medcodeid,term,learning
10374011,Laurence-Moon-Biedl syndrome,1
108541018,hurler's 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
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
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
829441000006116,hurler's syndrome,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