icd10_code,description,neuro
A800,"Acute paralytic poliomyelitis, vaccine-associated",1
A801,"Acute paralytic poliomyelitis, wild virus, imported",1
A802,"Acute paralytic poliomyelitis, wild virus, indigenous",1
A803,"Acute paralytic poliomyelitis, other and unspecified",1
A804,Acute nonparalytic poliomyelitis,1
A809,"Acute poliomyelitis, unspecified",1
A810,Creutzfeldt-Jakob disease,1
A811,Subacute sclerosing panencephalitis,1
A812,Progressive multifocal leukoencephalopathy,1
A818,Other atypical virus infections of central nervous system,1
A819,"Atypical virus infection of central nervous system, unspecified",1
B91,Sequelae of poliomyelitis,1
E104,Type 1 diabetes mellitus With neurological complications ,1
E114,Type 2 diabetes mellitus With neurological complications ,1
E134,Other specified diabetes mellitus With neurological complications ,1
E144,Unspecified diabetes mellitus With neurological complications ,1
E750,GM2 gangliosidosis,1
E751,Other gangliosidosis,1
E752,Other sphingolipidosis,1
E753,"Sphingolipidosis, unspecified",1
E754,Neuronal ceroid lipofuscinosis,1
E755,Other lipid storage disorders,1
E756,"Lipid storage disorder, unspecified",1
F021,Dementia in Creutzfeldt-Jakob disease,1
F022,Dementia in Huntington disease,1
F023,Dementia in Parkinson disease,1
G10,Huntington disease,1
G111,Early-onset cerebellar ataxia,1
G112,Late-onset cerebellar ataxia,1
G113,Cerebellar ataxia with defective DNA repair,1
G114,Hereditary spastic paraplegia,1
G118,Other hereditary ataxias,1
G119,"Hereditary ataxia, unspecified",1
G120,"Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]",1
G121,Other inherited spinal muscular atrophy,1
G122,Motor neuron disease,1
G128,Other spinal muscular atrophies and related syndromes,1
G129,"Spinal muscular atrophy, unspecified",1
G130,Paraneoplastic neuromyopathy and neuropathy,1
G131,Other systemic atrophy primarily affecting central nervous system in neoplastic disease,1
G132,Systemic atrophy primarily affecting central nervous system in myxoedema,1
G138,Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere,1
G14,Postpolio syndrome,1
G20,Parkinson disease,1
G210,Malignant neuroleptic syndrome,1
G211,Other drug-induced secondary parkinsonism,1
G212,Secondary parkinsonism due to other external agents,1
G213,Postencephalitic parkinsonism,1
G214,Vascular parkinsonism,1
G218,Other secondary parkinsonism,1
G219,"Secondary parkinsonism, unspecified",1
G22,Parkinsonism in diseases classified elsewhere,1
G230,Hallervorden-Spatz disease,1
G231,Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski],1
G232,"Multiple system atrophy, parkinsonian type [MSA-P]",1
G233,"Multiple system atrophy, cerebellar type [MSA-C]",1
G238,Other specified degenerative diseases of basal ganglia,1
G239,"Degenerative disease of basal ganglia, unspecified",1
G312,Degeneration of nervous system due to alcohol,1
G318,Other specified degenerative diseases of nervous system,1
G320,Subacute combined degeneration of spinal cord in diseases classified elsewhere,1
G35,Multiple sclerosis,1
G370,Diffuse sclerosis,1
G371,Central demyelination of corpus callosum,1
G375,Concentric sclerosis,1
G379,"Demyelinating disease of central nervous system, unspecified",1
G450,Vertebro-basilar artery syndrome,1
G451,Carotid artery syndrome (hemispheric),1
G452,Multiple and bilateral precerebral artery syndromes,1
G458,Other transient cerebral ischaemic attacks and related syndromes,1
G459,"Transient cerebral ischaemic attack, unspecified",1
G460,Middle cerebral artery syndrome,1
G461,Anterior cerebral artery syndrome,1
G462,Posterior cerebral artery syndrome,1
G463,Brain stem stroke syndrome,1
G464,Cerebellar stroke syndrome,1
G465,Pure motor lacunar syndrome,1
G466,Pure sensory lacunar syndrome ,1
G467,Other lacunar syndromes,1
G468,Other vascular syndromes of brain in cerebrovascular diseases ,1
