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23501004: Arginase deficiency (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2475895017 Deficiency of arginase en Synonym Active Case insensitive SNOMED CT core
39458015 Arginase deficiency en Synonym Active Case insensitive SNOMED CT core
39459011 Argininemia en Synonym Active Case insensitive SNOMED CT core
39460018 Hyperargininemia en Synonym Active Case insensitive SNOMED CT core
39461019 ARGI deficiency en Synonym Active Case sensitive SNOMED CT core
481635014 Argininaemia en Synonym Active Case insensitive SNOMED CT core
481636010 Hyperargininaemia en Synonym Active Case insensitive SNOMED CT core
753030010 Arginase deficiency (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
Arginase deficiency Is a Inherited metabolic disorder of nervous system true Inferred relationship Some
Arginase deficiency Is a Disorder of the urea cycle metabolism true Inferred relationship Some
Arginase deficiency Is a Enzymopathy false Inferred relationship Some
Arginase deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Arginase deficiency Is a Specific enzyme deficiency true Inferred relationship Some
Arginase deficiency Finding site Structure of nervous system true Inferred relationship Some 2
Arginase deficiency Occurrence Congenital true Inferred relationship Some 1

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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