Status: current, 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 |
| 482488013 | Hereditary disorder of the visual system | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 755157012 | Hereditary disorder of the visual system (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary disorder of the visual system (disorder) | Is a | Visual system disorder | true | Inferred relationship | Some | ||
| Hereditary disorder of the visual system (disorder) | Is a | Hereditary disorder by system | true | Inferred relationship | Some | ||
| Hereditary disorder of the visual system (disorder) | Finding site | Structure of visual system (body structure) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | Is a | True | Hereditary disorder of the visual system (disorder) | Inferred relationship | Some | |
| Keratitis fugax hereditaria | Is a | True | Hereditary disorder of the visual system (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR