Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3302367011 | Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3302368018 | Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3302370010 | Autosomal recessive ataxia with oculomotor apraxia type 1 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3302371014 | AOA1 (ataxia oculomotor apraxia type 1) | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3302375017 | Ataxia oculomotor apraxia type 1 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 | Is a | Cerebellar ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 | Is a | Oculomotor apraxia | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 | Finding site | Structure of visual system | true | Inferred relationship | Existential restriction modifier | 2 | |
| Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 | Finding site | Cerebellar structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 | 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