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236466005: Congenital Fanconi syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
354463014 De Toni-Fanconi syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
354464015 Primary Fanconi syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
354465019 Congenital Fanconi syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
625063019 Congenital Fanconi syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital Fanconi syndrome Is a Infantile nephropathic cystinosis true Inferred relationship Existential restriction modifier
Congenital Fanconi syndrome Finding site Structure of interstitial tissue of kidney false Inferred relationship Existential restriction modifier 1
Congenital Fanconi syndrome Associated morphology Inflammation false Inferred relationship Existential restriction modifier 2
Congenital Fanconi syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Congenital Fanconi syndrome Associated morphology Inflammation false Inferred relationship Existential restriction modifier 1
Congenital Fanconi syndrome Finding site Structure of interstitial tissue of kidney true Inferred relationship Existential restriction modifier 1
Congenital Fanconi syndrome Finding site Structure of parenchyma of kidney false Inferred relationship Existential restriction modifier 2
Congenital Fanconi syndrome Associated morphology Inflammatory morphology true Inferred relationship Existential restriction modifier 2
Congenital Fanconi syndrome Finding site Renal tubule structure true Inferred relationship Existential restriction modifier 2
Congenital Fanconi syndrome Associated morphology Inflammatory morphology true Inferred relationship Existential restriction modifier 1
Congenital Fanconi syndrome Is a Congenital connective tissue disorder true Inferred relationship Existential restriction modifier
Congenital Fanconi syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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