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707756004: Gitelman syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2015. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3031308017 Gitelman's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3031375018 Gitelman syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3031384018 Gitelman syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Gitelman syndrome Is a Hypocalciuria false Inferred relationship Existential restriction modifier
Gitelman syndrome Is a Familial hypokalemic and hypomagnesemic tubulopathy true Inferred relationship Existential restriction modifier
Gitelman syndrome Associated morphology Inflammation false Inferred relationship Existential restriction modifier 2
Gitelman syndrome Finding site Structure of parenchyma of kidney false Inferred relationship Existential restriction modifier 2
Gitelman syndrome Associated morphology Inflammation false Inferred relationship Existential restriction modifier 3
Gitelman syndrome Finding site Structure of interstitial tissue of kidney false Inferred relationship Existential restriction modifier 3
Gitelman syndrome Is a Renal hypocalciuria true Inferred relationship Existential restriction modifier
Gitelman syndrome Associated morphology Inflammatory morphology true Inferred relationship Existential restriction modifier 1
Gitelman syndrome Associated morphology Inflammatory morphology true Inferred relationship Existential restriction modifier 2
Gitelman syndrome Finding site Structure of interstitial tissue of kidney true Inferred relationship Existential restriction modifier 1
Gitelman syndrome Finding site Renal tubule structure true Inferred relationship Existential restriction modifier 2
Gitelman syndrome Is a Connective tissue hereditary disorder true Inferred relationship Existential restriction modifier
Gitelman syndrome Is a Hereditary nephropathy true Inferred relationship Existential restriction modifier
Gitelman syndrome Is a Autosomal recessive hereditary disorder 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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