{"orpha":101960,"name":"Genetic chronic primary adrenal insufficiency","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-101960/","orphanet_url":"https://www.orpha.net/en/disease/detail/101960","names":{"fr":{"name":"Insuffisance surrénale primaire chronique génétique"},"de":{"name":"Nebenniereninsuffizienz, chronische primäre, genetisch bedingte"},"es":{"name":"Insuficiencia suprarrenal primaria crónica genética"},"it":{"name":"Insufficienza surrenale primaria cronica genetica"},"nl":{"name":"Genetische chronische primaire adrenale insufficiëntie","synonyms":["Genetische chronische primaire bijnierinsufficiëntie"]},"pt":{"name":"Insuficiência supra-renal primária crónica genética"},"pl":{"name":"Genetyczna przewlekła pierwotna niedoczynność nadnerczy"},"cs":{"name":"Geneticky podmíněné chronické primární adrenální insuficience"},"uk":{"name":"Генетично обумовлена хронічна первинна надниркова недостатність"},"zh":{"name":"遗传性慢性原发性肾上腺功能不全"},"tr":{"name":"Genetik kronik primer adrenal yetmezlik"}},"xrefs":[{"source":"UMLS","code":"C5681791","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19804","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":101959,"name":"Chronic primary adrenal insufficiency","classifications":[193]},{"orpha":183637,"name":"Rare genetic adrenal disease","classifications":[156]}],"children":[{"orpha":168558,"name":"46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency","type":"Disease"},{"orpha":595337,"name":"Adrenal hypoplasia congenita","type":"Clinical group"},{"orpha":977,"name":"Adrenomyodystrophy","type":"Disease"},{"orpha":3453,"name":"Autoimmune polyendocrinopathy type 1","type":"Disease"},{"orpha":418,"name":"Congenital adrenal hyperplasia","type":"Clinical group"},{"orpha":199332,"name":"Endocrine-cerebro-osteodysplasia syndrome","type":"Malformation syndrome"},{"orpha":361,"name":"Familial glucocorticoid deficiency","type":"Disease"},{"orpha":289548,"name":"Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency","type":"Disease"},{"orpha":44,"name":"Neonatal adrenoleukodystrophy","type":"Disease"},{"orpha":869,"name":"Triple A syndrome","type":"Disease"},{"orpha":43,"name":"X-linked adrenoleukodystrophy","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}