has_mnd_ms_myas_or_huntingtons
- Coding system
- SNOMED CT
- Coding system release
- unknown
- Organisation
- QCovid
- Codelist ID
- qcovid/has_mnd_ms_myas_or_huntingtons
- Version ID
- 4b70c3f1
Versions
- 4b70c3f1
Description
SNOMED codelist for the has_mnd_ms_myas_or_huntingtons group in the QCovid® to develop the
COVID-19 Population Risk Assessment.
References
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 5262007 | Spinal muscular atrophy (disorder) |
| 7379000 | Pseudobulbar palsy (disorder) |
| 31097004 | Post poliomyelitis syndrome (disorder) |
| 37340000 | Motor neuron disease (disorder) |
| 54280009 | Kugelberg-Welander disease (disorder) |
| 54304004 | Progressive bulbar palsy (disorder) |
| 58756001 | Huntington's chorea (disorder) |
| 64383006 | Werdnig-Hoffmann disease (disorder) |
| 81211007 | Primary lateral sclerosis (disorder) |
| 85505000 | Adult spinal muscular atrophy (disorder) |
| 85672005 | Anterior horn cell disease (disorder) |
| 86044005 | Amyotrophic lateral sclerosis (disorder) |
| 88923002 | Progressive muscular atrophy (disorder) |
| 91637004 | Myasthenia gravis (disorder) |
| 128212001 | Spinal muscular atrophy, type II (disorder) |
| 193206003 | Persistent neonatal myasthenia gravis (disorder) |
| 193207007 | Juvenile or adult myasthenia gravis (disorder) |
| 193216006 | Congenital and developmental myasthenia (disorder) |
| 230246005 | Progressive bulbar palsy of childhood (disorder) |
| 230247001 | Distal spinal muscular atrophy (disorder) |
| 230248006 | Scapuloperoneal spinal muscular atrophy (disorder) |
| 230249003 | Facioscapulohumeral spinal muscular atrophy (disorder) |
| 230250003 | Facioscapulohumeral spinal muscular atrophy with sensory loss (disorder) |
| 230251004 | Scapulohumeral spinal muscular atrophy (disorder) |
| 230252006 | Oculopharyngeal spinal muscular atrophy (disorder) |
| 230253001 | Bulbospinal neuronopathy (disorder) |
| 230257000 | Paraneoplastic motor neurone disease (disorder) |
| 230258005 | Amyotrophic lateral sclerosis with dementia (disorder) |
| 230669004 | Genetically determined myasthenia (disorder) |
| 230671004 | Acetylcholine resynthesis deficiency (disorder) |
| 230672006 | Congenital myasthenia (disorder) |
| 230673001 | Congenital end-plate acetylcholine receptor deficiency (disorder) |
| 230674007 | Pseudomyopathic myasthenia (disorder) |
| 230676009 | Putative defect in acetylcholine synthesis or packaging (disorder) |
| 230677000 | Congenital end-plate acetylcholinesterase deficiency (disorder) |
| 230678005 | Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency (disorder) |
| 230679002 | Abnormality of synaptic vesicles (disorder) |
| 230685009 | Myasthenia gravis associated with thymoma (disorder) |
| 230686005 | Generalized myasthenia (disorder) |
| 230784003 | Congenital pseudobulbar palsy (disorder) |
| 249892007 | Progressive pseudobulbar palsy (disorder) |
| 305719002 | Neuromyotonia (disorder) |
| 864471000000106 | Anterior opercular syndrome (disorder) |
Codes not in the full codelist are in faint grey.