Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2983908011 | MEMSA - myoclonic epilepsy myopathy sensory ataxia | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
2983919014 | Spinocerebellar ataxia with epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2983928010 | Myoclonic epilepsy myopathy sensory ataxia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2983952015 | Myoclonic epilepsy myopathy sensory ataxia | 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 |
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Is a | Spinocerebellar disease | true | Inferred relationship | Some | ||
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Is a | Depletion of mitochondrial DNA | true | Inferred relationship | Some | ||
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Is a | Hereditary cerebellar degeneration | true | Inferred relationship | Some | ||
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Associated morphology | Degeneration | false | Inferred relationship | Some | 3 | |
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Associated morphology | Degeneration | false | Inferred relationship | Some | 4 | |
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Finding site | Spinal cord structure | true | Inferred relationship | Some | 3 | |
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Finding site | Cerebellar structure | false | Inferred relationship | Some | 4 | |
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 3 | |
Myoclonic epilepsy myopathy sensory ataxia (disorder) | Is a | Inherited metabolic disorder of nervous system | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets