Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module | Reference Sets |
347840013 | Congenital color blindness | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | US English: Preferred (foundation metadata concept) |
347841012 | Congenital colour blindness | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
620175012 | Congenital color blindness (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Protan defect | Is a | True | Congenital color blindness | Inferred relationship | Some | |
Tritan defect | Is a | True | Congenital color blindness | Inferred relationship | Some | |
Achromatopsia | Is a | True | Congenital color blindness | Inferred relationship | Some | |
Deutan defect | Is a | True | Congenital color blindness | Inferred relationship | Some | |
Blue cone monochromatism (disorder) | Is a | True | Congenital color blindness | Inferred relationship | Some |
This concept is not in any reference sets