Status: current, Primitive. Date: 31-Jan 2004. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2147497010 | Oculomotor apraxia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 2535852016 | Oculomotor dyspraxia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 298188010 | Oculomotor apraxia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Oculomotor apraxia | Is a | Strabismus | true | Inferred relationship | Some | ||
| Oculomotor apraxia | Finding site | Eye region structure | false | Inferred relationship | Some | 1 | |
| Oculomotor apraxia | Associated morphology | Misalignment | false | Inferred relationship | Some | 1 | |
| Oculomotor apraxia | Interprets | Ocular motility observable | false | Inferred relationship | Some | ||
| Oculomotor apraxia | Has interpretation | Abnormal | false | Inferred relationship | Some | 1 | |
| Oculomotor apraxia | Interprets | Ocular muscle balance | false | Inferred relationship | Some | 1 | |
| Oculomotor apraxia | Finding site | Structure of visual system | true | Inferred relationship | Some | 1 | |
| Oculomotor apraxia | Interprets | Ocular muscle balance | false | Inferred relationship | Some | 1 | |
| Oculomotor apraxia | Has interpretation | Abnormal | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome | Is a | True | Oculomotor apraxia | Inferred relationship | Some | |
| Acquired oculomotor apraxia | Is a | True | Oculomotor apraxia | Inferred relationship | Some | |
| Cerebellar ataxia with oculomotor apraxia type 4 | Is a | True | Oculomotor apraxia | Inferred relationship | Some | |
| Oculomotor apraxia - Cogan type | Is a | True | Oculomotor apraxia | Inferred relationship | Some | |
| Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 | Is a | True | Oculomotor apraxia | Inferred relationship | Some | |
| Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 | Is a | True | Oculomotor apraxia | Inferred relationship | Some | |
| Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome | Is a | True | Oculomotor apraxia | Inferred relationship | Some | |
| Balint syndrome | Is a | True | Oculomotor apraxia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR