237770005: Syndrome of apparent mineralocorticoid excess (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Viscus structure finding (finding)\Abdominal organ finding\Disorder of adrenal gland\Disorder of cortisol-cortisone shuttle (disorder)\A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of retroperitoneal compartment (disorder)\Disorder of adrenal gland\Disorder of cortisol-cortisone shuttle (disorder)\A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Disorder of adrenal gland\Disorder of cortisol-cortisone shuttle (disorder)\A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disorder of abdomen (disorder)\Disorder of retroperitoneal compartment (disorder)\Disorder of adrenal gland\Disorder of cortisol-cortisone shuttle (disorder)\A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.
• \Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of retroperitoneal compartment (disorder)\Disorder of adrenal gland\Disorder of cortisol-cortisone shuttle (disorder)\A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.
• \Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system (disorder)\A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.
• \Disease\Disorder of body system\Disorder of endocrine system\Disorder of adrenal gland\Disorder of cortisol-cortisone shuttle (disorder)\A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.
• \Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of retroperitoneal compartment (disorder)\Disorder of adrenal gland\Disorder of cortisol-cortisone shuttle (disorder)\A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.
• \Disease\Metabolic disease\Disorder of steroid metabolism\Disorder of cortisol-cortisone shuttle (disorder)\A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5449016019	A rare form of pseudohyperaldosteronism characterised by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5449017011	A rare form of pseudohyperaldosteronism characterized by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
356333019	Syndrome of apparent mineralocorticoid excess	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
626545016	Syndrome of apparent mineralocorticoid excess (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3968445018	AME - apparent mineralocorticoid excess	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3968446017	Apparent mineralocorticoid excess	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3968447014	11-beta-hydroxysteroid dehydrogenase deficiency type 2	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3968448016	Ulick syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
7261491000241117	déficit en 11-bêta-hydroxystéroïde déshydrogénase de type 2	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
7261501000241112	syndrome d'Ulick	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
7261511000241114	syndrome d'excès apparent de minéralocorticoïdes	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3417771001000118	Apparenter Mineralocorticoid Exzess	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

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

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