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72945002: Kynureninase deficiency (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
121167018 Kynureninase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
813278018 Kynureninase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
121167018 Kynureninase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
121167018 Kynureninase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
813278018 Kynureninase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
813278018 Kynureninase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4628831000241113 déficit en kynuréninase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4628831000241113 déficit en kynuréninase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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