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15689008: Pseudohypoaldosteronism, type 2 (disorder)


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
26586015 Pseudohypoaldosteronism, type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
742559015 Pseudohypoaldosteronism, type 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
926451000172119 pseudohypoaldostéronisme type 2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
974231000172116 hyperkaliémie minéralocorticoïde résistante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3424341001000113 Pseudohypoaldosteronismus Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pseudohypoaldosteronism, type 2 Is a Pseudohypoaldosteronism true Inferred relationship Some
Pseudohypoaldosteronism, type 2 Finding site Body system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
An autosomal dominant disease characterized by increased serum potassium levels, hypertension, short stature, increased urinary calcium excretion and hyperchloremic metabolic acidosis. Is a True Pseudohypoaldosteronism, type 2 Inferred relationship Some

This concept is not in any reference sets

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