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124284001: Deficiency of aspartate 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
203959014 Deficiency of glutamic-oxaloacetic transaminase en Synonym Active Entire term case insensitive SNOMED CT core module
203960016 Deficiency of glutamic-aspartic transaminase en Synonym Active Entire term case insensitive SNOMED CT core module
203961017 Deficiency of SGOT en Synonym Active Only initial character case insensitive SNOMED CT core module
203962012 Deficiency of GOT en Synonym Active Only initial character case insensitive SNOMED CT core module
203963019 Deficiency of aspartate aminotransferase en Synonym Active Entire term case insensitive SNOMED CT core module
727870015 Deficiency of aspartate 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 aspartate aminotransferase Is a Deficiency of transferase true Inferred relationship Existential restriction modifier
Deficiency of aspartate aminotransferase Finding site Body system structure false Inferred relationship Existential restriction modifier
Deficiency of aspartate aminotransferase Is a Serum aspartate aminotransferase level outside reference range false Inferred relationship Existential restriction modifier
Deficiency of aspartate aminotransferase Interprets Laboratory test false Inferred relationship Existential restriction modifier
Deficiency of aspartate aminotransferase Finding method Procedure false Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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