G600,Hereditary motor and sensory neuropathy,1
G601,Refsum disease,1
G602,Neuropathy in association with hereditary ataxia,1
G610,Guillain-Barré syndrome,1
G700,Myasthenia gravis,1
G701,Toxic myoneural disorders,1
G702,Congenital and developmental myasthenia,1
G708,Other specified myoneural disorders,1
G709,"Myoneural disorder, unspecified",1
G710,Muscular dystrophy,1
G711,Myotonic disorders,1
G712,Congenital myopathies,1
G713,"Mitochondrial myopathy, not elsewhere classified",1
G723,Periodic paralysis,1
G730,Myasthenic syndromes in endocrine diseases,1
G731,Lambert-Eaton syndrome,1
G732,Other myasthenic syndromes in neoplastic disease,1
G733,Myasthenic syndromes in other diseases classified elsewhere,1
G735,Myopathy in endocrine diseases,1
G736,Myopathy in metabolic diseases,1
G737,Myopathy in other diseases classified elsewhere,1
G800,Spastic quadriplegic cerebral palsy,1
G801,Spastic diplegic cerebral palsy,1
G802,Spastic hemiplegic cerebral palsy,1
G803,Dyskinetic cerebral palsy,1
G804,Ataxic cerebral palsy,1
G808,Other cerebral palsy,1
G809,"Cerebral palsy, unspecified",1
G810,Flaccid hemiplegia,1
G811,Spastic hemiplegia,1
G819,"Hemiplegia, unspecified",1
G820,Flaccid paraplegia,1
G821,Spastic paraplegia,1
G822,"Paraplegia, unspecified",1
G823,Flaccid tetraplegia,1
G824,Spastic tetraplegia,1
G825,"Tetraplegia, unspecified",1
I610,"Intracerebral haemorrhage in hemisphere, subcortical",1
I611,"Intracerebral haemorrhage in hemisphere, cortical",1
I612,"Intracerebral haemorrhage in hemisphere, unspecified",1
I614,Intracerebral haemorrhage in cerebellum,1
I615,"Intracerebral haemorrhage, intraventricular",1
I616,"Intracerebral haemorrhage, multiple localized",1
I618,Other intracerebral haemorrhage,1
I619,"Intracerebral haemorrhage, unspecified",1
I623,Intracerebral haemorrhage in brain stem,1
I630,Cerebral infarction due to thrombosis of precerebral arteries,1
I631,Cerebral infarction due to embolism of precerebral arteries,1
I632,Cerebral infarction due to unspecified occlusion or stenosis of precerebral arteries,1
I633,Cerebral infarction due to thrombosis of cerebral arteries,1
I634,Cerebral infarction due to embolism of cerebral arteries,1
I635,Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries,1
I636,"Cerebral infarction due to cerebral venous thrombosis, nonpyogenic",1
I638,Other cerebral infarction,1
I639,"Cerebral infarction, unspecified",1
I64,"Stroke, not specified as haemorrhage or infarction",1
I650,Occlusion and stenosis of vertebral artery,1
I651,Occlusion and stenosis of basilar artery,1
I652,Occlusion and stenosis of carotid artery,1
I653,Occlusion and stenosis of multiple and bilateral precerebral arteries,1
I658,Occlusion and stenosis of other precerebral artery,1
I659,Occlusion and stenosis of unspecified precerebral artery,1
I660,Occlusion and stenosis of middle cerebral artery,1
I661,Occlusion and stenosis of anterior cerebral artery,1
I662,Occlusion and stenosis of posterior cerebral artery,1
I663,Occlusion and stenosis of cerebellar arteries,1
I664,Occlusion and stenosis of multiple and bilateral cerebral arteries,1
I668,Occlusion and stenosis of other cerebral artery,1
I669,Occlusion and stenosis of unspecified cerebral artery,1
I673,Progressive vascular leukoencephalopathy,1
I674,Hypertensive encephalopathy,1
I675,Moyamoya disease,1
I676,Nonpyogenic thrombosis of intracranial venous system,1
I677,"Cerebral arteritis, not elsewhere classified",1
I680,Cerebral amyloid angiopathy,1
I682,Cerebral arteritis in other diseases classified elsewhere,1
I691,Sequelae of intracerebral haemorrhage,1
I693,Sequelae of cerebral infarction,1
I694,"Sequelae of stroke, not specified as haemorrhage or infarction",1
M330,Juvenile dermatomyositis,1
M331,Other dermatomyositis,1
M332,Polymyositis,1
M339,"Dermatopolymyositis, unspecified",1
M414,Neuromuscular scoliosis,1
M896,Osteopathy after poliomyelitis,1