18789002: Tryptophanuria (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Metabolic disease\Disorder of organic acid metabolism (disorder)\Disorder of amino acid metabolism (disorder)\Disorder of amino acid and organic acid metabolism\Disorder of tryptophan metabolism\Tryptophanuria

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

31681014 Tryptophanuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

746347017 Tryptophanuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

31681014 Tryptophanuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

31681014 Tryptophanuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

746347017 Tryptophanuria (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

746347017 Tryptophanuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4450731000241118 tryptophanurie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4450731000241118 tryptophanurie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Tryptophanuria	Is a	Disorder of tryptophan metabolism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Tryptophanuria	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Tryptophanuria	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Tryptophanuria with dwarfism	Is a	True	Tryptophanuria	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets