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1186812001: Familial hyperreninemic hypoaldosteronism type 2 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. 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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hyperreninemic hypoaldosteronism type 2 (disorder) Is a Familial disease false 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
Familial hyperreninemic hypoaldosteronism type 2 (disorder) Is a Familial aldosterone deficiency (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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