Learning disability (LD) codes
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- unknown
-
Organisation
- NHSD Primary Care Domain Refsets
-
Codelist ID
- nhsd-primary-care-domain-refsets/ld_cod
-
Version Tag
- 20210127
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Version ID
- 39feb05e
Versions
About
Description
Taken from the LD_COD refset published by NHSD.
We are aware that some of the individual codes contained in this codelist are offensive and upsetting. Although these terms are outdated and no longer in routine use, it is necessary to include them in codelists due to the historic nature of the data that is being analysed.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
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 |
|---|---|
| 10007009 | Coffin-Siris syndrome |
| 1089701000000105 | Profound intellectual development disorder without impairment of behaviour |
| 1089711000000107 | Profound intellectual development disorder with significant impairment of behaviour |
| 1089721000000101 | Profound intellectual development disorder with minimal impairment of behaviour |
| 1089731000000104 | Profound intellectual development disorder with impairment of behaviour |
| 1089741000000108 | Severe intellectual development disorder without significant impairment of behaviour |
| 1089751000000106 | Severe intellectual development disorder with significant impairment of behaviour |
| 1089761000000109 | Severe intellectual development disorder with minimal impairment of behaviour |
| 1089771000000102 | Severe intellectual development disorder with impairment of behaviour |
| 1089781000000100 | Moderate intellectual development disorder without significant impairment of behaviour |
| 1089791000000103 | Moderate intellectual development disorder with significant impairment of behaviour |
| 1089811000000102 | Moderate intellectual development disorder with minimal impairment of behaviour |
| 1089821000000108 | Moderate intellectual development disorder with impairment of behaviour |
| 1089831000000105 | Mild intellectual development disorder without significant impairment of behaviour |
| 1089841000000101 | Mild intellectual development disorder with significant impairment of behaviour |
| 1089851000000103 | Mild intellectual development disorder with minimal impairment of behaviour |
| 1093991000000101 | Mild intellectual development disorder with impairment of behaviour |
| 1094001000000106 | Intellectual development disorder without significant impairment of behaviour |
| 1094011000000108 | Intellectual development disorder with significant impairment of behaviour |
| 1094021000000102 | Intellectual development disorder with minimal impairment of behaviour |
| 1094031000000100 | Intellectual development disorder with impairment of behaviour |
| 109478007 | Kohlschutter's syndrome |
| 110359009 | Intellectual disability |
| 1239331000000100 | Significant intellectual disability |
| 15182000 | Coffin-Lowry syndrome |
| 17122004 | 4p partial monosomy syndrome |
| 17827007 | Cross syndrome |
| 205615000 | Trisomy 21- meiotic nondisjunction |
| 205616004 | Trisomy 21- mitotic nondisjunction mosaicism |
| 21111006 | Complete trisomy 13 syndrome |
| 21634003 | Borjeson-Forssman-Lehmann syndrome |
| 232059000 | Laurence-Moon syndrome |
| 234146006 | Hennekam lymphangiectasia-lymphedema syndrome |
| 253176002 | Gillespie syndrome |
| 254264002 | Partial trisomy 21 in Down's syndrome |
| 254268004 | Partial trisomy 13 in Patau's syndrome |
| 2593002 | Dubowitz's syndrome |
| 31216003 | Profound intellectual disability |
| 33982008 | Hyperphosphatasemia with intellectual disability |
| 401315004 | Smith-Magenis syndrome |
| 40354009 | De Lange syndrome |
| 40700009 | Severe intellectual disability |
| 41040004 | Complete trisomy 21 syndrome |
| 412787009 | Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth |
| 416075005 | On learning disability register |
| 422437002 | X-linked intellectual disability with marfanoid habitus |
| 508171000000105 | Severe learning disability |
| 51500006 | Complete trisomy 18 syndrome |
| 5619004 | Bardet-Biedl syndrome |
| 56604005 | Cohen syndrome |
| 57917004 | Seckel syndrome |
| 59252009 | Cutis laxa-corneal clouding-oligophrenia syndrome |
| 61152003 | Moderate intellectual disability |
| 65327002 | Mucopolysaccharidosis type I-H |
| 66758006 | Acrodysostosis |
| 68618008 | Rett's disorder |
| 699297004 | Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type |
| 699298009 | Blepharophimosis-mental retardation syndrome, Say-Barber-Biesecker-Young-Simpson type |
| 699669001 | Renpenning syndrome |
| 70173007 | 5p partial monosomy syndrome |
| 702327009 | Monocarboxylate transporter 8 deficiency |
| 702344008 | Pitt-Hopkins syndrome |
| 702357000 | Chromosome 2q37 deletion syndrome |
| 702412005 | X-linked intellectual deficit-dystonia-dysarthria syndrome |
| 702416008 | X-linked intellectual disability Snyder type |
| 702816000 | Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome |
| 703526007 | Progressive epilepsy-intellectual disability syndrome Finnish type |
| 703535000 | Mowat-Wilson syndrome |
| 715409005 | Trigonocephaly C syndrome |
| 715428003 | Skeletal dysplasia with epilepsy and short stature syndrome |
| 715628009 | Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome |
| 715989002 | Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome |
| 716024001 | Goniodysgenesis with intellectual disability and short stature syndrome |
| 716089008 | Craniofacial digital and genital anomalies syndrome |
| 716096005 | Hypospadias and intellectual disability syndrome Goldblatt type |
| 716112005 | Microcephaly with deafness and intellectual disability syndrome |
| 716191002 | Alopecia and intellectual disability syndrome |
| 716334004 | Intellectual disability and short stature with hand contracture and genital anomaly syndrome |
| 716709002 | FRAXE intellectual disability syndrome |
| 716996008 | Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome |
| 717157006 | Trisomy 10p |
| 717223008 | X-linked epilepsy with learning disability and behavior disorder syndrome |
| 717763008 | Chudley Lowry Hoar syndrome |
| 717822006 | Goldberg Shprintzen megacolon syndrome |
| 717887003 | Biemond syndrome type 2 |
| 717945001 | Brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome |
| 718226002 | Wolf Hirschhorn syndrome |
| 718573009 | Achalasia microcephaly syndrome |
| 718577005 | X-linked intellectual disability Atkin type |
| 718680001 | Oro-facial digital syndrome type 9 |
| 718681002 | Oro-facial digital syndrome type 11 |
| 718766002 | Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome |
| 718846001 | X-linked intellectual disability Zorick type |
| 718848000 | Fried syndrome |
| 718897009 | X-linked intellectual disability Seemanova type |
| 718900002 | Syndromic X-linked intellectual disability type 11 |
| 718905007 | X-linked intellectual disability Shrimpton type |
| 718908009 | X-linked intellectual disability Siderius type |
| 718909001 | X-linked intellectual disability Stevenson type |
| 718910006 | X-linked intellectual disability Stocco Dos Santos type |
| 718911005 | X-linked intellectual disability Stoll type |
| 718912003 | X-linked intellectual disability Turner type |
| 718914002 | X-linked intellectual disability Van Esch type |
| 719009006 | X-linked intellectual disability Wilson type |
| 719010001 | X-linked intellectual disability Schimke type |
| 719011002 | X-linked intellectual disability Pai type |
| 719012009 | X-linked intellectual disability Miles Carpenter type |
| 719013004 | X-linked intellectual disability Cilliers type |
| 719016007 | X-linked intellectual disability Cantagrel type |
| 719017003 | X-linked intellectual disability Armfield type |
| 719018008 | X-linked intellectual disability Abidi type |
| 719020006 | Pallister W syndrome |
| 719069008 | Shprintzen Goldberg craniosynostosis syndrome |
| 719097002 | Branchioskeletogenital syndrome |
| 719136005 | X-linked intellectual disability with cerebellar hypoplasia syndrome |
| 719137001 | X-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome |
| 719138006 | X-linked intellectual disability with cubitus valgus and dysmorphism syndrome |
| 719139003 | X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome |
| 719140001 | X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome |
| 719155005 | X-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome |
| 719157002 | X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome |
| 719160009 | Syndromic X-linked intellectual disability type 7 |
| 719162001 | Radioulnar synostosis with microcephaly and scoliosis syndrome |
| 719202006 | Spondyloepiphyseal dysplasia tarda Kohn type |
| 719212004 | Smith Fineman Myers syndrome |
| 719378009 | Microcephalus with brachydactyly and kyphoscoliosis syndrome |
| 719380003 | Microcephalus cardiomyopathy syndrome |
| 719396000 | Microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome |
| 719450007 | Disorder of sex development with intellectual disability syndrome |
| 719599008 | 19q13.11 microdeletion syndrome |
| 719800009 | Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome |
| 719808002 | Chromosome Xp11.3 microdeletion syndrome |
| 719810000 | X-linked intellectual disability with seizure and psoriasis syndrome |
| 719811001 | X-linked intellectual disability Cabezas type |
| 719812008 | X-linked intellectual disability with plagiocephaly syndrome |
| 719834005 | Wilson Turner syndrome |
| 719842006 | Congenital hypoplasia of ulna and intellectual disability syndrome |
| 719909009 | Chromosome Xq28 trisomy syndrome |
| 719947004 | Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome |
| 720401009 | Cystic fibrosis with gastritis and megaloblastic anemia syndrome |
| 720468000 | Aniridia and intellectual disability syndrome |
| 720501007 | Arachnodactyly with abnormal ossification and intellectual disability syndrome |
| 720517001 | Ataxia with deafness and intellectual disability syndrome |
| 720523006 | Autosomal recessive limb girdle muscular dystrophy type 2K |
| 720635002 | Cerebro-facio-thoracic dysplasia |
| 720639008 | Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome |
| 720746006 | Contracture with ectodermal dysplasia and orofacial cleft syndrome |
| 720748007 | Aural atresia with multiple congenital anomalies and intellectual disability syndrome |
| 720954000 | Filippi syndrome |
| 720955004 | Fine Lubinsky syndrome |
| 720957007 | Deafness with skeletal dysplasia and lip granuloma syndrome |
| 720979002 | Alopecia, contracture, dwarfism, intellectual disability syndrome |
| 720981000 | Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome |
| 720982007 | Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome |
| 721007005 | Hair defect with photosensitivity and intellectual disability syndrome |
| 721008000 | Hall Riggs syndrome |
| 721017000 | Postaxial polydactyly and intellectual disability syndrome |
| 721073008 | Short stature with webbed neck and congenital heart disease syndrome |
| 721087008 | Deafness and intellectual disability Martin Probst type syndrome |
| 721089006 | Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome |
| 721146009 | Intellectual disability, epilepsy, bulbous nose syndrome |
| 721207002 | Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome |
| 721208007 | Ectodermal dysplasia with blindness syndrome |
| 721224008 | Holmes Gang syndrome |
| 721875000 | Juberg Marsidi syndrome |
| 721973006 | Lipodystrophy, intellectual disability, deafness syndrome |
| 721974000 | Lowry MacLean syndrome |
| 722002002 | Intellectual disability, balding, patella luxation, acromicria syndrome |
| 722003007 | Intellectual disability with cataract and kyphosis syndrome |
| 722031003 | Kapur Toriello syndrome |
| 722033000 | Macrocephaly, short stature, paraplegia syndrome |
| 722035007 | Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome |
| 722037004 | Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome |
| 722055008 | Oculopalatocerebral syndrome |
| 722065002 | Okamoto syndrome |
| 722110003 | Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome |
| 722111004 | Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome |
| 722209002 | Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome |
| 722213009 | Severe X-linked intellectual disability Gustavson type |
| 722281001 | Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome |
| 722282008 | Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome |
| 722379001 | Congenital cataract with hypertrichosis and intellectual disability syndrome |
| 722380003 | Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome |
| 722454003 | Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome |
| 722455002 | Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome |
| 722456001 | Intellectual disability, developmental delay, contracture syndrome |
| 722459008 | Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome |
| 722478008 | Skeletal dysplasia with intellectual disability syndrome |
| 723304001 | Microcephaly, seizure, intellectual disability, heart disease syndrome |
| 723332005 | Isodicentric chromosome 15 syndrome |
| 723333000 | Faciocardiorenal syndrome |
| 723336008 | Fallot complex with intellectual disability and growth delay syndrome |
| 723365002 | Hypotrichosis and intellectual disability syndrome Lopes type |
| 723403008 | Microbrachycephaly, ptosis, cleft lip syndrome |
| 723441001 | Non-progressive cerebellar ataxia with intellectual disability |
| 723501008 | Renier Gabreels Jasper syndrome |
| 723504000 | Ramos Arroyo syndrome |
| 723621000 | Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome |
| 723676007 | Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome |
| 723994004 | Seizures and intellectual disability due to hydroxylysinuria syndrome |
| 724001005 | Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome |
| 724137002 | Macrocephaly, obesity, mental disability, ocular abnormality syndrome |
| 724207001 | Kleefstra syndrome |
| 724228005 | Infantile choroidocerebral calcification syndrome |
| 725140007 | Temple Baraitser syndrome |
| 725163002 | X-linked spasticity, intellectual disability, epilepsy syndrome |
| 725289009 | 5-amino-4-imidazole carboxamide ribosiduria |
| 725589005 | Bullous dystrophy macular type |
| 725906006 | Intellectual disability Buenos Aires type |
| 725908007 | Neurofaciodigitorenal syndrome |
| 725912001 | X-linked intellectual disability Brooks type |
| 726031001 | Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome |
| 726670008 | Weaver Williams syndrome |
| 726672000 | Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome |
| 726709001 | Intellectual disability, cataract, calcified pinna, myopathy syndrome |
| 726727003 | X-linked intellectual disability Hedera type |
| 726732002 | X-linked intellectual disability Nascimento type |
| 732246009 | X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome |
| 732251003 | Cortical blindness, intellectual disability, polydactyly syndrome |
| 732954002 | Osteopenia, intellectual disability, sparse hair syndrome |
| 732961003 | Branchial dysplasia, intellectual disability, inguinal hernia syndrome |
| 733031004 | Epilepsy, microcephaly, skeletal dysplasia syndrome |
| 733032006 | Epilepsy telangiectasia syndrome |
| 733049004 | Encephalopathy, intracerebral calcification, retinal degeneration syndrome |
| 733072002 | Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome |
| 733086003 | Pseudoprogeria syndrome |
| 733088002 | Preaxial polydactyly, colobomata, intellectual disability syndrome |
| 733090001 | Microcephalus, digital anomaly, intellectual disability syndrome |
| 733097003 | Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome |
| 733110004 | Van den Bosch syndrome |
| 733117001 | Thumb stiffness, brachydactyly, intellectual disability syndrome |
| 733417008 | Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome |
| 733419006 | Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome |
| 733455003 | Spastic paraplegia, glaucoma, intellectual disability syndrome |
| 733472005 | Microcephalus, glomerulonephritis, marfanoid habitus syndrome |
| 733522005 | Megalocornea with intellectual disability syndrome |
| 734017008 | Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome |
| 734349003 | Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 |
| 763136000 | Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome |
| 763186006 | Grubben, De Cock, Borghgraef syndrome |
| 763320005 | Craniofaciofrontodigital syndrome |
| 763350002 | Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome |
| 763404001 | Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome |
| 763615003 | Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome |
| 763618001 | Wiedemann Steiner syndrome |
| 763626009 | Intellectual disability due to nutritional deficiency |
| 763665007 | Craniodigital syndrome and intellectual disability syndrome |
| 763722004 | Hypotonia, speech impairment, severe cognitive delay syndrome |
| 763741001 | Intellectual disability, alacrima, achalasia syndrome |
| 763742008 | Intellectual disability, polydactyly, uncombable hair syndrome |
| 763743003 | Intellectual disability, spasticity, ectrodactyly syndrome |
| 763744009 | Intellectual disability, brachydactyly, Pierre Robin syndrome |
| 763745005 | Intellectual disability Wolff type |
| 763773007 | Macrocephaly and developmental delay syndrome |
| 763795006 | Malan overgrowth syndrome |
| 763797003 | Agenesis of corpus callosum and abnormal genitalia syndrome |
| 763837007 | Oro-facial digital syndrome type 14 |
| 763861000 | Pachygyria, intellectual disability, epilepsy syndrome |
| 764861005 | Intellectual disability Birk-Barel type |
| 764950001 | Cryptorchidism, arachnodactyly, intellectual disability syndrome |
| 764959000 | Intellectual disability, myopathy, short stature, endocrine defect syndrome |
| 765089003 | Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome |
| 765170001 | Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy |
| 765434008 | Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability |
| 765471005 | X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome |
| 765761009 | Brachydactyly, mesomelia, intellectual disability, heart defect syndrome |
| 766753005 | Nijmegen breakage syndrome-like disorder |
| 766870005 | Epiphyseal dysplasia, hearing loss, dysmorphism syndrome |
| 766871009 | Diencephalic mesencephalic junction dysplasia |
| 768677000 | Protein phosphatase 2 regulatory subunit b (b56) delta-related intellectual disability |
| 76880004 | Angelman syndrome |
| 770401007 | 10q22.3q23.3 microdeletion syndrome |
| 770411000 | Distal monosomy 19p13.3 |
| 770564004 | Microcephalic primordial dwarfism Alazami type |
| 770566002 | Monosomy 13q14 syndrome |
| 770595006 | Ring chromosome 12 syndrome |
| 770663003 | Tetrasomy 11q24.1 |
| 770678005 | Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome |
| 770679002 | Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome |
| 770719004 | 3q27.3 microdeletion syndrome |
| 770750002 | Intellectual disability, seizures, macrocephaly, obesity syndrome |
| 770755007 | Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome |
| 770901001 | Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome |
| 770907002 | Kagami Ogata syndrome |
| 770908007 | 49,XXXYY syndrome |
| 770948004 | Rhizomelic syndrome Urbach type |
| 771072001 | Monosomy 9p |
| 771149000 | Hepatic fibrosis, renal cyst, intellectual disability syndrome |
| 771262009 | Pseudoleprechaunism syndrome Patterson type |
| 771336003 | Polymicrogyria with optic nerve hypoplasia |
| 771472009 | Developmental and speech delay due to SRY-box 5 deficiency |
| 771512003 | Autism spectrum disorder due to AUTS2 activator of transcription and developmental regulator deficiency |
| 772127009 | White Sutton syndrome |
| 773230003 | Cyclin-dependent kinase-like 5 deficiency |
| 773329005 | CK syndrome |
| 773394007 | Autosomal recessive frontotemporal pachygyria |
| 773400009 | Severe feeding difficulties, failure to thrive, microcephaly due to ASXL transcriptional regulator 3 deficiency syndrome |
| 773405004 | Intellectual disability with strabismus syndrome |
| 773419004 | Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome |
| 773498006 | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency |
| 773581009 | Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome |
| 773665006 | Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome |
| 773670004 | Distal Xq28 microduplication syndrome |
| 773699009 | Pitt Hopkins-like syndrome |
| 773769008 | Ataxia, photosensitivity, short stature syndrome |
| 773772001 | Rare non-syndromic intellectual disability |
| 774068004 | AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome |
| 778011005 | Severe intellectual disability and progressive spastic paraplegia |
| 782676009 | Distal trisomy 18q |
| 782723007 | Severe intellectual disability, progressive spastic diplegia syndrome |
| 782736007 | Intellectual disability, facial dysmorphism syndrome due to SET domain containing 5 haploinsufficiency |
| 782753000 | Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome |
| 782755007 | Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome |
| 782772000 | Congenital muscular dystrophy with intellectual disability and severe epilepsy |
| 782886007 | Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome |
| 782941005 | Richieri Costa-da Silva syndrome |
| 782945001 | Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome |
| 783005002 | Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome |
| 783174004 | Congenital muscular dystrophy with intellectual disability |
| 783702009 | X-linked intellectual disability due to glutamate ionotropic receptor AMPA type subunit 3 mutations |
| 783703004 | White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome |
| 787093004 | Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency |
| 788417006 | Alopecia, epilepsy, intellectual disability syndrome Moynahan type |
| 79385002 | Lowe syndrome |
| 816067005 | Diabetes, hypogonadism, deafness, intellectual disability syndrome |
| 838441009 | Mental retardation, adducted thumbs, shuffling gait, aphasia syndrome |
| 840505007 | Down syndrome co-occurrent with leukemoid reaction associated transient neonatal pustulosis |
| 86765009 | Mild intellectual disability |
| 89392001 | Prader-Willi syndrome |
| 931001000000105 | Significant learning disability |
| 984661000000105 | Mild learning disability |
| 984671000000103 | Moderate learning disability |
| 984681000000101 | Profound learning disability |
Codes not in the full codelist are in faint grey.