Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1222464011 | Autosomal dominant optic atrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
4555010 | Dominant hereditary optic atrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
749857010 | Dominant hereditary optic atrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Dominant hereditary optic atrophy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Dominant hereditary optic atrophy | Is a | Hereditary optic atrophy | true | Inferred relationship | Some | ||
Dominant hereditary optic atrophy | Is a | Inherited optic neuropathy | false | Inferred relationship | Some | ||
Dominant hereditary optic atrophy | Finding site | Optic nerve structure | true | Inferred relationship | Some | 1 | |
Dominant hereditary optic atrophy | Associated morphology | Primary atrophy | true | Inferred relationship | Some | 1 | |
Dominant hereditary optic atrophy | Finding site | Optic nerve structure | false | Inferred relationship | Some | 1 | |
Dominant hereditary optic atrophy | Associated morphology | Primary atrophy | false | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Autosomal dominant optic atrophy plus syndrome | Is a | True | Dominant hereditary optic atrophy | Inferred relationship | Some | |
Autosomal dominant optic atrophy classic form | Is a | True | Dominant hereditary optic atrophy | Inferred relationship | Some | |
Autosomal dominant optic atrophy and peripheral neuropathy syndrome | Is a | True | Dominant hereditary optic atrophy | Inferred relationship | Some | |
Autosomal dominant optic atrophy and cataract | Is a | True | Dominant hereditary optic atrophy | Inferred relationship | Some | |
Optic atrophy, intellectual disability syndrome | Is a | True | Dominant hereditary optic atrophy | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set