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276426004: Ornithine oxo-acid aminotransferase deficiency (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
412550019 Ornithine aminotransferase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
412551015 Ornithine ketoacid transaminase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
412552010 OKT deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
412553017 Ornithine-oxo-acid amino acid transferase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
412554011 Ornithine-delta-aminotransferase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
412555012 OAT - Ornithine oxo-acid aminotransferase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
412556013 OAT deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
669339011 Ornithine oxo-acid aminotransferase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2476096010 Deficiency of ornithine-oxo-acid aminotransferase en Synonym Active Entire term case insensitive SNOMED CT core module
2669599018 Ornithine oxo-acid aminotransferase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ornithine oxo-acid aminotransferase deficiency Is a Disorder of ornithine metabolism true Inferred relationship Existential restriction modifier
Ornithine oxo-acid aminotransferase deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier
Ornithine oxo-acid aminotransferase deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier
Ornithine oxo-acid aminotransferase deficiency Is a Deficiency of transferase true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Ornithinemia with gyrate atrophy Is a False Ornithine oxo-acid aminotransferase deficiency Inferred relationship Existential restriction modifier
Gyrate atrophy Associated etiologic finding False Ornithine oxo-acid aminotransferase deficiency Inferred relationship Existential restriction modifier
Gyrate atrophy Due to True Ornithine oxo-acid aminotransferase deficiency Inferred relationship Existential restriction modifier 1

This concept is not in any reference sets

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