medcode,readcode,readterm,neuro
684,F20..00,multiple sclerosis,1
1391,C327100,gaucher's disease,1
1607,F370000,guillain-barre syndrome,1
1632,F39z.00,myopathy or muscular dystrophy nos,1
1691,F120.00,paralysis agitans,1
1749,F22..00,hemiplegia,1
2019,F234.00,infantile hemiplegia nos,1
2069,F23..00,congenital cerebral palsy,1
2298,F203.00,exacerbation of multiple sclerosis,1
2336,F143.00,cerebellar ataxia nos,1
2732,A40..00,acute poliomyelitis,1
3063,F241.00,paraplegia,1
3293,F223.00,right hemiplegia,1
3428,R013000,[d]ataxia nos,1
3440,F20..11,disseminated sclerosis,1
3464,F21..00,other central nervous system demyelinating diseases,1
3514,F141.00,hereditary spastic paraplegia,1
3621,2837.00,o/e - diplegia,1
4165,F140.00,friedreich's ataxia,1
4321,F12..00,parkinson's disease,1
4796,F152.00,motor neurone disease,1
4908,N003.00,dermatomyositis,1
5095,F21y200,binswanger's disease,1
5128,F142.00,primary cerebellar degeneration,1
5393,F391000,duchenne muscular dystrophy,1
5512,F230100,cerebral palsy with spastic diplegia,1
5560,F23..12,infantile cerebral palsy,1
5584,F361000,charcot-marie-tooth disease,1
5655,F380.00,myasthenia gravis,1
5964,F39B.00,muscular dystrophy,1
6376,F370.00,acute infective polyneuritis,1
6599,F39..00,muscular dystrophies and other myopathies,1
7037,F24y200,steele-richardson-olszewski syndrome,1
7470,F152111,duchenne aran muscular atrophy,1
7736,F162.00,subacute combined degeneration of spinal cord,1
8257,1412.00,h/o: poliomyelitis,1
8267,F363.00,refsum's disease,1
8282,2836.00,o/e - quadraplegia,1
8472,29L..12,o/e - ataxia,1
8492,F22z.00,hemiplegia nos,1
8933,F222.00,left hemiplegia,1
8956,F130300,parkinsonism with orthostatic hypotension ,1
9179,F151.00,spinal muscular atrophy,1
9271,F240.00,quadriplegia,1
9375,F241100,spastic paraplegia,1
9385,F24y000,progressive supranuclear palsy ,1
10189,G674000,cerebral amyloid angiopathy,1
10718,297A.00,o/e - parkinsonian tremor ,1
10890,Z7E4400,cerebellar ataxia,1
11346,F38z.00,myoneural disorder nos,1
11542,F360000,dejerine-sottas disease,1
12054,F21z.00,central nervous system demyelination nos,1
12666,F23yz00,other infantile cerebral palsy nos,1
12699,F38..00,myoneural disorders,1
14912,F12z.00,parkinson's disease nos,1
15100,N231100,progressive myositis ossificans,1
15261,F11y100,cerebral ataxia,1
15511,N004.00,polymyositis,1
15530,F23..11,congenital spastic cerebral palsy,1
16117,F240.11,tetraplegia,1
16118,F392000,dystrophia myotonica (steinert's disease),1
16162,A401.00,acute paralytic non-bulbar poliomyelitis,1
16860,2994.11,o/e - parkinson gait ,1
16903,F14y011,Louis - Bar syndrome,1
16956,G669.00,"cerebral palsy, not congenital or infantile, acute",1
16977,F137000,athetoid cerebral palsy,1
17004,2987.11,o/e - parkinson posture ,1
17392,F397.00,proximal myopathy,1
17990,F392.00,myotonic disorders,1
18084,F152300,pseudobulbar palsy,1
18307,F39X.00,"mitochondrial myopathy, not elsewhere classified",1
18493,Z7E4.00,ataxia,1
19052,R012000,[d]ataxic gait,1
19478,F121.11,drug induced parkinsonism ,1
20008,29L3.00,o/e - legs ataxic,1
20120,F152z00,motor neurone disease nos,1
20122,F221.00,spastic hemiplegia,1
20206,F144z00,cerebellar ataxia in disease nos,1
20261,F38y.00,other specific myoneural disorder,1
20493,F20z.00,multiple sclerosis nos,1
20845,F152400,primary lateral sclerosis,1
21022,F396700,myopathy due to sjogren's disease,1
21169,F101300,tay-sach's disease,1
21216,F14..00,spinocerebellar disease,1
21249,F232.00,congenital quadriplegia,1
21425,F391z00,hereditary progressive muscular dystrophy nos,1
21548,F23y000,ataxic infantile cerebral palsy,1
21863,F130.00,other basal ganglia degenerative diseases,1
21889,F15..00,anterior horn cell disease,1
22018,G673000,"dissection of cerebral arteries, nonruptured",1
22135,2833.00,o/e - hemiplegia,1
22174,F390z00,congenital hereditary muscular dystrophy nos,1
22400,G674.00,cerebral arteritis,1
22454,F174.00,multiple system atrophy ,1
23484,F392111,thomsen's disease,1
23730,F202.00,generalised multiple sclerosis,1
24001,F12W.00,secondary parkinsonism due to other external agents ,1
24019,AE1..00,late effects of acute poliomyelitis,1
24216,F370100,postinfectious polyneuritis,1
25268,F101211,batten's disease of retina,1
25324,F230.00,congenital diplegia,1
25429,F390300,myotubular myopathy,1
25570,F23y200,spastic cerebral palsy,1
25880,F13z100,stiff-man syndrome,1
26181,F12X.00,"secondary parkinsonism, unspecified ",1
26210,F391011,pseudohypertrophic dystrophy,1
27331,F14z.00,spinocerebellar disease nos,1
27377,F152200,progressive bulbar palsy,1
27515,F380z00,myasthenia gravis nos,1
27966,F231.00,congenital hemiplegia,1
28082,F21X.00,"acute disseminated demyelination, unspecified",1
28210,F391300,other limb-girdle muscular dystrophy,1
28262,F39W.00,"inflammatory myopathy, not elsewhere classified",1
28306,F23z.00,congenital cerebral palsy nos,1
28316,N003X00,"dermatopolymyositis, unspecified",1
28955,F392100,myotonia congenita (thomsen's disease),1
29114,A940.11,locomotor ataxia,1
29181,R007600,[d]post polio exhaustion,1
30537,F373.00,POLYNEUROPATHY IN MALIGNANT DISEASE,1
30987,F152100,progressive muscular atrophy,1
31209,F396400,myopathy due to rheumatoid arthritis,1
31329,F393.00,familial periodic paralysis,1
31742,F394100,alcoholic myopathy,1
32016,F39y.00,other myopathies and muscular dystrophies,1
32270,F381000,eaton-lambert syndrome,1
32310,G675.00,moyamoya disease,1
32527,F368.00,hereditary motor and sensory neuropathy,1
32649,N003000,juvenile dermatomyositis,1
32749,F391800,becker muscular dystrophy,1
32916,F394.00,toxic myopathy,1
33334,F150.00,werdnig - hoffmann disease,1
33544,F121.00,parkinsonism secondary to drugs ,1
33839,F144000,cerebellar ataxia due to alcoholism,1
33841,F370200,miller-fisher syndrome,1
34704,F390100,central core disease,1
34985,F391A00,emery-dreifuss muscular dystrophy,1
35059,G673100,carotico-cavernous sinus fistula,1
35137,F392y00,other specified myotonic disorder,1
35465,F368100,hereditary motor and sensory neuropathy type ii,1
35540,F240100,spastic tetraplegia,1
35839,F130500,shy-drager syndrome ,1
35938,F030211,poliomyelitis encephalitis,1
36079,F394000,drug-induced myopathy,1
36117,C371500,coproporphyria,1
36133,2835.00,o/e - paraplegia,1
36312,F210.11,devic's disease,1
36433,F152000,amyotrophic lateral sclerosis,1
36566,F390400,nemaline body disease,1
36567,PKy6100,cockayne syndrome,1
36671,F391400,facioscapulohumeral muscular dystrophy,1
37160,F230000,congenital paraplegia,1
37295,A403200,"acute paralytic poliomyelitis, wild virus, indigenous",1
38448,F391700,oculopharyngeal muscular dystrophy,1
39085,F220.00,flaccid hemiplegia,1
39398,F034D00,post polio vaccination encephalitis,1
39416,A4...00,poliomyelitis & other non-arthropod-borne viral diseases-cns,1
39725,F395z00,myopathy due to endocrine disease nos,1
39971,F23..13,littles disease,1
40344,F200.00,multiple sclerosis of the brain stem,1
40387,N003.11,poikilodermatomyositis,1
40407,2982.00,o/e - hemiplegic posture,1
40553,F130400,progressive supranuclear ophthalmoplegia ,1
40968,F21y500,concentric sclerosis,1
41000,F101500,retinal dystrophy in cerebroretinal lipidosis,1
41094,2993.00,o/e - gait ataxic,1
41904,F391600,ocular muscular dystrophy,1
42756,F4Gy100,extraocular muscle myopathy,1
42940,H57y100,lung disease with polymyositis,1
43203,F100.00,leucodystrophy,1
43232,666B.00,multiple sclerosis multidisciplinary review,1
43394,F151100,kugelberg - welander disease,1
43583,F21y.00,other specified central nervous system demyelinating disease,1
43626,A403100,"acute paralytic poliomyelitis, wild virus, imported",1
44512,F364.00,idiopathic progressive polyneuropathy,1
44708,F395.00,myopathy due to endocrine disease ec,1
44795,F210.00,neuromyelitis optica,1
44867,F392z00,myotonic disorder nos,1
44925,F398.00,myopathy in metabolic diseases,1
44985,666A.00,multiple sclerosis review,1
45006,N307z00,poliomyelitis osteopathy nos,1
45551,F230z00,congenital diplegia nos,1
45722,A403.00,"acute paralytic poliomyelitis, unspecified",1
45903,F100000,krabbe's disease,1
46128,F240000,flaccid tetraplegia,1
46175,F241000,flaccid paraplegia,1
46516,C327200,niemann-pick disease,1
46528,F393.11,familial hypokalaemic periodic paralysis,1
46748,F392200,paramyotonia congenita (eulenburg's disease),1
46749,C377111,pseudo - hurler's disease,1
46937,F365.00,neuropathy in association with hereditary ataxia,1
47695,F381600,myasthenic syndrome due to thyrotoxicosis,1
47696,65VD.00,notification of acute polio,1
48036,F391100,erb's muscular dystrophy,1
48126,F232.11,tetraplegia - congenital,1
48167,F395400,myopathy due to thyrotoxicosis,1
48211,F10y000,alper's disease,1
48300,F10y100,leigh's disease,1
49034,F24y011,steele richardson olszewsk syn,1
49181,F101400,gangliosidosis,1
49203,F130200,striatonigral degeneration,1
49482,F396200,MYOPATHY DUE TO MALIGNANT DISEASE,1
49737,F142200,dyssynergia cerebellaris myoclonica,1
49967,F23y300,dyskinetic cerebral palsy,1
50096,F145.00,congenital nonprogressive ataxia,1
50161,8CS1.00,multiple sclerosis care plan agreed,1
50725,A270300,listerial cerebral arteritis,1
50762,F130z00,other basal ganglia degenerative disease nos,1
51105,F123.00,postencephalitic parkinsonism ,1
51416,F395300,myopathy due to myxoedema,1
51534,C371300,protocoproporphyria,1
51640,F381.00,myasthenic syndrome due to disease ec,1
52519,F396500,myopathy due to sarcoidosis,1
52589,A94y100,syphilitic parkinsonism ,1
52659,F23y400,ataxic diplegic cerebral palsy,1
52677,A412.00,subacute sclerosing panencephalitis,1
52795,F14y.00,other spinocerebellar diseases,1
53178,F23y.00,other congenital cerebral palsy,1
53317,F383.00,congenital and developmental myasthenia,1
53365,F101.00,cerebral lipidoses,1
53382,F100200,pelizaeus-merzbacher disease,1
53620,A402.00,acute non-paralytic poliomyelitis,1
53655,2987.00,o/e -parkinson flexion posture ,1
53790,Fyu4.00,[x]demyelinating diseases of the central nervous system,1
53862,Nyu4400,[x]other dermatomyositis,1
53868,Fyu8A00,"[x]mitochondrial myopathy, not elsewhere classified",1
53919,Fyu4100,[x]other specified demyelinating diseases/the cns,1
54014,F392300,infantile myotonia,1
54213,N307.00,osteopathy from poliomyelitis,1
54300,F21yz00,other specified central nervous system demyelination nos,1
55371,2983.00,o/e - paraplegic in flexion,1
55372,PGy4.00,fibrodysplasia ossificans congenita,1
55426,F21y300,central demyelination of corpus callosum,1
55601,F396600,myopathy due to scleroderma,1
55636,F130100,hallervorden-spatz disease,1
55964,A40z.00,acute poliomyelitis nos,1
56153,F21y000,marchiafava-bignami disease,1
56288,F10..00,cerebral degenerations usually manifest in childhood,1
56910,F368000,hereditary motor and sensory neuropathy type i,1
56951,F101200,spielmeyer-vogt (batten) disease,1
56973,F381500,myasthenic syndrome due to pernicious anaemia,1
57551,F381100,MYASTHENIC SYNDROME DUE TO OTHER MALIGNANCY,1
57632,F151z00,spinal muscular atrophy nos,1
57638,F396z00,symptomatic inflammatory myopathy in disease nos,1
57847,F14yz00,other spinocerebellar disease nos,1
57888,F396300,myopathy due to polyarteritis nodosa,1
58576,F038.00,tropical spastic paraplegia,1
58729,F15z.00,anterior horn cell disease nos,1
58758,F374800,polyneuropathy in porphyria,1
58772,F142z00,primary cerebellar degeneration nos,1
59035,F100z00,leucodystrophy nos,1
59494,N231011,massive muscular calcification associated with paraplegia,1
59806,ZS82.11,landau-kleffner syndrome,1
59824,2994.00,o/e-festination-parkinson gait ,1
59855,F100300,metachromatic leucodystrophy,1
59956,F10z.00,childhood cerebral degenerations nos,1
60690,F395100,myopathy due to cushing's syndrome,1
60845,A403000,"acute paralytic poliomyelitis, vaccine-associated",1
61069,F381400,myasthenic syndrome due to hypothyroidism,1
62297,F396000,myopathy due to amyloid,1
62945,F211.11,balo's concentric sclerosis,1
63323,F382.00,toxic myoneural disorder,1
63333,F390000,benign congenital myopathy,1
63541,F396.00,symptomatic inflammatory myopathy in disease ec,1
63544,F370z00,acute infective polyneuritis nos,1
63608,A400.00,acute paralytic bulbar poliomyelitis,1
63652,F103000,cerebral degeneration in hunter's disease,1
64690,F390.00,congenital hereditary muscular dystrophy,1
65343,F102100,cerebral degeneration in niemann-pick disease,1
65825,F381z00,myasthenic syndrome due to disease nos,1
66575,F151200,adult spinal muscular atrophy,1
66726,F391500,distal (gower's) muscular dystrophy,1
66740,F380100,juvenile or adult myasthenia gravis,1
67687,F391411,facioscapulohumeral atrophy,1
67762,F103100,cerebral degeneration in mucopolysaccharidoses,1
68009,F391y11,distal dystrophy,1
68118,F391.00,hereditary progressive muscular dystrophy,1
68541,F392011,steinert's disease,1
69198,F395000,myopathy due to addison's disease,1
69429,N307600,poliomyelitis osteopathy of the lower leg,1
69613,C377100,mucolipidosis type iii,1
69848,F21y400,subacute necrotizing myelitis,1
69886,F201.00,multiple sclerosis of the spinal cord,1
70109,F151300,x-linked bulbo-spinal atrophy,1
70572,F151000,unspecified spinal muscular atrophy,1
71128,F391y00,other specified hereditary progressive muscular dystrophy,1
71400,F15y.00,other anterior horn cell disease,1
72309,F030200,encephalitis due to poliomyelitis,1
72717,N307700,poliomyelitis osteopathy of the ankle and foot,1
72879,Fyu2900,"[x]secondary parkinsonism, unspecified ",1
73583,F14y000,Ataxia-telangiectasia,1
73584,F14y100,corticostriatal-spinal degeneration,1
73943,F137.11,athetoid cerebral palsy,1
73990,F101.11,amaurotic familial idiocy,1
86062,Fyu2200,[x]parkinsonism in diseases classified elsewhere ,1
90520,Fyu9000,[x]other infantile cerebral palsy,1
91544,F391200,pelvic muscular dystrophy,1
91559,N003100,DERMATOPOLYMYOSITIS IN NEOPLASTIC DISEASE,1
93137,F144.00,cerebellar ataxia in diseases ec,1
93228,Fyu1300,[X]PARANEOPLASTIC NEUROMYOPATHY AND NEUROPATHY,1
93910,F24y012,steele - richardson oszewski syndrome,1
93963,F101600,sandhoff disease,1
94150,Fyu1000,[x]other hereditary ataxias,1
95005,F381200,myasthenic syndrome due to botulism,1
95437,Nyu4E00,"[x]dermatopolymyositis, unspecified",1
95465,Ayu8100,"[x]acute poliomyelitis, unspecified",1
95615,F150.11,infantile spinal muscular atrophy,1
95864,8Cc2.00,management of multiple sclerosis in stable disability phase,1
95972,F207.00,relapsing and remitting multiple sclerosis,1
