124287008: deficiëntie van tyrosinetransaminase (aandoening)

SNOMED CT Concept\Clinical finding (finding)\Disease\Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of transferase (disorder)\Deficiency of tyrosine aminotransferase

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

203979018 Deficiency of tyrosine aminotransferase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

727876014 Deficiency of tyrosine aminotransferase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

6864911000146114 deficiëntie van tyrosineaminotransferase nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

11343671000146115 deficiëntie van tyrosinetransaminase nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

11343681000146118 deficiëntie van tyrosinetransaminase (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Deficiency of tyrosine aminotransferase	Is a	Deficiency of transferase (disorder)	true	Inferred relationship	Some
Deficiency of tyrosine aminotransferase	Finding site	Body system structure	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hypertyrosinemia, Richner-Hanhart type (disorder)	Due to	True	Deficiency of tyrosine aminotransferase	Inferred relationship	Some	1

This concept is not in any reference sets