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- Bc73e906b0bde141fe98c6397773dc1f1 hasDbXref "Orphanet:235936" @default.
- Bc73e906b0bde141fe98c6397773dc1f1 type Axiom @default.
- Bc73e906b0bde141fe98c6397773dc1f1 annotatedProperty IAO_0000115 @default.
- Bc73e906b0bde141fe98c6397773dc1f1 annotatedSource MONDO_0016525 @default.
- Bc73e906b0bde141fe98c6397773dc1f1 annotatedTarget "Familial hyperaldosteronism (FH) is the heritable form of primary aldosteronism (PA) which comprises three identified subtypes to date: FH type I (FH-I) characterized by early-onset hypertension, glucocorticoid remediable adrenocorticotropic hormone (ACTH)-dependent hyperaldosteronism, variable hypokalemia, and overproduction of 18-oxocortisol and 18-hydroxycortisol; FH type II (FH-II) characterized by hypertension of varying severity and hyperaldosteronism not suppressible by dexamethasone; and FH type III (FH-III) characterized by profound hypokalemia, early-onset severe hypertension, non glucocorticoid-remediable hyperaldosteronism, and overproduction of 18-oxocortisol and 18-hydroxycortisol." @default.