Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module
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 | SNOMED CT core module |
3434279010 | Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3434280013 | Hereditary inclusion body myopathy type 3 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3434281012 | Inclusion body myopathy type 3 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Is a | External ophthalmoplegia | true | Inferred relationship | Existential restriction modifier | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Is a | Arthrogryposis | false | Inferred relationship | Existential restriction modifier | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Is a | Myopathy with cytoplasmic inclusions | true | Inferred relationship | Existential restriction modifier | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Existential restriction modifier | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Existential restriction modifier | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Finding site | Structure of nervous system | true | Inferred relationship | Existential restriction modifier | 4 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Finding site | Eye region structure | false | Inferred relationship | Existential restriction modifier | 5 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 4 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 5 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Associated morphology | Contracture | false | Inferred relationship | Existential restriction modifier | 4 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Finding site | Joint structure | false | Inferred relationship | Existential restriction modifier | 4 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Associated morphology | Developmental anomaly | false | Inferred relationship | Existential restriction modifier | 5 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Finding site | Skeletal muscle structure | false | Inferred relationship | Existential restriction modifier | 5 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 2 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Is a | Inherited arthrogryposis | true | Inferred relationship | Existential restriction modifier | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 2 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Existential restriction modifier | 2 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Finding site | Joint structure | false | Inferred relationship | Existential restriction modifier | 1 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Associated morphology | Contracture | true | Inferred relationship | Existential restriction modifier | 1 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Interprets | Range of joint movement | true | Inferred relationship | Existential restriction modifier | 3 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Has interpretation | Decreased | true | Inferred relationship | Existential restriction modifier | 3 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Finding site | Structure of joint region | true | Inferred relationship | Existential restriction modifier | 1 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Finding site | Structure of extraocular muscle | true | Inferred relationship | Existential restriction modifier | 5 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Is a | Myopathy of extraocular muscles | true | Inferred relationship | Existential restriction modifier | ||
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Interprets | Movement observable | true | Inferred relationship | Existential restriction modifier | 6 | |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Has interpretation | Absent | true | Inferred relationship | Existential restriction modifier | 6 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets