Status: current, Primitive. Date: 30-Apr 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5013174010 | Incomplete achromatopsia | en | Synonym | Active | Case insensitive | SNOMED CT core |
5013175011 | Incomplete achromatopsia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Incomplete achromatopsia | Is a | Achromatopsia | true | Inferred relationship | Some | ||
Incomplete achromatopsia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Incomplete achromatopsia | Finding site | Cone of retina | true | Inferred relationship | Some | 1 | |
Incomplete achromatopsia | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Incomplete achromatopsia | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set