Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
347703014 | Autosomal dominant retinitis pigmentosa | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
620067015 | Autosomal dominant retinitis pigmentosa (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 |
Autosomal dominant retinitis pigmentosa | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant retinitis pigmentosa | est un(e) (attribut) | rétinite pigmentaire (trouble) | true | Inferred relationship | Some | ||
Autosomal dominant retinitis pigmentosa | localisation d'une constatation (attribut) | structure de la rétine | false | Inferred relationship | Some | ||
Autosomal dominant retinitis pigmentosa | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Autosomal dominant retinitis pigmentosa | localisation d'une constatation (attribut) | structure de la rétine | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (disorder) | est un(e) (attribut) | True | Autosomal dominant retinitis pigmentosa | Inferred relationship | Some |
This concept is not in any reference sets