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124287008: Deficiency of tyrosine aminotransferase (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

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


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 Existential restriction modifier
Deficiency of tyrosine aminotransferase Finding site Body system structure false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Hypertyrosinemia, Richner-Hanhart type Due to True Deficiency of tyrosine aminotransferase Inferred relationship Existential restriction modifier 1

This concept is not in any reference sets

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