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236466005: Congenital Fanconi syndrome (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
354463014 De Toni-Fanconi syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
354464015 Primary Fanconi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
354465019 Congenital Fanconi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
625063019 Congenital Fanconi syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
354463014 De Toni-Fanconi syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
354464015 Primary Fanconi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
354465019 Congenital Fanconi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
625063019 Congenital Fanconi syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3441451001000118 Renotubuläres Fanconi-Syndrom, primäres de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5011201000241116 syndrome de Fanconi congénital fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5011201000241116 syndrome de Fanconi congénital fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3441451001000118 Renotubuläres Fanconi-Syndrom, primäres de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 (core metadata concept)
Congenital Fanconi syndrome Finding site Structure of interstitial tissue of kidney false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital Fanconi syndrome Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital Fanconi syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital Fanconi syndrome Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital Fanconi syndrome Finding site Structure of interstitial tissue of kidney true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital Fanconi syndrome Finding site Structure of parenchyma of kidney false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital Fanconi syndrome Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital Fanconi syndrome Finding site Renal tubule structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital Fanconi syndrome Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital Fanconi syndrome Is a Congenital connective tissue disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital Fanconi syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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