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5181007: Disorder of tryptophan metabolism (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
789751015 Disorder of tryptophan metabolism (disorder) en Fully specified name Active Case insensitive SNOMED CT core
9688014 Disorder of tryptophan metabolism en Synonym Active Case insensitive SNOMED CT core


9 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Disorder of tryptophan metabolism Is a Disorder of amino acid metabolism false Inferred relationship Some
Disorder of tryptophan metabolism Is a Disorder of amino acid and organic acid metabolism true Inferred relationship Some
Disorder of tryptophan metabolism Occurrence Congenital false Inferred relationship Some
Disorder of tryptophan metabolism Finding site Body system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Tryptophanuria Is a True Disorder of tryptophan metabolism Inferred relationship Some
Hooft's syndrome Is a True Disorder of tryptophan metabolism Inferred relationship Some
Hydroxykynureninuria Is a True Disorder of tryptophan metabolism Inferred relationship Some
Tryptophan malabsorption syndrome Is a True Disorder of tryptophan metabolism Inferred relationship Some
Kynureninase deficiency Is a True Disorder of tryptophan metabolism Inferred relationship Some
Indicanuria Is a True Disorder of tryptophan metabolism Inferred relationship Some
Tryptophanaemia Is a True Disorder of tryptophan metabolism Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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