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 |
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