Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3706344017 | AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3706345016 | Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3706346015 | Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3706347012 | Autosomal recessive spastic ataxia type 5 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3706348019 | AFG3L2-related spastic ataxia, myoclonic epilepsy, neuropathy syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3706349010 | A rare hereditary spastic ataxia disorder with childhood onset of slowly progressive lower limb spastic paraparesis and cerebellar ataxia (with dysarthria, swallowing difficulties, motor degeneration), associated with sensorimotor neuropathy (including muscle weakness and distal amyotrophy in lower extremities) and progressive myoclonic epilepsy. Ocular signs (ptosis, oculomotor apraxia), dysmetria, dysdiadochokinesia, dystonic movements and myoclonus may also be associated. Caused by homozygous mutation in the AFG3L2 gene on chromosome 18p11. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Is a | Mitochondrial cytopathy (disorder) | true | Inferred relationship | Some | ||
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Occurrence | Childhood | true | Inferred relationship | Some | 2 | |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Is a | Spinocerebellar ataxia | true | Inferred relationship | Some | ||
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Occurrence | Childhood | true | Inferred relationship | Some | 3 | |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 4 | |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Is a | Childhood seizure | false | Inferred relationship | Some | ||
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Occurrence | Childhood | true | Inferred relationship | Some | 1 | |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Is a | Chronic metabolic disorder | true | Inferred relationship | Some | ||
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Is a | Progressive myoclonic epilepsy | true | Inferred relationship | Some | ||
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Is a | Chronic brain syndrome | true | Inferred relationship | Some | ||
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Associated morphology | Degeneration | false | Inferred relationship | Some | 2 | |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Finding site | Spinal cord structure | true | Inferred relationship | Some | 2 | |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Finding site | Cerebrum | true | Inferred relationship | Some | 3 | |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 2 | |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Is a | Spinal cord myoclonus | false | Inferred relationship | Some | ||
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Is a | Acquired ataxia | false | Inferred relationship | Some | ||
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Is a | Extrapyramidal disease | false | Inferred relationship | Some | ||
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Interprets | Movement | false | Inferred relationship | Some | 5 | |
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) | Is a | Chronic disorder of spinal cord (disorder) | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets