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- B484d40bf0341048f04e18d05babdcfcc hasDbXref "Orphanet:88660" @default.
- B484d40bf0341048f04e18d05babdcfcc type Axiom @default.
- B484d40bf0341048f04e18d05babdcfcc annotatedProperty IAO_0000115 @default.
- B484d40bf0341048f04e18d05babdcfcc annotatedSource MONDO_0011517 @default.
- B484d40bf0341048f04e18d05babdcfcc annotatedTarget "Hypertension due to gain-of-function mutations in the mineralocorticoid receptor is a rare genetic hypertension characterized by a familial severe hypertension with an onset before age 20 years, associated with suppressed plasma renin and low aldosterone levels in the presence of low or normal levels of the mineralocorticoid aldosterone, that is highly resistant to antihypertensive medication. During pregnancy, there is a marked exacerbation of hypertension, accompanied by low serum potassium levels and undetectable aldosterone levels, but without signs of preeclampsia, requiring early delivery." @default.