Codes for chronic neurological diseases with susceptibility for COVID 19
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- 39.2.0
-
Organisation
- NHSD Primary Care Domain Refsets
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Codelist ID
- nhsd-primary-care-domain-refsets/codes-for-chronic-neurological-diseases-with-susceptibility-for-covid-19
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Version Tag
- 20241205
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Version ID
- 1ddf7a1f
Versions
About
Description
Taken from the CNDATRISK2_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 |
|---|---|
| 1010712009 | Autosomal dominant Emery-Dreifuss muscular dystrophy |
| 10394003 | Friedreich ataxia |
| 110270004 | Sequela of infection caused by Human poliovirus |
| 111501005 | Congenital hereditary muscular dystrophy |
| 111502003 | Fukuyama congenital muscular dystrophy |
| 111503008 | Merosin deficient congenital muscular dystrophy |
| 111504002 | Walker-Warburg congenital muscular dystrophy |
| 111505001 | Muscle-eye-brain disease, congenital muscular dystrophy |
| 111508004 | Emery-Dreifuss muscular dystrophy |
| 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 |
| 1212005 | Childhood type dermatomyositis |
| 1230273004 | Megaconial congenital muscular dystrophy |
| 124122005 | Deficiency of 3-hydroxyacyl-CoA dehydrogenase |
| 124166007 | Deficiency of butyryl-CoA dehydrogenase |
| 124621004 | Deficiency of enoyl-coenzyme A hydratase |
| 1259038005 | Autosomal dominant complex hereditary spastic paraplegia |
| 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 |
| 1260379008 | Parkinsonism caused by dopamine receptor antagonist |
| 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 |
| 1279839002 | Spinocerebellar ataxia type 46 |
| 1279840000 | Spinocerebellar ataxia type 45 |
| 128212001 | Spinal muscular atrophy, type II |
| 128213006 | Neuromuscular junction disorder |
| 128596003 | Medium-chain acyl-coenzyme A dehydrogenase deficiency |
| 14289006 | Myopathy in hypopituitarism |
| 14637005 | Late-infantile neuronal ceroid lipofuscinosis |
| 16415791000119104 | Myasthenia gravis in remission |
| 16851005 | Mitochondrial myopathy |
| 186476008 | Acute paralytic non-bulbar poliomyelitis |
| 186478009 | Acute paralytic poliomyelitis, vaccine-associated |
| 186479001 | Acute paralytic poliomyelitis, wild virus, imported |
| 186480003 | Acute paralytic poliomyelitis, wild virus, indigenous |
| 192686004 | Polioencephalitis |
| 193206003 | Persistent neonatal myasthenia gravis |
| 193207007 | Juvenile or adult myasthenia gravis |
| 193209005 | Myasthenic syndrome due to another disorder |
| 193212008 | Myasthenic syndrome due to hypothyroidism |
| 193213003 | Myasthenic syndrome due to pernicious anemia |
| 193214009 | Myasthenic syndrome due to thyrotoxicosis |
| 193216006 | Congenital and developmental myasthenia |
| 193225000 | Hereditary progressive muscular dystrophy |
| 193227008 | Pelvic muscular dystrophy |
| 193230001 | Distal muscular dystrophy with juvenile onset |
| 193237003 | Myotonic disorder |
| 193238008 | Infantile myotonia |
| 193246009 | Symptomatic inflammatory myopathy associated with another disorder |
| 193248005 | Myopathy due to disseminated lupus erythematosus |
| 193249002 | Myopathy due to polyarteritis nodosa |
| 193250002 | Myopathy due to rheumatoid arthritis |
| 193251003 | Sarcoid myopathy |
| 193252005 | Myopathy due to scleroderma |
| 193253000 | Myopathy due to Sjögren's disease |
| 195206000 | Intermittent cerebral ischemia |
| 196136009 | Lung disease co-occurrent with polymyositis |
| 19972008 | Postencephalitic parkinsonism |
| 21764004 | Renal carnitine transport defect |
| 22062008 | X-linked glutaric aciduria, type 2 |
| 22886006 | Glutaric aciduria, type 2 |
| 230237004 | Progressive spinocerebellar ataxia with decreased tendon reflexes |
| 230238009 | Progressive spinocerebellar ataxia with retained tendon reflexes |
| 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 |
| 230291001 | Juvenile Parkinson's disease |
| 230292008 | Secondary parkinsonism |
| 230296006 | Vascular parkinsonism |
| 230301006 | Akinetic-rigid form of Huntington's disease |
| 230669004 | Genetically determined myasthenia |
| 230670003 | Familial infantile myasthenia |
| 230671004 | Acetylcholine resynthesis deficiency |
| 230672006 | Congenital myasthenic syndrome |
| 230673001 | Congenital end-plate acetylcholine receptor deficiency |
| 230674007 | Pseudomyopathic myasthenia |
| 230675008 | Slow channel syndrome |
| 230676009 | Putative defect in acetylcholine synthesis or packaging |
| 230677000 | Congenital end-plate acetylcholinesterase deficiency |
| 230678005 | Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency |
| 230679002 | Abnormality of synaptic vesicles |
| 230682007 | Penicillamine-induced myasthenia |
| 230685009 | Myasthenia gravis associated with thymoma |
| 230686005 | Generalized myasthenia |
| 230687001 | Myopathy in myasthenia gravis |
| 230702001 | Ataxic hemiparesis due to and following lacunar infarction |
| 230703006 | Dysarthria-clumsy hand syndrome due to and following lacunar infarction |
| 230784003 | Congenital pseudobulbar palsy |
| 237997005 | Very long chain acyl-coenzyme A dehydrogenase deficiency |
| 237999008 | Mitochondrial trifunctional protein deficiency |
| 238001003 | Carnitine palmitoyltransferase I deficiency |
| 238002005 | Carnitine palmitoyltransferase II deficiency |
| 238003000 | Carnitine acylcarnitine translocase deficiency |
| 238026007 | Infantile GM1 gangliosidosis |
| 238936001 | Sclerodermatomyositis |
| 239898008 | Polymyositis with malignant disease |
| 239899000 | Polymyositis associated with autoimmune disease |
| 239901009 | Dermatomyositis with malignant disease |
| 240046001 | Muscular dystrophy with predominantly proximal limb girdle distribution |
| 240047005 | X-linked muscular dystrophy with limb girdle distribution |
| 240048000 | X-linked muscular dystrophy with abnormal dystrophin |
| 240049008 | Intermediate X-linked muscular dystrophy |
| 240050008 | Manifesting female carrier of X-linked muscular dystrophy |
| 240051007 | X-linked limb girdle muscular dystrophy with normal dystrophin |
| 240052000 | Ji muscular dystrophy |
| 240053005 | Hereditary myopathy limited to females |
| 240054004 | Autosomal recessive muscular dystrophy with limb girdle distribution |
| 240055003 | Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein |
| 240056002 | Severe autosomal recessive muscular dystrophy of childhood - North African type |
| 240058001 | Reunion-Indiana Amish type muscular dystrophy |
| 240059009 | Congenital muscular dystrophy |
| 240060004 | Western type of congenital muscular dystrophy |
| 240061000 | Congenital muscular dystrophy with arthrogryposis multiplex congenita |
| 240062007 | Ullrich congenital muscular dystrophy |
| 240063002 | Eichsfeld type congenital muscular dystrophy |
| 240064008 | Hutterite type of muscular dystrophy |
| 240065009 | Adult onset autosomal recessive muscular dystrophy with normal dystrophin |
| 240067001 | Autosomal dominant muscular dystrophy with limb girdle distribution |
| 240068006 | Autosomal dominant muscular dystrophy with gene located at 5q31 |
| 240069003 | Late onset proximal muscular dystrophy with dysarthria |
| 240070002 | Muscular dystrophy not predominantly limb girdle in distribution |
| 240071003 | X-linked muscular dystrophy not predominantly limb girdle |
| 240072005 | Benign scapuloperoneal muscular dystrophy with cardiomyopathy |
| 240073000 | Autosomal recessive muscular dystrophy not predominantly limb girdle |
| 240074006 | Scapulohumeral muscular dystrophy |
| 240075007 | Autosomal dominant muscular dystrophy not predominantly limb girdle |
| 240076008 | Benign scapuloperoneal muscular dystrophy |
| 240077004 | Severe scapuloperoneal muscular dystrophy with cardiomyopathy |
| 240078009 | Benign congenital muscular dystrophy with finger flexion contractures |
| 240460008 | Acute paralytic poliomyelitis |
| 240630008 | Hyperreactive malarial splenomegaly syndrome |
| 24654003 | Weber-Gubler syndrome |
| 249892007 | Progressive pseudobulbar palsy |
| 25425008 | Autosomal recessive glutaric aciduria, type 2 |
| 256321009 | Disorder of neuromuscular transmission |
| 26111005 | Metabolic myopathy |
| 267604001 | Myasthenic syndrome due to diabetic mellitus |
| 276220007 | Foville syndrome |
| 276221006 | Millard-Gubler syndrome |
| 277373000 | Severe childhood autosomal recessive muscular dystrophy |
| 281357005 | Idiopathic polymyositis |
| 29570005 | Leigh's disease |
| 305719002 | Neuromyotonia |
| 307127004 | Isolated long chain hydroxyacyl-CoA dehydrogenase deficiency |
| 307128009 | Combined long chain hydroxyacyl-coenzyme A dehydrogenase deficiency |
| 307130006 | 3-Ketoacyl-coenzyme A triolase deficiency |
| 31097004 | Post poliomyelitis syndrome |
| 31384009 | Polymyositis |
| 31839002 | Myasthenia gravis, adult form |
| 34253008 | Myopathy in Addison's disease |
| 37340000 | Motor neuron disease |
| 387732009 | Becker muscular dystrophy |
| 396230008 | Dermatomyositis |
| 398432008 | Bulbar weakness |
| 399091004 | Facioscapulohumeral muscular dystrophy |
| 39912006 | Hereditary spastic paraplegia |
| 40956001 | Guillain-Barré syndrome |
| 41574007 | Paramyotonia congenita |
| 41713005 | Benedikt's syndrome |
| 419921000000105 | [X]Dermatopolymyositis, unspecified |
| 4223005 | Parkinsonism caused by drug |
| 44395000 | Spastic tetraplegia with rigidity syndrome |
| 46251005 | Corticospinal motor disease |
| 48794007 | Human immunodeficiency virus infection with infectious mononucleosis-like syndrome |
| 49049000 | Parkinson's disease |
| 49793008 | Hereditary motor neuron disease |
| 50967008 | Gangliosidosis |
| 5262007 | Spinal muscular atrophy |
| 53509000 | Myopathy in Cushing's disease |
| 54280009 | Kugelberg-Welander disease |
| 54304004 | Progressive bulbar palsy |
| 55016009 | Congenital muscular hypertrophy-cerebral syndrome |
| 55051001 | Myasthenia gravis, juvenile form |
| 56989000 | Eaton-Lambert syndrome |
| 57938005 | Congenital myotonia, autosomal dominant form |
| 57958006 | Endocrine myopathy |
| 58756001 | Huntington's chorea |
| 58795000 | Distal muscular dystrophy |
| 60738003 | Secondary myopathy |
| 62009002 | Adult neuronal ceroid lipofuscinosis |
| 63135006 | Amyotonia congenita |
| 64383006 | Werdnig-Hoffmann disease |
| 64764001 | Acute paralytic poliomyelitis, bulbar |
| 67747009 | Ocular muscular dystrophy |
| 68437005 | Thyrotoxic myopathy |
| 68618008 | Rett syndrome |
| 699866005 | Progressive bulbar palsy with sensorineural deafness |
| 702343002 | Early onset myopathy with fatal cardiomyopathy |
| 702373006 | Hereditary myopathy with early respiratory failure |
| 702383005 | Distal myopathy 2 |
| 703524005 | Spinal muscular atrophy with progressive myoclonic epilepsy |
| 711406009 | Autosomal recessive axonal neuropathy with neuromyotonia |
| 711483003 | Spinal muscular atrophy with respiratory distress type 1 |
| 715429006 | Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome |
| 715565004 | Lethal arthrogryposis co-occurrent with anterior horn cell disease |
| 716722005 | Acute motor sensory axonal Guillain-Barré syndrome |
| 716723000 | Guillain-Barré syndrome acute inflammatory demyelinating polyradiculoneuropathic form |
| 717964007 | Juvenile primary lateral sclerosis |
| 718177001 | Autosomal recessive limb girdle muscular dystrophy type 2F |
| 718555006 | Juvenile amyotrophic lateral sclerosis |
| 718572004 | Bethlem myopathy |
| 719836007 | X-linked distal arthrogryposis multiplex congenita |
| 722987009 | Amyotrophic lateral sclerosis plus syndrome |
| 723308003 | Epidermolysis bullosa simplex with muscular dystrophy |
| 723612001 | Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome |
| 725046003 | Mitochondrial complex I deficiency due to deficiency of acyl-coenzyme A dehydrogenase 9 |
| 725420009 | Congenital muscular dystrophy Paradas type |
| 726021008 | Long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency |
| 73297009 | Muscular dystrophy |
| 733490006 | Distal myopathy with early respiratory muscle involvement |
| 7379000 | Pseudobulbar palsy |
| 75072002 | Nemaline myopathy |
| 763067000 | Autosomal dominant congenital benign spinal muscular atrophy |
| 763314009 | Congenital muscular dystrophy with hyperlaxity |
| 763533003 | Distal hereditary motor neuropathy Jerash type |
| 763829004 | Oculopharyngodistal myopathy |
| 764812008 | Autosomal recessive myogenic arthrogryposis multiplex congenita |
| 764944006 | Congenital muscular dystrophy type 1B |
| 765197008 | Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier |
| 76670001 | Duchenne muscular dystrophy |
| 766764008 | X-linked distal spinal muscular atrophy type 3 |
| 770558006 | Late-onset distal myopathy Markesbery Griggs type |
| 770596007 | Rippling muscle disease with myasthenia gravis |
| 770627003 | Desmin-related myofibrillar myopathy |
| 770722002 | Proximal myopathy with extrapyramidal signs |
| 770727008 | Spinal muscular atrophy with respiratory distress type 2 |
| 770786001 | Hereditary inclusion body myopathy type 4 |
| 770787005 | Benign Samaritan congenital myopathy |
| 770939009 | Huntington disease-like 3 |
| 77097004 | Oculopharyngeal muscular dystrophy |
| 771144005 | Hereditary motor and sensory neuropathy with acrodystrophy |
| 771238004 | Spinal atrophy, ophthalmoplegia, pyramidal syndrome |
| 771267003 | Congenital muscular dystrophy with integrin alpha-7 deficiency |
| 771272007 | Congenital muscular dystrophy due to lamin A/C mutation |
| 771302009 | Autosomal recessive lower motor neuron disease with childhood onset |
| 771306007 | Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome |
| 771475006 | Young adult-onset distal hereditary motor neuropathy |
| 772129007 | Autosomal dominant childhood-onset proximal spinal muscular atrophy |
| 773306002 | Congenital lethal myopathy Compton North type |
| 773555005 | Severe neurodegenerative syndrome with lipodystrophy |
| 773729007 | X-linked myopathy with postural muscle atrophy |
| 774148007 | Polyglucosan body myopathy type 1 |
| 77461000119109 | Myasthenia gravis with exacerbation |
| 77471000119103 | Myasthenia gravis without exacerbation |
| 776087007 | Autosomal recessive cerebral atrophy |
| 778029000 | FAST kinase domains 2-related infantile mitochondrial encephalomyopathy |
| 778060000 | Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy |
| 77956009 | Steinert myotonic dystrophy syndrome |
| 782743001 | Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions |
| 782772000 | Congenital muscular dystrophy with intellectual disability and severe epilepsy |
| 782883004 | Fatal infantile hypertonic myofibrillar myopathy |
| 783010003 | Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome |
| 783012006 | Parkinsonian pyramidal syndrome |
| 783174004 | Congenital muscular dystrophy with intellectual disability |
| 783175003 | Congenital muscular dystrophy without intellectual disability |
| 783176002 | Congenital muscular dystrophy with cerebellar involvement |
| 783734000 | Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency |
| 784341001 | Amyotrophic lateral sclerosis type 4 |
| 784371009 | Huntington disease-like 1 |
| 78468005 | Erb's muscular dystrophy |
| 785298001 | Muscle eye brain disease with bilateral multicystic leukodystrophy |
| 787037000 | Congenital muscular dystrophy type 1A |
| 80976008 | Myasthenic crisis |
| 81211007 | Primary lateral sclerosis |
| 82077006 | Myotubular myopathy |
| 84590007 | Lower motor neuron disease |
| 85505000 | Adult spinal muscular atrophy |
| 85672005 | Anterior horn cell disease |
| 86044005 | Amyotrophic lateral sclerosis |
| 864471000000106 | Anterior opercular syndrome |
| 870288002 | Parkinsonism caused by methanol |
| 870295006 | Parkinsonism caused by carbon disulfide |
| 87555007 | Claude's syndrome |
| 87694001 | Pyruvate carboxylase deficiency |
| 879937000 | Alpha-N-acetylgalactosaminidase deficiency type 1 |
| 88923002 | Progressive muscular atrophy |
| 890368007 | Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation |
| 890395002 | Congenital muscular dystrophy type 1D large gene mutation |
| 90099008 | Subcortical leukoencephalopathy |
| 9105005 | Muscle adenosine monophosphate deaminase deficiency |
| 91637004 | Myasthenia gravis |
| 93153005 | Limb-girdle muscular dystrophy |
| 95647008 | Upper motor neuron disease |
Codes not in the full codelist are in faint grey.