medcode,readcode,readterm,neuro
302,E310.00,"Moderate mental retardation, IQ in range 35-49",1
684,F20..00,multiple sclerosis,1
1278,E310.11,Imbecile,1
1350,E00..12,senile/presenile dementia,1
1362,E3...00,Mental retardation,1
1391,C327100,gaucher's disease,1
1543,PJ0..00,Down's syndrome - trisomy 21,1
1607,F370000,guillain-barre syndrome,1
1632,F39z.00,myopathy or muscular dystrophy nos,1
1680,E30..11,Educationally subnormal,1
1691,F120.00,paralysis agitans,1
1749,F22..00,hemiplegia,1
1787,E30..00,"Mild mental retardation, IQ in range 50-70",1
1916,E00..11,senile dementia,1
1917,F110.00,alzheimer's disease,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
2731,F11z.11,cerebral atrophy,1
2732,A40..00,acute poliomyelitis,1
2882,E00z.00,senile or presenile psychoses nos,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
3591,F134.00,huntington's chorea,1
3621,2837.00,o/e - diplegia,1
4165,F140.00,friedreich's ataxia,1
4321,F12..00,parkinson's disease,1
4357,Eu02z14,[x] senile dementia nos,1
4477,Eu81z11,[X]Learning disability NOS,1
4693,Eu02z00,[x] unspecified dementia,1
4796,F152.00,motor neurone disease,1
4825,E311.00,"Severe mental retardation, IQ in range 20-34",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
5651,F11z.00,cerebral degeneration nos,1
5655,F380.00,myasthenia gravis,1
5931,1461.00,h/o: dementia,1
5964,F39B.00,muscular dystrophy,1
6123,Eu71.00,[X]Moderate mental retardation,1
6376,F370.00,acute infective polyneuritis,1
6578,Eu01.00,[x]vascular dementia,1
6599,F39..00,muscular dystrophies and other myopathies,1
7037,F24y200,steele-richardson-olszewski syndrome,1
7226,Eu84.00,[X]Pervasive developmental disorders,1
7323,E000.00,uncomplicated senile dementia,1
7470,F152111,duchenne aran muscular atrophy,1
7572,F116.00,lewy body disease ,1
7664,Eu00.00,[x]dementia in alzheimer's disease,1
7736,F162.00,subacute combined degeneration of spinal cord,1
8195,Eu00z11,[x]alzheimer's dementia unspec,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
8634,E004.11,multi infarct dementia,1
8933,F222.00,left hemiplegia,1
8934,Eu01200,[x]subcortical vascular dementia,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
9509,Eu02300,[x]dementia in parkinson's disease,1
9565,Eu01.11,[x]arteriosclerotic dementia,1
10068,PKy8000,Noonan's syndrome,1
10189,G674000,cerebral amyloid angiopathy,1
10628,PJyy200,Fragile X chromosome,1
10718,297A.00,o/e - parkinsonian tremor ,1
10759,PJ0z.00,Down's syndrome NOS,1
10890,Z7E4400,cerebellar ataxia,1
10956,PKy9300,Prader - Willi syndrome,1
11136,F111.00,pick's disease,1
11175,Eu01100,[x]multi-infarct dementia,1
11346,F38z.00,myoneural disorder nos,1
11379,Eu00112,"[x]senile dementia,alzheimer's type",1
11542,F360000,dejerine-sottas disease,1
12054,F21z.00,central nervous system demyelination nos,1
12621,Eu02.00,[x]dementia in other diseases classified elsewhere,1
12666,F23yz00,other infantile cerebral palsy nos,1
12699,F38..00,myoneural disorders,1
12710,6AB..00,dementia annual review,1
14912,F12z.00,parkinson's disease nos,1
15100,N231100,progressive myositis ossificans,1
15165,E001.00,presenile dementia,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
16797,F110000,alzheimer's disease with early onset,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
18386,E002000,senile dementia with paranoia,1
18415,PJ0..12,Trisomy 21,1
18493,Z7E4.00,ataxia,1
19038,PJ1z.11,Trisomy 13 NOS,1
19052,R012000,[d]ataxic gait,1
19393,Eu01z00,"[x]vascular dementia, unspecified",1
19436,ZS34.11,Learning disability,1
19477,E004.00,arteriosclerotic dementia,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
21418,PKy6011,Cornelia de Lange syndrome,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
21887,E002100,senile dementia with depression,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
22760,918e.00,On learning disability register,1
23484,F392111,thomsen's disease,1
23489,PJ0..11,Mongolism,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
24581,F11x600,cerebral degeneration due to vitamin b12 deficiency,1
25268,F101211,batten's disease of retina,1
25306,PKyz511,Angelman syndrome,1
25324,F230.00,congenital diplegia,1
25386,E041.00,dementia in conditions ec,1
25429,F390300,myotubular myopathy,1
25570,F23y200,spastic cerebral palsy,1
25704,Eu00011,"[x]presenile dementia,alzheimer's type",1
25880,F13z100,stiff-man syndrome,1
26181,F12X.00,"secondary parkinsonism, unspecified ",1
26210,F391011,pseudohypertrophic dystrophy,1
26270,Eu02500,[x]lewy body dementia ,1
26323,Eu10711,[x]alcoholic dementia nos,1
27280,PKy0.12,Prader-Willi syndrome,1
27331,F14z.00,spinocerebellar disease nos,1
27342,E012.11,alcoholic dementia nos,1
27377,F152200,progressive bulbar palsy,1
27515,F380z00,myasthenia gravis nos,1
27677,E001300,presenile dementia with depression,1
27691,Eu72.11,[X]Severe mental subnormality,1
27759,Eu02z16,"[x] senile dementia, depressed or paranoid type",1
27935,Eu02z15,[x] senile psychosis 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
28402,Eu02000,[x]dementia in pick's disease,1
28740,Eu70.00,[X]Mild mental retardation,1
28955,F392100,myotonia congenita (thomsen's disease),1
28962,Eu7..00,[X]Mental retardation,1
29114,A940.11,locomotor ataxia,1
29181,R007600,[d]post polio exhaustion,1
29386,Eu00z00,"[x]dementia in alzheimer's disease, unspecified",1
29512,F112.00,senile degeneration of brain,1
30032,E001200,presenile dementia with paranoia,1
30537,F373.00,polyneuropathy in malignant disease,1
30706,Eu00200,"[x]dementia in alzheimer's dis, atypical or mixed type",1
30987,F152100,progressive muscular atrophy,1
31016,Eu01300,[x]mixed cortical and subcortical vascular dementia,1
31042,Eu84200,[X]Rett's syndrome,1
31209,F396400,myopathy due to rheumatoid arthritis,1
31329,F393.00,familial periodic paralysis,1
31426,PKy1.00,Laurence-Moon-Biedl syndrome,1
31524,F11yz00,other cerebral degeneration nos,1
31742,F394100,alcoholic myopathy,1
31795,PJ31.00,Cri-du-chat syndrome,1
31892,F11..00,other cerebral degenerations,1
32010,PJ01.00,"Trisomy 21, mosaicism",1
32016,F39y.00,other myopathies and muscular dystrophies,1
32057,F110100,alzheimer's disease with late onset,1
32270,F381000,eaton-lambert syndrome,1
32310,G675.00,moyamoya disease,1
32527,F368.00,hereditary motor and sensory neuropathy,1
32603,PJyy400,Fragile X syndrome,1
32649,N003000,juvenile dermatomyositis,1
32749,F391800,becker muscular dystrophy,1
32820,Eu7zz00,[X]Unsp mental retardation without mention impairment behav,1
32916,F394.00,toxic myopathy,1
33334,F150.00,werdnig - hoffmann disease,1
33353,F11y000,reye's syndrome,1
33390,C375112,hurler's syndrome,1
33544,F121.00,parkinsonism secondary to drugs ,1
33642,PJ2..00,Edward's syndrome - trisomy 18,1
33839,F144000,cerebellar ataxia due to alcoholism,1
33841,F370200,miller-fisher syndrome,1
33948,PJ32.11,Wolff - Hirschorn syndrome,1
33949,Eu70.12,[X]Mild mental subnormality,1
34174,Eu84112,[X]Mental retardation with autistic features,1
34704,F390100,central core disease,1
34734,Eu71.11,[X]Moderate mental subnormality,1
34944,Eu02z13,[x] primary degenerative dementia nos,1
34976,F11y.00,other cerebral degeneration,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
35665,PJ1..00,Patau's syndrome - trisomy 13,1
35839,F130500,shy-drager syndrome ,1
35938,F030211,poliomyelitis encephalitis,1
36045,Eu81z13,[X]Learn acquisition disab NOS,1
36079,F394000,drug-induced myopathy,1
36117,C371500,coproporphyria,1
36133,2835.00,o/e - paraplegia,1
36143,Eu72.00,[X]Severe mental retardation,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
36871,PJ33300,Smith-Magenis syndrome,1
37014,Eu02200,[x]dementia in huntington's disease,1
37015,E003.00,senile dementia with delirium,1
37160,F230000,congenital paraplegia,1
37295,A403200,"acute paralytic poliomyelitis, wild virus, indigenous",1
37867,E3z..00,Mental retardation NOS,1
37887,Eu7z.11,[X]Mental deficiency NOS,1
37911,Eu7z.12,[X]Mental subnormality NOS,1
37924,PKy5F00,Coffin-Lowry syndrome,1
37946,E012000,chronic alcoholic brain syndrome,1
38286,A411.00,jakob-creutzfeldt disease,1
38438,E001z00,presenile dementia nos,1
38448,F391700,oculopharyngeal muscular dystrophy,1
38678,Eu00100,[x]dementia in alzheimer's disease with late onset,1
39016,Eu70y00,"[X]Mild mental retardation, other impairments of behaviour",1
39017,PJ2z.00,Edward's syndrome NOS,1
39085,F220.00,flaccid hemiplegia,1
39398,F034D00,post polio vaccination encephalitis,1
39412,Eu70100,[X]Mld mental retard sig impairment behav req attent/treatmt,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
41089,E002z00,senile dementia with depressive or paranoid features nos,1
41094,2993.00,o/e - gait ataxic,1
41185,Eu02400,[x]dementia in human immunodef virus [hiv] disease,1
41461,PKy0.11,Prader-Willi Syndrome,1
41904,F391600,ocular muscular dystrophy,1
42279,E004z00,arteriosclerotic dementia nos,1
42520,Eu7yy00,"[X]Other mental retardation, other impairments of behaviour",1
42589,Eu7z.00,[X]Unspecified mental retardation,1
42602,E001000,uncomplicated presenile dementia,1
42701,PJ00.00,"Trisomy 21, meiotic nondisjunction",1
42756,F4Gy100,extraocular muscle myopathy,1
42886,Eu7z000,[X]Unsp mental retard with statement no or min impairm behav,1
42940,H57y100,lung disease with polymyositis,1
43089,E004000,uncomplicated arteriosclerotic dementia,1
43203,F100.00,leucodystrophy,1
43232,666B.00,multiple sclerosis multidisciplinary review,1
43292,E004300,arteriosclerotic dementia with depression,1
43346,Eu00113,"[x]primary degen dementia of alzheimer's type, senile onset",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
44327,Eu84z00,"[X]Pervasive developmental disorder, unspecified",1
44512,F364.00,idiopathic progressive polyneuropathy,1
44592,F11xz00,cerebral degeneration other disease nos,1
44674,E002.00,senile dementia with depressive or paranoid features,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
45133,E312.00,Profound mental retardation with IQ less than 20,1
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
46133,PJ12.00,"Trisomy 13, translocation",1
46175,F241000,flaccid paraplegia,1
46488,Eu01000,[x]vascular dementia of acute onset,1
46504,Eu70000,[X]Mld mental retard with statement no or min impairm behav,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
46762,Eu00111,[x]alzheimer's disease type 1,1
46766,PKyz500,Happy puppet syndrome,1
46787,PJ2z.11,TRISOMY 18 NOS,1
46937,F365.00,neuropathy in association with hereditary ataxia,1
47555,F11x000,cerebral degeneration due to alcoholism,1
47619,Eu02z12,[x] presenile psychosis nos,1
47658,F11x500,cerebral degeneration due to myxoedema,1
47695,F381600,myasthenic syndrome due to thyrotoxicosis,1
47696,65VD.00,notification of acute polio,1
47948,Eu84y00,[X]Other pervasive developmental disorders,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
48501,Eu02z11,[x] presenile dementia nos,1
48531,F11x700,cerebral degeneration due to jakob - creutzfeldt disease,1
49034,F24y011,steele richardson olszewsk syn,1
49181,F101400,gangliosidosis,1
49203,F130200,striatonigral degeneration,1
49263,Eu00000,[x]dementia in alzheimer's disease with early onset,1
49482,F396200,myopathy due to malignant disease,1
49513,E001100,presenile dementia with delirium,1
49541,A413.11,progressive multifocal leukoencephalopathy,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
50457,PKy6000,Amsterdam dwarf,1
50606,Eu70z00,[X]Mild mental retardation without mention impairment behav,1
50725,A270300,listerial cerebral arteritis,1
50751,Eu72100,[X]Sev mental retard sig impairment behav req attent/treatmt,1
50762,F130z00,other basal ganglia degenerative disease nos,1
50947,Eu72000,[X]Sev mental retard with statement no or min impairm behav,1
51105,F123.00,postencephalitic parkinsonism ,1
51268,Eu73.00,[X]Profound mental retardation,1
51416,F395300,myopathy due to myxoedema,1
51494,E00y.11,presbyophrenic psychosis,1
51534,C371300,protocoproporphyria,1
51622,E312.11,Idiocy,1
51640,F381.00,myasthenic syndrome due to disease ec,1
51954,E30..12,Feeble-minded,1
52519,F396500,myopathy due to sarcoidosis,1
52589,A94y100,syphilitic parkinsonism ,1
52602,Eu84400,[X]Overactive disorder assoc mental retard/stereotype movts,1
52659,F23y400,ataxic diplegic cerebral palsy,1
52673,A413.00,progressive multifocal leucoencephalopathy,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
53446,Eu04100,[x]delirium superimposed on dementia,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
54106,Eu02100,[x]dementia in creutzfeldt-jakob disease,1
54179,E31z.00,Other specified mental retardation NOS,1
54213,N307.00,osteopathy from poliomyelitis,1
54300,F21yz00,other specified central nervous system demyelination nos,1
54505,E012.00,other alcoholic dementia,1
54744,F11x200,cerebral degeneration due to cerebrovascular disease,1
54881,Eu71100,[X]Mod mental retard sig impairment behav req attent/treatmt,1
55222,ZS7C500,language disorder of dementia,1
55313,Eu01y00,[x]other vascular dementia,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
55467,E004200,arteriosclerotic dementia with paranoia,1
55560,Eu72z00,[X]Sev mental retardation without mention impairment behav,1
55601,F396600,myopathy due to scleroderma,1
55636,F130100,hallervorden-spatz disease,1
55838,Eu01111,[x]predominantly cortical dementia,1
55848,Eu72y00,"[X]Severe mental retardation, other impairments of behaviour",1
55964,A40z.00,acute poliomyelitis nos,1
56153,F21y000,marchiafava-bignami disease,1
56288,F10..00,cerebral degenerations usually manifest in childhood,1
56547,Eu7y100,[X]Oth mental retard sig impairment behav req attent/treatmt,1
56577,E31..00,Other specified mental retardation,1
56910,F368000,hereditary motor and sensory neuropathy type i,1
56912,E004100,arteriosclerotic dementia with delirium,1
56951,F101200,spielmeyer-vogt (batten) disease,1
56973,F381500,myasthenic syndrome due to pernicious anaemia,1
57043,PKy6600,Dubowitz syndrome,1
57199,E3y..00,Other specified mental retardation,1
57458,PKy1.11,Biedl-Bardet syndrome,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
57993,Eu03.11,"[x]korsakov's psychosis, nonalcoholic",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
59122,Fyu3000,[x]other alzheimer's disease,1
59407,Eu71y00,[X]Mod retard oth behav impair,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
60059,Eu00012,"[x]primary degen dementia, alzheimer's type, presenile onset",1
60062,Eu73z00,[X]Prfnd mental retardation without mention impairment behav,1
60473,Eu71z00,[X]Mod mental retardation without mention impairment behav,1
60673,PKyz000,"Ullrich - Feichtiger syndrome, chimaera",1
60690,F395100,myopathy due to cushing's syndrome,1
60845,A403000,"acute paralytic poliomyelitis, vaccine-associated",1
60913,Eu71000,[X]Mod mental retard with statement no or min impairm behav,1
61069,F381400,myasthenic syndrome due to hypothyroidism,1
61322,PKyG.11,Ohdo blepharophimosis syndrome,1
61499,PJ02.00,"Trisomy 21, translocation",1
61528,Eu00013,[x]alzheimer's disease type 2,1
61627,PJ0z.11,Trisomy 21 NOS,1
62132,E02y100,drug-induced dementia,1
62297,F396000,myopathy due to amyloid,1
62945,F211.11,balo's concentric sclerosis,1
63273,Eu7yz00,[X]Other mental retardation without mention impairment behav,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
64267,Eu02y00,[x]dementia in other specified diseases classif elsewhere,1
64690,F390.00,congenital hereditary muscular dystrophy,1
65343,F102100,cerebral degeneration in niemann-pick disease,1
65468,Eu73.11,[X]Profound mental subnormality,1
65825,F381z00,myasthenic syndrome due to disease nos,1
66383,Eu7zy00,"[X]Unspecified mental retardatn, other impairments of behav",1
66566,PJ32.00,Deletion of short arm of chromosome 4,1
66575,F151200,adult spinal muscular atrophy,1
66726,F391500,distal (gower's) muscular dystrophy,1
66740,F380100,juvenile or adult myasthenia gravis,1
66783,Eu7z100,[X]Unsp mentl retard sig impairment behav req attent/treatmt,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
68194,F21y211,binswanger's encephalopathy,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
70008,Eu7y000,[X]Oth mental retard with statement no or min impairm behav,1
70102,Eu73000,[X]Profound ment retrd wth statement no or min impairm behav,1
70109,F151300,x-linked bulbo-spinal atrophy,1
70572,F151000,unspecified spinal muscular atrophy,1
