Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3310750018 | Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3310751019 | Autosomal dominant optic atrophy and peripheral neuropathy syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3310752014 | A form of autosomal dominant optic atrophy with characteristics of progressive and isolated visual loss in the first decade of life, decreased reflexes in the lower limbs and a mild cerebellar stance. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant optic atrophy and peripheral neuropathy syndrome | Is a | Dominant hereditary optic atrophy | true | Inferred relationship | Some | ||
Autosomal dominant optic atrophy and peripheral neuropathy syndrome | Is a | Peripheral neuropathy | true | Inferred relationship | Some | ||
Autosomal dominant optic atrophy and peripheral neuropathy syndrome | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant optic atrophy and peripheral neuropathy syndrome | Associated morphology | Primary atrophy | true | Inferred relationship | Some | 2 | |
Autosomal dominant optic atrophy and peripheral neuropathy syndrome | Finding site | Optic nerve structure | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set