to INSR deficiency","type":"Disease"},{"orpha":276608,"name":"Non-insulinoma pancreatogenous hypoglycemia syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}