Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3766844018 | SCAR10 - autosomal recessive spinocerebellar ataxia type 10 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3766845017 | Adult-onset autosomal recessive cerebellar ataxia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3766846016 | Autosomal recessive spinocerebellar ataxia type 10 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
8227751000146110 | autosomaal recessieve spinocerebellaire ataxie type 10 | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8227761000146113 | autosomaal recessieve cerebellaire ataxie beginnend op volwassen leeftijd | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8227781000146117 | autosomaal recessieve cerebellaire ataxie beginnend op volwassen leeftijd (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8794331000146110 | ARCA10 | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Occurrence | Adulthood | true | Inferred relationship | Some | 1 | |
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Occurrence | Adulthood | true | Inferred relationship | Some | 2 | |
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Finding site | Spinal cord structure | true | Inferred relationship | Some | 2 | |
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Is a | Chronic brain syndrome | true | Inferred relationship | Some | ||
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Associated morphology | degeneratie (afwijkende morfologie) | false | Inferred relationship | Some | 2 | |
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Associated morphology | degeneratie (afwijkende morfologie) | false | Inferred relationship | Some | 1 | |
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Is a | Spinocerebellar ataxia | true | Inferred relationship | Some | ||
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 3 | |
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 2 | |
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Adult-onset autosomal recessive cerebellar ataxia (disorder) | Is a | Chronic disorder of spinal cord (disorder) | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets