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57119000: Hyperammonemia, type III (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1231687019 N-Acetylglutamate synthase deficiency en Synonym Active Initial character case insensitive SNOMED CT core
1231688012 NAGS - N-Acetylglutamate synthase deficiency en Synonym Active Case sensitive SNOMED CT core
198715011 NAGS deficiency en Synonym Active Case sensitive SNOMED CT core
497797019 Hyperammonaemia, type III en Synonym Active Initial character case insensitive SNOMED CT core
795706011 Hyperammonemia, type III (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
94990017 Hyperammonemia, type III en Synonym Active Initial character case insensitive SNOMED CT core
94991018 N-acetylglutamate synthetase deficiency en Synonym Active Case sensitive SNOMED CT core
94992013 Amino acid acetyltransferase deficiency en Synonym Active Case insensitive SNOMED CT core
94993015 N-acetylglutamate transferase deficiency en Synonym Active Case sensitive SNOMED CT core
94994014 AGA deficiency en Synonym Active Case sensitive SNOMED CT core
94995010 Congenital AGA deficiency en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperammonaemia, type III Is a Enzymopathy true Inferred relationship Some
Hyperammonaemia, type III Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Hyperammonaemia, type III Is a Hyperammonaemia true Inferred relationship Some
Hyperammonaemia, type III Is a Inborn error of metabolism true Inferred relationship Some
Hyperammonaemia, type III Occurrence Congenital true Inferred relationship Some 1
Hyperammonaemia, type III 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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