Monarch Disease Ontology identifier MONDO_0007080 (glucocorticoid-remediable aldosteronism) can be described as follows. 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. Also known as: FH-I, FH1, GRA, aldosteronism, glucocorticoid-remediable, dexamethasone-sensitive hypertension, familial hyperaldosteronism type 1, glucocorticoid-sensitive hypertension.