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

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

Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3663230012	Pseudohyperaldosteronism type 2	en	Synonym	Active	Case insensitive	SNOMED CT core
3663233014	Early-onset hypertension with exacerbation in pregnancy	en	Synonym	Active	Case insensitive	SNOMED CT core
3663234015	Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3663235019	Hypertension due to gain-of-function mutation in mineralocorticoid receptor	en	Synonym	Active	Case insensitive	SNOMED CT core
3663236018	A rare genetic hypertension with characteristics of 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.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

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