Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3331475017 | Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3331476016 | Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Is a | Hereditary cerebellar degeneration | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Is a | Narcolepsy | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Is a | Sensorineural hearing loss | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Is a | Cerebellar ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Is a | Congenital hearing disorder | false | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Is a | Auditory system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Finding site | Structure of auditory system | true | Inferred relationship | Existential restriction modifier | 2 | |
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Interprets | Hearing, function | true | Inferred relationship | Existential restriction modifier | 3 | |
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Interprets | Functional observable | false | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Associated morphology | Atrophic degeneration | false | Inferred relationship | Existential restriction modifier | 4 | |
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 4 | |
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Finding site | Cerebellar structure | false | Inferred relationship | Existential restriction modifier | 4 | |
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Is a | Hereditary ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 3 | |
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Finding site | Cerebellar structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | Associated morphology | Atrophic degeneration | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR