Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3434278019 | Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3434279010 | Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3434280013 | Hereditary inclusion body myopathy type 3 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3434281012 | Inclusion body myopathy type 3 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403310014 | A rare genetic neuromuscular disease characterized by early onset of proximal or generalized muscle weakness, external ophthalmoplegia with or without ptosis, and joint contractures. Hypotonia, neonatal respiratory distress necessitating ventilation, and severe dysphagia have also been reported. The disease is of variable severity and non- or slowly progressive. Patients typically remain ambulatory. Muscle biopsy may show predominance of type 1 fibers, marked variability in fiber size, increased internal nuclei, and proliferation of perimysial and endomysial connective tissue. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403311013 | A rare genetic neuromuscular disease characterised by early onset of proximal or generalised muscle weakness, external ophthalmoplegia with or without ptosis, and joint contractures. Hypotonia, neonatal respiratory distress necessitating ventilation, and severe dysphagia have also been reported. The disease is of variable severity and non- or slowly progressive. Patients typically remain ambulatory. Muscle biopsy may show predominance of type 1 fibres, marked variability in fibre size, increased internal nuclei, and proliferation of perimysial and endomysial connective tissue. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Is a | External ophthalmoplegia | true | Inferred relationship | Some | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Is a | Arthrogryposis | false | Inferred relationship | Some | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Is a | Myopathy with cytoplasmic inclusions | true | Inferred relationship | Some | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Is a | Hereditary disorder of musculoskeletal system | false | Inferred relationship | Some | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Finding site | Structure of nervous system (body structure) | true | Inferred relationship | Some | 4 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Finding site | Eye region structure (body structure) | false | Inferred relationship | Some | 5 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 5 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Associated morphology | Contracture | false | Inferred relationship | Some | 4 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Finding site | Joint structure | false | Inferred relationship | Some | 4 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 5 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 5 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Is a | Inherited arthrogryposis | true | Inferred relationship | Some | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 2 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Finding site | Joint structure | false | Inferred relationship | Some | 1 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Associated morphology | Contracture | true | Inferred relationship | Some | 1 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Interprets | Range of joint movement | true | Inferred relationship | Some | 3 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 3 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Finding site | Structure of joint region | true | Inferred relationship | Some | 1 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Finding site | Structure of extraocular muscle | true | Inferred relationship | Some | 5 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Is a | Myopathy of extraocular muscles | true | Inferred relationship | Some | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Interprets | Movement observable | true | Inferred relationship | Some | 6 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Has interpretation | Absent | true | Inferred relationship | Some | 6 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Finding site | Joint structure of multiple body sites (body structure) | true | Inferred relationship | Some | 7 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) | Associated morphology | Contracture | true | Inferred relationship | Some | 7 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)