766937004: Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Cardiovascular finding\Cardiovascular measurement - finding\Hypertensive disorder, systemic arterial (disorder)\Secondary hypertension\Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)
• \Cardiovascular finding\Disorder of cardiovascular system (disorder)\Cardiovascular system hereditary disorder\Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)
• \Cardiovascular finding\Disorder of cardiovascular system (disorder)\Hypertensive disorder, systemic arterial (disorder)\Secondary hypertension\Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Cardiovascular system hereditary disorder\Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)
• \Disease\Disorder of body system\Hereditary disorder by system\Cardiovascular system hereditary disorder\Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)
• \Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Cardiovascular system hereditary disorder\Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)
• \Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Hypertensive disorder, systemic arterial (disorder)\Secondary hypertension\Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3663230012	Pseudohyperaldosteronism type 2	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3663233014	Early-onset hypertension with exacerbation in pregnancy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3663234015	Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3663235019	Hypertension due to gain-of-function mutation in mineralocorticoid receptor	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5404714010	A rare genetic cause of hypertension characterized by severe early-onset therapy-resistant hypertension due to a gain-of-function mutation in the mineralocorticoid receptor. The condition is associated with suppressed plasma renin activity and low serum aldosterone levels and is markedly exacerbated during pregnancy.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5404715011	A rare genetic cause of hypertension characterised by severe early-onset therapy-resistant hypertension due to a gain-of-function mutation in the mineralocorticoid receptor. The condition is associated with suppressed plasma renin activity and low serum aldosterone levels and is markedly exacerbated during pregnancy.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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