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40488004: 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
67513013 Fanconi syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
777141012 Fanconi syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
67513013 Fanconi syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
777141012 Fanconi syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
777141012 Fanconi syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
820401000241119 syndrome de Fanconi fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
820401000241119 syndrome de Fanconi fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fanconi syndrome Is a Renal tubular disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Fanconi syndrome Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier (core metadata concept)
Fanconi syndrome Is a Amino acid transport disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Fanconi syndrome Is a Hereditary disorder of the urinary system false Inferred relationship Existential restriction modifier (core metadata concept)
Fanconi syndrome Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept)
Fanconi syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Fanconi syndrome Finding site Structure of interstitial tissue of kidney false Inferred relationship Existential restriction modifier (core metadata concept)
Fanconi syndrome Finding site Renal tubule structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Fanconi syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Fanconi syndrome Is a Metabolic renal disease true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Fanconi-de Toni-Debre syndrome Is a False Fanconi syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Acquired Fanconi syndrome Is a True Fanconi syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome Is a True Fanconi syndrome Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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