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1217069000: Familial hyperreninemic hypoaldosteronism type 1B (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Apr 2022. Module: SNOMED CT core module

Descriptions:

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hyperreninemic hypoaldosteronism type 1B Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier 1
Familial hyperreninemic hypoaldosteronism type 1B Is a Familial disease true Inferred relationship Existential restriction modifier
Familial hyperreninemic hypoaldosteronism type 1B Is a Hyperreninemic hypoaldosteronism true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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