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57119000: Hyperammonemia, type III (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
94990017 Hyperammonemia, type III en Synonym Active Only initial character case insensitive SNOMED CT core module
94991018 N-acetylglutamate synthetase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
94992013 Amino acid acetyltransferase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
94993015 N-acetylglutamate transferase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
94994014 AGA deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
94995010 Congenital AGA deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
198715011 NAGS deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
497797019 Hyperammonaemia, type III en Synonym Active Only initial character case insensitive SNOMED CT core module
795706011 Hyperammonemia, type III (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
1231687019 N-Acetylglutamate synthase deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
1231688012 NAGS - N-Acetylglutamate synthase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperammonemia, type III Is a Enzymopathy true Inferred relationship Existential restriction modifier
Hyperammonemia, type III Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Hyperammonemia, type III Is a Hyperammonemia true Inferred relationship Existential restriction modifier
Hyperammonemia, type III Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hyperammonemia, type III Finding site Body system structure false Inferred relationship Existential restriction modifier
Hyperammonemia, type III Is a Inborn error of metabolism true 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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