Mental and behavioural disorders
Codelist metadata
-
Coding system
- CTV3 (Read V3)
-
Coding system release
- unknown
-
Organisation
- Office for National Statistics
-
Codelist ID
- ons/mental-and-behavioural-disorders
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Version ID
- 29cebc01
Versions
About
No metadata has been provided for this codelist.
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.
| code | term |
|---|---|
| 1461. | H/O: dementia |
| 6664. | Mental handicap problem |
| A410. | Kuru |
| A411. | Creutzfeldt-Jakob disease |
| C3911 | DiGeorge syndrome |
| E00.. | Senile and presenile organic psychot conditions (& dementia) |
| E000. | Uncomplicated senile dementia |
| E001. | Presenile dementia |
| E0010 | Uncomplicated presenile dementia |
| E0011 | Presenile dementia with delirium |
| E0012 | Presenile dementia with paranoia |
| E0013 | Presenile dementia with depression |
| E001z | Presenile dementia NOS |
| E002. | Senile dementia with depressive or paranoid features |
| E0020 | Senile dementia with paranoia |
| E0021 | Senile dementia with depression |
| E002z | Senile dementia with depressive or paranoid features NOS |
| E003. | Senile dementia with delirium |
| E004. | Arteriosclerotic dementia (including [multi infarct dement]) |
| E0040 | Uncomplicated arteriosclerotic dementia |
| E0041 | Arteriosclerotic dementia with delirium |
| E0042 | Arteriosclerotic dementia with paranoia |
| E0043 | Arteriosclerotic dementia with depression |
| E004z | Arteriosclerotic dementia NOS |
| E00y. | (Oth senile/presen org psychoses) or (presbyophren psychos) |
| E00z. | Senile or presenile psychoses NOS |
| E011. | Korsakov psychosis |
| E0110 | Korsakov psychosis |
| E0111 | Korsakov's alcoholic psychosis with peripheral neuritis |
| E0112 | Wernicke-Korsakov syndrome |
| E011z | Alcohol amnestic syndrome NOS |
| E012. | Alcoholic dementia: [other] or [NOS] |
| E040. | Korsakoff's syndrome - non-alcoholic |
| E041. | Dementia in conditions EC |
| E1400 | Active infantile autism |
| E1401 | Residual infantile autism |
| E140z | Infantile autism NOS |
| E141. | Childhood disintegrative disorder |
| E1410 | Active disintegrative psychoses |
| E1411 | Residual disintegrative psychoses |
| E141z | Disintegrative psychosis NOS |
| E2F0. | Specific reading disorder |
| E2F00 | Reading disorder unspecified |
| E2F0z | Specific reading disorder NOS |
| E2F3. | (Develop disord: [language][speech]) or (articulatn defect) |
| E2F30 | (Developmental aphasia) or (word deafness) |
| E2F3z | Speech or language developmental disorder NOS |
| E2F5. | Mixed disorder of psychological development |
| E3... | Learning disability |
| E30.. | (Mild mental retard (& [feeble-mind][moron])) or (educ subn) |
| E31.. | Other specified mental retardation |
| E310. | Moderate mental retardation, IQ in range 35-49 |
| E311. | Severe mental retardation, IQ in range 20-34 |
| E312. | Profound mental retardation with IQ less than 20 |
| E31z. | Other specified mental retardation NOS |
| E3z.. | Mental retardation NOS |
| Eu00. | [X]Dementia in Alzheimer's disease |
| Eu001 | Dementia in Alzheimer's disease with late onset |
| Eu002 | [X]Dementia in Alzheimer's dis, atypical or mixed type |
| Eu00z | [X]Dementia in Alzheimer's disease, unspecified |
| Eu01. | Vascular dementia |
| Eu011 | [X]Dementia: [multi-infarct] or [predominantly cortical] |
| Eu01y | [X]Other vascular dementia |
| Eu01z | [X]Vascular dementia, unspecified |
| Eu02. | [X]Dementia in other diseases classified elsewhere |
| Eu020 | [X]Dementia in Pick's disease |
| Eu021 | [X]Dementia in Creutzfeldt-Jakob disease |
