Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
An autosomal dominant cerebellar ataxia type 1 that is characterized by a cerebellar syndrome along with altered vertical eye movements. | Is a | Autosomal dominant hereditary disorder (disorder) | true | Inferred relationship | Some | ||
An autosomal dominant cerebellar ataxia type 1 that is characterized by a cerebellar syndrome along with altered vertical eye movements. | Is a | Hereditary cerebellar degeneration | false | Inferred relationship | Some | ||
An autosomal dominant cerebellar ataxia type 1 that is characterized by a cerebellar syndrome along with altered vertical eye movements. | Is a | Spinocerebellar ataxia | true | Inferred relationship | Some | ||
An autosomal dominant cerebellar ataxia type 1 that is characterized by a cerebellar syndrome along with altered vertical eye movements. | Associated morphology | dégénérescence | false | Inferred relationship | Some | 2 | |
An autosomal dominant cerebellar ataxia type 1 that is characterized by a cerebellar syndrome along with altered vertical eye movements. | Associated morphology | dégénérescence | false | Inferred relationship | Some | 3 | |
An autosomal dominant cerebellar ataxia type 1 that is characterized by a cerebellar syndrome along with altered vertical eye movements. | Finding site | Cerebellar structure | true | Inferred relationship | Some | 2 | |
An autosomal dominant cerebellar ataxia type 1 that is characterized by a cerebellar syndrome along with altered vertical eye movements. | Finding site | Spinal cord structure | false | Inferred relationship | Some | 3 | |
An autosomal dominant cerebellar ataxia type 1 that is characterized by a cerebellar syndrome along with altered vertical eye movements. | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
An autosomal dominant cerebellar ataxia type 1 that is characterized by a cerebellar syndrome along with altered vertical eye movements. | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
An autosomal dominant cerebellar ataxia type 1 that is characterized by a cerebellar syndrome along with altered vertical eye movements. | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)