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766937004: hypertension par mutation gain de fonction du récepteur aux minéralocorticoïdes (trouble)


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
768671000241115 hypertension par mutation gain de fonction du récepteur aux minéralocorticoïdes (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
934681000172116 hypertension à début précoce accentuée par la grossesse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
981291000172112 hypertension par mutation gain de fonction du récepteur aux minéralocorticoïdes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
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 Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) localisation d'une constatation (attribut) Systemic circulatory system structure true Inferred relationship Some 2
Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) est un(e) (attribut) hypertension artérielle secondaire true Inferred relationship Some
Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) interprète (attribut) Blood pressure true Inferred relationship Some 1
Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) est un(e) (attribut) Cardiovascular system hereditary disorder true Inferred relationship Some
Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) a pour interprétation (attribut) augmenté true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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