| Eu022 | [X]Dementia in Huntington's disease |
| Eu023 | [X]Dementia in Parkinson's disease |
| Eu02y | [X]Dementia in other specified diseases classif elsewhere |
| Eu02z | [X] Dementia: [unspecified] or [named variants (& NOS)] |
| Eu041 | [X]Delirium superimposed on dementia |
| Eu700 | [X]Mld mental retard with statement no or min impairm behav |
| Eu701 | [X]Mld mental retard sig impairment behav req attent/treatmt |
| Eu70y | [X]Mild mental retardation, other impairments of behaviour |
| Eu70z | [X]Mild mental retardation without mention impairment behav |
| Eu710 | [X]Mod mental retard with statement no or min impairm behav |
| Eu711 | [X]Mod mental retard sig impairment behav req attent/treatmt |
| Eu71y | [X]Mod retard oth behav impair |
| Eu71z | [X]Mod mental retardation without mention impairment behav |
| Eu720 | [X]Sev mental retard with statement no or min impairm behav |
| Eu721 | [X]Sev mental retard sig impairment behav req attent/treatmt |
| Eu72y | [X]Severe mental retardation, other impairments of behaviour |
| Eu72z | [X]Sev mental retardation without mention impairment behav |
| Eu730 | [X]Profound ment retrd wth statement no or min impairm behav |
| Eu731 | [X]Profound ment retard sig impairmnt behav req attent/treat |
| Eu73y | [X]Profound mental retardation, other impairments of behavr |
| Eu73z | [X]Prfnd mental retardation without mention impairment behav |
| Eu7y. | [X]Other mental retardation |
| Eu7y0 | [X]Oth mental retard with statement no or min impairm behav |
| Eu7y1 | [X]Oth mental retard sig impairment behav req attent/treatmt |
| Eu7yy | [X]Other mental retardation, other impairments of behaviour |
| Eu7yz | [X]Other mental retardation without mention impairment behav |
| Eu7z. | [X] (Unspec mental retard) or (mental defic [& subnorm] NOS) |
| Eu7z0 | [X]Unsp mental retard with statement no or min impairm behav |
| Eu7z1 | [X]Unsp mentl retard sig impairment behav req attent/treatmt |
| Eu7zy | [X]Unspecified mental retardatn, other impairments of behav |
| Eu7zz | [X]Unsp mental retardation without mention impairment behav |
| Eu8.. | Disorder of psychological development |
| Eu800 | [X]Specific speech articulation disord (& [named variants]) |
| Eu801 | [X]Expressive lang disord: [devel dysphasia][devel aphasia] |
| Eu802 | [X] Receptive language disorder (& [named variants]) |
| Eu80y | [X] (Other develop disord speech and language) or (lisping) |
| Eu80z | [X]Developmental disorder speech &/or lang, unspecif or NOS |
| Eu81. | [X]Specific developmental disorders of scholastic skills |
| Eu811 | [X]Specific spelling disord (& [retardn, no reading disord]) |
| Eu813 | Mixed disorder of scholastic skills |
| Eu81y | [X]Devel disord scholastic skills: [oth][expressive writing] |
| Eu81z | [X]Developmental disorder of scholastic skills, unspecified |
| Eu842 | Rett syndrome |
| Eu843 | [X]Child disinteg dis:[oth][dement infantalis (& named var)] |
| Eu844 | [X]Overactive disorder assoc mental retard/stereotype movts |
| Eu84y | [X]Other pervasive developmental disorders |
| Eu84z | [X]Pervasive developmental disorder, unspecified |
| Eu8z. | [X]Unspecified disorder of psychological development |
| F110. | Alzheimer's disease |
| F1100 | Dementia in Alzheimer's disease with early onset |
| F1101 | Dementia in Alzheimer's disease with late onset |
| F111. | Pick's disease |
| F11x7 | Cerebral degeneration due to Creutzfeldt-Jakob disease |
| F11x8 | Cerebral degeneration due to multifocal leucoencephalopathy |
| F21y2 | Binswanger's disease |
| F4B5C | Posterior polymorphous corneal dystrophy |
| Fyu30 | [X]Other Alzheimer's disease |
| PJ0.. | (Down's trisom 21) or (mongol) or (trisom 21) or (trisom 22) |
| PJ00. | Trisomy 21- meiotic nondisjunction |
| PJ01. | Trisomy 21- mitotic nondisjunction mosaicism |
| PJ1.. | Patau's syndrome |
| PJ10. | Trisomy 13, meiotic nondisjunction |
| PJ11. | Trisomy 13 - mitotic nondisjunction mosaicism |
| PJ2.. | Edwards' syndrome |
| PJ20. | Trisomy 18 - meiotic nondisjunction |
| PJ21. | Trisomy 18 - mitotic nondisjunction mosaicism |
| PJ3.. | Monosomy and deletion from autosome |
| PJ30. | Antimongolism syndrome |
| PJ31. | Cri du chat syndrome |
| PJ32. | Deletion of short arm of chromosome 4 |
| PJ33. | Other deletions of part of a chromosome |
| PJ330 | Deletion of long arm of chromosome 13 |
| PJ331 | Deletion of arm of chromosome 18: [long] or [p] |
| PJ332 | Deletion of arm of chromosome 18: [q] or [short] |
| PJ33z | Other deletion of part of a chromosome NOS |
| PJ34. | Deletion seen only at prometaphase |
| PJ35. | Deletions with other complex rearrangements |
| PJ36. | Whole chromosome monosomy - meiotic nondisjunction |
| PJ37. | (Whole chrom monosomy: [variants]) or (autosom delet mosaic) |
| PJ370 | Monosomy 21, mosaicism |
| PJ37z | Whole chromosome monosomy, mosaicism NOS |
| PJ3y. | Other deletions from the autosomes |
| PJ3z. | Monosomies and deletions from the autosomes NOS |
| PJ50. | Whole chromosome trisomy syndrome |
| PJ501 | Trisomy 7 |
| PJ502 | Trisomy 8 |
| PJ503 | Trisomy 9 |
| PJ504 | Trisomy 10 |
| PJ506 | Trisomy 12 |
| PJ508 | Trisomy 22 |
| PJ50w | Whole chromosome trisomy, meitotic nondisjunction |
| PJ50x | Whole chromosome trisomy, mosaicism |
| PJ50y | Other specified whole chromosome trisomy syndrome |
| PJ50z | Whole chromosome trisomy syndrome NOS |
| PJ510 | Major partial trisomy |
| PJ523 | Triploidy |
| PJ524 | Polyploidy |
| PJ60. | Mixed gonadal dysgenesis |
| PJ63. | Turner's syndrome |
| PJ630 | Turner's phenotype, karyotype normal |
| PJ631 | Karyotype 45, X |
| PJ632 | Karyotype 46, X iso (Xq) |
| PJ633 | Karyotype 46, X with abnormal sex chromosome except iso (Xq) |
| PJ634 | Turner's phenotype, mosaicism 45, X; 46, XX or 45, X; 46, XY |
| PJ635 | Mosaicism 45, X/other cell line with abnormal sex chromosome |
| PJ636 | Turner's phenotype: [variant karyotypes] |
| PJ63z | (Turner syn NOS) or (Bonn-Ullr syn NOS) or (Ovar dwarf NEC) |
| PJ640 | XY, female phenotype |
| PJ7.. | Klinefelter's syndrome |
| PJ70. | XXY Klinefelter's syndrome |
| PJ71. | Klinefelter syndr: [male, more than 2 X chrom][ XXXY][XXXXY] |
| PJ72. | Klinefelter's syndrome - male with 46 XX karyotype |
| PJ73. | Klinefelter's syndrome, XXYY |
| PJ74. | Klinefelter's syndrome, XY/XXY mosaic |
| PJ7z. | Klinefelter's syndrome NOS |
| PJy0. | Additional sex chromosome |
| PJy1. | Sex chromosome mosaicism |
| PJy10 | Mosaic XO/XY |
| PJy11 | Mosaic XO/XX |
| PJy12 | Mosaic XY/XXY |
| PJy13 | Mosaic including XXXXY |
| PJy1z | Sex chromosome mosaicism NOS |
| PJy2. | Karyotype 47, XXX |
| PJy3. | XXY Klinefelter's syndrome |
| PJyy2 | Fragile X chromosome |
| PJz2. | Deletion of chromosome NOS |
| PKy0. | (Multi syst cong anom NEC) or (Prader-Willi) or (Noonan syn) |
| PKy1. | Laurence-Moon-Biedl syndrome |
| PKy4. | William syndrome |
| PKy61 | Cockayne syndrome |
| PKy80 | Noonan's syndrome |
| PKy92 | Menkes syndrome |
| PKy93 | Prader-Willi syndrome |
| PKy94 | Zellweger's syndrome |
| PKyz0 | Ullrich-Feichtiger syndrome, chimaera |
| PKyz5 | Angelman's syndrome |
| PyuA1 | [X]Other deletions of part of a chromosome |
| PyuA2 | [X]Other deletions from the autosomes |
| PyuA5 | [X]Other variants of Turner's syndrome |
| PyuA6 | [X]Other specif sex chromosome abnormalit, female phenotype |
| PyuA7 | [X]Other male with 46,XX karyotype |
| PyuA8 | [X]Other specif sex chromosome abnormalit, male phenotype |
| PyuAA | [X]Sex chromosome abnormality, male phenotype, unspecified |
| R034y | [D]Other specified failure of physiological development |
| Ub1S3 | Dysfluency |
| Ub1S4 | Developmental dysfluency |
| Ub1SD | Neurogenic stammering |
| Ub1T6 | Language disorder of dementia |
| Ub1TK | Motor speech disorder |
| Ub1Td | Articulatory dyspraxia |
| Ub1Te | Immature articulatory praxis |
| Ub1Tf | Developmental motor speech disorder |
| Ub1Tg | Developmental articulatory dyspraxia |
| Ub1Ts | Idiot savant |
| Ub1Tw | Persistent developmental avoidance |
| Ub1U0 | Developmental speech disorder |
| Ub1U6 | Speech delay |
| Ub1UG | Developmental language impairment |
| Ub1UL | Expressive language disorder |
| Ub1UM | Expressive language delay |
| Ub1UO | Receptive language delay |
| Ub1UR | Developmental language disorder |
| Ub1US | Delayed pre-verbal development |
| Ub1UT | Restricted language development |
| Ub1UU | Restricted expressive language development |
| Ub1UV | Restricted receptive language development |
| Ub1UW | Developmental syntactic impairment |
| Ub1UX | Developmental semantic impairment |
| Ub1Ua | Congenital auditory imperception |
| X002m | Amyotrophic lateral sclerosis with dementia |
| X002w | Dementia |
| X002x | Dementia in Alzheimer's disease with early onset |
| X002y | Familial Alzheimer's disease of early onset |
| X002z | Non-familial Alzheimer's disease of early onset |
| X0030 | Dementia in Alzheimer's disease with late onset |
| X0031 | Familial Alzheimer's disease of late onset |
| X0032 | Non-familial Alzheimer's disease of late onset |
| X0033 | Focal Alzheimer's disease |
| X0034 | Frontotemporal dementia |
| X0035 | Pick's disease with Pick bodies |
| X0036 | Pick's disease with Pick cells and no Pick bodies |
| X0037 | Frontotemporal degeneration |
| X0039 | Frontal lobe degeneration with motor neurone disease |
| X003A | Lewy body disease |
| X003G | Progressive aphasia in Alzheimer's disease |
| X003H | Argyrophilic brain disease |
| X003I | Post-traumatic dementia |
| X003J | Punch drunk syndrome |
| X003K | Spongiform encephalopathy |
| X003L | Prion protein disease |
| X003M | Gerstmann-Straussler-Scheinker syndrome |
| X003P | Acquired immune deficiency syndrome dementia complex |
| X003R | Vascular dementia of acute onset |
| X003T | Subcortical vascular dementia |
| X003V | Mixed cortical and subcortical vascular dementia |
| X003W | Semantic dementia |
| X003X | Patchy dementia |
| X003Y | Epileptic dementia |
| X003l | Parkinson's disease - dementia complex on Guam |
| X005S | Rett syndrome |
| X006o | Acquired epileptic aphasia |
| X00R0 | Presbyophrenic psychosis |
| X00R2 | Senile dementia |
| X00Rk | Alcoholic dementia NOS |
| X00TK | Language development disorder |
| X00TL | Developmental disorder of scholastic skill |
| X00TM | Autistic spectrum disorder |
| X00TN | Atypical autism |
| X00TP | Asperger syndrome |
| X00TQ | Developmental agnosia |
| X00e1 | Laurence-Moon syndrome |
| X00kY | Cat eye syndrome |
| X00mm | Shprintzen syndrome |
| X40Xn | Nutritional mental retardation |
| X50HX | Coffin-Siris syndrome |
| X50Hu | Amelocerebrohypohidrotic syndrome |
| X50In | Keratoderma with mental retardation and spastic paraplegia |
| X73mf | Creutzfeldt-Jakob disease agent |
| X73mj | Bovine spongiform encephalopathy agent |
| X77q7 | Local gigantism NEC |
| X78Ek | Down's syndrome NOS |
| X78El | Partial trisomy 21 in Down's syndrome |
| X78Em | Edward's syndrome NOS |
| X78En | Partial trisomy 18 in Edward's syndrome |
| X78Eo | Patau's syndrome NOS |
| X78Ep | Partial trisomy 13 in Patau's syndrome |
| X78Et | Autosomal deletion - mosaicism |
| X78Eu | Deletion of part of autosome |
| X78Ex | Sex chromosome abnormality - female phenotype |
| X78Ey | Ovarian dwarfism NEC |
| X78Ez | Bonnevie-Ullrich syndrome NOS |
| X78F0 | Turner's phenotype, partial X deletion karyotype |
| X78F1 | Mosaicism 45, X; 46, XY |
| X78F2 | Turner's phenotype - ring chromosome karyotype |
| X78F3 | Female with more than three X chromosomes |
| X78F4 | Mosaicism - lines with various numbers of X chromosomes |
| X78F5 | Female with 46 XY karyotype |
| X78F6 | Sex chromosome abnormality - male phenotype |
| X78F7 | Male with 46, XX karyotype |
| X78F8 | Karyotype 47, XYY |
| X78F9 | Male with structurally abnormal sex chromosome |
| X78FA | Male with sex chromosome mosaicism |
| X78FB | Fragile X syndrome |
| X78FC | FRAXA |
| X78FD | FRAXE |
| XE0pf | Relative - mental handicap |
| XE1MZ | Down's syndrome |
| XE1Ma | Chromosome replaced with ring or dicentric |
| XE1Me | Turner's phenotype, other variant karyotypes |
| XE1Mf | Turner's syndrome NOS |
| XE1Mg | Klinefelter's syndrome-male with more than two X chromosomes |
| XE1Ml | Multiple system congenital anomalies NEC |
| XE1Mm | Other specified anomalies NOS |
| XE1OW | (Gonadal dysgenesis (& Turner)) or Turner's syndrome |
| XE1OY | (Patau's syndrome) or (Klinefelter's syndrome) |
| XE1Xr | Senile and presenile organic psychotic conditions |
| XE1Xs | Vascular dementia |
| XE1Xt | Other senile and presenile organic psychoses |
| XE1Xu | Other alcoholic dementia |
| XE1Z3 | Disorder of speech and language development |
| XE1Z4 | Developmental aphasia |
| XE1Z6 | [X]Unspecified dementia |
| XE1a2 | [X]Unspecified mental retardation |
| XE1a3 | Developmental speech articulation disorder |
| XE1a4 | Developmental expressive language disorder |
| XE1a5 | [X]Receptive language disorder |
| XE1a6 | [X]Other developmental disorders of speech and language |
| XE1a7 | [X]Developmental disorder of speech and language unspecified |
| XE1a8 | Specific spelling disorder |
| XE1a9 | [X]Other developmental disorders of scholastic skills |
| XE1aA | [X]Other childhood disintegrative disorder |
| XE1aG | Dementia (& [presenile] or [senile]) |
| XE1bk | (Developm aphasia) or (delayed speech) or (speech delay) |
| XE2R1 | Whole chromosome monosomy - mitotic nondisjunction mosaicism |
| XE2a3 | Mild mental retardation, IQ in range 50-70 |
| XE2ac | Deletion of long arm of chromosome 18 |
| XE2ad | Deletion of short arm of chromosome 18 |
| XE2v2 | Childhood autism |
| XM1FU | Deletion with complex rearrangement |
| XM1KI | Family - [Downs/Mongol child] |
| XM1MJ | Klinefelter's syndrome XXXY |
| XM1MK | Klinefelter's syndrome XXXXY |
| XSDcM | 11q partial monosomy syndrome |
| XSDcU | Pallister-Killian syndrome |
| Xa0ER | Educationally subnormal |
| Xa0Yy | Alpha thalassaemia-mental retardation syndrome |
| Xa0ZS | Schprintzen |
| Xa0Zb | Borjeson-Forssman-Lehmann syndrome |
| Xa0Ze | Weaver syndrome |
| Xa0lH | Multi-infarct dementia |
| Xa0sC | Frontal lobe degeneration |
| Xa0sE | Dementia of frontal lobe type |
| Xa1GB | Cerebral degeneration presenting primarily with dementia |
| Xa1aW | Borderline mental retardation |
| Xa1c5 | Down's child in family |
| Xa25J | Alcoholic dementia |
| Xa3HI | Severely educationally subnormal |
| Xa3ez | Other senile/presenile dementia |
| Xa9D6 | Mosaicism 45, X; 46, XX |
| XaA1S | New variant of Creutzfeldt-Jakob disease |
| XaCKc | Down's screening blood test abnormal |
| XaCar | Discourse difficulties |
| XaDjY | Floating-Harbor syndrome |
| XaDki | Men ret congen heart dis blepharophim blepharop hypopl teeth |
| XaE74 | Senile dementia of the Lewy body type |
| XaIKB | Alzheimer's disease with early onset |
| XaIKC | Alzheimer's disease with late onset |
| XaIUM | O/E - speech delay |
| XaIwZ | Smith-Magenis syndrome |
| XaJJM | Suspected Downs syndrome |
| XaJW7 | Learning disabilities administration status |
| XaJW8 | Learning disabilities health action plan offered |
| XaJW9 | Learning disabilities health action plan declined |
| XaJWA | Learning disabilities health action plan reviewed |
| XaJmb | Learning disabilities health assessment |
| XaJmd | Discharge from learning disability team |
| XaJsd | Learning disabilities health action plan completed |
| XaKYb | On learning disability register |
| XaKYj | [D]Dysfluency |
| XaKyY | [X]Lewy body dementia |
| XaL2A | [X]Cocktail party syndrome |
| XaL2v | Lujan-Fryns syndrome |
| XaL3Q | Learning disabilities annual health assessment |
| XaLFf | Exception reporting: dementia quality indicators |
| XaLFo | Excepted from dementia quality indicators: Patient unsuitabl |
| XaLFp | Excepted from dementia quality indicators: Informed dissent |
| XaLKE | Seen in learning disabilities clinic |
| XaMAo | Prion protein markers for Creutzfeldt-Jakob disease |
| XaMFy | Dementia monitoring administration |
| XaMG0 | Dementia monitoring first letter |
| XaMGF | Dementia annual review |
| XaMGG | Dementia monitoring second letter |
| XaMGI | Dementia monitoring third letter |
| XaMGJ | Dementia monitoring verbal invite |
| XaMGK | Dementia monitoring telephone invite |
| XaMJC | Dementia monitoring |
| XaNWy | Mowat-Wilson syndrome |
| XaPx2 | Learning disability health examination |
| XaQZ3 | Moderate learning disability |
| XaQZ4 | Severe learning disability |
| XaREt | Mild learning disability |
| XaREu | Profound learning disability |
| XaXOz | Downs syndrome antenatal screening information leaflet given |
| XaYQ0 | Chromosome 22q11 deletion syndrome |
| XaYQ1 | Chromosome 3p deletion syndrome |
| XaYQ2 | Chromosome 4q deletion syndrome |
| XaYQ3 | 10q partial trisomy syndrome |
| XaYQU | 4p partial trisomy syndrome |
| XaYQb | 9p partial trisomy syndrome |
| XaYQe | 15q partial trisomy syndrome |
| XaYYN | Kleefstra syndrome |
| XaZWz | Participates in Butterfly Scheme for dementia |
| XaZX0 | Butterfly Scheme for dementia declined |
| XaaLb | Methyl-CpG-binding protein-2 duplication syndrome |
| Xaaa7 | Ulnar mammary syndrome |
| XaaiS | Specific learning disability |
| XabVp | Sporadic Creutzfeldt-Jakob disease |
| Xabk1 | Significant learning disability |
| XabtQ | Dementia medication review |
| XacF6 | Intellectual development disorder of unknown aetiology |
| XacKx | Developmental receptive language impairment |
| XacL0 | Developmental language comprehension impairment |
| XaesO | Pathological demand avoidance |
| Xaghb | Predominantly cortical dementia |
| Y000c | Dementia review done |
| Y1642 | Other Mental Disability |
| Y1f1d | Dementia monitoring invitation |
| Y1f22 | Dementia monitoring invitation |
| Y1f98 | Quality and Outcomes Framework dementia quality indicator-related care invitation (procedure) |
| Y23fb | Mixed dementia |
| Y2916 | Autistic spectrum disorder - Gluten-casein intolerance checklist |
| Y2917 | Autistic spectrum disorder - Autism checklist |
| Y6230 | Creutzfeldt - Jakob disease |
| Y8180 | Other senile/presenile dement. |
| Y9086 | Senile dementia - simple type |
| Y9087 | Senile dementia-acute confused |
| Y9103 | Severe mental retardation |
| Y9981 | Profound mental retardation |
| YA841 | Severe learning disability |
Codes not in the full codelist are in faint grey.