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 |
3637770011 | Autosomal dominant spastic paraplegia type 42 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3637771010 | Autosomal dominant spastic paraplegia type 42 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403935014 | A pure form of hereditary spastic paraplegia characterized by slowly progressive spastic paraplegia of lower extremities with an age of onset ranging from childhood to adulthood and patients presenting with spastic gait, increased tendon reflexes in lower limbs, extensor plantar response, weakness and atrophy of lower limb muscles and, in rare cases, pes cavus. No abnormalities are noted on magnetic resonance imaging. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403936010 | A pure form of hereditary spastic paraplegia characterised by slowly progressive spastic paraplegia of lower extremities with an age of onset ranging from childhood to adulthood and patients presenting with spastic gait, increased tendon reflexes in lower limbs, extensor plantar response, weakness and atrophy of lower limb muscles and, in rare cases, pes cavus. No abnormalities are noted on magnetic resonance imaging. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant spastic paraplegia type 42 | Is a | Pure hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal dominant spastic paraplegia type 42 | Is a | Autosomal dominant hereditary spastic paraplegia | true | Inferred relationship | Some | ||
Autosomal dominant spastic paraplegia type 42 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 42 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 42 | Finding site | Spinal cord structure | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 42 | Finding site | Lower limb structure | false | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 42 | Associated morphology | Degeneration | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 42 | Associated morphology | Degenerative abnormality | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 42 | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 3 | |
Autosomal dominant spastic paraplegia type 42 | Finding site | Lower limb structure | false | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 42 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 42 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal dominant spastic paraplegia type 42 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
Autosomal dominant spastic paraplegia type 42 | Finding site | Structure of right lower limb (body structure) | true | Inferred relationship | Some | 4 | |
Autosomal dominant spastic paraplegia type 42 | Finding site | Structure of left lower limb (body structure) | true | Inferred relationship | Some | 5 | |
Autosomal dominant spastic paraplegia type 42 | Interprets | Movement observable | true | Inferred relationship | Some | 2 | |
Autosomal dominant spastic paraplegia type 42 | Has interpretation | Absent | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)