Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3498660011 | Myoclonus, cerebellar ataxia, deafness syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3498661010 | Myoclonus, cerebellar ataxia, deafness syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403703018 | This syndrome is characterized by the association of myoclonus, cerebellar ataxia and sensorineural hearing loss. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403704012 | This syndrome is characterised by the association of myoclonus, cerebellar ataxia and sensorineural hearing loss. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Myoclonus, cerebellar ataxia, deafness syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Is a | Sensorineural hearing loss | false | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Is a | Extrapyramidal disease | true | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Is a | Cerebellar ataxia | true | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Is a | Congenital hearing disorder | false | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Is a | Myoclonic disorder | true | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Interprets | Hearing | true | Inferred relationship | Some | 3 | |
Myoclonus, cerebellar ataxia, deafness syndrome | Interprets | Functional observable | false | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 4 | |
Myoclonus, cerebellar ataxia, deafness syndrome | Finding site | Cerebellar structure | true | Inferred relationship | Some | 4 | |
Myoclonus, cerebellar ataxia, deafness syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 5 | |
Myoclonus, cerebellar ataxia, deafness syndrome | Finding site | Ear structure | true | Inferred relationship | Some | 5 | |
Myoclonus, cerebellar ataxia, deafness syndrome | Is a | Hereditary ataxia (disorder) | true | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Is a | Congenital sensorineural hearing loss (disorder) | true | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Is a | Disorder of ear | true | Inferred relationship | Some | ||
Myoclonus, cerebellar ataxia, deafness syndrome | Interprets | Movement | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)