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124284001: Deficiency of aspartate aminotransferase (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
203959014 Deficiency of glutamic-oxaloacetic transaminase en Synonym Active Case insensitive SNOMED CT core
203960016 Deficiency of glutamic-aspartic transaminase en Synonym Active Case insensitive SNOMED CT core
203961017 Deficiency of SGOT en Synonym Active Initial character case insensitive SNOMED CT core
203962012 Deficiency of GOT en Synonym Active Initial character case insensitive SNOMED CT core
203963019 Deficiency of aspartate aminotransferase en Synonym Active Case insensitive SNOMED CT core
727870015 Deficiency of aspartate 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 aspartate aminotransferase Is a Deficiency of transferase true Inferred relationship Some
Deficiency of aspartate aminotransferase Is a Serum aspartate aminotransferase level outside reference range false Inferred relationship Some
Deficiency of aspartate aminotransferase Interprets Laboratory test false Inferred relationship Some
Deficiency of aspartate aminotransferase Finding method Procedure false Inferred relationship Some
Deficiency of aspartate aminotransferase Finding site Body system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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