Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3638642017 | Autosomal recessive cerebellar ataxia due to GBA2 (glucosylceramidase beta 2) deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3638643010 | Autosomal recessive cerebellar ataxia with late-onset spasticity | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3638644016 | Autosomal recessive cerebellar ataxia with late-onset spasticity (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive cerebellar ataxia with late-onset spasticity | Is a | Cerebellar ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive cerebellar ataxia with late-onset spasticity | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive cerebellar ataxia with late-onset spasticity | Is a | Sphingolipidosis | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive cerebellar ataxia with late-onset spasticity | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive cerebellar ataxia with late-onset spasticity | Finding site | Cerebellar structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive cerebellar ataxia with late-onset spasticity | Is a | Hereditary ataxia | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR