[ { "phenotype_id": "PH3890", "phenotype_version_id": 9043, "name": "Wider Learning Disability", "definition": "This codelist was taken from [OpenCodelists](https://www.opencodelists.org/), created by [OpenSAFELY](https://www.opensafely.org/). We recommend viewing this Phenotype on the OpenCodelist website to view the most recent version.\n\n\nTaken from the `LEARNDIS_COD` field in SARS\\-CoV2 COVID19 Vaccination Uptake Reporting Codes 20_21 v1, published by PRIMIS.\n\n\n© PRIMIS \\- the University of Nottingham 2021\n\n\n© University of Oxford for the Bennett Institute for Applied Data Science 2025\\. This work may be copied freely for non\\-commercial research and study.\n\n", "implementation": null, "publications": null, "validation": null, "citation_requirements": null, "created": "2026-01-26T23:38:16.054315Z", "author": "PRIMIS Covid Vaccination Uptake Reporting (old)", "collections": [ { "name": "OpenCodelist", "value": 31 }, { "name": "Phenotype Library", "value": 18 } ], "tags": null, "organisation": { "id": 1, "slug": "opensafely", "name": "OpenSAFELY" }, "world_access": 1, "updated": "2026-01-26T23:38:16.049486Z", "references": [], "signed_off": [], "methodology": "", "coding_system": [ { "name": "SNOMED CT codes", "value": 9 } ], "open_codelist_id": "primis-covid19-vacc-uptake-old/learndis_cod", "source_reference": "https://www.opencodelists.org/codelist/primis-covid19-vacc-uptake-old/learndis_cod/v1", "concept_information": [ { "concept_id": 9220, "concept_version_id": 16705, "concept_name": "primis-covid19-vacc-uptake-old/learndis_cod/v1", "coding_system": { "id": 9, "name": "SNOMED CT codes", "description": "SNOMED CT codes" }, "phenotype_id": "PH3890", "phenotype_version_id": 9043, "phenotype_name": "Wider Learning Disability", "code_attribute_header": [], "codes": [ { "code": "10007009", "description": "Coffin-Siris syndrome", "attributes": null }, { "code": "1089701000000105", "description": "Profound intellectual development disorder without impairment of behaviour", "attributes": null }, { "code": "1089711000000107", "description": "Profound intellectual development disorder with significant impairment of behaviour", "attributes": null }, { "code": "1089721000000101", "description": "Profound intellectual development disorder with minimal impairment of behaviour", "attributes": null }, { "code": "1089731000000104", "description": "Profound intellectual development disorder with impairment of behaviour", "attributes": null }, { "code": "1089741000000108", "description": "Severe intellectual development disorder without significant impairment of behaviour", "attributes": null }, { "code": "1089751000000106", "description": "Severe intellectual development disorder with significant impairment of behaviour", "attributes": null }, { "code": "1089761000000109", "description": "Severe intellectual development disorder with minimal impairment of behaviour", "attributes": null }, { "code": "1089771000000102", "description": "Severe intellectual development disorder with impairment of behaviour", "attributes": null }, { "code": "1089781000000100", "description": "Moderate intellectual development disorder without significant impairment of behaviour", "attributes": null }, { "code": "1089791000000103", "description": "Moderate intellectual development disorder with significant impairment of behaviour", "attributes": null }, { "code": "1089811000000102", "description": "Moderate intellectual development disorder with minimal impairment of behaviour", "attributes": null }, { "code": "1089821000000108", "description": "Moderate intellectual development disorder with impairment of behaviour", "attributes": null }, { "code": "1089831000000105", "description": "Mild intellectual development disorder without significant impairment of behaviour", "attributes": null }, { "code": "1089841000000101", "description": "Mild intellectual development disorder with significant impairment of behaviour", "attributes": null }, { "code": "1089851000000103", "description": "Mild intellectual development disorder with minimal impairment of behaviour", "attributes": null }, { "code": "1093991000000101", "description": "Mild intellectual development disorder with impairment of behaviour", "attributes": null }, { "code": "1094001000000106", "description": "Intellectual development disorder without significant impairment of behaviour", "attributes": null }, { "code": "1094011000000108", "description": "Intellectual development disorder with significant impairment of behaviour", "attributes": null }, { "code": "1094021000000102", "description": "Intellectual development disorder with minimal impairment of behaviour", "attributes": null }, { "code": "1094031000000100", "description": "Intellectual