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 |
1222464011 | Autosomal dominant optic atrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4555010 | Dominant hereditary optic atrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
749857010 | Dominant hereditary optic atrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Dominant hereditary optic atrophy | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Dominant hereditary optic atrophy | est un(e) (attribut) | Hereditary optic atrophy | true | Inferred relationship | Some | ||
Dominant hereditary optic atrophy | est un(e) (attribut) | Inherited optic neuropathy | false | Inferred relationship | Some | ||
Dominant hereditary optic atrophy | localisation d'une constatation (attribut) | Optic nerve structure | true | Inferred relationship | Some | 1 | |
Dominant hereditary optic atrophy | morphologie associée (attribut) | Primary atrophy | true | Inferred relationship | Some | 1 | |
Dominant hereditary optic atrophy | localisation d'une constatation (attribut) | Optic nerve structure | false | Inferred relationship | Some | 1 | |
Dominant hereditary optic atrophy | morphologie associée (attribut) | Primary atrophy | false | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Autosomal dominant optic atrophy plus syndrome (disorder) | est un(e) (attribut) | True | Dominant hereditary optic atrophy | Inferred relationship | Some | |
atrophie optique autosomique dominante classique | est un(e) (attribut) | True | Dominant hereditary optic atrophy | Inferred relationship | Some | |
Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder) | est un(e) (attribut) | True | Dominant hereditary optic atrophy | Inferred relationship | Some | |
Autosomal dominant optic atrophy and cataract (disorder) | est un(e) (attribut) | True | Dominant hereditary optic atrophy | Inferred relationship | Some | |
Optic atrophy, intellectual disability syndrome (disorder) | est un(e) (attribut) | True | Dominant hereditary optic atrophy | Inferred relationship | Some |
Reference Sets
Canada French language reference set (foundation metadata concept)