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 |
3428260010 | Autosomal recessive spastic paraplegia type 55 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3428261014 | Autosomal recessive spastic paraplegia type 55 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403164016 | Autosomal recessive spastic paraplegia type 55 (SPG 55) is a rare, complex type of hereditary spastic paraplegia characterized by childhood onset of progressive spastic paraplegia associated with optic atrophy (with reduced visual acuity and central scotoma), ophthalmoplegia, reduced upper-extremity strength and dexterity, muscular atrophy in the lower extremities, and sensorimotor neuropathy. SPG55 is caused by mutations in the C12ORF65 gene (12q24.31) encoding probable peptide chain release factor C12orf65, mitochondrial. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403165015 | Autosomal recessive spastic paraplegia type 55 (SPG 55) is a rare, complex type of hereditary spastic paraplegia characterised by childhood onset of progressive spastic paraplegia associated with optic atrophy (with reduced visual acuity and central scotoma), ophthalmoplegia, reduced upper-extremity strength and dexterity, muscular atrophy in the lower extremities, and sensorimotor neuropathy. SPG55 is caused by mutations in the C12ORF65 gene (12q24.31) encoding probable peptide chain release factor C12orf65, mitochondrial. | 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 55 (disorder) | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 55 (disorder) | Is a | Complicated hereditary spastic paraplegia | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 55 (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 55 (disorder) | Finding site | Lower limb structure | false | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 55 (disorder) | Associated morphology | Degeneration | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Finding site | Spinal cord structure | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Finding site | Cerebellar structure | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Finding site | Lower limb structure | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Associated morphology | Primary atrophy | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Finding site | Optic nerve structure | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Is a | SPOAN and SPOAN-related disorder | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 55 (disorder) | Finding site | Lower limb structure | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Finding site | Optic nerve structure | true | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Associated morphology | Primary atrophy | true | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Interprets | Movement | true | Inferred relationship | Some | 5 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Finding site | Structure of left lower limb (body structure) | true | Inferred relationship | Some | 6 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Finding site | Structure of right lower limb (body structure) | true | Inferred relationship | Some | 7 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Interprets | Movement observable | true | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 55 (disorder) | Has interpretation | Absent | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)