Status: current, Primitive. 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 | Active | Case insensitive | SNOMED CT core |
3896440013 | Childhood-onset autosomal dominant optic atrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Childhood-onset autosomal dominant optic atrophy | Occurrence | Childhood | true | Inferred relationship | Some | 1 | |
Childhood-onset autosomal dominant optic atrophy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Childhood-onset autosomal dominant optic atrophy | Is a | Hereditary optic atrophy | true | Inferred relationship | Some | ||
Childhood-onset autosomal dominant optic atrophy | Associated morphology | Primary atrophy | true | Inferred relationship | Some | 1 | |
Childhood-onset autosomal dominant optic atrophy | Finding site | Optic nerve structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set