development disorder with impairment of behaviour", "attributes": null }, { "code": "109478007", "description": "Kohlschutter's syndrome", "attributes": null }, { "code": "110359009", "description": "Intellectual disability", "attributes": null }, { "code": "1239331000000100", "description": "Significant intellectual disability", "attributes": null }, { "code": "17827007", "description": "Cross syndrome", "attributes": null }, { "code": "205615000", "description": "Trisomy 21- meiotic nondisjunction", "attributes": null }, { "code": "205619006", "description": "Trisomy 13, meiotic nondisjunction", "attributes": null }, { "code": "205620000", "description": "Trisomy 13 - mitotic nondisjunction mosaicism", "attributes": null }, { "code": "205623003", "description": "Trisomy 18 - meiotic nondisjunction", "attributes": null }, { "code": "205624009", "description": "Trisomy 18 - mitotic nondisjunction mosaicism", "attributes": null }, { "code": "21111006", "description": "Complete trisomy 13 syndrome", "attributes": null }, { "code": "21634003", "description": "Borjeson-Forssman-Lehmann syndrome", "attributes": null }, { "code": "232059000", "description": "Laurence-Moon syndrome", "attributes": null }, { "code": "234146006", "description": "Hennekam lymphangiectasia-lymphedema syndrome", "attributes": null }, { "code": "236529001", "description": "Prune belly syndrome with pulmonic stenosis, mental retardation and deafness", "attributes": null }, { "code": "253176002", "description": "Gillespie syndrome", "attributes": null }, { "code": "254264002", "description": "Partial trisomy 21 in Down's syndrome", "attributes": null }, { "code": "254266000", "description": "Partial trisomy 18 in Edward's syndrome", "attributes": null }, { "code": "254268004", "description": "Partial trisomy 13 in Patau's syndrome", "attributes": null }, { "code": "31216003", "description": "Profound intellectual disability", "attributes": null }, { "code": "33982008", "description": "Hyperphosphatasemia with intellectual disability", "attributes": null }, { "code": "40700009", "description": "Severe intellectual disability", "attributes": null }, { "code": "41040004", "description": "Complete trisomy 21 syndrome", "attributes": null }, { "code": "412787009", "description": "Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth", "attributes": null }, { "code": "416075005", "description": "On learning disability register", "attributes": null }, { "code": "422437002", "description": "X-linked intellectual disability with marfanoid habitus", "attributes": null }, { "code": "432091002", "description": "Savant syndrome", "attributes": null }, { "code": "508171000000105", "description": "Severe learning disability", "attributes": null }, { "code": "51500006", "description": "Complete trisomy 18 syndrome", "attributes": null }, { "code": "5619004", "description": "Bardet-Biedl syndrome", "attributes": null }, { "code": "57917004", "description": "Seckel syndrome", "attributes": null }, { "code": "59252009", "description": "Cutis laxa-corneal clouding-oligophrenia syndrome", "attributes": null }, { "code": "61152003", "description": "Moderate intellectual disability", "attributes": null }, { "code": "613003", "description": "Fragile X syndrome", "attributes": null }, { "code": "68618008", "description": "Rett's disorder", "attributes": null }, { "code": "699297004", "description": "Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type", "attributes": null }, { "code": "699298009", "description": "Blepharophimosis-mental retardation syndrome, Say-Barber-Biesecker-Young-Simpson type", "attributes": null }, { "code": "699316006", "description": "Myhre syndrome", "attributes": null }, { "code": "699669001", "description": "Renpenning syndrome", "attributes": null }, { "code": "702344008", "description": "Pitt-Hopkins syndrome", "attributes": null }, { "code": "702356009", "description": "X-linked intellectual disability-psychosis-macroorchidism syndrome", "attributes": null }, { "code": "702412005", "description": "X-linked intellectual deficit-dystonia-dysarthria syndrome", "attributes": null }, { "code": "702416008", "description": "X-linked intellectual disability Snyder type", "attributes": null }, { "code": "702441001", "description": "Fatal X-linked ataxia with deafness and loss of vision", "attributes": null }, { "code": "702816000", "description": "Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome", "attributes": null }, { "code": "703389002", "description": "Calcium/calmodulin-dependent serine protein kinase related intellectual disability", "attributes": null }, { "code": "703526007", "description": "Progressive epilepsy-intellectual disability syndrome Finnish type", "attributes": null }, { "code": "703535000", "description": "Mowat-Wilson syndrome", "attributes": null }, { "code": "709469005", "description": "Periodontitis co-occurrent with Down syndrome", "attributes": null }, { "code": "715409005", "description": "Trigonocephaly C syndrome", "attributes": null }, { "code": "715428003", "description": "Skeletal dysplasia with epilepsy and short stature syndrome", "attributes": null }, { "code": "715441004", "description": "McDonough syndrome", "attributes": null }, { "code": "715628009", "description": "Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome", "attributes": null }, { "code": "715989002", "description": "Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome", "attributes": null }, { "code": "716024001", "description": "Goniodysgenesis with intellectual disability and short stature syndrome", "attributes": null }, { "code": "716089008", "description": "Craniofacial digital and genital anomalies syndrome", "attributes": null }, { "code": "716096005", "description": "Hypospadias and intellectual disability syndrome Goldblatt type", "attributes": null }, { "code": "716107009", "description": "Early onset parkinsonism and intellectual disability syndrome", "attributes": null }, { "code": "716112005", "description": "Microcephaly with deafness and intellectual disability syndrome", "attributes": null }, { "code": "716191002", "description": "Alopecia and intellectual disability syndrome", "attributes": null }, { "code": "716334004", "description": "Intellectual disability and short stature with hand contracture and genital anomaly syndrome", "attributes": null }, { "code": "716706009", "description": "Female restricted epilepsy with intellectual disability syndrome", "attributes": null }, { "code": "716709002", "description": "FRAXE intellectual disability syndrome", "attributes": null }, { "code": "716996008", "description": "Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome", "attributes": null }, { "code": "717157006", "description": "Trisomy 10p", "attributes": null }, { "code": "717222003", "description": "Microphthalmia with ankyloblepharon and intellectual disability syndrome", "attributes": null }, { "code": "717223008", "description": "X-linked epilepsy with learning disability and behavior disorder syndrome", "attributes": null }, { "code": "717763008", "description": "Chudley Lowry Hoar syndrome", "attributes": null }, { "code": "717822006", "description": "Goldberg Shprintzen megacolon syndrome", "attributes": null }, { "code": "717887003", "description": "Biemond syndrome type 2", "attributes": null }, { "code": "717913006", "description": "Blepharonasofacial malformation syndrome", "attributes": null }, { "code": "717945001", "description": "Brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome", "attributes": null }, { "code": "718226002", "description": "Wolf Hirschhorn syndrome", "attributes": null }, { "code": "718573009", "description": "Achalasia microcephaly syndrome", "attributes": null }, { "code": "718577005", "description": "X-linked intellectual disability Atkin type", "attributes": null }, { "code": "718680001", "description": "Oro-facial digital syndrome type 9", "attributes": null }, { "code": "718681002", "description": "Oro-facial digital syndrome type 11", "attributes": null }, { "code": "718766002", "description": "Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome", "attributes": null }, { "code": "718845002", "description": "X-linked intellectual disability with ataxia and apraxia syndrome", "attributes": null }, { "code": "718848000", "description": "Fried syndrome", "attributes": null }, { "code": "718896000", "description": "X-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome", "attributes": null }, { "code": "718897009", "description": "X-linked intellectual disability Seemanova type", "attributes": null }, { "code": "718900002", "description": "Syndromic X-linked intellectual disability type 11", "attributes": null }, { "code": "718905007", "description": "X-linked intellectual disability Shrimpton type", "attributes": null }, { "code": "718908009", "description": "X-linked intellectual disability Siderius type", "attributes": null }, { "code": "718909001", "description": "X-linked intellectual disability Stevenson type", "attributes": null }, { "code": "718910006", "description": "X-linked intellectual disability Stocco Dos Santos type", "attributes": null }, { "code": "718911005", "description": "X-linked intellectual disability Stoll type", "attributes": null }, { "code": "718912003", "description": "X-linked intellectual disability Turner type", "attributes": null }, { "code": "718914002", "description": "X-linked intellectual disability Van Esch type", "attributes": null }, { "code": "719009006", "description": "X-linked intellectual disability Wilson type", "attributes": null }, { "code": "719010001", "description": "X-linked intellectual disability Schimke type", "attributes": null }, { "code": "719011002", "description": "X-linked intellectual disability Pai type", "attributes": null }, { "code": "719012009", "description": "X-linked intellectual disability Miles Carpenter type", "attributes": null }, { "code": "719013004", "description": "X-linked intellectual disability Cilliers type", "attributes": null }, { "code": "719016007", "description": "X-linked intellectual disability Cantagrel type", "attributes": null }, { "code": "719017003", "description": "X-linked intellectual disability Armfield type", "attributes": null }, { "code": "719018008", "description": "X-linked intellectual disability Abidi type", "attributes": null }, { "code": "719020006", "description": "Pallister W syndrome", "attributes": null }, { "code": "719042007", "description": "Uveal coloboma with cleft lip and palate and intellectual disability syndrome", "attributes": null }, { "code": "719046005", "description": "12q14 microdeletion syndrome", "attributes": null }, { "code": "719069008", "description": "Shprintzen Goldberg craniosynostosis syndrome", "attributes": null }, { "code": "719097002", "description": "Branchioskeletogenital syndrome", "attributes": null }, { "code": "719101006", "description": "Carpenter Waziri syndrome", "attributes": null }, { "code": "719102004", "description": "Congenital cataract with ataxia and deafness syndrome", "attributes": null }, { "code": "719136005", "description": "X-linked intellectual disability with cerebellar hypoplasia syndrome", "attributes": null }, { "code": "719138006", "description": "X-linked intellectual disability with cubitus valgus and dysmorphism syndrome", "attributes": null }, { "code": "719139003", "description": "X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome", "attributes": null }, { "code": "719140001", "description": "X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome", "attributes": null }, { "code": "719155005", "description": "X-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome", "attributes": null }, { "code": "719156006", "description": "X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome", "attributes": null }, { "code": "719157002", "description": "X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome", "attributes": null }, { "code": "719160009", "description": "Syndromic X-linked intellectual disability type 7", "attributes": null }, { "code": "719161008", "description": "Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation", "attributes": null }, { "code": "719162001", "description": "Radioulnar synostosis with microcephaly and scoliosis syndrome", "attributes": null }, { "code": "719202006", "description": "Spondyloepiphyseal dysplasia tarda Kohn type", "attributes": null }, { "code": "719212004", "description": "Smith Fineman Myers syndrome", "attributes": null }, { "code": "719378009", "description": "Microcephalus with brachydactyly and kyphoscoliosis syndrome", "attributes": null }, { "code": "719380003", "description": "Microcephalus cardiomyopathy syndrome", "attributes": null }, { "code": "719450007", "description": "Disorder of sex development with intellectual disability syndrome", "attributes": null }, { "code": "719466009", "description": "Cleft palate with short stature and vertebral anomaly syndrome", "attributes": null }, { "code": "719583002", "description": "17q11.2 microduplication syndrome", "attributes": null }, { "code": "719599008", "description": "19q13.11 microdeletion syndrome", "attributes": null }, { "code": "719600006", "description": "1p21.3 microdeletion syndrome", "attributes": null }, { "code": "719800009", "description": "Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome", "attributes": null }, { "code": "719808002", "description": "Chromosome Xp11.3 microdeletion syndrome", "attributes": null }, { "code": "719810000", "description": "X-linked intellectual disability with seizure and psoriasis syndrome", "attributes": null }, { "code": "719811001", "description": "X-linked intellectual disability Cabezas type", "attributes": null }, { "code": "719812008", "description": "X-linked intellectual disability with plagiocephaly syndrome", "attributes": null }, { "code": "719825000", "description": "X-linked intellectual disability, macrocephaly, macroorchidism syndrome", "attributes": null }, { "code": "719826004", "description": "X-linked intellectual disability with acromegaly and hyperactivity syndrome", "attributes": null }, { "code": "719834005", "description": "Wilson Turner syndrome", "attributes": null }, { "code": "719842006", "description": "Congenital hypoplasia of ulna and intellectual disability syndrome", "attributes": null }, { "code": "719909009", "description": "Chromosome Xq28 trisomy syndrome", "attributes": null }, { "code": "719947004", "description": "Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome", "attributes": null }, { "code": "720401009", "description": "Cystic fibrosis with gastritis and megaloblastic anemia syndrome", "attributes": null }, { "code": "720468000", "description": "Aniridia and intellectual disability syndrome", "attributes": null }, { "code": "720501007", "description": "Arachnodactyly with abnormal ossification and intellectual disability syndrome", "attributes": null }, { "code": "720502000", "description": "Arachnodactyly and intellectual disability with facial dysmorphism syndrome", "attributes": null }, { "code": "720517001", "description": "Ataxia with deafness and intellectual disability syndrome", "attributes": null }, { "code": "720573009", "description": "Brachymorphism with onychodysplasia and dysphalangism syndrome", "attributes": null }, { "code": "720635002", "description": "Cerebro-facio-thoracic dysplasia", "attributes": null }, { "code": "720639008", "description": "Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome", "attributes": null }, { "code": "720746006", "description": "Contracture with ectodermal dysplasia and orofacial cleft syndrome", "attributes": null }, { "code": "720748007", "description": "Aural atresia with multiple congenital anomalies and intellectual disability syndrome", "attributes": null }, { "code": "720825005", "description": "Cystic leukoencephalopathy without megalencephaly", "attributes": null }, { "code": "720855003", "description": "Cerebrooculonasal syndrome", "attributes": null }, { "code": "720954000", "description": "Filippi syndrome", "attributes": null }, { "code": "720955004", "description": "Fine Lubinsky syndrome", "attributes": null }, { "code": "720957007", "description": "Deafness with skeletal dysplasia and lip granuloma syndrome", "attributes": null }, { "code": "720979002", "description": "Alopecia, contracture, dwarfism, intellectual disability syndrome", "attributes": null }, { "code": "720981000", "description": "Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome", "attributes": null }, { "code": "720982007", "description": "Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome", "attributes": null }, { "code": "721007005", "description": "Hair defect with photosensitivity and intellectual disability syndrome", "attributes": null }, { "code": "721008000", "description": "Hall Riggs syndrome", "attributes": null }, { "code": "721017000", "description": "Postaxial polydactyly and intellectual disability syndrome", "attributes": null }, { "code": "721073008", "description": "Short stature with webbed neck and congenital heart disease syndrome", "attributes": null }, { "code": "721086004", "description": "Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome", "attributes": null }, { "code": "721087008", "description": "Deafness and intellectual disability Martin Probst type syndrome", "attributes": null }, { "code": "721089006", "description": "Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome", "attributes": null }, { "code": "721146009", "description": "Intellectual disability, epilepsy, bulbous nose syndrome", "attributes": null }, { "code": "721207002", "description": "Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome", "attributes": null }, { "code": "721208007", "description": "Ectodermal dysplasia with blindness syndrome", "attributes": null }, { "code": "721224008", "description": "Holmes Gang syndrome", "attributes": null }, { "code": "721841001", "description": "Hypogonadism with mitral valve prolapse and intellectual disability syndrome", "attributes": null }, { "code": "721843003", "description": "Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome", "attributes": null }, { "code": "721875000", "description": "Juberg Marsidi syndrome", "attributes": null }, { "code": "721883006", "description": "Radioulnar synostosis with developmental delay and hypotonia syndrome", "attributes": null }, { "code": "721973006", "description": "Lipodystrophy, intellectual disability, deafness syndrome", "attributes": null }, { "code": "721974000", "description": "Lowry MacLean syndrome", "attributes": null }, { "code": "722002002", "description": "Intellectual disability, balding, patella luxation, acromicria syndrome", "attributes": null }, { "code": "722003007", "description": "Intellectual disability with cataract and kyphosis syndrome", "attributes": null }, { "code": "722031003", "description": "Kapur Toriello syndrome", "attributes": null }, { "code": "722033000", "description": "Macrocephaly, short stature, paraplegia syndrome", "attributes": null }, { "code": "722035007", "description": "Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome", "attributes": null }, { "code": "722037004", "description": "Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome", "attributes": null }, { "code": "722055008", "description": "Oculopalatocerebral syndrome", "attributes": null }, { "code": "722056009", "description": "Oculocerebrofacial syndrome Kaufman type", "attributes": null }, { "code": "722065002", "description": "Okamoto syndrome", "attributes": null }, { "code": "722075004", "description": "Oro-facial digital syndrome type 10", "attributes": null }, { "code": "722105002", "description": "Oro-facial digital syndrome type 5", "attributes": null }, { "code": "722106001", "description": "Oro-facial digital syndrome type 8", "attributes": null }, { "code": "722107005", "description": "Ossification anomaly with psychomotor developmental delay syndrome", "attributes": null }, { "code": "722110003", "description": "Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome", "attributes": null }, { "code": "722111004", "description": "Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome", "attributes": null }, { "code": "722209002", "description": "Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome", "attributes": null }, { "code": "722213009", "description": "Severe X-linked intellectual disability Gustavson type", "attributes": null }, { "code": "722281001", "description": "Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome", "attributes": null }, { "code": "722282008", "description": "Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome", "attributes": null }, { "code": "722378009", "description": "Congenital cataract with deafness and hypogonadism syndrome", "attributes": null }, { "code": "722379001", "description": "Congenital cataract with hypertrichosis and intellectual disability syndrome", "attributes": null }, { "code": "722380003", "description": "Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome", "attributes": null }, { "code": "722454003", "description": "Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome", "attributes": null }, { "code": "722455002", "description": "Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome", "attributes": null }, { "code": "722456001", "description": "Intellectual disability, developmental delay, contracture syndrome", "attributes": null }, { "code": "722459008", "description": "Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome", "attributes": null }, { "code": "722477003", "description": "Toriello Carey syndrome", "attributes": null }, { "code": "722478008", "description": "Skeletal dysplasia with intellectual disability syndrome", "attributes": null }, { "code": "723304001", "description": "Microcephaly, seizure, intellectual disability, heart disease syndrome", "attributes": null }, { "code": "723332005", "description": "Isodicentric chromosome 15 syndrome", "attributes": null }, { "code": "723333000", "description": "Faciocardiorenal syndrome", "attributes": null }, { "code": "723336008", "description": "Fallot complex with intellectual disability and growth delay syndrome", "attributes": null }, { "code": "723365002", "description": "Hypotrichosis and intellectual disability syndrome Lopes type", "attributes": null }, { "code": "723403008", "description": "Microbrachycephaly, ptosis, cleft lip syndrome", "attributes": null }, { "code": "723441001", "description": "Non-progressive cerebellar ataxia with intellectual disability", "attributes": null }, { "code": "723454008", "description": "Phosphoribosylpyrophosphate synthetase superactivity", "attributes": null }, { "code": "723501008", "description": "Renier Gabreels Jasper syndrome", "attributes": null }, { "code": "723504000", "description": "Ramos Arroyo syndrome", "attributes": null }, { "code": "723621000", "description": "Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome", "attributes": null }, { "code": "723676007", "description": "Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome", "attributes": null }, { "code": "723994004", "description": "Seizures and intellectual disability due to hydroxylysinuria syndrome", "attributes": null }, { "code": "724001005", "description": "Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome", "attributes": null }, { "code": "724039002", "description": "Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency", "attributes": null }, { "code": "724137002", "description": "Macrocephaly, obesity, mental disability, ocular abnormality syndrome", "attributes": null }, { "code": "724178000", "description": "Laryngeal abductor paralysis with intellectual