has material basis in germline mutation in CYP11B1 glucocorticoid-remediable aldosteronism https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/2790/glucocorticoid-remediable-aldosteronism https://www.malacards.org/card/hyperaldosteronism_familial_type_i dexamethasone sensitive hypertension UMLS:C3838731 ICD9:255.11 FH-I Orphanet:403 aldosteronism, glucocorticoid-remediable ICD10CM:E26.02 MEDGEN:824577 hyperaldosteronism, familial type 1 FH1 MONDO:0007080 DOID:14080 familial hyperaldosteronism type 1 HALD1 GRA glucocorticoid-remediable aldosteronism OMIM:103900 Familial hyperaldosteronism type I (FH-I) is a rare heritable, glucocorticoid remediable form of primary aldosteronism (PA) characterized by early-onset hypertension, hyperaldosteronism, variable hypokalemia, low plasma renin activity (PRA), and abnormal production of 18-oxocortisol and 18-hydroxycortisol. dexamethasone-sensitive hypertension glucocorticoid-sensitive hypertension glucocorticoid sensitive hypertension GARD:0002790 MESH:C563177 familial hyperaldosteronism