Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3655849015 | Biallelic RPE65, retinoid isomerohydrolase mutation associated retinal dystrophy (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3655850015 | Biallelic RPE65 mutation associated retinal dystrophy | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3655851016 | Biallelic RPE65, retinoid isomerohydrolase mutation associated retinal dystrophy | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3655854012 | Biallelic mutation carriers have a mutation (not necessarily the same mutation) in both copies of a particular gene (a paternal and a maternal mutation). The RPE65 gene provides instructions for making an enzyme that is essential for normal vision and mutations in this gene result in reduced or absent levels of RPE65 activity, blocking the visual cycle and resulting in impaired vision. Almost all patients eventually progress to complete blindness. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Biallelic RPE65 mutation associated retinal dystrophy | Is a | Congenital disease | true | Inferred relationship | Some | ||
Biallelic RPE65 mutation associated retinal dystrophy | Is a | Hereditary retinal dystrophy primarily involving retinal pigment epithelium | true | Inferred relationship | Some | ||
Biallelic RPE65 mutation associated retinal dystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Biallelic RPE65 mutation associated retinal dystrophy | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Biallelic RPE65 mutation associated retinal dystrophy | Finding site | Retinal 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