Motor neurone disease codes
Codelist metadata
-
Coding system
- SNOMED CT
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Coding system release
- 39.2.0
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Organisation
- NHSD Primary Care Domain Refsets
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Codelist ID
- nhsd-primary-care-domain-refsets/motor-neurone-disease-codes
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Version Tag
- 20241205
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Version ID
- 63a853d2
Versions
About
Description
Taken from the MND_COD refset published by NHSD.
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 |
|---|---|
| 103851000119100 | Restrictive lung disease due to amyotrophic lateral sclerosis |
| 1105051000000102 | Subacute combined degeneration of spinal cord due to use of nitrous oxide |
| 1172689007 | Prenatal-onset spinal muscular atrophy with congenital bone fractures |
| 1197152005 | Distal hereditary motor neuropathy type 5 |
| 1197523001 | Autosomal dominant amyotrophic lateral sclerosis type 1 |
| 1197524007 | Autosomal recessive amyotrophic lateral sclerosis type 1 |
| 1201863001 | Amyotrophic lateral sclerosis type 1 |
| 1201947005 | Juvenile amyotrophic lateral sclerosis type 2 |
| 1201950008 | Amyotrophic lateral sclerosis type 3 |
| 1201961000 | Juvenile amyotrophic lateral sclerosis type 5 |
| 1204334005 | Amyotrophic lateral sclerosis type 6 |
| 1204349002 | Amyotrophic lateral sclerosis type 7 |
| 1204350002 | Amyotrophic lateral sclerosis type 8 |
| 1204351003 | Amyotrophic lateral sclerosis type 9 |
| 1208412003 | Amyotrophic lateral sclerosis type 10 |
| 1208615009 | Neurogenic scapuloperoneal syndrome Kaeser type |
| 1230343006 | Distal hereditary motor neuropathy type 2 |
| 1259121008 | Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea |
| 1259122001 | Amyotrophic lateral sclerosis with parkinsonism |
| 1259123006 | Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula |
| 1259124000 | Amyotrophic lateral sclerosis with frontotemporal dementia |
| 1259125004 | Amyotrophic lateral sclerosis with multiple system atrophy |
| 1259126003 | Amyotrophic lateral sclerosis with autonomic dysfunction |
| 1259127007 | Amyotrophic lateral sclerosis with cerebellar dysfunction |
| 1259129005 | Amyotrophic lateral sclerosis with spinocerebellar ataxia |
| 1263497002 | Motor neuron disease due to neoplastic disease |
| 1263531001 | Motor neuron disease due to and following radiotherapy to spinal cord |
| 1263534009 | Motor neuron disease due to herpes zoster |
| 1263535005 | Motor neuron disease due to human immunodeficiency virus infection |
| 1263536006 | Motor neuron disease due to hereditary spastic paraplegia |
| 1263538007 | Motor neuron disease due to gammopathy |
| 128212001 | Spinal muscular atrophy, type II |
| 155014006 | (Anterior horn cell disease) or (muscular atrophy) |
| 155015007 | Motor neurone disease |
| 155016008 | Other anterior horn cell disease &/or Werdnig-Hoffman disease |
| 192884004 | Anterior horn cell disease |
| 192885003 | Unspecified spinal muscular atrophy |
| 192887006 | Spinal muscular atrophy NOS |
| 192888001 | Motor neurone disease |
| 192889009 | Motor neurone disease |
| 192890000 | Motor neurone disease NOS |
| 192891001 | Other anterior horn cell disease |
| 192892008 | Anterior horn cell disease NOS |
| 194461001 | [X]Other inherited spinal muscular atrophy |
| 230246005 | Progressive bulbar palsy of childhood |
| 230247001 | Distal spinal muscular atrophy |
| 230248006 | Scapuloperoneal spinal muscular atrophy |
| 230249003 | Facioscapulohumeral spinal muscular atrophy |
| 230250003 | Facioscapulohumeral spinal muscular atrophy with sensory loss |
| 230251004 | Scapulohumeral spinal muscular atrophy |
| 230252006 | Oculopharyngeal spinal muscular atrophy |
| 230253001 | Bulbospinal neuronopathy |
