Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 372988011 | Truncal ataxia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 640569018 | Truncal ataxia (finding) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Truncal ataxia | Is a | Ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Truncal ataxia | Finding site | Structure of nervous system | false | Inferred relationship | Existential restriction modifier | ||
| Truncal ataxia | Interprets | Nervous system function | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Intellectual disability, hyperkinetic movement, truncal ataxia syndrome | Is a | True | Truncal ataxia | Inferred relationship | Existential restriction modifier | |
| Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency | Is a | True | Truncal ataxia | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR