Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2981441013 | Hereditary retinal dystrophy primarily involving retinal pigment epithelium | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
2981448019 | Hereditary retinal dystrophy primarily involving retinal pigment epithelium (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
2981489016 | Inherited retinal dystrophy primarily involving retinal pigment epithelium | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary retinal dystrophy primarily involving retinal pigment epithelium | Is a | Hereditary retinal dystrophy | true | Inferred relationship | Existential restriction modifier | ||
Hereditary retinal dystrophy primarily involving retinal pigment epithelium | Finding site | Retinal structure | false | Inferred relationship | Existential restriction modifier | ||
Hereditary retinal dystrophy primarily involving retinal pigment epithelium | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
Hereditary retinal dystrophy primarily involving retinal pigment epithelium | Finding site | Retinal structure | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Biallelic RPE65, retinoid isomerohydrolase mutation associated retinal dystrophy | Is a | True | Hereditary retinal dystrophy primarily involving retinal pigment epithelium | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets