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Mineralocorticoid Excess Syndrome, Apparent
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Mineralocorticoid Excess Syndrome, Apparent 3 coordinate concepts∟ ∟ ∟ ∟ ∟ Mineralocorticoid Excess Syndrome, Apparent 3 coordinate conceptsX |
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History note: | Metabolism, Inborn Errors (1977-2003)X |
historyNote*: | 2004
X |
publicMeSHNote*: | 2004
X |
Scope note: | A hereditary disease characterized by childhood onset HYPERTENSION, hypokalemic alkalosis, and low RENIN and ALDOSTERONE secretion. It results from a defect in the activity of the 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE 2 enzyme which results in inadequate conversion of CORTISOL to CORTISONE. The build up of unprocessed cortisol to levels that stimulate MINERALOCORTICOID RECEPTORS creates the appearance of having excessive MINERALOCORTICOIDS.
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 2003-07-09X |
dateEstablished*: | 2004-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | jmpX |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Näennäinen mineralokortikoidiylimääräoireyhtymä (fi) XNäennäinen mineralokortikoidiylimääräsyndrooma (fi, replaced) Apparent Mineralocorticoid Excess Syndrome (en, replaced) |
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