Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3766843012 | Adult-onset autosomal recessive cerebellar ataxia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3766844018 | SCAR10 - autosomal recessive spinocerebellar ataxia type 10 | en | Synonym | Active | Case sensitive | SNOMED CT core |
3766845017 | Adult-onset autosomal recessive cerebellar ataxia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3766846016 | Autosomal recessive spinocerebellar ataxia type 10 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3766847013 | A rare genetic autosomal recessive cerebellar ataxia disease with characteristics of adulthood-onset of slowly progressive spinocerebellar ataxia, manifesting with gait and appendicular ataxia, dysarthria, ocular movement anomalies (for example horizontal, vertical, and/or downbeat nystagmus, hypermetric saccades), increased deep tendon reflexes and progressive cognitive decline. Additional variable features may include proximal leg muscle wasting and fasciculations, pes cavus, inspiratory stridor, epilepsy, retinal degeneration and cataracts. Brain imaging reveals marked cerebellar atrophy and electromyography shows evidence of lower motor neuron involvement. Caused by homozygous or compound heterozygous mutation in the ANO10 gene on chromosome 3p22. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Adult-onset autosomal recessive cerebellar ataxia | Occurrence | Adulthood | true | Inferred relationship | Some | 1 | |
Adult-onset autosomal recessive cerebellar ataxia | Occurrence | Adulthood | true | Inferred relationship | Some | 2 | |
Adult-onset autosomal recessive cerebellar ataxia | Finding site | Spinal cord structure | true | Inferred relationship | Some | 2 | |
Adult-onset autosomal recessive cerebellar ataxia | Is a | Chronic brain syndrome | true | Inferred relationship | Some | ||
Adult-onset autosomal recessive cerebellar ataxia | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Adult-onset autosomal recessive cerebellar ataxia | Associated morphology | Degeneration | false | Inferred relationship | Some | 2 | |
Adult-onset autosomal recessive cerebellar ataxia | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
Adult-onset autosomal recessive cerebellar ataxia | Is a | Spinocerebellar ataxia | true | Inferred relationship | Some | ||
Adult-onset autosomal recessive cerebellar ataxia | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Adult-onset autosomal recessive cerebellar ataxia | Clinical course | Progressive | true | Inferred relationship | Some | 3 | |
Adult-onset autosomal recessive cerebellar ataxia | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 2 | |
Adult-onset autosomal recessive cerebellar ataxia | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set