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
108541018,hurler's syndrome,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
123479016,reye's syndrome,1
1235534016,binswanger's encephalopathy,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
12702281000006111,degenerative brain disorder,1
12704251000006113,cerebellar ataxia associated with another disorder,1
12704731000006113,inflammatory disorder of muscle,1
12717021000006115,myopathy or muscular dystrophy nos,1
12724061000006112,cerebral degeneration other disease nos,1
12725491000006112,myopathy or muscular dystrophy nos,1
12725821000006112,cerebral degeneration 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
148381000006115,senile/presenile dementia,1
1491762016,central demyelination of corpus callosum,1
1492251019,becker's disease,1
149347010,binswanger'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
1823871000006112,dementia confirmed,1
1834091000006117,dementia care plan,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
1916981000006111,dementia medication review,1
1949611000006114,dementia post diagnostic support (scotland),1
1949621000006118,dementia stage at diagnosis,1
1949631000006115,dementia stage at diagnosis - early (mild),1
1949641000006113,dementia stage at diagnosis - mid (moderate),1
1949651000006110,dementia stage at diagnosis - late (severe),1
1949661000006112,dementia stage at diagnosis - undetermined,1
1949671000006117,dementia stage at diagnosis - not known,1
1949681000006119,person centred dementia support plan (scotland),1
1949691000006116,dementia support plan (scot) in place at 12 months,1
1949701000006116,dementia support plan (scot) partly in place at 12 months,1
1949711000006118,dementia support plan (scot) absent at 12 months,1
1949721000006114,dementia post diagnostic support (pds) - transition arrangements,1
1949731000006112,dementia pds transition - progress to supported self management,1
1949751000006117,dementia pds transition - further pds required,1
1949771000006110,dementia post diagnostic support (pds)(scot)- 5 pillar model,1
1950411000006115,dementia pds(scot)-understanding illness/managing symptms status,1
1950421000006111,dementia pds (scot) understanding illness status - pillar met,1
1950431000006114,dementia pds (scot) understanding illness - pillar partially met,1
1950451000006119,dementia pds understanding illness-pillar not met(service reasn),1
1950461000006117,dementia pds understanding illness - pillar not met (pt choice),1
1950481000006110,dementia pds understanding illness - other pillar status,1
1950491000006113,dementia pds understanding illness - pillar status not known,1
1950501000006117,dementia pds (scot) - planning for future care status,1
1950511000006119,dementia pds (scot) planning future care status - pillar met,1
1950521000006110,dementia pds (scot) planning future care - pillar partially met,1
1950531000006113,dementia pds planning future care-pillar not met(service reason),1
1950541000006115,dementia pds planning future care - pillar not met (pt choice),1
1950551000006118,dementia pds planning future care - other pillar status,1
1950561000006116,dementia pds planning future care - pillar status not known,1
1950571000006111,dementia pds (scot) - peer support status,1
1950581000006114,dementia pds (scot) peer support status - pillar met,1
1950591000006112,dementia pds (scot) peer support status - pillar partially met,1
1950601000006116,dementia pds (scot) peer support-pillar not met (service reason),1
1950611000006118,dementia pds (scot) peer support - pillar not met (pt choice),1
1950621000006114,dementia pds (scot) peer support - other pillar status,1
1950631000006112,dementia pds (scot) peer support - pillar status not known,1
1950641000006119,dementia pds (scot) - supporting community connections status,1
1950651000006117,dementia pds (scot) support community connections - pillar met,1
1950661000006115,dementia pds support community connections -pillar partially met,1
1950671000006110,dementia pds supprt comm. connectns-pillar not met(servce reasn),1
1950681000006113,dementia pds support comm. connectns-pillar not met (pt choice),1
1950691000006111,dementia pds support comm. connectns - other pillar status,1
1950701000006111,dementia pds support comm. connectns - pillar status not known,1
1950711000006114,dementia pds (scot) - planning future decision-making status,1
1950721000006118,dementia pds planning future decision-making - pillar met,1
1950731000006115,dementia pds planning future decisn-making -pillar partially met,1
1950741000006113,dementia pds plan.futur decisn-mkng-pillar not met(servce reasn),1
1950751000006110,dementia pds plan.future decisn-making-pillar not met(pt choice),1
1950761000006112,dementia pds plan future decision-making - other pillar status,1
1950771000006117,dementia pds plan future decision-making-pillar status not known,1
1971401000006111,"dementia in alzheimer's disease with early onset, without additional symptoms",1
1971541000006114,"dementia in alzheimer's disease with early onset, other symptoms, predominantly delusional",1
1971771000006112,"dementia in alzheimer's disease with early onset, other symptoms, predominantly hallucinatory",1
1972021000006119,"unspecified dementia, without additional symptoms",1
1972041000006114,"unspecified dementia, other symptoms, predominantly delusional",1
1972061000006113,"unspecified dementia, other symptoms, predominantly hallucinatory",1
1972071000006118,"unspecified dementia, other symptoms, predominantly depressive",1
1972081000006115,"unspecified dementia, other mixed symptoms",1
1972131000006115,"dementia in alzheimer's disease with early onset, other symptoms, predominantly depressive",1
1972141000006113,"dementia in alzheimer's disease with early onset, other mixed symptoms",1
1972171000006117,"dementia in alzheimer's disease with late onset, without additional symptoms",1
1972181000006119,"dementia in alzheimer's disease with late onset, other symptoms, predominantly delusional",1
1972191000006116,"dementia in alzheimer's disease with late onset, other symptoms, predominantly hallucinatory",1
1972201000006118,"dementia in alzheimer's disease with late onset, other symptoms, predominantly depressive",1
1972211000006115,"dementia in alzheimer's disease with late onset, other mixed symptoms",1
1972231000006114,"dementia in alzheimer's dis, atypical or mixed type, without additional symptoms",1
1972251000006119,"dementia in alzheimer's dis, atypical or mixed type, other symptoms, predominantly delusional",1
1972291000006113,"dementia in alzheimer's dis, atypical or mixed type, other symptoms, predominantly hallucinatory",1
1972311000006112,"dementia in alzheimer's dis, atypical or mixed type, other symptoms, predominantly depressive",1
1972341000006111,"dementia in alzheimer's dis, atypical or mixed type, other mixed symptoms",1
1972371000006115,"dementia in alzheimer's disease, unspecified, without additional symptoms",1
1972401000006117,"dementia in alzheimer's disease, unspecified, other symptoms, predominantly delusional",1
1972421000006110,"dementia in alzheimer's disease, unspecified, other symptoms, predominantly hallucinatory",1
1972451000006118,"dementia in alzheimer's disease, unspecified, other symptoms, predominantly depressive",1
1972471000006111,"dementia in alzheimer's disease, unspecified, other mixed symptoms",1
1972481000006114,"vascular dementia of acute onset, without additional symptoms",1
1972501000006116,"vascular dementia of acute onset, other symptoms, predominantly delusional",1
1972521000006114,"vascular dementia of acute onset, other symptoms, predominantly hallucinatory",1
1972541000006119,"vascular dementia of acute onset, other symptoms, predominantly depressive",1
1972571000006110,"vascular dementia of acute onset, other mixed symptoms",1
1972601000006115,"multi-infarct dementia, without additional symptoms",1
1972621000006113,"multi-infarct dementia, other symptoms, predominantly delusional",1
1972641000006118,"multi-infarct dementia, other symptoms, predominantly hallucinatory",1
1972661000006119,"multi-infarct dementia, other symptoms, predominantly depressive",1
1972681000006112,"multi-infarct dementia, other mixed symptoms",1
1972711000006113,"subcortical vascular dementia, without additional symptoms",1
1972731000006119,"subcortical vascular dementia, other symptoms, predominantly delusional",1
1972751000006114,"subcortical vascular dementia, other symptoms, predominantly hallucinatory",1
1972771000006116,"subcortical vascular dementia, other symptoms, predominantly depressive",1
1972791000006115,"subcortical vascular dementia, other mixed symptoms",1
1972821000006112,"mixed cortical and subcortical vascular dementia, without additional symptoms",1
1972831000006110,"mixed cortical and subcortical vascular dementia, other symptoms, predominantly delusional",1
1972871000006113,"mixed cortical and subcortical vascular dementia, other symptoms, predominantly hallucinatory",1
1972911000006111,"mixed cortical and subcortical vascular dementia, other symptoms, predominantly depressive",1
1972931000006117,"mixed cortical and subcortical vascular dementia, other mixed symptoms",1
1973221000006118,"other vascular dementia, without additional symptoms",1
1973271000006117,"other vascular dementia, other symptoms, predominantly delusional",1
1973341000006118,"other vascular dementia, other symptoms, predominantly hallucinatory",1
1973381000006112,"other vascular dementia, other symptoms, predominantly depressive",1
1973401000006112,"other vascular dementia, other mixed symptoms",1
1973461000006113,"vascular dementia, unspecified, without additional symptoms",1
1973501000006113,"vascular dementia, unspecified, other symptoms, predominantly delusional",1
1973531000006117,"vascular dementia, unspecified, other symptoms, predominantly hallucinatory",1
1973551000006112,"vascular dementia, unspecified, other symptoms, predominantly depressive",1
1976831000006111,"vascular dementia, unspecified, other mixed symptoms",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
21256010,presenile dementia,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
22408016,pick's disease,1
2248021000000110,dementia care plan,1
2267591000000110,neuroferritinopathy,1
2283041000000116,choreo-athetotic cerebral palsy,1
2283831000000117,choreoathetoid cerebral palsy,1
2290431000000110,antipsychotic drug therapy for dementia,1
2326271000000114,bilateral spastic cerebral palsy,1
2345801000000113,dementia advance care plan declined,1
2345881000000115,dementia advance care plan agreed,1
2345931000000111,review of dementia advance care plan,1
2366171000000112,sporadic creutzfeldt-jakob disease,1
2366181000000114,sporadic cjd (creutzfeldt-jakob disease),1
2366391000000114,dementia leaflet given,1
2386018,jakob-creutzfeldt disease,1
2403101000000116,dementia medication review,1
243291000006119,paramyotonia congenita (eulenburg's disease),1
2439591000000113,dementia care plan agreed,1
2439631000000113,dementia care plan reviewed,1
2439671000000110,dementia care plan declined,1
2439711000000111,dementia care plan review declined,1
244311000006117,parkinsonism secondary to drugs,1
2445471000000112,dementia advance care plan,1
2445691000000113,dementia advance care plan review declined,1
2475876012,balo's concentric sclerosis,1
2475877015,ataxic diplegic cerebral palsy,1
2502971000006115,dementia associated with alcoholism,1
2502981000006117,alcohol-induced persisting dementia,1
2510951000006114,creutzfeldt-jakob disease,1
2510971000006116,subacute spongiform encephalopathy,1
2510981000006118,cjd - creutzfeldt-jakob disease,1
2510991000006115,jcd - jakob-creutzfeldt disease,1
2511001000006119,transmissible virus dementia,1
2511011000006116,creutzfeldt jakob disease,1
251539016,h/o: poliomyelitis,1
251625013,h/o: dementia,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
2543131000006118,organic brain syndrome,1
2543151000006113,obs - organic brain syndrome,1
2543161000006110,acute psycho-organic syndrome,1
2543181000006117,abs - acute brain syndrome,1
2543191000006119,acute brain 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
2551441000006116,amnestic syndrome,1
2551451000006119,amnesic syndrome,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
2620431000000115,shared care prescribing of drugs for dementia,1
2637771000000114,proximal myotonic myopathy,1
264417019,notification of acute polio,1
2650601000006118,paraplegic-spastic gait,1
26545010,senile dementia,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
2707651000006116,circumscribed cerebral atrophy,1
2707661000006119,pick disease,1
2707671000006114,picks disease,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
2743011000000119,dementia advance care plan agreed,1
2748441000006111,sd - senile dementia,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
2854601000006117,progressive multifocal leukoencephalopathy,1
2854611000006119,multifocal leukoencephalopathy,1
2854631000006113,multifocal leucoencephalopathy,1
2854641000006115,pml - progressive multifocal leucoencephalopathy,1
2854651000006118,pmle - progressive multifocal leukoencephalopathy,1
2854661000006116,pmle - progressive multifocal leucoencephalopathy,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
2931231000006118,ad - alzheimer's disease,1
2931241000006111,alzheimer disease,1
2931251000006113,alzheimer dementia,1
293326016,gaucher's disease,1
293544011,coproporphyria,1
293813012,[x]other gangliosidosis,1
294635013,uncomplicated senile dementia,1
294637017,uncomplicated presenile dementia,1
294638010,presenile dementia with delirium,1
294641018,presenile dementia with paranoia,1
294642013,presenile dementia with depression,1
294643015,presenile dementia nos,1
294644014,senile dementia with depressive or paranoid features,1
294645010,senile dementia with paranoia,1
294646011,senile dementia with depression,1
294647019,senile dementia with depressive or paranoid features nos,1
294648012,senile dementia with delirium,1
294652012,uncomplicated arteriosclerotic dementia,1
294653019,arteriosclerotic dementia with delirium,1
294654013,arteriosclerotic dementia with paranoia,1
294655014,arteriosclerotic dementia with depression,1
294656010,arteriosclerotic dementia nos,1
294660013,senile or presenile psychoses nos,1
294668018,chronic alcoholic brain syndrome,1
294688019,drug-induced dementia,1
294704013,acute confusional state nos,1
294718018,dementia in conditions ec,1
2949121000006114,brown-séquard syndrome,1
295668011,[x]dementia in alzheimer's disease,1
295671015,"[x]dementia in alzheimer's dis, atypical or mixed type",1
295672010,"[x]dementia in alzheimer's disease, unspecified",1
295680015,[x]other vascular dementia,1
295681016,"[x]vascular dementia, unspecified",1
295684012,[x]dementia in other diseases classified elsewhere,1
295685013,[x]dementia in pick's disease,1
295686014,[x]dementia in creutzfeldt-jakob disease,1
295687017,[x]dementia in huntington's disease,1
295688010,[x]dementia in parkinson's disease,1
295690011,[x]dementia in other specified diseases classif elsewhere,1
295713019,"[x]delirium not superimposed on dementia, so described",1
295714013,[x]delirium superimposed on dementia,1
295718011,"[x]delirium, unspecified",1
