medcode,readcode,readterm,learning 302,E310.00,"Moderate mental retardation, IQ in range 35-49",1 1278,E310.11,Imbecile,1 1362,E3...00,Mental retardation,1 1543,PJ0..00,Down's syndrome - trisomy 21,1 1680,E30..11,Educationally subnormal,1 1787,E30..00,"Mild mental retardation, IQ in range 50-70",1 4477,Eu81z11,[X]Learning disability NOS,1 4825,E311.00,"Severe mental retardation, IQ in range 20-34",1 6123,Eu71.00,[X]Moderate mental retardation,1 7226,Eu84.00,[X]Pervasive developmental disorders,1 10068,PKy8000,Noonan's syndrome,1 10628,PJyy200,Fragile X chromosome,1 10759,PJ0z.00,Down's syndrome NOS,1 10956,PKy9300,Prader - Willi syndrome,1 18415,PJ0..12,Trisomy 21,1 19038,PJ1z.11,Trisomy 13 NOS,1 19436,ZS34.11,Learning disability,1 21418,PKy6011,Cornelia de Lange syndrome,1 22760,918e.00,On learning disability register,1 23489,PJ0..11,Mongolism,1 25306,PKyz511,Angelman syndrome,1 27280,PKy0.12,Prader-Willi syndrome,1 27691,Eu72.11,[X]Severe mental subnormality,1 28740,Eu70.00,[X]Mild mental retardation,1 28962,Eu7..00,[X]Mental retardation,1 31042,Eu84200,[X]Rett's syndrome,1 31426,PKy1.00,Laurence-Moon-Biedl syndrome,1 31795,PJ31.00,Cri-du-chat syndrome,1 32010,PJ01.00,"Trisomy 21, mosaicism",1 32603,PJyy400,Fragile X syndrome,1 32820,Eu7zz00,[X]Unsp mental retardation without mention impairment behav,1 33390,C375112,hurler's syndrome,1 33642,PJ2..00,Edward's syndrome - trisomy 18,1 33948,PJ32.11,Wolff - Hirschorn syndrome,1 33949,Eu70.12,[X]Mild mental subnormality,1 34174,Eu84112,[X]Mental retardation with autistic features,1 34734,Eu71.11,[X]Moderate mental subnormality,1 35665,PJ1..00,Patau's syndrome - trisomy 13,1 36045,Eu81z13,[X]Learn acquisition disab NOS,1 36143,Eu72.00,[X]Severe mental retardation,1 36871,PJ33300,Smith-Magenis syndrome,1 37867,E3z..00,Mental retardation NOS,1 37887,Eu7z.11,[X]Mental deficiency NOS,1 37911,Eu7z.12,[X]Mental subnormality NOS,1 37924,PKy5F00,Coffin-Lowry syndrome,1 39016,Eu70y00,"[X]Mild mental retardation, other impairments of behaviour",1 39017,PJ2z.00,Edward's syndrome NOS,1 39412,Eu70100,[X]Mld mental retard sig impairment behav req attent/treatmt,1 41461,PKy0.11,Prader-Willi Syndrome,1 42520,Eu7yy00,"[X]Other mental retardation, other impairments of behaviour",1 42589,Eu7z.00,[X]Unspecified mental retardation,1 42701,PJ00.00,"Trisomy 21, meiotic nondisjunction",1 42886,Eu7z000,[X]Unsp mental retard with statement no or min impairm behav,1 44327,Eu84z00,"[X]Pervasive developmental disorder, unspecified",1 45133,E312.00,Profound mental retardation with IQ less than 20,1 46133,PJ12.00,"Trisomy 13, translocation",1 46504,Eu70000,[X]Mld mental retard with statement no or min impairm behav,1 46766,PKyz500,Happy puppet syndrome,1 46787,PJ2z.11,TRISOMY 18 NOS,1 47948,Eu84y00,[X]Other pervasive developmental disorders,1 50457,PKy6000,Amsterdam dwarf,1 50606,Eu70z00,[X]Mild mental retardation without mention impairment behav,1 50751,Eu72100,[X]Sev mental retard sig impairment behav req attent/treatmt,1 50947,Eu72000,[X]Sev mental retard with statement no or min impairm behav,1 51268,Eu73.00,[X]Profound mental retardation,1 51622,E312.11,Idiocy,1 51954,E30..12,Feeble-minded,1 52602,Eu84400,[X]Overactive disorder assoc mental retard/stereotype movts,1 54179,E31z.00,Other specified mental retardation NOS,1 54881,Eu71100,[X]Mod mental retard sig impairment behav req attent/treatmt,1 55560,Eu72z00,[X]Sev mental retardation without mention impairment behav,1 55848,Eu72y00,"[X]Severe mental retardation, other impairments of behaviour",1 56547,Eu7y100,[X]Oth mental retard sig impairment behav req attent/treatmt,1 56577,E31..00,Other specified mental retardation,1 57043,PKy6600,Dubowitz syndrome,1 57199,E3y..00,Other specified mental retardation,1 57458,PKy1.11,Biedl-Bardet syndrome,1 59407,Eu71y00,[X]Mod retard oth behav impair,1 60062,Eu73z00,[X]Prfnd mental retardation without mention impairment behav,1 60473,Eu71z00,[X]Mod mental retardation without mention impairment behav,1 60673,PKyz000,"Ullrich - Feichtiger syndrome, chimaera",1 60913,Eu71000,[X]Mod mental retard with statement no or min impairm behav,1 61322,PKyG.11,Ohdo blepharophimosis syndrome,1 61499,PJ02.00,"Trisomy 21, translocation",1 61627,PJ0z.11,Trisomy 21 NOS,1 63273,Eu7yz00,[X]Other mental retardation without mention impairment behav,1 65468,Eu73.11,[X]Profound mental subnormality,1 66383,Eu7zy00,"[X]Unspecified mental retardatn, other impairments of behav",1 66566,PJ32.00,Deletion of short arm of chromosome 4,1 66783,Eu7z100,[X]Unsp mentl retard sig impairment behav req attent/treatmt,1 70008,Eu7y000,[X]Oth mental retard with statement no or min impairm behav,1 70102,Eu73000,[X]Profound ment retrd wth statement no or min impairm behav,1 71196,Eu7y.00,[X]Other mental retardation,1 71632,E30..13,Moron,1 72265,PJ1z.00,Patau's syndrome NOS,1 72742,PKyG.00,Men ret congen heart dis blepharophim blepharop hypopl teeth,1 84154,Eu70.11,[X]Feeble-mindedness,1 89727,PKy0.13,Noonan's syndrome,1 90276,Eu73y00,"[X]Profound mental retardation, other impairments of behavr",1 93694,PJ9..00,Mowat-Wilson syndrome,1 97059,PKyz700,Angelman's syndrome,1 98100,Eu73100,[X]Profound ment retard sig impairmnt behav req attent/treat,1 98293,Eu81500,[X]Severe learning disability,1 98342,Eu81400,[X]Moderate learning disability,1 98617,PKyz711,Angelman syndrome,1 98941,PJ31.11,Deletion of short arm of chromosome 5,1 99652,PKyJ.00,Lujan-Fryns syndrome,1 99774,Eu81600,[X]Mild learning disability,1 100648,Eu81700,[X]Profound learning disability,1 101309,PJ02.11,Partial trisomy 21 in Down's syndrome,1 102102,PJ12.11,Partial trisomy 13 in Patau's syndrome,1 103891,C375.13,hurler's syndrome,1 105514,PJ33A00,Kleefstra syndrome,1 106590,PKy5K00,Cohen syndrome,1 107822,PKy6900,Borjeson-Forssman-Lehmann syndrome,1 107919,PJ01.11,"Trisomy 21, mitotic nondisjunction",1 107968,Eu81800,[X]Specific learning disability,1 108375,PG5F.00,Acrodysostosis,1