Status: current, Primitive. Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3873907011 | Autosomal recessive progressive external ophthalmoplegia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3873908018 | Autosomal recessive progressive external ophthalmoplegia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3873909014 | arPEO- autosomal recessive progressive external ophthalmoplegia | en | Synonym | Active | Case sensitive | SNOMED CT core |
3873910016 | A rare genetic neuro-ophthalmological disease with characteristics of progressive weakness of the external eye muscles, resulting in bilateral ptosis and diffuse, symmetric ophthalmoparesis. Additional signs may include generalised skeletal muscle weakness, muscle atrophy, sensory axonal neuropathy, ataxia, cardiomyopathy, and psychiatric symptoms. It is usually more severe than autosomal dominant form. | en | Definition | Active | Case sensitive | SNOMED CT core |
3873911017 | A rare genetic neuro-ophthalmological disease with characteristics of progressive weakness of the external eye muscles, resulting in bilateral ptosis and diffuse, symmetric ophthalmoparesis. Additional signs may include generalized skeletal muscle weakness, muscle atrophy, sensory axonal neuropathy, ataxia, cardiomyopathy, and psychiatric symptoms. It is usually more severe than autosomal dominant form. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive progressive external ophthalmoplegia | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Some | ||
Autosomal recessive progressive external ophthalmoplegia | Is a | Progressive external ophthalmoplegia | true | Inferred relationship | Some | ||
Autosomal recessive progressive external ophthalmoplegia | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Autosomal recessive progressive external ophthalmoplegia | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Autosomal recessive progressive external ophthalmoplegia | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Autosomal recessive progressive external ophthalmoplegia | Is a | Chronic metabolic disorder | true | Inferred relationship | Some | ||
Autosomal recessive progressive external ophthalmoplegia | Is a | Mitochondrial cytopathy | true | Inferred relationship | Some | ||
Autosomal recessive progressive external ophthalmoplegia | Clinical course | Progressive | true | Inferred relationship | Some | 1 | |
Autosomal recessive progressive external ophthalmoplegia | Finding site | Structure of nervous system | true | Inferred relationship | Some | 2 | |
Autosomal recessive progressive external ophthalmoplegia | Finding site | Structure of extraocular muscle | true | Inferred relationship | Some | 3 | |
Autosomal recessive progressive external ophthalmoplegia | Interprets | Movement | true | Inferred relationship | Some | 5 | |
Autosomal recessive progressive external ophthalmoplegia | Interprets | Movement observable | true | Inferred relationship | Some | 4 | |
Autosomal recessive progressive external ophthalmoplegia | Has interpretation | Absent | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set