Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3896439011 | Childhood-onset autosomal dominant optic atrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3896440013 | Childhood-onset autosomal dominant 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 |
Childhood-onset autosomal dominant optic atrophy | survenue (attribut) | enfance | true | Inferred relationship | Some | 1 | |
Childhood-onset autosomal dominant optic atrophy | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Childhood-onset autosomal dominant optic atrophy | est un(e) (attribut) | Hereditary optic atrophy | true | Inferred relationship | Some | ||
Childhood-onset autosomal dominant optic atrophy | morphologie associée (attribut) | Primary atrophy | true | Inferred relationship | Some | 1 | |
Childhood-onset autosomal dominant optic atrophy | localisation d'une constatation (attribut) | Optic nerve structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets