Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2022. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Is a | Decreased hearing (finding) | true | Inferred relationship | Some | ||
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Is a | Blindness AND/OR vision impairment level | true | Inferred relationship | Some | ||
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Is a | Spinocerebellar ataxia | true | Inferred relationship | Some | ||
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Some | ||
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Finding site | Structure of visual system (body structure) | true | Inferred relationship | Some | 4 | |
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Finding site | Structure of auditory system (body structure) | true | Inferred relationship | Some | 5 | |
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Interprets | Hearing | true | Inferred relationship | Some | 3 | |
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 3 | |
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Finding site | Spinal cord structure | true | Inferred relationship | Some | 2 | |
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 2 | |
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) | Is a | Disorder of sensory function (disorder) | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets