Status: current, Primitive. Date: 30-Nov 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4670313019 | Autosomal recessive spastic paraplegia type 74 | en | Synonym | Active | Case insensitive | SNOMED CT core |
4670314013 | Autosomal recessive spastic paraplegia type 74 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4670316010 | A rare genetic spastic paraplegia-optic atrophy-neuropathy-related (SPOAN-like) disorder with characteristics of childhood onset of mild to moderate spastic paraparesis which manifests with gait impairment that very slowly progresses into late adulthood, hyperactive patellar reflex and bilateral extensor plantar response, in association with optic atrophy and typical symptoms of peripheral neuropathy, including reduced or absent ankle reflexes, lower limb atrophy and distal sensory impairment. Reduced visual acuity and pes cavus are frequently reported. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive spastic paraplegia type 74 | Is a | SPOAN and SPOAN-related disorder | true | Inferred relationship | Some | ||
Autosomal recessive spastic paraplegia type 74 | Clinical course | Progressive | true | Inferred relationship | Some | 1 | |
Autosomal recessive spastic paraplegia type 74 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 74 | Finding site | Optic nerve structure | true | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 74 | Associated morphology | Primary atrophy | true | Inferred relationship | Some | 2 | |
Autosomal recessive spastic paraplegia type 74 | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 74 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 74 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 3 | |
Autosomal recessive spastic paraplegia type 74 | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 74 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 74 | Interprets | Movement | true | Inferred relationship | Some | 5 | |
Autosomal recessive spastic paraplegia type 74 | Finding site | Structure of left lower limb | true | Inferred relationship | Some | 6 | |
Autosomal recessive spastic paraplegia type 74 | Finding site | Structure of right lower limb | true | Inferred relationship | Some | 7 | |
Autosomal recessive spastic paraplegia type 74 | Interprets | Movement observable | true | Inferred relationship | Some | 4 | |
Autosomal recessive spastic paraplegia type 74 | Has interpretation | Absent | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set