2966061000006116,progressive supranuclear ophthalmoplegia,1
2966081000006114,nuchal dystonia-dementia syndrome,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
296958010,cerebral degenerations usually manifest in childhood,1
296959019,leucodystrophy,1
296966018,krabbe's disease,1
296982017,leucodystrophy nos,1
296987011,retinal dystrophy in cerebroretinal lipidosis,1
296988018,cerebral lipidoses nos,1
296990017,cerebral degeneration in gaucher's disease,1
296991018,cerebral degeneration in niemann-pick disease,1
296992013,cerebral degeneration in lipidosis nos,1
296993015,cerebral degeneration in diseases ec,1
296994014,cerebral degeneration in hunter's disease,1
296995010,cerebral degeneration in mucopolysaccharidoses,1
296996011,cerebral degeneration in disease nos,1
296997019,other cerebral degenerations in childhood,1
296998012,other cerebral degenerations in childhood nos,1
296999016,childhood cerebral degenerations nos,1
297000018,other cerebral degenerations,1
297011014,alcoholic encephalopathy,1
297012019,cerebral degeneration due to beriberi,1
297013012,cerebral degeneration due to cerebrovascular disease,1
297014018,cerebral degeneration due to congenital hydrocephalus,1
297015017,cerebral degeneration due to neoplastic disease,1
297018015,cerebral degeneration due to vitamin b12 deficiency,1
297022013,cerebral degeneration other disease nos,1
297025010,other cerebral degeneration nos,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
299325013,[x]other alzheimer's disease,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
299641000000112,[x]lewy body dementia,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
3240651000006113,age-related degeneration of brain,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
3341641000006113,dementia paralytica,1
3341701000006116,paralytic dementia,1
3350441000006115,organic dementia,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
3414231000006117,mid - multi-infarct dementia,1
3414251000006112,vad - vascular dementia,1
3414261000006114,multi infarct dementia,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
345092016,frontotemporal degeneration,1
345121017,vascular parkinsonism,1
345122012,multiple system atrophy,1
345221014,subacute necrotizing myelitis,1
345223012,concentric sclerosis,1
3454511000006118,chronic progressive chorea,1
3454521000006114,chronic progressive hereditary chorea,1
3454531000006112,hc - huntington chorea,1
3454541000006119,hd - huntington chorea,1
3454551000006117,huntington chorea,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
346897015,presbyophrenic psychosis,1
346929012,alcoholic dementia nos,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
3562061000006117,"mucopolysaccharidosis, mps-i-h",1
3562071000006112,"l-iduronidase deficiency, hurler type",1
3562081000006110,lipochondrodystrophy,1
3562091000006113,gargoylism,1
3562111000006116,hurler-pfaundler syndrome,1
3562121000006112,dysostosis multiplex syndrome,1
3562131000006110,mps 1-h - mucopolysaccharidosis type i-h,1
3562141000006117,mucopolysaccharidosis type i-h,1
3562151000006115,hurler disease mps type 1h,1
3562161000006118,mucopolysaccharidosis type i severe form,1
356811012,lipofuscinosis nec,1
3569341000006114,mucolipidosis iii,1
3569351000006111,pseudo-hurler disease,1
3569361000006113,pseudo-hurler's disease,1
35741000006114,other cerebral degeneration,1
359081000006118,[x] presenile dementia nos,1
359091000006115,[x] presenile psychosis nos,1
359101000006114,[x] primary degenerative dementia nos,1
359141000006111,[x] senile dementia nos,1
359151000006113,"[x] senile dementia, depressed or paranoid type",1
359161000006110,[x] senile psychosis nos,1
359241000006119,[x] unspecified dementia,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
362201000006116,[x]acute / subacute brain syndrome,1
362231000006112,[x]acute / subacute organic reaction,1
362941000006113,[x]alcoholic dementia nos,1
363021000006113,[x]alzheimer's dementia unspec,1
363031000006111,[x]alzheimer's disease type 1,1
363041000006118,[x]alzheimer's disease type 2,1
363791000006112,[x]arteriosclerotic dementia,1
3667821000006111,dissociative ataxia,1
3670601000006111,dementia infantilis,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
3708651000006112,reye's encephalopathy,1
3708661000006114,reye syndrome,1
370961000006119,[x]chronic alcoholic brain syndrome,1
3720541000006119,nemaline myopathy,1
3720561000006115,rod myopathy,1
3720571000006110,rod-body myopathy,1
37365019,progressive multifocal leukoencephalopathy,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
376431000006118,[x]delirium of mixed origin,1
376531000006119,[x]dementia in alzheimer's disease with early onset,1
376541000006112,[x]dementia in alzheimer's disease with late onset,1
376571000006116,[x]dementia in human immunodef virus [hiv] disease,1
376631000006115,[x]dementia infantalis,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
3802621000006119,lewy body variant of alzheimer's disease,1
3802631000006116,sdlt - senile dementia of the lewy body type,1
3802641000006114,lbd - lewy body disease,1
3802651000006111,dementia of the lewy body type,1
3802661000006113,dlbd - diffuse lewy body disease,1
3802671000006118,cortical lewy body disease,1
3802681000006115,clbd - cortical lewy body disease,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
3938581000006118,hepatocerebral degeneration,1
3945241000006118,duchenne-aran muscular atrophy,1
3945251000006116,pure progressive muscular atrophy,1
3945261000006119,pma - progressive muscular atrophy,1
394691000006116,"[x]korsakov's psychosis, nonalcoholic",1
3964591000006117,subcortical leucoencephalopathy,1
3964601000006113,subcortical leukoencephalopathy,1
3964611000006111,binswanger's dementia,1
3964621000006115,encephalitis subcorticalis chronica,1
3964651000006112,subcortical arteriosclerotic encephalopathy,1
3964661000006114,subcortical atherosclerotic dementia,1
3964671000006119,chronic progressive subcortical encephalopathy,1
39846012,primary cerebellar degeneration,1
398571000006112,[x]mixed cortical and subcortical vascular dementia,1
3988981000006118,erb-goldflam disease,1
3988991000006115,mg - myasthenia gravis,1
399031000006111,[x]multi-infarct dementia,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
399393010,cerebral degeneration nos,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
399481000000113,prion protein markers for creutzfeldt-jakob disease,1
40055016,sandhoff disease,1
4015801000006118,limb-girdle muscular dystrophy,1
4015811000006115,leyden-möbius muscular dystrophy,1
401757012,senile and presenile organic psychotic conditions,1
401759010,other senile and presenile organic psychoses,1
401760017,other alcoholic dementia,1
401831017,[x]other delirium,1
402512016,o/e-festination-parkinson gait,1
402513014,o/e - festination,1
402514015,o/e - parkinson gait,1
403921000006119,[x]organic amnesic synd not induced alc/oth psychoact subs,1
408401000000119,dementia annual review,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
415873013,cerebral atrophy,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
423221000006117,[x]predominantly cortical dementia,1
423351000006115,"[x]presenile dementia,alzheimer's type",1
423381000006111,"[x]primary degen dementia of alzheimer's type, senile onset",1
423391000006114,"[x]primary degen dementia, alzheimer's type, presenile onset",1
42524012,refsum's disease,1
425901000006116,"[x]senile dementia,alzheimer's type",1
426301000006114,[x]sequelae of poliomyelitis,1
428171000006118,[x]subacute combined degeneration/spinal cord in diseases ce,1
428201000006119,[x]subcortical vascular dementia,1
428581000006114,[x]systemic atrophies primarily affecting the cns,1
428601000006116,[x]systemic atrophy affecting the cns in other diseases ce,1
431681000006117,[x]vascular dementia,1
431691000006119,[x]vascular dementia of acute onset,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
45046017,alzheimer's disease,1
450830018,roussy-levy syndrome,1
451123015,"cerebral palsy, not congenital or infantile, acute",1
4539231000006115,history of poliomyelitis,1
4539871000006116,history of dementia,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
4763081000006118,senile delirium,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
4768791000006110,cerebral degeneration in gaucher disease,1
4768841000006113,cerebral degeneration in hunter disease,1
4768851000006110,cerebral degeneration in mucopolysaccharidosis,1
4768901000006117,alcohol induced encephalopathy,1
4768951000006118,myxoedema encephalopathy,1
4768961000006116,myxedema encephalopathy,1
4768981000006114,cerebral degeneration due to creutzfeldt-jakob disease,1
4769001000006112,cerebral degeneration due to progressive multifocal leukoencephalopathy,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
481281019,progressive multifocal leucoencephalopathy,1
4819691000006111,poliomyelitis osteopathy of the pelvic region and/or thigh,1
4819721000006118,poliomyelitis osteopathy of the ankle and/or foot,1
483651010,acute confusional state,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
497559016,arteriosclerotic dementia,1
498020017,thomsen's disease,1
498788015,subacute combined degeneration,1
499491010,oppenheim's amyotonia,1
499946014,alzheimer's disease with early onset,1
499948010,acute paralytic bulbar poliomyelitis,1
500317011,alzheimer's disease with late onset,1
5005041000006118,system disorder of the nervous system,1
5005341000006116,bulbospinal neuronopathy,1
5005361000006117,x-linked bulbospinal atrophy,1
5005371000006112,bulbospinal muscular atrophy,1
5005661000006113,lobar 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
542611000006114,cerebral degeneration due to alcoholism,1
542651000006110,cerebral degeneration due to jakob - creutzfeldt disease,1
542661000006112,cerebral degeneration due to multifocal leucoencephalopathy,1
542671000006117,cerebral degeneration due to myxoedema,1
542741000006119,cerebral degeneration in lipidoses ec,1
542781000006113,cerebral degeneration in other disease ec,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
612521000006115,delirium - acute organic,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
636681000000117,cerebral degeneration in parkinson'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
6897211000006117,"primary degenerative dementia of the alzheimer type, presenile onset",1
6897221000006113,"primary degenerative dementia of the alzheimer type, early onset",1
6897241000006118,dementia of the alzheimers type with early onset,1
6897251000006116,"presenile dementia, alzheimer's type",1
6897271000006114,dementia in alzheimer's disease - type 2,1
6900181000006114,"primary degenerative dementia of the alzheimer type, senile onset",1
6900191000006112,"primary degenerative dementia of the alzheimer type, late onset",1
6900201000006110,"dementia of the alzheimers type, late onset",1
6900221000006117,"sdat - senile dementia, alzheimer's type",1
6900241000006112,dementia in alzheimer's disease - type 1,1
6949031000006112,cerebral degeneration associated with generalised lipidosis,1
6949041000006119,cerebral degeneration associated with generalized lipidosis,1
6949051000006117,cerebral degeneration in generalized lipidosis,1
6949061000006115,cerebral degeneration in lipidoses,1
695191000006119,multiple sclerosis of the brain stem,1
696161000006115,multi infarct dementia,1
696641000006114,mucolipidosis type iii,1
6973421000006116,dementia associated with aids,1
6973431000006118,acquired immune deficiency syndrome-related dementia,1
6973441000006111,aids - acquired immune deficiency syndrome dementia complex,1
6973451000006113,adc - acquired immune deficiency syndrome dementia complex,1
6973461000006110,acquired immune deficiency syndrome dementia complex,1
6973471000006115,dementia associated with acquired immunodeficiency syndrome,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
7043651000006119,dementia associated with parkinson's disease,1
7043661000006117,dementia associated with parkinson disease,1
7045281000006112,multiple sclerosis (ms) secondary progressive,1
7058051000006116,multiple sclerosis (ms) relapsing remitting,1
7092351000006112,multiple sclerosis (ms) primary progressive,1
7103601000006116,dementia due to creutzfeldt-jakob disease,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
7263011000006112,dementia due to huntington disease,1
7263021000006116,dementia due to huntingtons disease,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
745381000006119,lewy body disease,1
753451000006118,kugelberg - welander disease,1
761411000006111,flaccid infantile cerebral palsy,1
7620901000006112,gmfcs (gross motor function classification system) for cerebral palsy,1
76484016,senile degeneration of brain,1
7699251000006118,sporadic jakob-creutzfeldt disease,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
8009521000006114,dementia due to picks disease,1
8009531000006112,dementia due to pick disease,1
8009541000006119,dementia co-occurrent and due to pick's disease,1
81717011,parkinson's disease,1
81719014,paralysis agitans,1
8193781000006112,history of parkinson disease,1
829441000006116,hurler's syndrome,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
8399871000006111,prion protein markers for cjd (creutzfeldt-jakob disease),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
882171000006115,dementia,1
882181000006117,other senile/presenile dement.,1
882191000006119,senile and presenile dementias,1
882201000006116,senile dementia - simple type,1
882211000006118,senile dementia-acute confused,1
882931000006115,child cerebral degeneration,1
882941000006113,senile brain degeneration,1
882951000006110,cerebral degenerations nos,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
905791000006115,[rfc] alzheimer's disease,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
914921000006117,[d] vascular dementia,1
914931000006119,[d] dementia with lewy bodies,1
914941000006112,[d] dementia,1
914951000006114,[d] dementia in alzheimer's disease,1
915111000006112,dementia review,1
915121000006116,dementia review with third party,1
939491000006118,[rfc] dementia,1
94780015,eaton-lambert syndrome,1
96850018,protocoproporphyria,1
97154016,niemann-pick disease,1
9742014,stiff-man syndrome,1
97642017,huntington's chorea,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
10374011,Laurence-Moon-Biedl syndrome,1
110901011,Acrodysostosis,1
1129781000000117,[X]Severe learning disability,1
1129811000000119,[X]Moderate learning disability,1
11998101000006118,Intellectual developmental disorder,1
12177531000006112,Profound intellectual disability,1
12177541000006119,Profound intellectual development disorder,1
12181611000006117,Severe intellectual disability,1
12181621000006113,Severe intellectual development disorder,1
12190771000006114,Moderate intellectual disability,1
12190781000006112,Moderate intellectual development disorder,1
12202441000006114,Mild intellectual disability,1
12202451000006111,Mild intellectual development disorder,1
1221474011,Deletion of short arm of chromosome 4,1
1224878018,Trisomy 21 NOS,1
1224879014,Trisomy 18 NOS,1
1224880012,Trisomy 13 NOS,1
1224941015,Dubowitz syndrome,1
1229637015,Degenerative amsterodamensis typus,1
1229639017,Bruck-de Lange syndrome,1
1231577014,Biedl-Bardet syndrome,1
12321891000006112,"Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth",1
1233229018,Deletion of short arm of chromosome 5,1
12337641000006113,X-linked intellectual disability with marfanoid habitus,1
1234038018,Angelman's syndrome,1
12359591000006114,Hirschsprung disease-intellectual disability syndrome,1
12702211000006116,Specific learning difficulty,1
12703781000006112,Mild mental retardation (I.Q. 50-70),1
12703791000006110,Moderate mental retardation (I.Q. 35-49),1
12703921000006110,Profound mental retardation (I.Q. below 20),1
12703941000006115,Severe mental retardation (I.Q. 20-34),1
127638013,Angelman syndrome,1
127639017,Happy puppet syndrome,1
146051000006113,"Severe mental retardation, IQ in range 20-34",1
148214012,Prader-Willi syndrome,1
151009017,Mental retardation,1
1550041000000110,[X]Mild learning disability,1
1550051000000113,[X]Profound learning disability,1
1694831000006112,Pitt-Hopkins syndrome,1
1705901000006118,Angelman syndrome,1
1780502018,Smith-Magenis syndrome,1
1803731000006114,Acrodysostosis,1
1887331000006119,[X]Specific learning disability,1
201751000006110,Profound mental retardation with IQ less than 20,1
2090010,Fragile X syndrome,1
2114791000000110,Kleefstra syndrome,1
212911000006116,Prader - Willi syndrome,1
212921000006112,Prader-Willi Syndrome,1
215821000000119,Moron,1
222121000000113,Trisomy 21,1
239991000006111,Patau's syndrome - trisomy 13,1
2478440016,Ohdo blepharophimosis syndrome,1
2540251000006114,Dubowitz's syndrome,1
2548475019,On learning disability register,1
25776014,Coffin-Lowry syndrome,1
2589171000006110,Bardet-Biedl syndrome,1
2589191000006111,LMBB - Laurence-Moon-Bardet-Biedl syndrome,1
2740611000006112,CLS - Coffin-Lowry syndrome,1
2771701000006114,4p partial monosomy syndrome,1
2771711000006112,Chromosome 4 short arm deletion syndrome,1
2771721000006116,4p minus syndrome,1
2771731000006118,Midline fusion defect syndrome,1
2835541000006116,Complete trisomy 13 syndrome,1
2835561000006117,D>1< trisomy syndrome,1
2844171000006117,BFLS,1
2844181000006119,Borjeson syndrome,1
295661017,Other specified mental retardation,1
295662012,Other specified mental retardation NOS,1
295664013,Mental retardation NOS,1
296557014,"[X]Mild mental retardation, other impairments of behaviour",1
296565012,[X]Mod retard oth behav impair,1
296574014,"[X]Severe mental retardation, other impairments of behaviour",1
296586012,[X]Other mental retardation,1
296592018,"[X]Other mental retardation, other impairments of behaviour",1
296678017,[X]Other pervasive developmental disorders,1
296679013,"[X]Pervasive developmental disorder, unspecified",1
297751000006119,Noonan's syndrome,1
3003301000006113,Profound mental handicap,1
3003311000006111,Profound mental retardation (Intelligence Quotient below 20),1
3003321000006115,Profound learning disability with intelligence quotient less than 20,1
3003331000006117,Profound learning impairment with intelligence quotient less than 20,1
3003341000006110,"Profound learning disability, intelligence quotient less than 20",1
3003351000006112,"Profound learning impairment, intelligence quotient less than 20",1
3003361000006114,Profound learning disability,1
302051000000118,Lujan-Fryns syndrome,1
3149211000006118,De Lange syndrome,1
3149231000006112,Brachmann-de Lange syndrome,1
3149251000006117,Degenerative amstelodamensis typus,1
3149271000006110,Typus degenerativus amstelodamensis,1
315486012,Fragile X chromosome,1
3155151000006112,Severe learning disability,1
3155171000006119,Severe mental handicap,1
3155181000006116,Severe mental retardation (Intelligence Quotient 20-34),1
3155191000006118,"Severe learning disability, intelligence quotient in range 20-34",1
3155201000006115,"Severe learning impairment, intelligence quotient in range 20-34",1
315625018,Noonan's syndrome,1
3161031000006112,Complete trisomy 21 syndrome,1
3161041000006119,Down syndrome,1
3161051000006117,T21 - Trisomy 21,1
3161061000006115,Downs syndrome,1
3334491000006116,Complete trisomy 18 syndrome,1
3334501000006112,Edwards syndrome,1
3493641000006112,Moderate mental handicap,1
3493651000006114,Moderate mental retardation (Intelligence Quotient 35-49),1
3493661000006111,"Moderate learning disability, intelligence quotient in range 35-49",1
3493671000006116,"Moderate learning impairment, intelligence quotient in range 35-49",1
3493681000006118,Moderate learning disability,1
3585501000006118,Peripheral dysostosis,1
3616531000006110,Rett's disorder,1
3616551000006115,Cerebroatrophic hyperammonemia,1
3616561000006118,Cerebroatrophic hyperammonaemia,1
3616571000006113,RTS - Rett syndrome,1
3616581000006111,Rett disorder,1
3616591000006114,Retts syndrome,1
36300015,Borjeson-Forssman-Lehmann syndrome,1
3640931000006110,5p partial monosomy syndrome,1
3640951000006115,Lejeune syndrome,1
3640961000006118,5p minus syndrome,1
3640971000006113,Partial deletion of short arm of chromosome 5 syndrome,1
3750051000006112,Angelman syndrome,1
378493013,Down's syndrome NOS,1
378494019,Partial trisomy 21 in Down's syndrome,1
378496017,Edward's syndrome NOS,1
378499012,Patau's syndrome NOS,1
378500015,Partial trisomy 13 in Patau's syndrome,1
386751000006111,[X]Feeble-mindedness,1
3910901000006110,Mild mental handicap,1
3910921000006117,Mild mental retardation (Intelligence Quotient 50-70),1
3910931000006119,"Mild learning disability, intelligence quotient in range 50-70",1
3910941000006112,"Mild learning impairment, intelligence quotient in range 50-70",1
3910951000006114,Mild learning disability,1
395051000006119,[X]Learn acquisition disab NOS,1
395061000006117,[X]Learning disability NOS,1
398201000006115,[X]Mental deficiency NOS,1
398231000006111,[X]Mental retardation,1
398241000006118,[X]Mental retardation with autistic features,1
398251000006116,[X]Mental subnormality NOS,1
398381000006119,[X]Mild mental retardation,1
398391000006116,[X]Mild mental retardation without mention impairment behav,1
398411000006116,[X]Mild mental subnormality,1
398651000006118,[X]Mld mental retard sig impairment behav req attent/treatmt,1
398661000006116,[X]Mld mental retard with statement no or min impairm behav,1
398761000006113,[X]Mod mental retard sig impairment behav req attent/treatmt,1
398771000006118,[X]Mod mental retard with statement no or min impairm behav,1
398781000006115,[X]Mod mental retardation without mention impairment behav,1
398811000006118,[X]Moderate mental retardation,1
398821000006114,[X]Moderate mental subnormality,1
401902015,[X]Unspecified mental retardation,1
404851000006117,[X]Oth mental retard sig impairment behav req attent/treatmt,1
404861000006115,[X]Oth mental retard with statement no or min impairm behav,1
411791000006118,[X]Other mental retardation without mention impairment behav,1
413177014,Educationally subnormal,1
417681000006116,[X]Overactive disorder assoc mental retard/stereotype movts,1
420581000006111,[X]Pervasive developmental disorders,1
423361000006118,[X]Prfnd mental retardation without mention impairment behav,1
423481000006119,[X]Profound ment retard sig impairmnt behav req attent/treat,1
423491000006116,[X]Profound ment retrd wth statement no or min impairm behav,1
423501000006112,[X]Profound mental retardation,1
423511000006110,"[X]Profound mental retardation, other impairments of behavr",1
423521000006119,[X]Profound mental subnormality,1
424971000006111,[X]Rett's syndrome,1
426521000006114,[X]Sev mental retard sig impairment behav req attent/treatmt,1
426531000006112,[X]Sev mental retard with statement no or min impairm behav,1
426541000006119,[X]Sev mental retardation without mention impairment behav,1
426591000006111,[X]Severe mental retardation,1
426611000006117,[X]Severe mental subnormality,1
430061000006113,[X]Unsp mental retard with statement no or min impairm behav,1
430071000006118,[X]Unsp mental retardation without mention impairment behav,1
430081000006115,[X]Unsp mentl retard sig impairment behav req attent/treatmt,1
431231000006115,"[X]Unspecified mental retardatn, other impairments of behav",1
4830941000006112,Trisomy 21- meiotic nondisjunction,1
4830961000006111,Mosaic Down syndrome,1
4830971000006116,Mosaic Down's syndrome,1
4831981000006110,Noonan-Ehmke syndrome,1
4831991000006113,Turner-like syndrome,1
4832001000006110,Noonan syndrome,1
507246016,"Mild mental retardation, IQ in range 50-70",1
5339911000006112,Trisomy 21 - translocation,1
5339921000006116,Partial trisomy 21 in Down syndrome,1
5339971000006115,Trisomy 13 - translocation,1
5339981000006117,Partial trisomy 13 in Patau syndrome,1
53891000006113,Wolff - Hirschorn syndrome,1
557191000000119,Mowat-Wilson syndrome,1
600811000006111,Cri-du-chat syndrome,1
628281000006114,Down's syndrome - trisomy 21,1
636711000006113,Edward's syndrome - trisomy 18,1
63896011,Cornelia de Lange syndrome,1
63898012,Amsterdam dwarf,1
667621000006119,Feeble-minded,1
68472012,Mongolism,1
6989771000006117,X-linked mental retardation with marfanoid habitus syndrome,1
700071000006118,"Moderate mental retardation, IQ in range 35-49",1
7558461000006113,PTHS - Pitt-Hopkins syndrome,1
7577251000006111,"Microcephaly, mental retardation and distinct features, with or without Hirschsprung disease",1
7577261000006113,Hirschsprung disease-mental retardation syndrome,1
785941000006115,Imbecile,1
787151000006113,Idiocy,1
79051000006114,"Ullrich - Feichtiger syndrome, chimaera",1
8191411000006110,[X]Severe learning disability,1
8337561000006119,Significant learning disability,1
8337571000006114,Significant intellectual development disorder,1
8337581000006112,Significant developmental disability,1
8337591000006110,Significant intellectual disability,1
88271000006113,"Trisomy 13, translocation",1
882771000006119,Mild mental retardation,1
882781000006116,Moderate mental retardation,1
882791000006118,Severe mental retardation,1
88351000006114,"Trisomy 21, meiotic nondisjunction",1
88361000006111,"Trisomy 21, mitotic nondisjunction",1
88371000006116,"Trisomy 21, mosaicism",1
88381000006118,"Trisomy 21, translocation",1
893481000006117,Down's syndrome,1
94131019,Cohen syndrome,1
968201000006114,Men ret congen heart dis blepharophim blepharop hypopl teeth,1
9881000006115,Other specified mental retardation,1