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1217069000: Familial hyperreninemic hypoaldosteronism type 1B (disorder)


Status: current, Primitive. Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5034600017 Familial hyperreninemic hypoaldosteronism type 1B en Synonym Active Initial character case insensitive SNOMED CT core
5034601018 Familial hyperreninemic hypoaldosteronism type 1B (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
5034602013 Familial hyperreninaemic hypoaldosteronism type 1B en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hyperreninaemic hypoaldosteronism type 1B Finding site Adrenal cortex structure true Inferred relationship Some 1
Familial hyperreninaemic hypoaldosteronism type 1B Is a Familial disease true Inferred relationship Some
Familial hyperreninaemic hypoaldosteronism type 1B Is a Hyperreninaemic hypoaldosteronism true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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