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124287008: Deficiency of tyrosine aminotransferase (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
203979018 Deficiency of tyrosine aminotransferase en Synonym Active Case insensitive SNOMED CT core
727876014 Deficiency of tyrosine aminotransferase (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deficiency of tyrosine aminotransferase Is a Deficiency of transferase 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
Hypertyrosinaemia, Richner-Hanhart type Due to True Deficiency of tyrosine aminotransferase Inferred relationship Some 1

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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