Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
347840013 | Congenital color blindness | en | Synonym | Active | Case insensitive | SNOMED CT core |
347841012 | Congenital colour blindness | en | Synonym | Active | Case insensitive | SNOMED CT core |
620175012 | Congenital color blindness (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Blue cone monochromatism | Is a | True | Congenital colour blindness | Inferred relationship | Some | |
Protan defect | Is a | True | Congenital colour blindness | Inferred relationship | Some | |
Tritan defect | Is a | True | Congenital colour blindness | Inferred relationship | Some | |
Achromatopsia | Is a | True | Congenital colour blindness | Inferred relationship | Some | |
Deutan defect | Is a | True | Congenital colour blindness | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set