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 |
| 776297011 | Color vision deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1475747016 | Colour vision deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1476707015 | Color vision deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4235981000005119 | farvesynsdefekt | da | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Danish module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Color vision deficiency (disorder) | Is a | Visual system disorder | false | Inferred relationship | Some | ||
| Color vision deficiency (disorder) | Finding site | The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways | true | Inferred relationship | Some | 1 | |
| Color vision deficiency (disorder) | Is a | Disorder of vision | true | Inferred relationship | Some | ||
| Color vision deficiency (disorder) | Interprets | Vision observable (observable entity) | false | Inferred relationship | Some | 1 | |
| Color vision deficiency (disorder) | Has interpretation | Abnormal | false | Inferred relationship | Some | 1 | |
| Color vision deficiency (disorder) | Interprets | Visual function | false | Inferred relationship | Some | 1 | |
| Color vision deficiency (disorder) | Has interpretation | Abnormal | false | Inferred relationship | Some | 1 | |
| Color vision deficiency (disorder) | Interprets | Visual function | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital color blindness | Is a | True | Color vision deficiency (disorder) | Inferred relationship | Some | |
| Acquired color vision deficiency | Is a | True | Color vision deficiency (disorder) | Inferred relationship | Some | |
| Tritanopia (disorder) | Is a | True | Color vision deficiency (disorder) | Inferred relationship | Some | |
| objektivt: rød-grøn farveblindhed | Associated finding | False | Color vision deficiency (disorder) | Inferred relationship | Some | |
| On examination - color blindness NOS | Associated finding | False | Color vision deficiency (disorder) | Inferred relationship | Some | 1 |
| On examination - color blindness NOS | Is a | False | Color vision deficiency (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR