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360410009: Hepatic tyrosine aminotransferase 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
476178012 Hepatic tyrosine aminotransferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
740197019 Hepatic tyrosine aminotransferase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
476178012 Hepatic tyrosine aminotransferase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
476178012 Hepatic tyrosine aminotransferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
740197019 Hepatic tyrosine aminotransferase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
740197019 Hepatic tyrosine aminotransferase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5225661000241117 déficit en tyrosine-aminotransférase hépatique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5225661000241117 déficit en tyrosine-aminotransférase hépatique 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
Hepatic tyrosine aminotransferase deficiency Is a Disorder of tyrosine metabolism (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hepatic tyrosine aminotransferase deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hepatic tyrosine aminotransferase 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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