medcodeid,term,neuro
100323011,paraplegia,1
100638016,subacute combined degeneration of spinal cord,1
104952014,amyotonia congenita,1
107018015,infantile spinal muscular atrophy,1
107602013,myotonic cataract,1
107661000006110,tay-sach's disease,1
107800019,pelizaeus-merzbacher disease,1
110721000006114,tetraplegia - congenital,1
111210017,toxic myopathy,1
112508017,ocular muscular dystrophy,1
114794013,moyamoya disease,1
1148731000000112,history of parkinson's disease,1
11903671000006114,steele-richardson-olszewski syndrome,1
11904601000006118,progressive supranuclear ophthalmoplegia,1
11904611000006115,progressive supranuclear palsy,1
121721014,muscular dystrophy,1
1219655013,hereditary motor and sensory neuropathy type iii,1
1221108018,acute non-paralytic poliomyelitis,1
1222437010,alper's disease,1
1223979019,disseminated sclerosis,1
1224865018,hereditary motor and sensory neuropathy type iv,1
1224974015,myopathy in metabolic diseases,1
1225697014,brown-sequard syndrome,1
1229775013,eulenburg's disease,1
1233040016,myopathy due to thyrotoxicosis,1
1234144017,polyneuropathy in malignant disease,1
1234731016,fibrodysplasia ossificans congenita,1
124598014,athetoid cerebral palsy,1
12465281000006112,[x]cerebral palsy and other paralytic syndromes,1
124689016,nemaline body disease,1
12477641000006119,[x]other specified myopathies,1
125891000006119,steele - richardson oszewski syndrome,1
125901000006115,steele richardson olszewsk syn,1
125971000006114,steinert's disease,1
12704251000006113,cerebellar ataxia associated with another disorder,1
12704731000006113,inflammatory disorder of muscle,1
12717021000006115,myopathy or muscular dystrophy nos,1
12725491000006112,myopathy or muscular dystrophy nos,1
127307018,duchenne muscular dystrophy,1
12733271000006111,central nervous system demyelination nos,1
12759421000006112,fxtas - fragile x associated tremor ataxia syndrome,1
127990018,oculopharyngeal muscular dystrophy,1
130209011,erb's muscular dystrophy,1
13165015,pseudobulbar palsy,1
132112014,spastic hemiplegia,1
134251013,flaccid hemiplegia,1
134601000006111,spielmeyer-vogt (batten) disease,1
134744017,primary lateral sclerosis,1
136147016,myotubular myopathy,1
136148014,centronuclear myopathy,1
137233019,progressive myositis ossificans,1
141723016,adult spinal muscular atrophy,1
142016013,anterior horn cell disease,1
142653015,amyotrophic lateral sclerosis,1
143230018,poikilodermatomyositis,1
147444011,progressive muscular atrophy,1
1480894012,marchiafava-bignami disease,1
1481810012,becker muscular dystrophy,1
1491762016,central demyelination of corpus callosum,1
1492251019,becker's disease,1
151586018,spinocerebellar disease,1
151829017,myasthenia gravis,1
151951000006115,secondary parkinsonism due to other external agents,1
151961000006118,"secondary parkinsonism, unspecified",1
1648061000000115,vanishing white matter disease,1
1672021000006115,axonal sensorimotor neuropathy,1
1679791000006113,management of ms in progressive disability phase,1
1682241000006111,relapsing and remitting multiple sclerosis,1
1682791000006112,mitoch myopath/encephalopath/lactic acidosis/stroke-like episode,1
1705661000006112,peho syndrome,1
1728581000006115,vanishing white matter disease,1
1763331000006113,early onset cerebellar ataxia with hypogonadism,1
1772621000006118,bethlem myopathy,1
1774931000006117,multi-core congenital myopathy,1
1776211019,dermatomyositis,1
1777664015,hereditary motor and sensory neuropathy,1
1777666018,acute poliomyelitis,1
1778099018,botulism,1
1778554019,facioscapulohumeral muscular dystrophy,1
1780951000006111,brown-sequard syndrome,1
1781041000006119,fragile x associated tremor ataxia syndrome,1
1784692011,juvenile dermatomyositis,1
1785557019,metachromatic leucodystrophy,1
1786041000006110,congenital myopathy,1
1786065018,hereditary motor and sensory neuropathy type i,1
1786163010,hereditary motor and sensory neuropathy type ii,1
178743010,congenital hereditary muscular dystrophy,1
178750014,emery-dreifuss muscular dystrophy,1
18091019,friedreich's ataxia,1
1815931000006114,spastic diplegic cerebral palsy,1
1815951000006119,spastic quadriplegic cerebral palsy,1
1815971000006112,other cerebral palsy,1
1815981000006110,cerebral palsy nos,1
1846861000006111,charcot-marie-tooth syndrome,1
1858901000006117,neuroferritinopathy,1
187765019,amaurotic familial idiocy,1
187824013,dejerine-sottas disease,1
1883621000006119,gross motor function classification system cerebral palsy,1
198171000006110,pseudo - hurler's disease,1
198381000006110,pseudohypertrophic dystrophy,1
19943011,quadriplegia,1
19944017,tetraplegia,1
206411014,cerebral palsy,1
207847010,acute infective polyneuritis,1
2108221000000110,stiff person syndrome,1
211331000006117,postinfectious polyneuritis,1
2122001000000116,spastic hemiplegic cerebral palsy,1
2168441000000115,lambert-eaton syndrome,1
220771000000110,pseudo - hurler's disease,1
221361000006118,poliomyelitis & other non-arthropod-borne viral diseases-cns,1
223801000000115,paraplegia - congenital,1
2267591000000110,neuroferritinopathy,1
2283041000000116,choreo-athetotic cerebral palsy,1
2283831000000117,choreoathetoid cerebral palsy,1
2326271000000114,bilateral spastic cerebral palsy,1
243291000006119,paramyotonia congenita (eulenburg's disease),1
244311000006117,parkinsonism secondary to drugs,1
2475876012,balo's concentric sclerosis,1
2475877015,ataxic diplegic cerebral palsy,1
251539016,h/o: poliomyelitis,1
2517761000006112,childhood type dermatomyositis,1
2524111000006113,postnatal infantile hemiplegia,1
2526611000006112,fisher's syndrome,1
2526621000006116,"ophthalmoplegia, ataxia, areflexia syndrome",1
2526631000006118,miller-fisher variant of guillain-barre syndrome,1
2526651000006113,fisher syndrome,1
2546861000006113,pigmentary pallidal degeneration,1
2546871000006118,pigmentary pallidal atrophy,1
254829017,o/e - hemiplegia,1
254833012,o/e - paraplegia,1
254834018,o/e - quadriplegia,1
254835017,o/e - diplegia,1
254935018,o/e - parkinsonian tremor,1
254939012,o/e - hemiplegic posture,1
254940014,o/e - paraplegic in flexion,1
254941013,o/e - paraplegic in extension,1
254944017,o/e -parkinson flexion posture,1
254950010,o/e - ataxic gait,1
254951014,o/e - gait ataxic,1
255061010,o/e - arms ataxic,1
255062015,o/e - legs ataxic,1
2554211000006118,myositis ossificans associated with dermato / polymyositis,1
2566251000006117,parkinsonism caused by drug,1
2582941000006110,stiff-man syndrome,1
2582951000006112,moersch-woltmann syndrome,1
2582961000006114,gamma neuron overactivity syndrome,1
2582971000006119,moersch-woltman syndrome,1
2583601000006114,sma - spinal muscular atrophy,1
2597431000006110,demyelinating disorders of the central nervous system,1
2597441000006117,demyelinating cns disease,1
2597451000006115,demyelinating disease central nervous system (cns),1
2637771000000114,proximal myotonic myopathy,1
264417019,notification of acute polio,1
2650601000006118,paraplegic-spastic gait,1
2665351000006114,friedreich's ataxia,1
2665361000006111,friedreich's disease,1
2665371000006116,familial ataxia,1
2665381000006118,fa - friedreich ataxia,1
2674605012,secondary progressive multiple sclerosis,1
2692565012,primary progressive multiple sclerosis,1
2726231000006116,myopathy in hypopituitarism,1
2730161000006118,acute nonparalytic poliomyelitis,1
2730171000006113,anterior acute poliomyelitis specified as nonparalytic,1
2730181000006111,epidemic acute poliomyelitis specified as non paralytic,1
2730191000006114,"anterior acute poliomyelitis, nonparalytic",1
2730201000006112,"epidemic acute poliomyelitis, non paralytic",1
2767491000006113,ragged red myopathy,1
27731000006112,other limb-girdle muscular dystrophy,1
2784591000006116,toxic neuromuscular junction disorder,1
2784601000006112,toxic myoneural junction disorder,1
2784611000006110,toxic disorders of the neuromuscular junction,1
280121000006113,o/e - parkinson posture,1
28047015,shy-drager syndrome,1
2806371000006116,alcoholic myopathic syndrome,1
2806381000006118,alcoholic myositis,1
2821931000006118,ataxia (loss of muscle coordination),1
2824381000006115,progressive sclerosing poliodystrophy,1
2824391000006117,alpers' disease,1
2824401000006115,gray matter degeneration,1
2824411000006117,spongy glioneuronal dystrophy,1
2824421000006113,poliodystrophy,1
2824431000006111,progressive neuronal degeneration with liver cirrhosis,1
2838078010,"multiple system atrophy, cerebellar variant",1
2841061014,"multiple system atrophy, parkinson variant",1
286395017,listerial cerebral arteritis,1
286639018,acute paralytic non-bulbar poliomyelitis,1
286641017,"acute paralytic poliomyelitis, unspecified",1
286642012,"acute paralytic poliomyelitis, vaccine-associated",1
286643019,"acute paralytic poliomyelitis, wild virus, imported",1
286644013,"acute paralytic poliomyelitis, wild virus, indigenous",1
286645014,acute poliomyelitis nos,1
2880611000006115,"gm>2< gangliosidosis, type 2",1
2880621000006111,hexosaminidase a and b deficiency,1
2880631000006114,total hexosaminidase deficiency,1
288115019,"[x]acute paralytic poliomyelitis, other and unspecified",1
288116018,"[x]acute poliomyelitis, unspecified",1
2894411000006110,ms - multiple sclerosis,1
2894421000006119,ds - disseminated sclerosis,1
2900005013,fragile x associated tremor ataxia syndrome,1
2900031000006111,subacute myelo-optic neuropathy,1
2900041000006118,devic syndrome,1
2900051000006116,optic neuromyelitis,1
2900061000006119,smon - subacute myelo-optico-neuropathy,1
2901621000006111,tabetic gait,1
2901631000006114,broadened gait,1
2905521000006110,phytanic acid storage disease,1
2905541000006115,heredopathia atactica polyneuritiformis,1
2905551000006118,refsum syndrome,1
2905561000006116,heredoataxia hemeralopica polyneuritiformis,1
2905571000006111,refsum-thiébaut disease,1
2905581000006114,"hereditary sensory-motor neuropathy, type iv",1
2905591000006112,refsum-thiebaut disease,1
2905601000006116,"hereditary motor and sensory neuropathy, type iv",1
2905611000006118,hsmn iv,1
2905631000006112,heredoataxic atactica polyneuritiformis,1
2905641000006119,heredoataxic hemeralopica polyneuritiformis,1
2912671000006115,mitochondrial ocular myopathy,1
293326016,gaucher's disease,1
293544011,coproporphyria,1
293813012,[x]other gangliosidosis,1
2949121000006114,brown-séquard syndrome,1
2966061000006116,progressive supranuclear ophthalmoplegia,1
2966101000006118,psp - progressive supranuclear palsy,1
296838010,subacute sclerosing panencephalitis,1
296840017,dawson's inclusion body encephalitis,1
296841018,poliomyelitis encephalitis,1
2968551000006111,myotonia chondrodystrophica,1
2968561000006113,osteochondromuscular dystrophy,1
2968571000006118,chondrodystrophic myotonia,1
296884017,post polio vaccination encephalitis,1
296959019,leucodystrophy,1
296966018,krabbe's disease,1
296982017,leucodystrophy nos,1
296987011,retinal dystrophy in cerebroretinal lipidosis,1
297037012,parkinson's disease nos,1
297041011,other basal ganglia degenerative diseases,1
297043014,parkinsonism with orthostatic hypotension,1
297045019,other basal ganglia degenerative disease nos,1
297107018,dyssynergia cerebellaris myoclonica,1
297108011,primary cerebellar degeneration nos,1
297112017,cerebellar ataxia in diseases ec,1
297117011,cerebellar ataxia due to neoplasia,1
297118018,cerebellar ataxia in disease nos,1
297120015,other spinocerebellar diseases,1
297122011,other spinocerebellar disease nos,1
297123018,spinocerebellar disease nos,1
297125013,unspecified spinal muscular atrophy,1
297127017,spinal muscular atrophy nos,1
297130012,motor neurone disease nos,1
297131011,other anterior horn cell disease,1
297132016,anterior horn cell disease nos,1
297177019,multiple sclerosis of the spinal cord,1
297179016,generalised multiple sclerosis,1
297180018,exacerbation of multiple sclerosis,1
297181019,multiple sclerosis nos,1
297182014,other central nervous system demyelinating diseases,1
297190014,other specified central nervous system demyelinating disease,1
297195016,other specified central nervous system demyelination nos,1
297196015,central nervous system demyelination nos,1
297210016,hemiplegia nos,1
297221013,congenital paraplegia,1
297223011,congenital diplegia nos,1
297232013,infantile hemiplegia nos,1
297233015,other congenital cerebral palsy,1
297234014,ataxic infantile cerebral palsy,1
297238012,other infantile cerebral palsy nos,1
297239016,congenital cerebral palsy nos,1
297241015,flaccid tetraplegia,1
297242010,spastic tetraplegia,1
297243017,flaccid paraplegia,1
297244011,spastic paraplegia,1
297522019,peroneal muscular atrophy nos,1
297525017,neuropathy in association with hereditary ataxia,1
297539017,acute infective polyneuritis nos,1
2975521000006117,infantile necrotizing encephalomyelopathy,1
2975531000006119,subacute necrotizing encephalopathy,1
2975541000006112,subacute necrotizing encephalomyelopathy,1
2975551000006114,subacute necrotising encephalomyelopathy,1
2975561000006111,subacute necrotising encephalopathy,1
2975571000006116,infantile necrotising encephalomyelopathy,1
2975581000006118,snem - subacute necrotising encephalomyelopathy,1
2975591000006115,snem - subacute necrotizing encephalomyelopathy,1
2975601000006111,leigh syndrome,1
2975611000006114,leigh disease,1
2975621000006118,leighs disease,1
297564019,polyneuropathy in porphyria,1
297581011,juvenile or adult myasthenia gravis,1
297582016,myasthenia gravis nos,1
297583014,myasthenic syndrome due to disease ec,1
297584015,myasthenic syndrome due to other malignancy,1
297588017,myasthenic syndrome due to hypothyroidism,1
297589013,myasthenic syndrome due to pernicious anaemia,1
297591017,myasthenic syndrome due to thyrotoxicosis,1
297592012,myasthenic syndrome due to disease nos,1
297593019,congenital and developmental myasthenia,1
297601018,myoneural disorder nos,1
297602013,muscular dystrophies and other myopathies,1
297605010,benign congenital myopathy,1
297607019,congenital hereditary muscular dystrophy nos,1
297608012,hereditary progressive muscular dystrophy,1
297610014,pelvic muscular dystrophy,1
297623019,hereditary progressive muscular dystrophy nos,1
297625014,infantile myotonia,1
297626010,other specified myotonic disorder,1
297627018,myotonic disorder nos,1
2976311000006114,striatonigral atrophy,1
2976321000006118,snd - striatonigral degeneration,1
297635015,myopathy due to endocrine disease ec,1
297636019,myopathy due to endocrine disease nos,1
297637011,symptomatic inflammatory myopathy in disease ec,1
297639014,Myopathy due to disseminated lupus erythematosus,1
297640011,myopathy due to polyarteritis nodosa,1
297641010,myopathy due to rheumatoid arthritis,1
297643013,myopathy due to sarcoidosis,1
297644019,myopathy due to scleroderma,1
297645018,myopathy due to sjogren's disease,1
297646017,symptomatic inflammatory myopathy in disease nos,1
297647014,proximal myopathy,1
297654015,other myopathies and muscular dystrophies,1
297655019,myopathy or muscular dystrophy nos,1
299241000000110,multiple sclerosis review,1
299303019,[x]other hereditary ataxias,1
299304013,[x]other inherited spinal muscular atrophy,1
299305014,[x]other spinal muscular atrophies and related syndromes,1
299306010,[x]paraneoplastic neuromyopathy and neuropathy,1
299312017,[x]other drug-induced secondary parkinsonism,1
299313010,[x]other secondary parkinsonism,1
299314016,[x]parkinsonism in diseases classified elsewhere,1
299321016,"[x]secondary parkinsonism, unspecified",1
299323018,[x]secondary parkinsonism due to other external agents,1
299329019,[x]demyelinating diseases of the central nervous system,1
299330012,[x]other specified acute disseminated demyelination,1
299332016,"[x]acute disseminated demyelination, unspecified",1
299377019,[x]diseases of myoneural junction and muscle,1
299378012,[x]other specified myoneural disorders,1
299379016,[x]other primary disorders of muscles,1
299380018,[x]other specified myopathies,1
299388013,[x]myopathy in endocrine diseases classified elsewhere,1
299389017,[x]myopathy in metabolic diseases classified elsewhere,1
299390014,[x]myopathy in other diseases classified elsewhere,1
299391013,"[x]mitochondrial myopathy, not elsewhere classified",1
299392018,"[x]inflammatory myopathy, not elsewhere classified",1
299393011,[x]cerebral palsy and other paralytic syndromes,1
299394017,[x]other infantile cerebral palsy,1
300141000000119,multiple sclerosis care plan agreed,1
3001451000006118,post poliomyelitis syndrome,1
3001471000006111,postpolio muscular atrophy,1
3001481000006114,post-polio progressive muscular atrophy,1
3001491000006112,progressive muscular atrophy following poliomyelitis,1
300389010,"dissection of cerebral arteries, nonruptured",1
3005741000006110,neuromyositis,1
3005751000006112,pm - polymyositis,1
300945017,[x]cerebral arteritis in infectious and parasitic diseases,1
301341000006119,[d]post polio exhaustion,1
301719013,lung disease with polymyositis,1
3028151000006111,parkinsonism,1
3028161000006113,disorders presenting primarily with parkinsonism,1
3051551000006111,myopathy in addison's disease,1
3051561000006113,myopathy in addison disease,1
3101701000006117,motor neuron disease,1
3101721000006110,mnd - motor neurone disease,1
311610013,other specific muscle disorder,1
311617011,other specific muscle disorder nos,1
311933012,osteopathy from poliomyelitis,1
311934018,poliomyelitis osteopathy of unspecified site,1
311935017,poliomyelitis osteopathy of the shoulder region,1
311936016,poliomyelitis osteopathy of the upper arm,1
311937013,poliomyelitis osteopathy of the forearm,1
311938015,poliomyelitis osteopathy of the hand,1
311939011,poliomyelitis osteopathy of the pelvic region and thigh,1
311940013,poliomyelitis osteopathy of the lower leg,1
311941012,poliomyelitis osteopathy of the ankle and foot,1
311942017,poliomyelitis osteopathy of other specified sites,1
311943010,poliomyelitis osteopathy of multiple sites,1
311944016,poliomyelitis osteopathy nos,1
312580013,[x]other dermatomyositis,1
312591018,"[x]dermatopolymyositis, unspecified",1
312638019,[x]other specified disorders of muscle,1
3142311000006118,strumpell-lorrain disease,1
3142321000006114,familial spastic paraplegia syndrome,1
3142331000006112,hsp - hereditary spastic paraplegia,1
3142341000006119,strumpell disease,1
3142351000006117,spastic congenital paraplegia,1
3142511000006112,"juvenile myopathy, encephalopathy, lactic acidosis and stroke",1
3142531000006118,"melas - mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes",1
3142551000006113,"mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes",1
315671000000110,multiple sclerosis multidisciplinary review,1
3159741000006112,guillain-barré syndrome,1
3159751000006114,landry-guillain-barré syndrome,1
3159761000006111,ascending paralysis,1
3159771000006116,landry-guillain-barre syndrome,1
3159791000006115,acute inflammatory demyelinating polyradiculoneuropathy,1
3159801000006119,acute idiopathic polyradiculoneuritis,1
3159811000006116,acute idiopathic polyneuritis,1
3159821000006112,acute post-infective radiculoneuropathy,1
3159831000006110,acute inflammatory neuropathy,1
3159841000006117,guillain barre syndrome,1
3170061000006117,eulenburg syndrome,1
3170081000006110,eulenburg disease,1
317120013,[d]ataxic gait,1
317127011,[d]ataxia nos,1
317651000000113,paroxysmal non-kinesigenic dyskinesia,1
3195451000006114,central core myopathy,1
3208041000006113,corticostriatal spinal degeneration,1
3240521000006115,roussy-lévy syndrome,1
3240531000006117,hereditary ataxia-muscular atrophy syndrome,1
3247231000006116,progressive external ophthalmoplegia,1
3247241000006114,graefe's disease,1
3247251000006111,chronic progressive ophthalmoplegia,1
3247271000006118,cpeo - chronic progressive external ophthalmoplegia,1
3247281000006115,peo - progressive external ophthalmoplegia,1
3253991000006119,ataxia with lactic acidosis i,1
3254021000006118,ataxia with lactic acidosis,1
3256761000006118,marie cerebellar ataxia,1
3288331000006116,quadriplegic cerebral palsy,1
3288341000006114,tetraplegic cerebral palsy,1
3288351000006111,cerebral palsy with spastic tetraplegia,1
3288361000006113,tetraplegic spastic cerebral palsy,1
3288371000006118,quadriplegic spastic cerebral palsy,1
3293611000006112,paralysis agitans,1
3293621000006116,shaking palsy,1
3293631000006118,idiopathic parkinson's disease,1
3293641000006111,parkinson disease,1
3293651000006113,pd - parkinson's disease,1
3293661000006110,parkinsons disease,1
3293671000006115,primary parkinsonism,1
3293681000006117,idiopathic parkinsonism,1
3319161000006112,hemiplegia (paralysis on one side),1
3325651000006114,ganglioside accumulation in nervous tissue lysosomes,1
3325661000006111,ganglioside storage disease,1
33622011,postencephalitic parkinsonism,1
3367711000006117,myopathy in cushing's disease,1
3367721000006113,myopathy in cushing disease,1
3377581000006110,upper diplegia,1
3380781000006113,kugelberg-welander disease,1
3380791000006111,familial spinal muscular atrophy,1
3380811000006110,"spinal muscular atrophy, type iii",1
3380821000006119,sma3,1
3380831000006116,sma type iii,1
3380841000006114,spinal muscular atrophy type iii,1
3381191000006118,bulbar paralysis,1
3381201000006115,bulbar palsy,1
3381211000006117,pbp - progressive bulbar palsy,1
3416421000006111,monoplegic cerebral palsy,1
3426051000006115,myasthenic syndrome,1
3426061000006118,lambert-eaton myasthenic syndrome,1
3426071000006113,lems - lambert-eaton myasthenic syndrome,1
3441181000006115,"congenital myotonia, autosomal dominant form",1
3441201000006119,thomsen's disease,1
3441211000006116,thomsen myotonia congenita,1
3441481000006110,endocrine myopathy,1
3441491000006113,muscle disease related to endocrine disease,1
3441501000006117,muscle disorders associated with endocrine disease,1
3445431000006112,diplegic cerebral palsy,1
3445451000006117,spastic diplegic cerebral palsy,1
3446901000006115,variegate porphyria,1
3446911000006117,south african porphyria,1
3446921000006113,south african genetic porphyria,1
3446931000006111,protocoproporphyria,1
3446941000006118,dean-barnes syndrome,1
3446951000006116,mixed porphyria,1
3446961000006119,protoporphyrinogen oxidase deficiency,1
3446971000006114,vp - variegate porphyria,1
3446981000006112,porphyria variegata,1
3449761000006113,sphingomyelin/cholesterol lipidosis,1
3449771000006118,neuronal cholesterol lipidosis,1
3449781000006115,sphingomyelinase deficiency,1
3449801000006116,sphingomyelin lipidosis,1
345037013,early onset cerebellar ataxia with hypogonadism,1
345068012,kennedy syndrome,1
345121017,vascular parkinsonism,1
345122012,multiple system atrophy,1
345221014,subacute necrotizing myelitis,1
345223012,concentric sclerosis,1
3455151000006111,distal muscular dystrophy,1
345594014,axonal sensorimotor neuropathy,1
345701012,cerebral amyloid angiopathy,1
345771011,infantile cerebral palsy,1
345773014,spastic cerebral palsy,1
345780011,dyskinetic cerebral palsy,1
3480751000006110,paralysis of both lower limbs,1
3480761000006112,lower paraplegia,1
3480771000006117,paraplegia (complete or partial paralysis of legs),1
348287011,late effects of acute poliomyelitis,1
3483991000006113,posterolateral sclerosis,1
3484001000006116,vitamin b>12< deficiency disease of spinal cord,1
3484011000006118,putnam-dana syndrome,1
3484021000006114,lichtheim's disease,1
3484041000006119,neuromyelopathy due to vitamin b12 deficiency,1
3484051000006117,sacd - subacute combined degeneration,1
3484061000006115,vitamin b>12< deficiency neuropathy,1
3486721000006115,secondary myopathy,1
3501681000006110,batten-mayou disease,1
3501691000006113,spielmeyer-vogt disease,1
3501701000006113,"amaurotic idiocy, juvenile type",1
3501711000006111,"cerebral lipidosis, myoclonic variant",1
3501721000006115,batten-spielmeyer-vogt disease,1
3501731000006117,cerebral lipidosis myoclonic variant,1
3501741000006110,batten-mayou syndrome,1
3501751000006112,amaurotic idiocy juvenile type,1
3501761000006114,spielmeyer-vogt type neuronal ceroid lipofuscinosis,1
3532651000006115,myasthenia angiosclerotica,1
35440018,cockayne syndrome,1
3547281000006113,werdnig-hoffmann disease,1
3547301000006112,progressive muscular atrophy of infancy,1
3547311000006110,"spinal muscular atrophy, type i",1
3547321000006119,spinal muscular atrophy type i,1
3547331000006116,whd - werdnig-hoffmann disease,1
3553301000006118,"acute paralytic poliomyelitis, bulbar",1
3553311000006115,acute infantile paralysis,1
3553321000006111,acute anterior poliomyelitis,1
3553331000006114,acute anterior bulbar polioencephalomyelitis,1
3555041000006119,sudanophilic leukodystrophy,1
356811012,lipofuscinosis nec,1
3569341000006114,mucolipidosis iii,1
3569351000006111,pseudo-hurler disease,1
3569361000006113,pseudo-hurler's disease,1
359459016,dermatopolymyositis in neoplastic disease,1
359673017,hauptmann-thannhauser muscular dystrophy,1
359699012,familial hypokalaemic periodic paralysis,1
359712012,drug-induced myopathy,1
3601731000006114,kiloh-nevin syndrome,1
3601741000006116,ocular myopathy,1
3601951000006116,olivopontocerebellar degeneration,1
3613541000006112,thyrotoxic myopathy,1
3614661000006114,ataxia-telangiectasia syndrome,1
3614671000006119,louis-bar syndrome,1
3614691000006118,ataxia telangiectasia syndrome,1
3667821000006111,dissociative ataxia,1
3671061000006110,carcinomatous myopathic syndrome,1
3671071000006115,myopathy associated with malignant disease,1
3691951000006119,md - muscular dystrophy,1
3691961000006117,progressive muscular dystrophy,1
3691971000006112,pmd - progressive muscular dystrophy,1
3694981000006113,dentato-rubral atrophy syndrome,1
3694991000006111,hunt's disease,1
3695001000006116,dentate cerebellar ataxia,1
370681000006116,[x]cerebral arteritis in other diseases ce,1
3720541000006119,nemaline myopathy,1
3720561000006115,rod myopathy,1
3720571000006110,rod-body myopathy,1
3746951000006112,pseudohypertrophic muscular dystrophy,1
3746961000006114,dmd - duchenne muscular dystrophy,1
3753631000006115,oculopharyngeal dystrophy,1
3763421000006110,carcinomatous peripheral neuropathy,1
3763431000006113,carcinomatous neuropathy,1
3763441000006115,paraneoplastic polyneuropathy,1
376791000006111,[x]dermato(poly)myositis in neoplastic disease ce,1
3768201000006114,steinert myotonic dystrophy syndrome,1
3768211000006112,steinert syndrome,1
3768221000006116,dystrophia myotonica,1
3768241000006111,dm - dystrophia myotonica,1
3768251000006113,myotonia dystrophica,1
3776451000006119,erb muscular dystrophy,1
3779961000006118,titubant ataxic gait,1
383065014,myoneural disorders,1
3845821000006119,münchmeyer disease,1
3845831000006116,diffuse progressive ossifying polymyositis,1
3845841000006114,fibrodysplasia ossificans progressiva,1
3845851000006111,fop - fibrodysplasia ossificans progressiva,1
3845871000006118,myositis ossificans progressiva,1
3846021000006116,familial hypokalemic periodic paralysis,1
3846031000006118,hypokalemic periodic paralysis,1
3846041000006111,hypokalaemic periodic paralysis,1
3846051000006113,periodic paralysis i,1
3884271000006114,cerebellar ataxia (loss of muscle coordination),1
3889791000006116,adult spinal muscular atrophy,1
3889801000006115,generalized spinal muscular atrophy of late onset,1
3889811000006117,generalised spinal muscular atrophy of late onset,1
3889821000006113,adult onset spinal muscular atrophy,1
3898641000006114,bulbar motor neuron disease,1
3898651000006111,lou gehrig's disease,1
3898661000006113,als - amyotrophic lateral sclerosis,1
3927641000006114,hypothyroid myopathy,1
3927651000006111,myxedema myopathy,1
3927661000006113,myxoedema myopathy,1
3931641000006118,amyotrophy,1
3931651000006116,muscular atrophy,1
3945241000006118,duchenne-aran muscular atrophy,1
3945251000006116,pure progressive muscular atrophy,1
3945261000006119,pma - progressive muscular atrophy,1
39846012,primary cerebellar degeneration,1
3988981000006118,erb-goldflam disease,1
3988991000006115,mg - myasthenia gravis,1
399191000006111,[x]myasthenic syndromes in endocrine diseases ce,1
399201000006114,[x]myasthenic syndromes/other diseases classified elsewhere,1
399371000006112,[x]myopathy/infectious+parasitic diseases ce,1
399400019,cerebellar ataxia nos,1
399401000006110,[x]myositis in protozoal and parasitic infections ce,1
399420018,other specific myoneural disorder,1
399421019,other specified hereditary progressive muscular dystrophy,1
399422014,familial periodic paralysis,1
399436016,lipofuscinosis nos,1
40055016,sandhoff disease,1
4015801000006118,limb-girdle muscular dystrophy,1
4015811000006115,leyden-möbius muscular dystrophy,1
402512016,o/e-festination-parkinson gait,1
402513014,o/e - festination,1
402514015,o/e - parkinson gait,1
409341000006112,[x]other disorders of muscle in diseases ce,1
411453017,congenital cerebral palsy,1
411454011,congenital spastic cerebral palsy,1
411455012,congenital quadriplegia,1
411456013,congenital diplegia,1
411822012,o/e - ataxia,1
412051000006115,[x]other myasthenic syndromes in neoplastic disease ce,1
41398015,multiple sclerosis,1
414541000006119,[x]other specified degenerative diseases/the basal ganglia,1
414561000006115,[x]other specified demyelinating diseases/the cns,1
415146010,right hemiplegia,1
415147018,left hemiplegia,1
4177151000006119,late effects of poliomyelitis,1
4177161000006117,sequelae of poliomyelitis,1
4177181000006110,sequela of infection caused by human poliovirus,1
41961013,neuromyelitis optica,1
41962018,devic's disease,1
4196391000006115,déjérine-sottas disease,1
4196401000006118,"hereditary sensory-motor neuropathy, type iii",1
4196411000006115,hereditary hypertrophic neuropathy,1
4196431000006114,progressive hypertrophic interstitial neuropathy,1
4196441000006116,"hereditary motor and sensory neuropathy, type iii",1
4196451000006119,hsmn iii,1
4196461000006117,hmsn iii,1
4196471000006112,hypertrophic hereditary neuropathy,1
4196491000006113,hypertrophic demyelinative neuropathy of infancy,1
4196651000006117,emd - emery-dreifuss muscular dystrophy,1
4196661000006115,benign scapuloperoneal muscular dystrophy with early contractures,1
422941000006114,[x]polyneuropathy in neoplastic disease ce,1
42524012,refsum's disease,1
426301000006114,[x]sequelae of poliomyelitis,1
428171000006118,[x]subacute combined degeneration/spinal cord in diseases ce,1
428581000006114,[x]systemic atrophies primarily affecting the cns,1
428601000006116,[x]systemic atrophy affecting the cns in other diseases ce,1
4405181000006112,cp - cerebral palsy,1
4405191000006110,cerebral palsy (cp),1
4410181000006116,inflammatory myopathy,1
4427721000006110,myopathic disease,1
4427731000006113,myopathy,1
4428511000006110,porphyric polyneuropathy,1
448235011,neuromyotonia,1
450830018,roussy-levy syndrome,1
451123015,"cerebral palsy, not congenital or infantile, acute",1
4539231000006115,history of poliomyelitis,1
456401000006118,"acute disseminated demyelination, unspecified",1
4566571000006117,on examination - hemiplegia,1
4566621000006119,on examination - paraplegia,1
4566641000006114,on examination - quadriplegia,1
4566651000006111,o/e - tetraplegia,1
4566661000006113,on examination - tetraplegia,1
4566681000006115,on examination - diplegia,1
4567631000006119,on examination - parkinsonian tremor,1
4567691000006115,on examination - hemiplegic posture,1
4567711000006117,on examination - paraplegic in flexion,1
4567731000006111,on examination - paraplegic in extension,1
4567791000006110,on examination - parkinson flexion posture,1
4567891000006116,on examination - gait ataxic,1
4569041000006110,on examination - arms ataxic,1
4569061000006114,on examination - legs ataxic,1
4742071000006115,spinal paralytic poliomyelitis,1
47484015,cerebral arteritis,1
4759751000006118,gaucher's disease,1
4759771000006111,cerebroside lipidosis syndrome,1
4759781000006114,glucocerebrosidase deficiency,1
4759791000006112,kerasin histiocytosis,1
4759801000006113,gaucher splenomegaly,1
4759811000006111,kerasin lipoidosis,1
4759821000006115,glucocerebrosidosis,1
4759831000006117,gaucher syndrome,1
4759841000006110,glucosylceramidase deficiency,1
4759851000006112,glucosylceramide beta-glucosidase deficiency,1
476701000006114,alcoholic myopathy,1
4767941000006119,sspe - subacute sclerosing panencephalitis,1
4767951000006117,dawson's inclusion body encephalitis,1
4768661000006111,leukodystrophy,1
4768671000006116,galactosylceramide beta-galactosidase deficiency,1
4768681000006118,krabbe's leukodystrophy,1
4768691000006115,globoid cell leucodystrophy,1
4768701000006115,krabbe leucodystrophy,1
4768711000006117,gcl - globoid cell leucodystrophy,1
4768731000006111,krabbe disease,1
4768741000006118,galactocerebroside beta-galactosidase deficiency,1
4768751000006116,diffuse globoid cell cerebral sclerosis,1
4768761000006119,b variant hexosaminidase a deficiency,1
4769091000006117,myxoedema cerebellar degeneration,1
4769101000006111,myxedema cerebellar degeneration,1
4769111000006114,paraneoplastic cerebellar degeneration,1
4769281000006110,multiple sclerosis of the brainstem,1
4769291000006113,brain stem multiple sclerosis,1
4769321000006116,generalized multiple sclerosis,1
4769341000006111,multiple sclerosis (ms) exacerbation,1
4769391000006119,hypotonic cerebral palsy,1
4769421000006110,spastic quadriplegia,1
4770411000006116,post-infectious polyneuritis,1
4770721000006119,myasthenic syndrome due to another disorder,1
4770761000006113,myasthenic syndrome due to pernicious anemia,1
4770841000006119,distal muscular dystrophy with juvenile onset,1
4770871000006110,symptomatic inflammatory myopathy associated with another disorder,1
4770891000006111,amyloid myopathy,1
4770931000006119,sarcoid myopathy,1
4770951000006114,myopathy due to systemic sclerosis,1
4770971000006116,myopathy due to sjögren's disease,1
4770991000006115,myopathy due to sjögren disease,1
4771001000006119,myopathy due to sjogrens disease,1
478046010,cerebellar ataxia due to alcoholism,1
4782441000006114,lung disease co-occurrent with polymyositis,1
4782451000006111,polymyositis with pulmonary involvement,1
478396017,miller-fisher syndrome,1
47937012,cerebral ataxia,1
4819691000006111,poliomyelitis osteopathy of the pelvic region and/or thigh,1
4819721000006118,poliomyelitis osteopathy of the ankle and/or foot,1
48512013,progressive supranuclear ophthalmoplegia,1
48513015,progressive supranuclear palsy,1
48515010,steele-richardson-olszewski syndrome,1
486177011,neuralgic amyotrophy,1
486695013,motor neurone disease,1
494103012,tropical spastic paraplegia,1
49474011,leigh's disease,1
49542018,striatonigral degeneration,1
496154014,tabes dorsalis - neurosyphilis,1
496159016,syphilitic posterior spinal sclerosis,1
496911000006118,ataxia-telangiectasia,1
497021000006113,athetoid cerebral palsy,1
498020017,thomsen's disease,1
498788015,subacute combined degeneration,1
499491010,oppenheim's amyotonia,1
499948010,acute paralytic bulbar poliomyelitis,1
5005041000006118,system disorder of the nervous system,1
5005341000006116,bulbospinal neuronopathy,1
5005361000006117,x-linked bulbospinal atrophy,1
5005371000006112,bulbospinal muscular atrophy,1
5005921000006112,secondary parkinson's disease,1
5005931000006110,secondary parkinson disease,1
5005991000006114,msa - multiple system atrophy,1
5006171000006115,autosomal dominant late onset basal ganglia degeneration,1
5007001000006112,subacute necrotizing myelitis,1
5007011000006110,balo concentric sclerosis,1
5007031000006116,balo's concentric sclerosis,1
5007041000006114,balos concentric sclerosis,1
5007921000006115,landau-kleffner syndrome,1
5011691000006117,caa - cerebral amyloid angiopathy,1
5011701000006117,congophilic angiopathy,1
5012271000006111,periventricular leukoencephalopathy,1
5012321000006115,pyramidal cerebral palsy,1
5012331000006117,congenital spastic paralysis,1
5012341000006110,spastic infantile paralysis,1
5012351000006112,little's disease,1
5012361000006114,infantile spastic cerebral palsy,1
504081000006111,batten's disease of retina,1
5141031000006112,dermatomyositis with malignant disease,1
52052015,postpolio syndrome,1
52463013,polymyositis,1
5381371000006113,combined disorder of muscle and peripheral nerve,1
5381381000006111,neuromuscular disorder,1
538601000006110,carotico-cavernous sinus fistula,1
542301000006117,cerebellar ataxia due to myxoedema,1
542991000006113,cerebral lipidoses,1
543071000006115,cerebral palsy with spastic diplegia,1
5501291000006119,myoplegic dystrophy,1
5501301000006118,familial recurrent paralysis,1
5501311000006115,familial myoplegia,1
5501321000006111,cavarre disease,1
5501331000006114,periodic myotonia,1
5509101000006115,on examination - festination-parkinson gait,1
55351000006111,x-linked bulbo-spinal atrophy,1
55426011,idiopathic progressive polyneuropathy,1
5573561000006115,congenital tetraplegia,1
5577511000006113,on examination - ataxia,1
5611491000006112,lt - left hemiplegia,1
5614151000006112,congenital non-progressive ataxia,1
5614181000006116,ataxic cerebral palsy,1
571541000006116,cockayne's syndrome,1
584031000006114,congenital nonprogressive ataxia,1
5904251000006117,carotid cavernous fistula,1
5904271000006110,ccf - carotid cavernous fistula,1
5944191000006113,continuous muscle fiber activity,1
5944201000006111,continuous muscle fibre activity,1
59911000006112,werdnig - hoffmann disease,1
6060631000006111,tabes dorsalis,1
6060641000006118,duchenne's disease,1
6080016,hallervorden-spatz disease,1
614691000006113,"dermatopolymyositis, unspecified",1
625401000006110,distal (gower's) muscular dystrophy,1
625421000006117,distal dystrophy,1
630491000006110,drug induced parkinsonism,1
631811000006111,duchenne aran muscular atrophy,1
63319012,sanger-brown cerebellar ataxia,1
633431000006115,dystrophia myotonica (steinert's disease),1
640991000006117,encephalitis due to poliomyelitis,1
641041000006119,encephalitis due to subacute sclerosing panencephalitis,1
641211000000118,benign multiple sclerosis,1
641301000000114,malignant multiple sclerosis,1
6461171000006118,marchiafava disease,1
6476861000006119,bmd - becker muscular dystrophy,1
6476871000006114,becker's muscular dystrophy,1
6476881000006112,benign duchenne muscular dystrophy,1
64875013,syphilitic parkinsonism,1
6566121000006117,wagner-unverricht syndrome,1
6566131000006119,polymyositis with skin involvement,1
6566141000006112,dm - dermatomyositis,1
6568031000006116,metachromatic leukodystrophy,1
6568041000006114,sulphatide lipidosis,1
6568051000006111,sulfatide lipidosis,1
6568061000006113,mld,1
6568081000006115,metachromatic leukoencephaly,1
6568091000006117,van bogaert-nijssen disease,1
6568101000006111,familial progressive cerebral sclerosis,1
6568111000006114,mld - metachromatic leucodystrophy,1
6596741000006113,"charcot-marie-tooth disease, type i",1
6596751000006110,"hereditary sensory-motor neuropathy, type i",1
6596761000006112,peroneal muscular atrophy of demyelinating type,1
6596771000006117,inherited dominant hypertrophic neuropathy,1
6596791000006116,charcot-marie-tooth disease of demyelinating type,1
6596801000006115,"hsmn, type i",1
6596811000006117,"charcot marie tooth disease, type 1",1
6597711000006111,hereditary sensory and motor neuropathy,1
6597721000006115,hereditary sensory-motor neuropathy,1
6597731000006117,hsmn,1
6597741000006110,hmsn,1
6597751000006112,hmsn - hereditary motor and sensory neuropathy,1
6597761000006114,hsmn - hereditary sensory and motor neuropathy,1
6597771000006119,hereditary sensorimotor neuropathy,1
6597811000006119,polio,1
6597821000006110,pm - poliomyelitis,1
6597831000006113,poliomyelitis,1
6599291000006119,"charcot-marie-tooth disease, type ii",1
6599301000006118,inherited neuronal peroneal muscular atrophy,1
6599321000006111,peroneal muscular atrophy of neuronal type,1
6599331000006114,"charcot marie tooth disease, type 2",1
660171000006114,extraocular muscle myopathy,1
660231000006117,extrapyramidal disease excluding parkinson's disease,1
6607251000006111,lame sickness,1
6607261000006113,infection due to clostridium botulinum,1
6607271000006118,infection caused by clostridium botulinum,1
661251000006116,facioscapulohumeral atrophy,1
6617161000006116,fsh - facioscapulohumeral muscular dystrophy,1
6617171000006111,landouzy-déjérine muscular dystrophy,1
6617181000006114,landouzy-dejerine muscular dystrophy,1
6617191000006112,fshd - facioscapulohumeral muscular dystrophy,1
6617201000006110,fmd - facioscapulohumeral muscular dystrophy,1
6617211000006113,fascioscapulohumeral muscular dystrophy,1
66483014,hereditary spastic paraplegia,1
682621000006119,myopathy due to addison's disease,1
682631000006116,myopathy due to amyloid,1
682641000006114,myopathy due to cushing's syndrome,1
682681000006115,myopathy due to hypopituitarism,1
682691000006117,myopathy due to malignant disease,1
682701000006117,myopathy due to myxoedema,1
682841000006110,myotonia congenita (thomsen's disease),1
682861000006114,myotonic chondrodysplasia,1
682891000006118,myotonic disorders,1
68321016,guillain-barre syndrome,1
683431000006111,myasthenic syndrome due to botulism,1
6839012,polymyositis ossificans,1
695191000006119,multiple sclerosis of the brain stem,1
696641000006114,mucolipidosis type iii,1
699671000000115,management of multiple sclerosis in onset phase,1
699731000000110,management of multiple sclerosis in early disease phase,1
699791000000111,management of multiple sclerosis in stable disability phase,1
699911000000117,management of multiple sclerosis in palliative phase,1
701491000006117,"mitochondrial myopathy, not elsewhere classified",1
7045281000006112,multiple sclerosis (ms) secondary progressive,1
7058051000006116,multiple sclerosis (ms) relapsing remitting,1
7092351000006112,multiple sclerosis (ms) primary progressive,1
7108161000006116,congenital nonprogressive myopathy with moebius and robin sequences,1
716831000006114,massive muscular calcification associated with paraplegia,1
71981018,central core disease,1
72531016,congenital hemiplegia,1
7289421000006111,"multiple system atrophy, parkinson's variant",1
73325012,corticostriatal-spinal degeneration,1
734711000006110,louis - bar syndrome,1
7349161000006111,fxtas - fragile x associated tremor ataxia syndrome,1
736381000006110,locomotor ataxia,1
740431000006115,littles disease,1
753451000006118,kugelberg - welander disease,1
761411000006111,flaccid infantile cerebral palsy,1
7620901000006112,gmfcs (gross motor function classification system) for cerebral palsy,1
77128019,progressive external ophthalmoplegia,1
7717281000006114,human t-cell lymphotropic virus 1-associated myelopathy,1
7717301000006113,htlv-i-associated myelopathy,1
7717311000006111,tropical spastic paraparesis,1
7717321000006115,myelopathy caused by human t-lymphotropic virus 1,1
7730241000006111,myotonic dystrophy type 2,1
7774171000006115,benign autosomal dominant myopathy,1
778591000006118,"inflammatory myopathy, not elsewhere classified",1
78021014,marie's cerebellar ataxia,1
78022019,hereditary cerebellar ataxia,1
81717011,parkinson's disease,1
81719014,paralysis agitans,1
8193781000006112,history of parkinson disease,1
8328151000006111,scpe (surveillance of cerebral palsy in europe) predominant pattern classification a - maldevelopment,1
8328171000006118,scpe (surveillance of cerebral palsy in europe) predominant pattern classification b - predominant white matter injury,1
8328191000006117,scpe (surveillance of cerebral palsy in europe) predominant pattern classification c - predominant grey matter injury,1
8328211000006116,scpe (surveillance of cerebral palsy in europe) predominant pattern classification d - unspecified,1
8328231000006110,scpe (surveillance of cerebral palsy in europe) predominant pattern classification a.1.1 - disorder of proliferation,1
8328251000006115,scpe (surveillance of cerebral palsy in europe) predominant pattern classification a.1.2 - disorder of migration,1
8328271000006113,scpe (surveillance of cerebral palsy in europe) predominant pattern classification a.1.3 - disorder of organisation,1
8328331000006119,scpe (surveillance of cerebral palsy in europe) predominant pattern classification a.2 - unspecified maldevelopment,1
8328461000006117,scpe (surveillance of cerebral palsy in europe) predominant pattern classification b.1 - periventricular leucomalacia,1
8328481000006110,scpe (surveillance of cerebral palsy in europe) predominant pattern classification b.2 - sequelae of intraventricular haemorrhage or periventricular infarction,1
8328501000006117,scpe (surveillance of cerebral palsy in europe) predominant pattern classification b.3 - combination of periventricular leucomalacia and intraventricular haemorrhage sequelae,1
8328531000006113,scpe (surveillance of cerebral palsy in europe) predominant pattern classification e - normal,1
8328551000006118,scpe (surveillance of cerebral palsy in europe) predominant pattern classification c.1 - basal ganglia and thalamus lesions,1
8328571000006111,scpe (surveillance of cerebral palsy in europe) predominant pattern classification c.2 - parasagittal lesions,1
8328591000006112,scpe (surveillance of cerebral palsy in europe) predominant pattern classification c.3 - infarct of the middle cerebral artery,1
8342831000006112,degenerative disease of basal ganglia,1
84200019,peroneal muscular atrophy,1
84201015,charcot-marie-tooth disease,1
84272011,hemiplegia,1
84935014,gangliosidosis,1
856091000006114,right hemiplegia,1
857181000006110,left hemiplegia,1
882961000006112,secondary parkinsonism - drugs,1
883181000006113,other myoneural disorders,1
883191000006111,myopathy nos,1
89919017,diplegia of upper limbs,1
90229010,juvenile spinal muscular atrophy,1
90263012,progressive bulbar palsy,1
905781000006118,[rfc] multiple sclerosis,1
905801000006119,[rfc] motor neurone disease,1
905821000006112,[rfc] parkinson's disease,1
905891000006114,[rfc] paraplegias,1
907241000006111,[rfc] cerebral palsy,1
907411000006113,[rfc] cerebral palsy,1
908811000006112,[rfc] multiple sclerosis,1
908821000006116,[rfc] motor neurone disease,1
909021000006117,[rfc] parkinson's disease,1
94780015,eaton-lambert syndrome,1
96850018,protocoproporphyria,1
9742014,stiff-man syndrome,1
9822014,spinal muscular atrophy,1
983261000006119,multiple sclerosis - personal health plan,1
983271000006114,multiple sclerosis - multidisciplinary review,1
983281000006112,multiple sclerosis - review,1
983291000006110,multiple sclerosis - primary progressive,1
983301000006111,multiple sclerosis - secondary progressive,1
983311000006114,multiple sclerosis - relapsing remitting,1
99251000006111,toxic myoneural disorder,1