FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

5181007: Disorder of tryptophan metabolism (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
9688014 Disorder of tryptophan metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
789751015 Disorder of tryptophan metabolism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
9688014 Disorder of tryptophan metabolism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
9688014 Disorder of tryptophan metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
789751015 Disorder of tryptophan metabolism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
789751015 Disorder of tryptophan metabolism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
973531000172116 trouble du métabolisme du tryptophane fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
973531000172116 trouble du métabolisme du tryptophane fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

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 (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of tryptophan metabolism Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of tryptophan metabolism Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of tryptophan metabolism Is a Disorder of amino acid and organic acid metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Tryptophanaemia Is a True Disorder of tryptophan metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Tryptophanuria Is a True Disorder of tryptophan metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Hooft's syndrome Is a True Disorder of tryptophan metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Hydroxykynureninuria Is a True Disorder of tryptophan metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Tryptophan malabsorption syndrome Is a True Disorder of tryptophan metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Kynureninase deficiency Is a True Disorder of tryptophan metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Indicanuria Is a True Disorder of tryptophan metabolism Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start