Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3656355013 | Autosomal recessive spastic paraplegia type 62 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3656356014 | Autosomal recessive spastic paraplegia type 62 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5404456013 | A pure or complex form of hereditary spastic paraplegia characterized by an onset in the first decade of life of spastic paraparesis (more prominent in lower than upper extremities) and unsteady gait, as well as increased deep tendon reflexes, amyotrophy, cerebellar ataxia, and flexion contractures of the knees, in some. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5404457016 | A pure or complex form of hereditary spastic paraplegia characterised by an onset in the first decade of life of spastic paraparesis (more prominent in lower than upper extremities) and unsteady gait, as well as increased deep tendon reflexes, amyotrophy, cerebellar ataxia, and flexion contractures of the knees, in some. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive spastic paraplegia type 62 | Is a | Hereditary spastic paraplegia | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 62 | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 62 | Associated morphology | Degeneration | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 62 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 62 | Finding site | Spinal cord structure | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 62 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 62 | Finding site | Lower limb structure | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 62 | Associated morphology | Degenerative abnormality | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 62 | Is a | Autosomal recessive hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 62 | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 62 | Finding site | Lower limb structure | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 62 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 62 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 62 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
Autosomal recessive spastic paraplegia type 62 | Finding site | Structure of right lower limb (body structure) | true | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 62 | Finding site | Structure of left lower limb (body structure) | true | Inferred relationship | Some | 5 | |
Autosomal recessive spastic paraplegia type 62 | Interprets | Movement observable | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 62 | Has interpretation | Absent | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)