96096,8Cc3.00,management of ms in progressive disability phase,1
96246,F208.00,secondary progressive multiple sclerosis,1
96256,F37y100,axonal sensorimotor neuropathy,1
96291,F204.00,benign multiple sclerosis,1
96607,F206.00,primary progressive multiple sclerosis,1
97170,Fyu2100,[x]other secondary parkinsonism ,1
97444,Fyu8200,[x]other specified myopathies,1
97487,8Cc1.00,management of multiple sclerosis in early disease phase,1
97866,AyuJ500,[x]sequelae of poliomyelitis,1
98521,8Cc4.00,management of multiple sclerosis in palliative phase,1
98835,8Cc0.00,management of multiple sclerosis in onset phase,1
99040,F230.11,paraplegia - congenital,1
99542,N307200,poliomyelitis osteopathy of the upper arm,1
99763,F142000,marie's cerebellar ataxia,1
100043,Fyu8500,[x]myasthenic syndromes/other diseases classified elsewhere,1
100128,F124.00,vascular parkinsonism,1
100165,ZRVE.00,kurtzke multiple sclerosis rating scale,1
100921,F392211,eulenburg's disease,1
101090,147F.00,history of parkinson's disease,1
101222,F151111,juvenile spinal muscular atrophy,1
101490,N307300,poliomyelitis osteopathy of the forearm,1
101494,N307800,poliomyelitis osteopathy of other specified sites,1
101525,Fyu3200,[x]subacute combined degeneration/spinal cord in diseases ce,1
101786,F392400,neuromyotonia,1
102338,F21y600,vanishing white matter disease,1
102734,2984.00,o/e - paraplegic in extension,1
102921,F10y200,peho syndrome,1
103120,Fyu2300,[x]other specified degenerative diseases/the basal ganglia,1
103722,F390500,congenital myopathy,1
104166,N307100,poliomyelitis osteopathy of the shoulder region,1
104334,F164.00,brown-sequard syndrome,1
104459,F29y100,postpolio syndrome,1
104498,F2B..00,cerebral palsy,1
104580,F2B0.00,spastic quadriplegic cerebral palsy,1
104654,F2Bz.00,cerebral palsy nos,1
104775,F230111,spastic diplegic cerebral palsy,1
104782,F2By.00,other cerebral palsy,1
104828,F23y100,flaccid infantile cerebral palsy,1
104967,F13z111,stiff person syndrome,1
105082,F381011,lambert-eaton syndrome,1
105133,F2B1.00,spastic hemiplegic cerebral palsy,1
105180,F1y0.00,fragile x associated tremor ataxia syndrome,1
105620,Ayu8000,"[x]acute paralytic poliomyelitis, other and unspecified",1
105947,Fyu2000,[x]other drug-induced secondary parkinsonism,1
106103,F368200,hereditary motor and sensory neuropathy type iii,1
106200,F4J7100,progressive external ophthalmoplegia,1
107057,F139000,paroxysmal non-kinesigenic dyskinesia,1
107551,F23y600,choreoathetoid cerebral palsy,1
107640,N307500,poliomyelitis osteopathy of the pelvic region and thigh,1
107844,38Gw.00,gross motor function classification system cerebral palsy,1
107848,Fyu4000,[x]other specified acute disseminated demyelination,1
108072,F396100,Myopathy due to disseminated lupus erythematosus,1
108131,F146.00,early onset cerebellar ataxia with hypogonadism,1
108773,F103z00,cerebral degeneration in disease nos,1
108795,Fyu8900,[x]myopathy in other diseases classified elsewhere,1
108834,F361012,charcot-marie-tooth syndrome,1
108947,PKyz.11,cockayne's syndrome,1
109170,F13z600,neuroferritinopathy,1
109176,F143.11,roussy-levy syndrome,1
109873,Fyu1600,[x]systemic atrophy affecting the cns in other diseases ce,1
110875,N307000,poliomyelitis osteopathy of unspecified site,1
111255,Fyu8B00,"[x]inflammatory myopathy, not elsewhere classified",1
111807,F142100,sanger-brown cerebellar ataxia,1
112614,F390200,centronuclear myopathy,1
112736,F2B2.00,bilateral spastic cerebral palsy,1
113264,F395200,myopathy due to hypopituitarism,1
113438,F144100,cerebellar ataxia due to myxoedema,1