| 230254007 | Western Pacific motor neurone disease |
| 230255008 | Madras-type motor neurone disease |
| 230257000 | Paraneoplastic motor neurone disease |
| 230258005 | Amyotrophic lateral sclerosis with dementia |
| 230264003 | Troyer syndrome |
| 230274000 | Frontal lobe degeneration with motor neurone disease |
| 230547002 | Bulbar palsy |
| 230784003 | Congenital pseudobulbar palsy |
| 249892007 | Progressive pseudobulbar palsy |
| 267693003 | (Anterior horn cell disease) or (muscular atrophy) |
| 267694009 | Other anterior horn cell disease &/or Werdnig-Hoffman disease |
| 305719002 | Neuromyotonia |
| 31097004 | Post poliomyelitis syndrome |
| 367094007 | Postpolio syndrome |
| 37340000 | Motor neuron disease |
| 398432008 | Bulbar weakness |
| 412291000000109 | [X]Other spinal muscular atrophies and related syndromes |
| 430031000000107 | [X]Other inherited spinal muscular atrophy |
| 44395000 | Spastic tetraplegia with rigidity syndrome |
| 46251005 | Corticospinal motor disease |
| 49793008 | Hereditary motor neuron disease |
| 5262007 | Spinal muscular atrophy |
| 54280009 | Kugelberg-Welander disease |
| 54304004 | Progressive bulbar palsy |
| 583151000000109 | Other anterior horn cell disease |
| 60576007 | Subacute combined degeneration of spinal cord |
| 630471000000103 | Anterior horn cell disease NOS |
| 64383006 | Werdnig-Hoffmann disease |
| 646181000000106 | Unspecified spinal muscular atrophy |
| 646191000000108 | Spinal muscular atrophy NOS |
| 646201000000105 | Motor neurone disease NOS |
| 699866005 | Progressive bulbar palsy with sensorineural deafness |
| 703524005 | Spinal muscular atrophy with progressive myoclonic epilepsy |
| 703544004 | Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia |
| 711406009 | Autosomal recessive axonal neuropathy with neuromyotonia |
| 711483003 | Spinal muscular atrophy with respiratory distress type 1 |
| 715565004 | Lethal arthrogryposis co-occurrent with anterior horn cell disease |
| 717964007 | Juvenile primary lateral sclerosis |
| 718555006 | Juvenile amyotrophic lateral sclerosis |
| 719836007 | X-linked distal arthrogryposis multiplex congenita |
| 722987009 | Amyotrophic lateral sclerosis plus syndrome |
| 723612001 | Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome |
| 7379000 | Pseudobulbar palsy |
| 757061000000109 | Neuromyotonia |
| 763067000 | Autosomal dominant congenital benign spinal muscular atrophy |
| 763533003 | Distal hereditary motor neuropathy Jerash type |
| 766764008 | X-linked distal spinal muscular atrophy type 3 |
| 770430000 | Autosomal recessive distal spinal muscular atrophy type 3 |
| 770630005 | Distal hereditary motor neuropathy type 1 |
| 770727008 | Spinal muscular atrophy with respiratory distress type 2 |
| 771081007 | Distal hereditary motor neuropathy type 7 |
| 771238004 | Spinal atrophy, ophthalmoplegia, pyramidal syndrome |
| 771302009 | Autosomal recessive lower motor neuron disease with childhood onset |
| 771475006 | Young adult-onset distal hereditary motor neuropathy |
| 772129007 | Autosomal dominant childhood-onset proximal spinal muscular atrophy |
| 778171000000101 | Postpolio syndrome |
| 783618006 | Lower motor neuron syndrome with late-adult onset |
| 784341001 | Amyotrophic lateral sclerosis type 4 |
| 784391002 | Autosomal dominant adult-onset proximal spinal muscular atrophy |
| 81211007 | Primary lateral sclerosis |
| 838276009 | Amyotrophic lateral sclerosis, parkinsonism, dementia complex |
| 84590007 | Lower motor neuron disease |
| 85505000 | Adult spinal muscular atrophy |
| 85672005 | Anterior horn cell disease |
| 86044005 | Amyotrophic lateral sclerosis |
| 864471000000106 | Anterior opercular syndrome |
| 864481000000108 | Anterior opercular syndrome |
| 88923002 | Progressive muscular atrophy |
| 95647008 | Upper motor neuron disease |
Codes not in the full codelist are in faint grey.