70709,4L49.00,prion protein markers for creutzfeldt-jakob disease,1
70957,F11x400,cerebral degeneration due to neoplastic disease,1
71128,F391y00,other specified hereditary progressive muscular dystrophy,1
71196,Eu7y.00,[X]Other mental retardation,1
71400,F15y.00,other anterior horn cell disease,1
71632,E30..13,Moron,1
72265,PJ1z.00,Patau's syndrome NOS,1
72309,F030200,encephalitis due to poliomyelitis,1
72717,N307700,poliomyelitis osteopathy of the ankle and foot,1
72742,PKyG.00,Men ret congen heart dis blepharophim blepharop hypopl teeth,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
84154,Eu70.11,[X]Feeble-mindedness,1
86062,Fyu2200,[x]parkinsonism in diseases classified elsewhere ,1
89727,PKy0.13,Noonan's syndrome,1
90276,Eu73y00,"[X]Profound mental retardation, other impairments of behavr",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
93372,F103.00,cerebral degeneration in diseases ec,1
93694,PJ9..00,Mowat-Wilson syndrome,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
96860,F11x900,cerebral degeneration in parkinson's disease,1
97059,PKyz700,Angelman's syndrome,1
97170,Fyu2100,[x]other secondary parkinsonism ,1
97422,F11x.00,cerebral degeneration in other disease ec,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
98100,Eu73100,[X]Profound ment retard sig impairmnt behav req attent/treat,1
98293,Eu81500,[X]Severe learning disability,1
98342,Eu81400,[X]Moderate learning disability,1
98521,8Cc4.00,management of multiple sclerosis in palliative phase,1
98617,PKyz711,Angelman syndrome,1
98835,8Cc0.00,management of multiple sclerosis in onset phase,1
98941,PJ31.11,Deletion of short arm of chromosome 5,1
99040,F230.11,paraplegia - congenital,1
99542,N307200,poliomyelitis osteopathy of the upper arm,1
99652,PKyJ.00,Lujan-Fryns syndrome,1
99684,F11x800,cerebral degeneration due to multifocal leucoencephalopathy,1
99763,F142000,marie's cerebellar ataxia,1
99774,Eu81600,[X]Mild learning disability,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
100648,Eu81700,[X]Profound learning disability,1
100921,F392211,eulenburg's disease,1
101090,147F.00,history of parkinson's disease,1
101222,F151111,juvenile spinal muscular atrophy,1
101309,PJ02.11,Partial trisomy 21 in Down's syndrome,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
102102,PJ12.11,Partial trisomy 13 in Patau's syndrome,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
103891,C375.13,hurler's syndrome,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
104534,F118.00,frontotemporal degeneration,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
105514,PJ33A00,Kleefstra 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
106311,8CMZ.00,dementia care plan,1
106590,PKy5K00,Cohen syndrome,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
107822,PKy6900,Borjeson-Forssman-Lehmann syndrome,1
107844,38Gw.00,gross motor function classification system cerebral palsy,1
107848,Fyu4000,[x]other specified acute disseminated demyelination,1
107919,PJ01.11,"Trisomy 21, mitotic nondisjunction",1
107968,Eu81800,[X]Specific learning disability,1
108072,F396100,myopathy due to disseminated lupus erythematosus,1
108131,F146.00,early onset cerebellar ataxia with hypogonadism,1
108228,8CSA.00,dementia advance care plan agreed,1
108268,8CMG200,review of dementia advance care plan,1
108375,PG5F.00,Acrodysostosis,1
108391,8IAe000,dementia advance care plan declined,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
109047,8BPa.00,antipsychotic drug therapy for dementia,1
109170,F13z600,neuroferritinopathy,1
109176,F143.11,roussy-levy syndrome,1
109288,A411000,sporadic creutzfeldt-jakob disease,1
109708,8CMZ100,dementia care plan reviewed,1
109731,8CMZ000,dementia care plan agreed,1
109737,8BM0200,dementia medication review,1
109786,8CMZ200,dementia care plan declined,1
109790,8CMe000,dementia advance care plan,1
109873,Fyu1600,[x]systemic atrophy affecting the cns in other diseases ce,1
110075,8IAe200,dementia advance care plan review declined,1
110123,8CMZ300,dementia care plan review declined,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