medcodeid,term,originalreadcode,cleansedreadcode,snomedctconceptid,snomedctdescriptionid,lidisability
108541018,hurler's syndrome,C3751-2,C375112,65327002,108541018,1
3562061000006117,"mucopolysaccharidosis, mps-i-h",^ESCTMU356206,,65327002,108537017,1
3562071000006112,"l-iduronidase deficiency, hurler type",^ESCTLI356207,,65327002,108538010,1
3562081000006110,lipochondrodystrophy,^ESCTLI356208,,65327002,108539019,1
3562091000006113,gargoylism,^ESCTGA356209,,65327002,108540017,1
3562111000006116,hurler-pfaundler syndrome,^ESCTHU356211,,65327002,108542013,1
3562121000006112,dysostosis multiplex syndrome,^ESCTDY356212,,65327002,108543015,1
3562131000006110,mps 1-h - mucopolysaccharidosis type i-h,^ESCTMP356213,,65327002,500079013,1
3562141000006117,mucopolysaccharidosis type i-h,^ESCTMU356214,,65327002,500080011,1
3562151000006115,hurler disease mps type 1h,^ESCTHU356215,,65327002,500081010,1
3562161000006118,mucopolysaccharidosis type i severe form,^ESCTMU356216,,65327002,500082015,1
829441000006116,hurler's syndrome,C375-3,C375.13,65327002,108541018,1
10374011,Laurence-Moon-Biedl syndrome,PKy1,PKy1.00,5619004,10374011,1
110901011,Acrodysostosis,PG5F,PG5F.00,66758006,110901011,1
1129781000000117,[X]Severe learning disability,Eu815,Eu81500,508171000000105,1129801000000116,1
1129811000000119,[X]Moderate learning disability,Eu814,Eu81400,984671000000103,2504061000000114,1
11998101000006118,Intellectual developmental disorder,^ESCT1199810,,110359009,3642975016,1
12177531000006112,Profound intellectual disability,^ESCT1217753,,31216003,12177531000006112,1
12177541000006119,Profound intellectual development disorder,^ESCT1217754,,31216003,3654215011,1
12181611000006117,Severe intellectual disability,^ESCT1218161,,40700009,12181611000006117,1
12181621000006113,Severe intellectual development disorder,^ESCT1218162,,40700009,3654214010,1
12190771000006114,Moderate intellectual disability,^ESCT1219077,,61152003,12190771000006114,1
12190781000006112,Moderate intellectual development disorder,^ESCT1219078,,61152003,3654216012,1
12202441000006114,Mild intellectual disability,^ESCT1220244,,86765009,12202441000006114,1
12202451000006111,Mild intellectual development disorder,^ESCT1220245,,86765009,3654174011,1
1221474011,Deletion of short arm of chromosome 4,PJ32,PJ32.00,17122004,1221474011,1
1224878018,Trisomy 21 NOS,PJ0z-1,PJ0z.11,41040004,222121000000113,1
1224879014,Trisomy 18 NOS,PJ2z-1,PJ2z.11,51500006,85775018,1
1224880012,Trisomy 13 NOS,PJ1z-1,PJ1z.11,21111006,35482019,1
1224941015,Dubowitz syndrome,PKy66,PKy6600,2593002,1224941015,1
1229637015,Degenerative amsterodamensis typus,PKy60-3,PKy6013,40354009,1229637015,1
1229639017,Bruck-de Lange syndrome,PKy60-2,PKy6012,40354009,1229639017,1
1231577014,Biedl-Bardet syndrome,PKy1-1,PKy1.11,5619004,1231577014,1
12321891000006112,"Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth",^ESCT1232189,,412787009,3643126011,1
1233229018,Deletion of short arm of chromosome 5,PJ31-1,PJ31.11,70173007,1233229018,1
12337641000006113,X-linked intellectual disability with marfanoid habitus,^ESCT1233764,,422437002,3643151012,1
1234038018,Angelman's syndrome,PKyz7,PKyz700,76880004,1234038018,1
12359591000006114,Hirschsprung disease-intellectual disability syndrome,^ESCT1235959,,703535000,3643142016,1
12702211000006116,Specific learning difficulty,^ESCT1270221,,889211000000104,2290321000000117,1
12703781000006112,Mild mental retardation (I.Q. 50-70),^ESCT1270378,,86765009,143892017,1
12703791000006110,Moderate mental retardation (I.Q. 35-49),^ESCT1270379,,61152003,101619019,1
12703921000006110,Profound mental retardation (I.Q. below 20),^ESCT1270392,,31216003,52225019,1
12703941000006115,Severe mental retardation (I.Q. 20-34),^ESCT1270394,,40700009,67882016,1
127638013,Angelman syndrome,PKyz5-1,PKyz511,76880004,1234038018,1
127639017,Happy puppet syndrome,PKyz5,PKyz500,76880004,127639017,1
146051000006113,"Severe mental retardation, IQ in range 20-34",E311,E311.00,40700009,3643515012,1
148214012,Prader-Willi syndrome,PKy0-2,PKy0.12,89392001,148214012,1
151009017,Mental retardation,E3,E3...00,110359009,3643707012,1
1550041000000110,[X]Mild learning disability,Eu816,Eu81600,984661000000105,2504041000000113,1
1550051000000113,[X]Profound learning disability,Eu817,Eu81700,984681000000101,2504081000000117,1
1694831000006112,Pitt-Hopkins syndrome,EMISNQPI5,,702344008,2995603016,1
1705901000006118,Angelman syndrome,PKyz7-1,PKyz711,76880004,1234038018,1
1780502018,Smith-Magenis syndrome,PJ333,PJ33300,401315004,1780502018,1
1803731000006114,Acrodysostosis,EMISNQAC767,,66758006,1803731000006114,1
1887331000006119,[X]Specific learning disability,Eu818,Eu81800,889211000000104,2290291000000110,1
201751000006110,Profound mental retardation with IQ less than 20,E312,E312.00,31216003,3643527010,1
2090010,Fragile X syndrome,PJyy4,PJyy400,613003,2090010,1
2114791000000110,Kleefstra syndrome,PJ33A,PJ33A00,724207001,3432347016,1
212911000006116,Prader - Willi syndrome,PKy93,PKy9300,89392001,148214012,1
212921000006112,Prader-Willi Syndrome,PKy0-1,PKy0.11,89392001,148214012,1
215821000000119,Moron,E30-3,E30..13,86765009,507246016,1
222121000000113,Trisomy 21,PJ0-2,PJ0..12,41040004,68470016,1
239991000006111,Patau's syndrome - trisomy 13,PJ1,PJ1..00,21111006,35483012,1
2478440016,Ohdo blepharophimosis syndrome,PKyG-1,PKyG.11,412787009,2478440016,1
2540251000006114,Dubowitz's syndrome,^ESCTDU254025,,2593002,5418016,1
2548475019,On learning disability register,918e,918e.00,416075005,2548475019,1
25776014,Coffin-Lowry syndrome,PKy5F,PKy5F00,15182000,25776014,1
2589171000006110,Bardet-Biedl syndrome,^ESCTBA258917,,5619004,10373017,1
2589191000006111,LMBB - Laurence-Moon-Bardet-Biedl syndrome,^ESCTLM258919,,5619004,1231576017,1
2740611000006112,CLS - Coffin-Lowry syndrome,^ESCTCL274061,,15182000,1221167013,1
2771701000006114,4p partial monosomy syndrome,^ESCT4P277170,,17122004,28958010,1
2771711000006112,Chromosome 4 short arm deletion syndrome,^ESCTCH277171,,17122004,28959019,1
2771721000006116,4p minus syndrome,^ESCT4P277172,,17122004,28960012,1
2771731000006118,Midline fusion defect syndrome,^ESCTMI277173,,17122004,28961011,1
2835541000006116,Complete trisomy 13 syndrome,^ESCTCO283554,,21111006,35482019,1
2835561000006117,D>1< trisomy syndrome,^ESCTD1283556,,21111006,35484018,1
2844171000006117,BFLS,^ESCTBF284417,,21634003,196134011,1
2844181000006119,Borjeson syndrome,^ESCTBO284418,,21634003,1222652011,1
295661017,Other specified mental retardation,E3y,E3y..00,110359009,175156010,1
295662012,Other specified mental retardation NOS,E31z,E31z.00,110359009,175156010,1
295664013,Mental retardation NOS,E3z,E3z..00,110359009,175156010,1
296557014,"[X]Mild mental retardation, other impairments of behaviour",Eu70y,Eu70y00,86765009,143892017,1
296565012,[X]Mod retard oth behav impair,Eu71y,Eu71y00,61152003,101619019,1
296574014,"[X]Severe mental retardation, other impairments of behaviour",Eu72y,Eu72y00,40700009,67882016,1
296586012,[X]Other mental retardation,Eu7y,Eu7y.00,110359009,175156010,1
296592018,"[X]Other mental retardation, other impairments of behaviour",Eu7yy,Eu7yy00,110359009,175156010,1
296678017,[X]Other pervasive developmental disorders,Eu84y,Eu84y00,35919005,59939011,1
296679013,"[X]Pervasive developmental disorder, unspecified",Eu84z,Eu84z00,35919005,3078949014,1
297751000006119,Noonan's syndrome,PKy0-3,PKy0.13,205824006,315625018,1
3003301000006113,Profound mental handicap,^ESCTPR300330,,31216003,1227448012,1
3003311000006111,Profound mental retardation (Intelligence Quotient below 20),^ESCTPR300331,,31216003,2974835016,1
3003321000006115,Profound learning disability with intelligence quotient less than 20,^ESCTPR300332,,31216003,536901000000113,1
3003331000006117,Profound learning impairment with intelligence quotient less than 20,^ESCTPR300333,,31216003,552571000000113,1
3003341000006110,"Profound learning disability, intelligence quotient less than 20",^ESCTPR300334,,31216003,556521000000113,1
3003351000006112,"Profound learning impairment, intelligence quotient less than 20",^ESCTPR300335,,31216003,556531000000110,1
3003361000006114,Profound learning disability,^ESCTPR300336,,31216003,1666271000000112,1
302051000000118,Lujan-Fryns syndrome,PKyJ,PKyJ.00,422437002,2649528010,1
3149211000006118,De Lange syndrome,^ESCTDE314921,,40354009,63895010,1
3149231000006112,Brachmann-de Lange syndrome,^ESCTBR314923,,40354009,63897019,1
3149251000006117,Degenerative amstelodamensis typus,^ESCTDE314925,,40354009,1229636012,1
3149271000006110,Typus degenerativus amstelodamensis,^ESCTTY314927,,40354009,1229638013,1
315486012,Fragile X chromosome,PJyy2,PJyy200,205720009,315486012,1
3155151000006112,Severe learning disability,^ESCTSE315515,,40700009,2310251000000113,1
3155171000006119,Severe mental handicap,^ESCTSE315517,,40700009,1229669012,1
3155181000006116,Severe mental retardation (Intelligence Quotient 20-34),^ESCTSE315518,,40700009,2975060010,1
3155191000006118,"Severe learning disability, intelligence quotient in range 20-34",^ESCTSE315519,,40700009,536891000000112,1
3155201000006115,"Severe learning impairment, intelligence quotient in range 20-34",^ESCTSE315520,,40700009,552561000000118,1
315625018,Noonan's syndrome,PKy80,PKy8000,205824006,315625018,1
3161031000006112,Complete trisomy 21 syndrome,^ESCTCO316103,,41040004,68470016,1
3161041000006119,Down syndrome,^ESCTDO316104,,41040004,68471017,1
3161051000006117,T21 - Trisomy 21,^ESCTT2316105,,41040004,1229711010,1
3161061000006115,Downs syndrome,^ESCTDO316106,,41040004,2921053011,1
3334491000006116,Complete trisomy 18 syndrome,^ESCTCO333449,,51500006,85775018,1
3334501000006112,Edwards syndrome,^ESCTED333450,,51500006,85776017,1
3493641000006112,Moderate mental handicap,^ESCTMO349364,,61152003,1232179016,1
3493651000006114,Moderate mental retardation (Intelligence Quotient 35-49),^ESCTMO349365,,61152003,2981606015,1
3493661000006111,"Moderate learning disability, intelligence quotient in range 35-49",^ESCTMO349366,,61152003,536881000000110,1
3493671000006116,"Moderate learning impairment, intelligence quotient in range 35-49",^ESCTMO349367,,61152003,552551000000116,1
3493681000006118,Moderate learning disability,^ESCTMO349368,,61152003,1666321000000118,1
3585501000006118,Peripheral dysostosis,^ESCTPE358550,,66758006,1232838015,1
3616531000006110,Rett's disorder,^ESCTRE361653,,68618008,113976016,1
3616551000006115,Cerebroatrophic hyperammonemia,^ESCTCE361655,,68618008,113978015,1
3616561000006118,Cerebroatrophic hyperammonaemia,^ESCTCE361656,,68618008,501065014,1
3616571000006113,RTS - Rett syndrome,^ESCTRT361657,,68618008,1233070014,1
3616581000006111,Rett disorder,^ESCTRE361658,,68618008,2838409013,1
3616591000006114,Retts syndrome,^ESCTRE361659,,68618008,2951769014,1
36300015,Borjeson-Forssman-Lehmann syndrome,PKy69,PKy6900,21634003,36300015,1
3640931000006110,5p partial monosomy syndrome,^ESCT5P364093,,70173007,116546014,1
3640951000006115,Lejeune syndrome,^ESCTLE364095,,70173007,116548010,1
3640961000006118,5p minus syndrome,^ESCT5P364096,,70173007,116549019,1
3640971000006113,Partial deletion of short arm of chromosome 5 syndrome,^ESCTPA364097,,70173007,116550019,1
3750051000006112,Angelman syndrome,^ESCTAN375005,,76880004,127638013,1
378493013,Down's syndrome NOS,PJ0z,PJ0z.00,41040004,598021000000114,1
378494019,Partial trisomy 21 in Down's syndrome,PJ02-1,PJ02.11,254264002,378494019,1
378496017,Edward's syndrome NOS,PJ2z,PJ2z.00,51500006,85775018,1
378499012,Patau's syndrome NOS,PJ1z,PJ1z.00,21111006,35482019,1
378500015,Partial trisomy 13 in Patau's syndrome,PJ12-1,PJ12.11,254268004,378500015,1
386751000006111,[X]Feeble-mindedness,Eu70-1,Eu70.11,86765009,507246016,1
3910901000006110,Mild mental handicap,^ESCTMI391090,,86765009,507245017,1
3910921000006117,Mild mental retardation (Intelligence Quotient 50-70),^ESCTMI391092,,86765009,2975045012,1
3910931000006119,"Mild learning disability, intelligence quotient in range 50-70",^ESCTMI391093,,86765009,536871000000113,1
3910941000006112,"Mild learning impairment, intelligence quotient in range 50-70",^ESCTMI391094,,86765009,552541000000119,1
3910951000006114,Mild learning disability,^ESCTMI391095,,86765009,1666311000000112,1
395051000006119,[X]Learn acquisition disab NOS,Eu81z-3,Eu81z13,110359009,3643707012,1
395061000006117,[X]Learning disability NOS,Eu81z-1,Eu81z11,1855002,478664016,1
398201000006115,[X]Mental deficiency NOS,Eu7z-1,Eu7z.11,110359009,175156010,1
398231000006111,[X]Mental retardation,Eu7,Eu7..00,110359009,3643707012,1
398241000006118,[X]Mental retardation with autistic features,Eu841-2,Eu84112,231536004,347022013,1
398251000006116,[X]Mental subnormality NOS,Eu7z-2,Eu7z.12,110359009,175156010,1
398381000006119,[X]Mild mental retardation,Eu70,Eu70.00,86765009,507246016,1
398391000006116,[X]Mild mental retardation without mention impairment behav,Eu70z,Eu70z00,86765009,3643513017,1
398411000006116,[X]Mild mental subnormality,Eu70-2,Eu70.12,86765009,507246016,1
398651000006118,[X]Mld mental retard sig impairment behav req attent/treatmt,Eu701,Eu70100,86765009,143892017,1
398661000006116,[X]Mld mental retard with statement no or min impairm behav,Eu700,Eu70000,86765009,143892017,1
398761000006113,[X]Mod mental retard sig impairment behav req attent/treatmt,Eu711,Eu71100,61152003,101619019,1
398771000006118,[X]Mod mental retard with statement no or min impairm behav,Eu710,Eu71000,61152003,101619019,1
398781000006115,[X]Mod mental retardation without mention impairment behav,Eu71z,Eu71z00,61152003,3643518014,1
398811000006118,[X]Moderate mental retardation,Eu71,Eu71.00,61152003,3643518014,1
398821000006114,[X]Moderate mental subnormality,Eu71-1,Eu71.11,61152003,3643518014,1
401902015,[X]Unspecified mental retardation,Eu7z,Eu7z.00,110359009,175156010,1
404851000006117,[X]Oth mental retard sig impairment behav req attent/treatmt,Eu7y1,Eu7y100,110359009,175156010,1
404861000006115,[X]Oth mental retard with statement no or min impairm behav,Eu7y0,Eu7y000,110359009,175156010,1
411791000006118,[X]Other mental retardation without mention impairment behav,Eu7yz,Eu7yz00,110359009,175156010,1
413177014,Educationally subnormal,E30-1,E30..11,276854003,413177014,1
417681000006116,[X]Overactive disorder assoc mental retard/stereotype movts,Eu844,Eu84400,35919005,59939011,1
420581000006111,[X]Pervasive developmental disorders,Eu84,Eu84.00,35919005,3078949014,1
423361000006118,[X]Prfnd mental retardation without mention impairment behav,Eu73z,Eu73z00,31216003,52225019,1
423481000006119,[X]Profound ment retard sig impairmnt behav req attent/treat,Eu731,Eu73100,31216003,52225019,1
423491000006116,[X]Profound ment retrd wth statement no or min impairm behav,Eu730,Eu73000,31216003,52225019,1
423501000006112,[X]Profound mental retardation,Eu73,Eu73.00,31216003,3643527010,1
423511000006110,"[X]Profound mental retardation, other impairments of behavr",Eu73y,Eu73y00,31216003,52225019,1
423521000006119,[X]Profound mental subnormality,Eu73-1,Eu73.11,31216003,3643527010,1
424971000006111,[X]Rett's syndrome,Eu842,Eu84200,68618008,113977013,1
426521000006114,[X]Sev mental retard sig impairment behav req attent/treatmt,Eu721,Eu72100,40700009,67882016,1
426531000006112,[X]Sev mental retard with statement no or min impairm behav,Eu720,Eu72000,40700009,67882016,1
426541000006119,[X]Sev mental retardation without mention impairment behav,Eu72z,Eu72z00,40700009,3643515012,1
426591000006111,[X]Severe mental retardation,Eu72,Eu72.00,40700009,3643515012,1
426611000006117,[X]Severe mental subnormality,Eu72-1,Eu72.11,40700009,3643515012,1
430061000006113,[X]Unsp mental retard with statement no or min impairm behav,Eu7z0,Eu7z000,110359009,175156010,1
430071000006118,[X]Unsp mental retardation without mention impairment behav,Eu7zz,Eu7zz00,110359009,175156010,1
430081000006115,[X]Unsp mentl retard sig impairment behav req attent/treatmt,Eu7z1,Eu7z100,110359009,175156010,1
431231000006115,"[X]Unspecified mental retardatn, other impairments of behav",Eu7zy,Eu7zy00,110359009,175156010,1
4830941000006112,Trisomy 21- meiotic nondisjunction,^ESCTTR483094,,205615000,315346017,1
4830961000006111,Mosaic Down syndrome,^ESCTMO483096,,205616004,2882581019,1
4830971000006116,Mosaic Down's syndrome,^ESCTMO483097,,205616004,2882582014,1
4831981000006110,Noonan-Ehmke syndrome,^ESCTNO483198,,205824006,2475674013,1
4831991000006113,Turner-like syndrome,^ESCTTU483199,,205824006,2475675014,1
4832001000006110,Noonan syndrome,^ESCTNO483200,,205824006,2475676010,1
507246016,"Mild mental retardation, IQ in range 50-70",E30,E30..00,86765009,507246016,1
5339911000006112,Trisomy 21 - translocation,^ESCTTR533991,,254264002,378495018,1
5339921000006116,Partial trisomy 21 in Down syndrome,^ESCTPA533992,,254264002,2837910011,1
5339971000006115,Trisomy 13 - translocation,^ESCTTR533997,,254268004,378501016,1
5339981000006117,Partial trisomy 13 in Patau syndrome,^ESCTPA533998,,254268004,2838921016,1
53891000006113,Wolff - Hirschorn syndrome,PJ32-1,PJ32.11,17122004,1221473017,1
557191000000119,Mowat-Wilson syndrome,PJ9,PJ9..00,703535000,3009119013,1
600811000006111,Cri-du-chat syndrome,PJ31,PJ31.00,70173007,116547017,1
628281000006114,Down's syndrome - trisomy 21,PJ0,PJ0..00,41040004,598021000000114,1
636711000006113,Edward's syndrome - trisomy 18,PJ2,PJ2..00,51500006,85776017,1
63896011,Cornelia de Lange syndrome,PKy60-1,PKy6011,40354009,63896011,1
63898012,Amsterdam dwarf,PKy60,PKy6000,40354009,63898012,1
667621000006119,Feeble-minded,E30-2,E30..12,86765009,507246016,1
68472012,Mongolism,PJ0-1,PJ0..11,41040004,598021000000114,1
6989771000006117,X-linked mental retardation with marfanoid habitus syndrome,^ESCTXL698977,,422437002,2645975014,1
700071000006118,"Moderate mental retardation, IQ in range 35-49",E310,E310.00,61152003,3643518014,1
7558461000006113,PTHS - Pitt-Hopkins syndrome,^ESCTPT755846,,702344008,2995797017,1
7577251000006111,"Microcephaly, mental retardation and distinct features, with or without Hirschsprung disease",^ESCTMI757725,,703535000,3009030013,1
7577261000006113,Hirschsprung disease-mental retardation syndrome,^ESCTHI757726,,703535000,3009165011,1
785941000006115,Imbecile,E310-1,E310.11,61152003,3643518014,1
787151000006113,Idiocy,E312-1,E312.11,31216003,3643527010,1
79051000006114,"Ullrich - Feichtiger syndrome, chimaera",PKyz0,PKyz000,21111006,35482019,1
8191411000006110,[X]Severe learning disability,^ESCTXS819141,,508171000000105,1129781000000117,1
8337561000006119,Significant learning disability,^ESCTSI833756,,931001000000105,2385981000000116,1
8337571000006114,Significant intellectual development disorder,^ESCTSI833757,,931001000000105,2714221000000114,1
8337581000006112,Significant developmental disability,^ESCTSI833758,,931001000000105,2714231000000111,1
8337591000006110,Significant intellectual disability,^ESCTSI833759,,931001000000105,2714241000000119,1
88271000006113,"Trisomy 13, translocation",PJ12,PJ12.00,254268004,378501016,1
882771000006119,Mild mental retardation,E30-99,E30..99,86765009,882771000006119,1
882781000006116,Moderate mental retardation,E310-99,E310.99,61152003,882781000006116,1
882791000006118,Severe mental retardation,E311-99,E311.99,40700009,882791000006118,1
88351000006114,"Trisomy 21, meiotic nondisjunction",PJ00,PJ00.00,205615000,315346017,1
88361000006111,"Trisomy 21, mitotic nondisjunction",PJ01-1,PJ01.11,205616004,315347014,1
88371000006116,"Trisomy 21, mosaicism",PJ01,PJ01.00,205616004,315347014,1
88381000006118,"Trisomy 21, translocation",PJ02,PJ02.00,254264002,378495018,1
893481000006117,Down's syndrome,PJ0-98,PJ0..98,41040004,893481000006117,1
94131019,Cohen syndrome,PKy5K,PKy5K00,56604005,94131019,1
968201000006114,Men ret congen heart dis blepharophim blepharop hypopl teeth,PKyG,PKyG.00,412787009,2474343011,1
9881000006115,Other specified mental retardation,E31,E31..00,110359009,175156010,1