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1186812001: Familial hyperreninemic hypoaldosteronism type 2 (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4667750018 Familial hyperreninemic hypoaldosteronism type 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4667751019 Familial hyperreninemic hypoaldosteronism type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4667752014 Familial hyperreninaemic hypoaldosteronism type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5325081000052111 familjär hyperrenin hypoaldosteronism, typ 2 sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hyperreninemic hypoaldosteronism type 2 (disorder) Is a Familial disease true Inferred relationship Some
Familial hyperreninemic hypoaldosteronism type 2 (disorder) Is a Hyperreninemic hypoaldosteronism true Inferred relationship Some
Familial hyperreninemic hypoaldosteronism type 2 (disorder) Finding site Adrenal cortex structure 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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