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276426004: Ornithine oxo-acid aminotransferase deficiency (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
412550019 Ornithine aminotransferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
412551015 Ornithine ketoacid transaminase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
412552010 OKT deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
412553017 Ornithine-oxo-acid amino acid transferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
412554011 Ornithine-delta-aminotransferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
412555012 OAT - Ornithine oxo-acid aminotransferase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
412556013 OAT deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
669339011 Ornithine oxo-acid aminotransferase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2476096010 Deficiency of ornithine-oxo-acid aminotransferase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2669599018 Ornithine oxo-acid aminotransferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
412550019 Ornithine aminotransferase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
412550019 Ornithine aminotransferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
412551015 Ornithine ketoacid transaminase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
412551015 Ornithine ketoacid transaminase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
412552010 OKT deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
412553017 Ornithine-oxo-acid amino acid transferase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
412553017 Ornithine-oxo-acid amino acid transferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
412554011 Ornithine-delta-aminotransferase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
412554011 Ornithine-delta-aminotransferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
412555012 OAT - Ornithine oxo-acid aminotransferase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
412556013 OAT deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
669339011 Ornithine oxo-acid aminotransferase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
669339011 Ornithine oxo-acid aminotransferase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2476096010 Deficiency of ornithine-oxo-acid aminotransferase en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2476096010 Deficiency of ornithine-oxo-acid aminotransferase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2669599018 Ornithine oxo-acid aminotransferase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2669599018 Ornithine oxo-acid aminotransferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3429271001000113 Atrophia gyrata der Chorioidea und Retina de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5123341000241113 déficit en ornithine oxo-acide aminotransférase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5123341000241113 déficit en ornithine oxo-acide aminotransférase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3429271001000113 Atrophia gyrata der Chorioidea und Retina de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ornithine aminotransferase deficiency Is a Disorder of ornithine metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Ornithine aminotransferase deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Ornithine aminotransferase deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Ornithine aminotransferase deficiency Is a Deficiency of transferase true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Ornithinemia with gyrate atrophy Is a False Ornithine aminotransferase deficiency Inferred relationship Existential restriction modifier (core metadata concept)
Gyrate atrophy Associated etiologic finding False Ornithine aminotransferase deficiency Inferred relationship Existential restriction modifier (core metadata concept)
Gyrate atrophy Due to True Ornithine aminotransferase deficiency Inferred relationship Existential restriction modifier (core metadata concept) 1

This concept is not in any reference sets

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