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9360008: Hyperammonemia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
16419019 Hyperammonemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
510396013 Hyperammonaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
837368011 Hyperammonemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
16419019 Hyperammonemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
16419019 Hyperammonemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
510396013 Hyperammonaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
510396013 Hyperammonaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
837368011 Hyperammonemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
837368011 Hyperammonemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4420071000241115 hyperammoniémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4420071000241115 hyperammoniémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperammonemia Is a Disorder of the urea cycle metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Hyperammonemia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Hyperammonemia Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Transient hyperammonemia in infancy Is a True Hyperammonemia Inferred relationship Existential restriction modifier (core metadata concept)
Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome Is a True Hyperammonemia Inferred relationship Existential restriction modifier (core metadata concept)
Hyperammonemia, type III Is a True Hyperammonemia Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hyperammonemia, type I Is a False Hyperammonemia Inferred relationship Existential restriction modifier (core metadata concept)
Ornithine carbamoyltransferase deficiency Is a True Hyperammonemia Inferred relationship Existential restriction modifier (core metadata concept)
Hyperammonemic encephalopathy (disorder) Associated with True Hyperammonemia Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperinsulinism and hyperammonaemia syndrome Is a True Hyperammonemia Inferred relationship Existential restriction modifier (core metadata concept)
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency (disorder) Due to True Hyperammonemia Inferred relationship Existential restriction modifier (core metadata concept) 2

This concept is not in any reference sets

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