Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3302596011 | Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302599016 | Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302623015 | Cerebellar hypoplasia and tapetoretinal degeneration | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | localisation d'une constatation (attribut) | Structure of visual system (body structure) | true | Inferred relationship | Some | 2 | |
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | morphologie associée (attribut) | Hypoplasia (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | localisation d'une constatation (attribut) | structure cérébelleuse | true | Inferred relationship | Some | 1 | |
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | est un(e) (attribut) | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | est un(e) (attribut) | Congenital cerebellar hypoplasia | true | Inferred relationship | Some | ||
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | est un(e) (attribut) | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | est un(e) (attribut) | Hereditary disorder of the visual system | true | Inferred relationship | Some | ||
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | localisation d'une constatation (attribut) | Structure of visual system (body structure) | false | Inferred relationship | Some | ||
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | morphologie associée (attribut) | Hypoplasia (morphologic abnormality) | false | Inferred relationship | Some | 2 | |
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 2 | |
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) | localisation d'une constatation (attribut) | structure cérébelleuse | false | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets