Intellectual disability

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Codelist metadata

Coding system

CTV3 (Read V3)

Coding system release

unknown

Organisation

OpenSAFELY

Codelist ID

opensafely/intellectual-disability

Version Tag

2020-08-27

Version ID

2c515838

Versions

  • 2020-08-27 Updated: 2023-11-28 16:39:47

About

Description

Codes for a history of intellectual/learning disability

Methodology

The following codes are prepared from CTV3 and expected to be used in general practices in records of people with intellectual/learning disability.

We are aware that some of the individual codes contained in this code list are offensive and upsetting. Although these terms are outdated we have chosen to still include them in the code list due to the historic nature of the data that is being analysed. Excluding these terms would reduce the completeness of the data and may mean that some people with a learning disability are not included in the analyses.

References

Signed off by

  • John Tazare, (Aug. 27, 2020)

Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.

We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.

CTV3ID CTV3PreferredTermDesc CTV3Source
6664. Mental handicap problem CTV3Map_Code_And_Term
C3911 DiGeorge syndrome High_Level_SNOMED
E1400 Active infantile autism CTV3Map_Code_And_Term
E1401 Residual infantile autism CTV3Map_Code_And_Term
E140z Infantile autism NOS CTV3Map_Code_And_Term
E141. Childhood disintegrative disorder CTV3Map_Code_And_Term
E141. Childhood disintegrative disorder CTV3Map_Code_Only
XaCKc Down's screening blood test abnormal CTV3Map_Code_And_Term
E1410 Active disintegrative psychoses CTV3_Children
E1411 Residual disintegrative psychoses CTV3_Children
E141z Disintegrative psychosis NOS CTV3_Children
E2F0. Specific reading disorder High_Level_SNOMED
E2F00 Reading disorder unspecified High_Level_SNOMED
E2F0z Specific reading disorder NOS High_Level_SNOMED
E2F3. (Develop disord: [language][speech]) or (articulatn defect) High_Level_SNOMED
E2F30 (Developmental aphasia) or (word deafness) High_Level_SNOMED
E2F3z Speech or language developmental disorder NOS High_Level_SNOMED
E2F5. Mixed disorder of psychological development High_Level_SNOMED
E3... Mental retardation CTV3Map_Code_And_Term
E3... Mental retardation CTV3Map_Code_Only
E30.. (Mild mental retard (& [feeble-mind][moron])) or (educ subn) CTV3_Children
E31.. Other specified mental retardation CTV3Map_Code_And_Term
E310. Moderate mental retardation, IQ in range 35-49 CTV3Map_Code_And_Term
E310. Moderate mental retardation, IQ in range 35-49 CTV3Map_Code_Only
E311. Severe mental retardation, IQ in range 20-34 CTV3Map_Code_And_Term
E311. Severe mental retardation, IQ in range 20-34 CTV3Map_Code_Only
E312. Profound mental retardation with IQ less than 20 CTV3Map_Code_And_Term
E312. Profound mental retardation with IQ less than 20 CTV3Map_Code_Only
E31z. Other specified mental retardation NOS CTV3Map_Code_And_Term
E3z.. Mental retardation NOS CTV3Map_Code_And_Term
Eu700 [X]Mld mental retard with statement no or min impairm behav CTV3Map_Code_And_Term
Eu701 [X]Mld mental retard sig impairment behav req attent/treatmt CTV3Map_Code_And_Term
Eu70y [X]Mild mental retardation, other impairments of behaviour CTV3Map_Code_And_Term
Eu70z [X]Mild mental retardation without mention impairment behav CTV3Map_Code_And_Term
Eu710 [X]Mod mental retard with statement no or min impairm behav CTV3Map_Code_And_Term
Eu711 [X]Mod mental retard sig impairment behav req attent/treatmt CTV3Map_Code_And_Term
Eu71y [X]Mod retard oth behav impair CTV3Map_Code_And_Term
Eu71z [X]Mod mental retardation without mention impairment behav CTV3Map_Code_And_Term
Eu720 [X]Sev mental retard with statement no or min impairm behav CTV3Map_Code_And_Term
Eu721 [X]Sev mental retard sig impairment behav req attent/treatmt CTV3Map_Code_And_Term
Eu72y [X]Severe mental retardation, other impairments of behaviour CTV3Map_Code_And_Term
Eu72z [X]Sev mental retardation without mention impairment behav CTV3Map_Code_And_Term
Eu730 [X]Profound ment retrd wth statement no or min impairm behav CTV3Map_Code_And_Term
Eu731 [X]Profound ment retard sig impairmnt behav req attent/treat CTV3Map_Code_And_Term
Eu73y [X]Profound mental retardation, other impairments of behavr CTV3Map_Code_And_Term
Eu73z [X]Prfnd mental retardation without mention impairment behav CTV3Map_Code_And_Term
Eu7y. [X]Other mental retardation CTV3Map_Code_And_Term
Eu7y0 [X]Oth mental retard with statement no or min impairm behav CTV3Map_Code_And_Term
Eu7y1 [X]Oth mental retard sig impairment behav req attent/treatmt CTV3Map_Code_And_Term
Eu7yy [X]Other mental retardation, other impairments of behaviour CTV3Map_Code_And_Term
Eu7yz [X]Other mental retardation without mention impairment behav CTV3Map_Code_And_Term
Eu7z. [X] (Unspec mental retard) or (mental defic [& subnorm] NOS) CTV3_Children
Eu7z0 [X]Unsp mental retard with statement no or min impairm behav CTV3Map_Code_And_Term
Eu7z1 [X]Unsp mentl retard sig impairment behav req attent/treatmt CTV3Map_Code_And_Term
Eu7zy [X]Unspecified mental retardatn, other impairments of behav CTV3Map_Code_And_Term
Eu7zz [X]Unsp mental retardation without mention impairment behav CTV3Map_Code_And_Term
Eu8.. Disorder of psychological development High_Level_SNOMED
Eu800 [X]Specific speech articulation disord (& [named variants]) High_Level_SNOMED
Eu801 [X]Expressive lang disord: [devel dysphasia][devel aphasia] High_Level_SNOMED
Eu802 [X] Receptive language disorder (& [named variants]) High_Level_SNOMED
Eu80y [X] (Other develop disord speech and language) or (lisping) High_Level_SNOMED
Eu80z [X]Developmental disorder speech &/or lang, unspecif or NOS High_Level_SNOMED
Eu81. [X]Specific developmental disorders of scholastic skills High_Level_SNOMED
Eu811 [X]Specific spelling disord (& [retardn, no reading disord]) High_Level_SNOMED
Eu813 Mixed disorder of scholastic skills High_Level_SNOMED
Eu81y [X]Devel disord scholastic skills: [oth][expressive writing] High_Level_SNOMED
Eu81z [X]Developmental disorder of scholastic skills, unspecified CTV3Map_Code_Only
Eu842 Rett syndrome CTV3_Children
Eu843 [X]Child disinteg dis:[oth][dement infantalis (& named var)] High_Level_SNOMED
Eu844 [X]Overactive disorder assoc mental retard/stereotype movts CTV3Map_Code_And_Term
Eu84y [X]Other pervasive developmental disorders CTV3_Children
Eu84z [X]Pervasive developmental disorder, unspecified CTV3Map_Code_Only
Eu8z. [X]Unspecified disorder of psychological development High_Level_SNOMED
F4B5C Posterior polymorphous corneal dystrophy High_Level_SNOMED
PJ0.. (Down's trisom 21) or (mongol) or (trisom 21) or (trisom 22) High_Level_SNOMED
PJ00. Trisomy 21- meiotic nondisjunction CTV3Map_Code_And_Term
PJ01. Trisomy 21- mitotic nondisjunction mosaicism CTV3Map_Code_And_Term
PJ01. Trisomy 21- mitotic nondisjunction mosaicism CTV3Map_Code_Only
PJ1.. Patau's syndrome CTV3Map_Code_And_Term
PJ10. Trisomy 13, meiotic nondisjunction CTV3Map_Code_And_Term
PJ11. Trisomy 13 - mitotic nondisjunction mosaicism CTV3Map_Code_And_Term
PJ11. Trisomy 13 - mitotic nondisjunction mosaicism CTV3Map_Code_Only
PJ2.. Edwards' syndrome CTV3Map_Code_And_Term
PJ20. Trisomy 18 - meiotic nondisjunction CTV3Map_Code_And_Term
PJ21. Trisomy 18 - mitotic nondisjunction mosaicism CTV3Map_Code_And_Term
PJ21. Trisomy 18 - mitotic nondisjunction mosaicism CTV3Map_Code_Only
PJ3.. Monosomy and deletion from autosome High_Level_SNOMED
PJ30. Antimongolism syndrome CTV3Map_Code_And_Term
PJ30. Antimongolism syndrome CTV3Map_Code_Only
PJ31. Cri du chat syndrome CTV3Map_Code_And_Term
PJ31. Cri du chat syndrome CTV3Map_Code_Only
PJ32. Deletion of short arm of chromosome 4 CTV3Map_Code_And_Term
PJ32. Deletion of short arm of chromosome 4 CTV3Map_Code_Only
PJ33. Other deletions of part of a chromosome High_Level_SNOMED
PJ330 Deletion of long arm of chromosome 13 CTV3Map_Code_And_Term
PJ331 Deletion of arm of chromosome 18: [long] or [p] CTV3_Children
PJ332 Deletion of arm of chromosome 18: [q] or [short] CTV3_Children
PJ33z Other deletion of part of a chromosome NOS High_Level_SNOMED
PJ34. Deletion seen only at prometaphase High_Level_SNOMED
PJ35. Deletions with other complex rearrangements High_Level_SNOMED
PJ36. Whole chromosome monosomy - meiotic nondisjunction CTV3Map_Code_And_Term
PJ37. (Whole chrom monosomy: [variants]) or (autosom delet mosaic) High_Level_SNOMED
PJ370 Monosomy 21, mosaicism High_Level_SNOMED
PJ37z Whole chromosome monosomy, mosaicism NOS CTV3Map_Code_And_Term
PJ3y. Other deletions from the autosomes High_Level_SNOMED
PJ3z. Monosomies and deletions from the autosomes NOS High_Level_SNOMED
PJ50. Whole chromosome trisomy syndrome CTV3Map_Code_And_Term
PJ501 Trisomy 7 CTV3Map_Code_And_Term
PJ502 Trisomy 8 CTV3Map_Code_And_Term
PJ503 Trisomy 9 CTV3Map_Code_And_Term
PJ503 Trisomy 9 CTV3Map_Code_Only
PJ504 Trisomy 10 High_Level_SNOMED
PJ506 Trisomy 12 CTV3Map_Code_And_Term
PJ508 Trisomy 22 CTV3Map_Code_And_Term
PJ508 Trisomy 22 CTV3Map_Code_Only
PJ50w Whole chromosome trisomy, meitotic nondisjunction CTV3Map_Code_And_Term
PJ50x Whole chromosome trisomy, mosaicism CTV3Map_Code_And_Term
PJ50x Whole chromosome trisomy, mosaicism CTV3Map_Code_Only
PJ50y Other specified whole chromosome trisomy syndrome CTV3Map_Code_And_Term
PJ50z Whole chromosome trisomy syndrome NOS CTV3Map_Code_And_Term
PJ510 Major partial trisomy CTV3Map_Code_And_Term
PJ523 Triploidy CTV3Map_Code_And_Term
PJ524 Polyploidy CTV3Map_Code_And_Term
PJ60. Mixed gonadal dysgenesis High_Level_SNOMED
PJ63. Turner's syndrome High_Level_SNOMED
PJ630 Turner's phenotype, karyotype normal High_Level_SNOMED
PJ631 Karyotype 45, X High_Level_SNOMED
PJ632 Karyotype 46, X iso (Xq) High_Level_SNOMED
PJ633 Karyotype 46, X with abnormal sex chromosome except iso (Xq) High_Level_SNOMED
PJ634 Turner's phenotype, mosaicism 45, X; 46, XX or 45, X; 46, XY High_Level_SNOMED
PJ635 Mosaicism 45, X/other cell line with abnormal sex chromosome High_Level_SNOMED
PJ636 Turner's phenotype: [variant karyotypes] High_Level_SNOMED
PJ63z (Turner syn NOS) or (Bonn-Ullr syn NOS) or (Ovar dwarf NEC) High_Level_SNOMED
PJ640 XY, female phenotype High_Level_SNOMED
PJ7.. Klinefelter's syndrome High_Level_SNOMED
PJ70. XXY Klinefelter's syndrome High_Level_SNOMED
PJ71. Klinefelter syndr: [male, more than 2 X chrom][ XXXY][XXXXY] High_Level_SNOMED
PJ72. Klinefelter's syndrome - male with 46 XX karyotype High_Level_SNOMED
PJ73. Klinefelter's syndrome, XXYY CTV3Map_Code_And_Term
PJ74. Klinefelter's syndrome, XY/XXY mosaic High_Level_SNOMED
PJ7z. Klinefelter's syndrome NOS High_Level_SNOMED
PJy0. Additional sex chromosome High_Level_SNOMED
PJy1. Sex chromosome mosaicism High_Level_SNOMED
PJy10 Mosaic XO/XY High_Level_SNOMED
PJy11 Mosaic XO/XX High_Level_SNOMED
PJy12 Mosaic XY/XXY High_Level_SNOMED
PJy13 Mosaic including XXXXY High_Level_SNOMED
PJy1z Sex chromosome mosaicism NOS High_Level_SNOMED
PJy2. Karyotype 47, XXX High_Level_SNOMED
PJy3. XXY Klinefelter's syndrome High_Level_SNOMED
PJyy2 Fragile X chromosome CTV3Map_Code_And_Term
PJz2. Deletion of chromosome NOS High_Level_SNOMED
PKy0. (Multi syst cong anom NEC) or (Prader-Willi) or (Noonan syn) High_Level_SNOMED
PKy1. Laurence-Moon-Biedl syndrome High_Level_SNOMED
PKy4. William syndrome CTV3Map_Code_And_Term
PKy61 Cockayne syndrome CTV3Map_Code_And_Term
PKy80 Noonan's syndrome CTV3Map_Code_Only
PKy92 Menkes syndrome CTV3Map_Code_And_Term
PKy92 Menkes syndrome CTV3Map_Code_Only
PKy93 Prader-Willi syndrome CTV3Map_Code_And_Term
PKy93 Prader-Willi syndrome CTV3Map_Code_Only
PKy94 Zellweger's syndrome CTV3Map_Code_And_Term
PKyz0 Ullrich-Feichtiger syndrome, chimaera CTV3Map_Code_And_Term
PKyz5 Angelman's syndrome CTV3Map_Code_And_Term
PKyz5 Angelman's syndrome CTV3Map_Code_Only
PyuA1 [X]Other deletions of part of a chromosome High_Level_SNOMED
PyuA2 [X]Other deletions from the autosomes High_Level_SNOMED
PyuA5 [X]Other variants of Turner's syndrome High_Level_SNOMED
PyuA6 [X]Other specif sex chromosome abnormalit, female phenotype High_Level_SNOMED
PyuA7 [X]Other male with 46,XX karyotype High_Level_SNOMED
PyuA8 [X]Other specif sex chromosome abnormalit, male phenotype High_Level_SNOMED
PyuAA [X]Sex chromosome abnormality, male phenotype, unspecified High_Level_SNOMED
R034y [D]Other specified failure of physiological development CTV3Map_Code_And_Term
R034y [D]Other specified failure of physiological development CTV3Map_Code_Only
Ub1S3 Dysfluency High_Level_SNOMED
Ub1S4 Developmental dysfluency High_Level_SNOMED
Ub1SD Neurogenic stammering High_Level_SNOMED
Ub1TK Motor speech disorder High_Level_SNOMED
Ub1Td Articulatory dyspraxia High_Level_SNOMED
Ub1Te Immature articulatory praxis High_Level_SNOMED
Ub1Tf Developmental motor speech disorder High_Level_SNOMED
Ub1Tg Developmental articulatory dyspraxia High_Level_SNOMED
Ub1Ts Idiot savant CTV3_Children
Ub1Tw Persistent developmental avoidance High_Level_SNOMED
Ub1U0 Developmental speech disorder High_Level_SNOMED
Ub1U6 Speech delay High_Level_SNOMED
Ub1UG Developmental language impairment High_Level_SNOMED
Ub1UL Expressive language disorder High_Level_SNOMED
Ub1UM Expressive language delay High_Level_SNOMED
Ub1UO Receptive language delay High_Level_SNOMED
Ub1UR Developmental language disorder High_Level_SNOMED
Ub1US Delayed pre-verbal development High_Level_SNOMED
Ub1UT Restricted language development High_Level_SNOMED
Ub1UU Restricted expressive language development High_Level_SNOMED
Ub1UV Restricted receptive language development High_Level_SNOMED
Ub1UW Developmental syntactic impairment High_Level_SNOMED
Ub1UX Developmental semantic impairment High_Level_SNOMED
Ub1Ua Congenital auditory imperception High_Level_SNOMED
X005S Rett syndrome CTV3Map_Code_And_Term
X006o Acquired epileptic aphasia High_Level_SNOMED
X00TK Language development disorder High_Level_SNOMED
X00TL Developmental disorder of scholastic skill High_Level_SNOMED
X00TM Autistic spectrum disorder CTV3Map_Code_And_Term
X00TM Autistic spectrum disorder CTV3Map_Code_Only
X00TN Atypical autism CTV3Map_Code_And_Term
X00TN Atypical autism CTV3Map_Code_Only
X00TP Asperger syndrome CTV3_Children
X00TQ Developmental agnosia High_Level_SNOMED
X00e1 Laurence-Moon syndrome High_Level_SNOMED
X00kY Cat eye syndrome High_Level_SNOMED
X00mm Shprintzen syndrome CTV3Map_Code_And_Term
X00mm Shprintzen syndrome CTV3Map_Code_Only
X40Xn Nutritional mental retardation High_Level_SNOMED
X50HX Coffin-Siris syndrome High_Level_SNOMED
X50Hu Amelocerebrohypohidrotic syndrome High_Level_SNOMED
X50In Keratoderma with mental retardation and spastic paraplegia High_Level_SNOMED
X77q7 Local gigantism NEC CTV3Map_Code_Only
X78Ek Down's syndrome NOS CTV3Map_Code_And_Term
X78Ek Down's syndrome NOS CTV3Map_Code_Only
X78El Partial trisomy 21 in Down's syndrome CTV3Map_Code_And_Term
X78El Partial trisomy 21 in Down's syndrome CTV3Map_Code_Only
X78Em Edward's syndrome NOS CTV3Map_Code_And_Term
X78Em Edward's syndrome NOS CTV3Map_Code_Only
X78En Partial trisomy 18 in Edward's syndrome CTV3Map_Code_And_Term
X78En Partial trisomy 18 in Edward's syndrome CTV3Map_Code_Only
X78Eo Patau's syndrome NOS CTV3Map_Code_And_Term
X78Eo Patau's syndrome NOS CTV3Map_Code_Only
X78Ep Partial trisomy 13 in Patau's syndrome CTV3Map_Code_And_Term
X78Ep Partial trisomy 13 in Patau's syndrome CTV3Map_Code_Only
X78Et Autosomal deletion - mosaicism CTV3Map_Code_Only
X78Eu Deletion of part of autosome High_Level_SNOMED
X78Ex Sex chromosome abnormality - female phenotype High_Level_SNOMED
X78Ey Ovarian dwarfism NEC High_Level_SNOMED
X78Ez Bonnevie-Ullrich syndrome NOS High_Level_SNOMED
X78F0 Turner's phenotype, partial X deletion karyotype CTV3Map_Code_Only
X78F1 Mosaicism 45, X; 46, XY High_Level_SNOMED
X78F2 Turner's phenotype - ring chromosome karyotype CTV3Map_Code_And_Term
X78F3 Female with more than three X chromosomes High_Level_SNOMED
X78F4 Mosaicism - lines with various numbers of X chromosomes High_Level_SNOMED
X78F5 Female with 46 XY karyotype High_Level_SNOMED
X78F6 Sex chromosome abnormality - male phenotype High_Level_SNOMED
X78F7 Male with 46, XX karyotype High_Level_SNOMED
X78F8 Karyotype 47, XYY High_Level_SNOMED
X78F9 Male with structurally abnormal sex chromosome High_Level_SNOMED
X78FA Male with sex chromosome mosaicism High_Level_SNOMED
X78FB Fragile X syndrome CTV3Map_Code_And_Term
X78FC FRAXA CTV3_Children
X78FD FRAXE CTV3_Children
XE0pf Relative - mental handicap CTV3Map_Code_Only
XE1MZ Down's syndrome CTV3Map_Code_And_Term
XE1MZ Down's syndrome CTV3Map_Code_Only
XE1Ma Chromosome replaced with ring or dicentric CTV3Map_Code_And_Term
XE1Ma Chromosome replaced with ring or dicentric CTV3Map_Code_Only
XE1Me Turner's phenotype, other variant karyotypes CTV3Map_Code_Only
XE1Mf Turner's syndrome NOS High_Level_SNOMED
XE1Mg Klinefelter's syndrome-male with more than two X chromosomes CTV3Map_Code_And_Term
XE1Mg Klinefelter's syndrome-male with more than two X chromosomes CTV3Map_Code_Only
XE1Ml Multiple system congenital anomalies NEC CTV3Map_Code_Only
XE1Mm Other specified anomalies NOS CTV3Map_Code_Only
XE1OW (Gonadal dysgenesis (& Turner)) or Turner's syndrome High_Level_SNOMED
XE1OY (Patau's syndrome) or (Klinefelter's syndrome) High_Level_SNOMED
XE1Z3 Disorder of speech and language development High_Level_SNOMED
XE1Z4 Developmental aphasia High_Level_SNOMED
XE1a2 [X]Unspecified mental retardation CTV3Map_Code_And_Term
XE1a2 [X]Unspecified mental retardation CTV3Map_Code_Only
XE1a3 Developmental speech articulation disorder High_Level_SNOMED
XE1a4 Developmental expressive language disorder High_Level_SNOMED
XE1a5 [X]Receptive language disorder High_Level_SNOMED
XE1a6 [X]Other developmental disorders of speech and language High_Level_SNOMED
XE1a7 [X]Developmental disorder of speech and language unspecified High_Level_SNOMED
XE1a8 Specific spelling disorder High_Level_SNOMED
XE1a9 [X]Other developmental disorders of scholastic skills High_Level_SNOMED
XE1aA [X]Other childhood disintegrative disorder CTV3Map_Code_And_Term
XE1aA [X]Other childhood disintegrative disorder CTV3Map_Code_Only
XE1bk (Developm aphasia) or (delayed speech) or (speech delay) High_Level_SNOMED
XE2R1 Whole chromosome monosomy - mitotic nondisjunction mosaicism CTV3Map_Code_And_Term
XE2R1 Whole chromosome monosomy - mitotic nondisjunction mosaicism CTV3Map_Code_Only
XE2a3 Mild mental retardation, IQ in range 50-70 CTV3Map_Code_And_Term
XE2a3 Mild mental retardation, IQ in range 50-70 CTV3Map_Code_Only
XE2ac Deletion of long arm of chromosome 18 CTV3Map_Code_And_Term
XE2ac Deletion of long arm of chromosome 18 CTV3Map_Code_Only
XE2ad Deletion of short arm of chromosome 18 CTV3Map_Code_And_Term
XE2ad Deletion of short arm of chromosome 18 CTV3Map_Code_Only
XE2v2 Childhood autism CTV3Map_Code_And_Term
XE2v2 Childhood autism CTV3Map_Code_Only
XM1FU Deletion with complex rearrangement High_Level_SNOMED
XM1KI Family - [Downs/Mongol child] CTV3_Children
XM1MJ Klinefelter's syndrome XXXY CTV3Map_Code_And_Term
XM1MJ Klinefelter's syndrome XXXY CTV3Map_Code_Only
XM1MK Klinefelter's syndrome XXXXY CTV3Map_Code_And_Term
XM1MK Klinefelter's syndrome XXXXY CTV3Map_Code_Only
XSDcM 11q partial monosomy syndrome CTV3Map_Code_And_Term
XSDcU Pallister-Killian syndrome High_Level_SNOMED
Xa0ER Educationally subnormal CTV3Map_Code_And_Term
Xa0ER Educationally subnormal CTV3Map_Code_Only
Xa0Yy Alpha thalassaemia-mental retardation syndrome High_Level_SNOMED
Xa0ZS Schprintzen High_Level_SNOMED
Xa0Zb Borjeson-Forssman-Lehmann syndrome High_Level_SNOMED
Xa0Ze Weaver syndrome CTV3Map_Code_And_Term
Xa1aW Borderline mental retardation CTV3_Children
Xa1c5 Down's child in family CTV3Map_Code_And_Term
Xa1c5 Down's child in family CTV3Map_Code_Only
Xa3HI Severely educationally subnormal CTV3_Children
Xa9D6 Mosaicism 45, X; 46, XX High_Level_SNOMED
XaCar Discourse difficulties High_Level_SNOMED
XaDjY Floating-Harbor syndrome High_Level_SNOMED
XaDki Men ret congen heart dis blepharophim blepharop hypopl teeth High_Level_SNOMED
XaIUM O/E - speech delay High_Level_SNOMED
XaIwZ Smith-Magenis syndrome CTV3Map_Code_And_Term
XaJJM Suspected Downs syndrome CTV3Map_Code_And_Term
XaJW7 Learning disabilities administration status CTV3Map_Code_And_Term
XaJW8 Learning disabilities health action plan offered CTV3Map_Code_And_Term
XaJW9 Learning disabilities health action plan declined CTV3Map_Code_And_Term
XaJWA Learning disabilities health action plan reviewed CTV3Map_Code_And_Term
XaJmb Learning disabilities health assessment CTV3Map_Code_And_Term
XaJmd Discharge from learning disability team CTV3Map_Code_And_Term
XaJsd Learning disabilities health action plan completed CTV3Map_Code_And_Term
XaKYb On learning disability register CTV3Map_Code_And_Term
XaKYj [D]Dysfluency High_Level_SNOMED
XaL2A [X]Cocktail party syndrome High_Level_SNOMED
XaL2v Lujan-Fryns syndrome High_Level_SNOMED
XaL3Q Learning disabilities annual health assessment CTV3Map_Code_And_Term
XaLKE Seen in learning disabilities clinic CTV3Map_Code_And_Term
XaNWy Mowat-Wilson syndrome CTV3Map_Code_And_Term
XaPx2 Learning disability health examination CTV3Map_Code_And_Term
XaQZ3 Moderate learning disability High_Level_SNOMED
XaQZ4 Severe learning disability High_Level_SNOMED
XaREt Mild learning disability High_Level_SNOMED
XaREu Profound learning disability High_Level_SNOMED
XaXOz Downs syndrome antenatal screening information leaflet given CTV3Map_Code_And_Term
XaYQ0 Chromosome 22q11 deletion syndrome High_Level_SNOMED
XaYQ1 Chromosome 3p deletion syndrome High_Level_SNOMED
XaYQ2 Chromosome 4q deletion syndrome High_Level_SNOMED
XaYQ3 10q partial trisomy syndrome High_Level_SNOMED
XaYQU 4p partial trisomy syndrome High_Level_SNOMED
XaYQb 9p partial trisomy syndrome High_Level_SNOMED
XaYQe 15q partial trisomy syndrome High_Level_SNOMED
XaYYN Kleefstra syndrome High_Level_SNOMED
XaaLb Methyl-CpG-binding protein-2 duplication syndrome High_Level_SNOMED
Xaaa7 Ulnar mammary syndrome High_Level_SNOMED
XaaiS Specific learning disability High_Level_SNOMED
Xabk1 Significant learning disability High_Level_SNOMED
XacF6 Intellectual development disorder of unknown aetiology High_Level_SNOMED
XacKx Developmental receptive language impairment High_Level_SNOMED
XacL0 Developmental language comprehension impairment High_Level_SNOMED
XaesO Pathological demand avoidance CTV3_Children
Y1642 Other Mental Disability CTV3_Children
Y2916 Autistic spectrum disorder - Gluten-casein intolerance checklist CTV3_Children
Y2917 Autistic spectrum disorder - Autism checklist CTV3_Children
Y9981 Profound mental retardation CTV3_Children
YA841 Severe learning disability CTV3_Children

Codes not in the full codelist are in faint grey.