Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
44142012 | Hereditary optic atrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
756783015 | Hereditary optic atrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary optic atrophy | Is a | Inherited optic neuropathy | true | Inferred relationship | Some | ||
Hereditary optic atrophy | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
Hereditary optic atrophy | Is a | Primary optic atrophy | true | Inferred relationship | Some | ||
Hereditary optic atrophy | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
Hereditary optic atrophy | Is a | Hereditary disorder of the visual system | false | Inferred relationship | Some | ||
Hereditary optic atrophy | Finding site | Optic nerve structure | true | Inferred relationship | Some | 1 | |
Hereditary optic atrophy | Associated morphology | Primary atrophy | true | Inferred relationship | Some | 1 | |
Hereditary optic atrophy | Associated morphology | Primary atrophy | false | Inferred relationship | Some | 1 | |
Hereditary optic atrophy | Finding site | Optic nerve structure | false | Inferred relationship | Some | 1 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set