Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3766832016 | SCAR6 - autosomal recessive spinocerebellar ataxia type 6 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3766833014 | Infantile-onset autosomal recessive non progressive cerebellar ataxia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3766834015 | Autosomal recessive spinocerebellar ataxia type 6 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3766835019 | Infantile-onset autosomal recessive nonprogressive cerebellar ataxia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3766836018 | Infantile-onset autosomal recessive non progressive cerebellar ataxia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Infantile-onset autosomal recessive non progressive cerebellar ataxia | Is a | Hereditary ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Infantile-onset autosomal recessive non progressive cerebellar ataxia | Occurrence | Infancy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Infantile-onset autosomal recessive non progressive cerebellar ataxia | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Infantile-onset autosomal recessive non progressive cerebellar ataxia | Finding site | Cerebellar structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Infantile-onset autosomal recessive non progressive cerebellar ataxia | Is a | Cerebellar ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Infantile-onset autosomal recessive non progressive cerebellar ataxia | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Existential restriction modifier | ||
| Infantile-onset autosomal recessive non progressive cerebellar ataxia | Clinical course | Non-progressive | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR