{"orpha":97978,"name":"Rare endocrine disease","type":"Category","group":"Group of disorders","status":"active","flags":["Head of classification"],"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-97978/","orphanet_url":"https://www.orpha.net/en/disease/detail/97978","names":{"fr":{"name":"Maladie endocrinienne rare"},"de":{"name":"Endokrine Krankheit, seltene"},"es":{"name":"Enfermedad endocrina rara"},"it":{"name":"Malattia endocrina rara"},"nl":{"name":"Zeldzame endocriene ziekte"},"pt":{"name":"Doença endócrina rara"},"pl":{"name":"Rzadkie choroby endokrynologiczne"},"cs":{"name":"Vzácná endokrinní onemocnění"},"uk":{"name":"Рідкісне ендокринне захворювання"},"zh":{"name":"罕见内分泌疾病"},"tr":{"name":"Nadir endokrin hastalığı"}},"xrefs":[{"source":"UMLS","code":"C5681540","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[{"orpha":90771,"name":"Difference of sex development","type":"Category"},{"orpha":785,"name":"Estrogen resistance syndrome","type":"Disease"},{"orpha":77828,"name":"Genetic obesity","type":"Category"},{"orpha":443095,"name":"Hyperinsulinemic hypoglycaemia","type":"Category"},{"orpha":293964,"name":"Hypoinsulinemic hypoglycemia and body hemihypertrophy","type":"Disease"},{"orpha":877,"name":"Neuroendocrine neoplasm","type":"Category"},{"orpha":101956,"name":"Polyendocrinopathy","type":"Category"},{"orpha":90970,"name":"Primary lipodystrophy","type":"Category"},{"orpha":101954,"name":"Rare adrenal disease","type":"Category"},{"orpha":101952,"name":"Rare diabetes mellitus","type":"Category"},{"orpha":181441,"name":"Rare disorder with hypergonadotropic hypogonadism","type":"Category"},{"orpha":101953,"name":"Rare dyslipidemia","type":"Category"},{"orpha":90692,"name":"Rare endocrine growth disease","type":"Category"},{"orpha":181384,"name":"Rare hypothalamic or pituitary disease","type":"Category"},{"orpha":68415,"name":"Rare parathyroid disease and phosphocalcic metabolism anomaly","type":"Category"},{"orpha":101955,"name":"Rare thyroid disease","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}