Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3701485013 | Retinal macular dystrophy type 2 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3701486014 | MCDR2 - retinal macular dystrophy type 2 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3701487017 | Retinal macular dystrophy type 2 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Retinal macular dystrophy type 2 | Is a | Hereditary macular dystrophy | true | Inferred relationship | Existential restriction modifier | ||
Retinal macular dystrophy type 2 | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
Retinal macular dystrophy type 2 | Finding site | Macula lutea structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Retinal macular dystrophy type 2 | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets