Status: current, Primitive. Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3791517011 | Complete achromatopsia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3791518018 | Complete color blindness | en | Synonym | Active | Case insensitive | SNOMED CT core |
3791519014 | Complete colour blindness | en | Synonym | Active | Case insensitive | SNOMED CT core |
3791520015 | Complete achromatopsia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3791521016 | Total colour blindness | en | Synonym | Active | Case insensitive | SNOMED CT core |
3791522011 | Rod monochromatism | en | Synonym | Active | Case insensitive | SNOMED CT core |
3791523018 | Total color blindness | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Complete achromatopsia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Complete achromatopsia | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Complete achromatopsia | Is a | Achromatopsia | true | Inferred relationship | Some | ||
Complete achromatopsia | Finding site | Cone of retina | true | Inferred relationship | Some | 1 | |
Complete achromatopsia | Pathological process | Pathological developmental process | 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