Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3302395011 | Autosomal dominant optic atrophy plus syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3302396012 | Autosomal dominant optic atrophy plus syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
5048275014 | ADOA (autosomal dominant optic atrophy) plus | en | Synonym | Active | Case sensitive | SNOMED CT core |
3302397015 | A variant of autosomal dominant optic atrophy associating typical optic atrophy with other extra-ocular manifestations such as sensorineural deafness, myopathy, chronic progressive external ophthalmoplegia, ataxia and peripheral neuropathy. More rarely, other manifestations have been associated with this condition, such as spastic paraplegia, multiple-sclerosis like illness. ADOA plus is caused by mutations in the OPA1 gene (3q29), encoding a dynamin-like GTPase involved in the fusion of the inner mitochondrial membrane. The phenotypes observed in ADOA plus are thus related to mitochondrial DNA instability resulting in multiple mitochondrial DNA deletions. Transmission is autosomal dominant with variable penetrance. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant optic atrophy plus syndrome | Is a | Dominant hereditary optic atrophy | true | Inferred relationship | Some | ||
Autosomal dominant optic atrophy plus syndrome | Is a | Mitochondrial cytopathy | true | Inferred relationship | Some | ||
Autosomal dominant optic atrophy plus syndrome | Associated morphology | Primary atrophy | true | Inferred relationship | Some | 1 | |
Autosomal dominant optic atrophy plus syndrome | 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
Australian dialect reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set