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- B374fa8f1ba6d1026d544719ebaf8c81b hasDbXref "Orphanet:403" @default.
- B374fa8f1ba6d1026d544719ebaf8c81b type Axiom @default.
- B374fa8f1ba6d1026d544719ebaf8c81b annotatedProperty IAO_0000115 @default.
- B374fa8f1ba6d1026d544719ebaf8c81b annotatedSource MONDO_0007080 @default.
- B374fa8f1ba6d1026d544719ebaf8c81b annotatedTarget "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." @default.