disability syndrome", "attributes": null }, { "code": "724207001", "description": "Kleefstra syndrome", "attributes": null }, { "code": "724228005", "description": "Infantile choroidocerebral calcification syndrome", "attributes": null }, { "code": "724643004", "description": "Transient abnormal myelopoiesis co-occurrent with Down syndrome", "attributes": null }, { "code": "724644005", "description": "Myeloid leukemia co-occurrent with Down syndrome", "attributes": null }, { "code": "725140007", "description": "Temple Baraitser syndrome", "attributes": null }, { "code": "725163002", "description": "X-linked spasticity, intellectual disability, epilepsy syndrome", "attributes": null }, { "code": "725289009", "description": "5-amino-4-imidazole carboxamide ribosiduria", "attributes": null }, { "code": "725589005", "description": "Bullous dystrophy macular type", "attributes": null }, { "code": "725906006", "description": "Intellectual disability Buenos Aires type", "attributes": null }, { "code": "725908007", "description": "Neurofaciodigitorenal syndrome", "attributes": null }, { "code": "725912001", "description": "X-linked intellectual disability Brooks type", "attributes": null }, { "code": "726031001", "description": "Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome", "attributes": null }, { "code": "726621009", "description": "Caudal appendage deafness syndrome", "attributes": null }, { "code": "726669007", "description": "Central nervous system calcification, deafness, tubular acidosis, anemia syndrome", "attributes": null }, { "code": "726670008", "description": "Weaver Williams syndrome", "attributes": null }, { "code": "726672000", "description": "Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome", "attributes": null }, { "code": "726709001", "description": "Intellectual disability, cataract, calcified pinna, myopathy syndrome", "attributes": null }, { "code": "726727003", "description": "X-linked intellectual disability Hedera type", "attributes": null }, { "code": "726732002", "description": "X-linked intellectual disability Nascimento type", "attributes": null }, { "code": "732246009", "description": "X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome", "attributes": null }, { "code": "732251003", "description": "Cortical blindness, intellectual disability, polydactyly syndrome", "attributes": null }, { "code": "732954002", "description": "Osteopenia, intellectual disability, sparse hair syndrome", "attributes": null }, { "code": "732957009", "description": "Brachydactyly and preaxial hallux varus syndrome", "attributes": null }, { "code": "732958004", "description": "Spastic paraplegia with precocious puberty syndrome", "attributes": null }, { "code": "732961003", "description": "Branchial dysplasia, intellectual disability, inguinal hernia syndrome", "attributes": null }, { "code": "733031004", "description": "Epilepsy, microcephaly, skeletal dysplasia syndrome", "attributes": null }, { "code": "733032006", "description": "Epilepsy telangiectasia syndrome", "attributes": null }, { "code": "733049004", "description": "Encephalopathy, intracerebral calcification, retinal degeneration syndrome", "attributes": null }, { "code": "733050004", "description": "Dysmorphism, short stature, deafness, disorder of sex development syndrome", "attributes": null }, { "code": "733062000", "description": "Marfanoid habitus with autosomal recessive intellectual disability syndrome", "attributes": null }, { "code": "733072002", "description": "Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome", "attributes": null }, { "code": "733086003", "description": "Pseudoprogeria syndrome", "attributes": null }, { "code": "733088002", "description": "Preaxial polydactyly, colobomata, intellectual disability syndrome", "attributes": null }, { "code": "733097003", "description": "Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome", "attributes": null }, { "code": "733110004", "description": "Van den Bosch syndrome", "attributes": null }, { "code": "733116005", "description": "Aniridia, renal agenesis, psychomotor retardation syndrome", "attributes": null }, { "code": "733117001", "description": "Thumb stiffness, brachydactyly, intellectual disability syndrome", "attributes": null }, { "code": "733194007", "description": "Dementia co-occurrent and due to Down syndrome", "attributes": null }, { "code": "733417008", "description": "Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome", "attributes": null }, { "code": "733419006", "description": "Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome", "attributes": null }, { "code": "733455003", "description": "Spastic paraplegia, glaucoma, intellectual disability syndrome", "attributes": null }, { "code": "733472005", "description": "Microcephalus, glomerulonephritis, marfanoid habitus syndrome", "attributes": null }, { "code": "733522005", "description": "Megalocornea with intellectual disability syndrome", "attributes": null }, { "code": "734017008", "description": "Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome", "attributes": null }, { "code": "734173003", "description": "Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome", "attributes": null }, { "code": "734349003", "description": "Alpha-thalassemia intellectual disability syndrome linked to chromosome 16", "attributes": null }, { "code": "763136000", "description": "Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome", "attributes": null }, { "code": "763186006", "description": "Grubben, De Cock, Borghgraef syndrome", "attributes": null }, { "code": "763278004", "description": "Facial dysmorphism, cleft palate, loose skin syndrome", "attributes": null }, { "code": "763320005", "description": "Craniofaciofrontodigital syndrome", "attributes": null }, { "code": "763344007", "description": "Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome", "attributes": null }, { "code": "763350002", "description": "Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome", "attributes": null }, { "code": "763353000", "description": "Cerebrofacioarticular syndrome", "attributes": null }, { "code": "763404001", "description": "Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome", "attributes": null }, { "code": "763615003", "description": "Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome", "attributes": null }, { "code": "763618001", "description": "Wiedemann Steiner syndrome", "attributes": null }, { "code": "763626009", "description": "Intellectual disability due to nutritional deficiency", "attributes": null }, { "code": "763665007", "description": "Craniodigital syndrome and intellectual disability syndrome", "attributes": null }, { "code": "763722004", "description": "Hypotonia, speech impairment, severe cognitive delay syndrome", "attributes": null }, { "code": "763741001", "description": "Intellectual disability, alacrima, achalasia syndrome", "attributes": null }, { "code": "763742008", "description": "Intellectual disability, polydactyly, uncombable hair syndrome", "attributes": null }, { "code": "763743003", "description": "Intellectual disability, spasticity, ectrodactyly syndrome", "attributes": null }, { "code": "763744009", "description": "Intellectual disability, brachydactyly, Pierre Robin syndrome", "attributes": null }, { "code": "763745005", "description": "Intellectual disability Wolff type", "attributes": null }, { "code": "763773007", "description": "Macrocephaly and developmental delay syndrome", "attributes": null }, { "code": "763795006", "description": "Malan overgrowth syndrome", "attributes": null }, { "code": "763797003", "description": "Agenesis of corpus callosum and abnormal genitalia syndrome", "attributes": null }, { "code": "763837007", "description": "Oro-facial digital syndrome type 14", "attributes": null }, { "code": "763861000", "description": "Pachygyria, intellectual disability, epilepsy syndrome", "attributes": null }, { "code": "764455002", "description": "Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome", "attributes": null }, { "code": "764732004", "description": "Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome", "attributes": null }, { "code": "764861005", "description": "Intellectual disability Birk-Barel type", "attributes": null }, { "code": "764950001", "description": "Cryptorchidism, arachnodactyly, intellectual disability syndrome", "attributes": null }, { "code": "764959000", "description": "Intellectual disability, myopathy, short stature, endocrine defect syndrome", "attributes": null }, { "code": "765089003", "description": "Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome", "attributes": null }, { "code": "765170001", "description": "Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy", "attributes": null }, { "code": "765434008", "description": "Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability", "attributes": null }, { "code": "765471005", "description": "X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome", "attributes": null }, { "code": "765758008", "description": "Microcephalic primordial dwarfism Montreal type", "attributes": null }, { "code": "765761009", "description": "Brachydactyly, mesomelia, intellectual disability, heart defect syndrome", "attributes": null }, { "code": "766753005", "description": "Nijmegen breakage syndrome-like disorder", "attributes": null }, { "code": "766824003", "description": "Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder", "attributes": null }, { "code": "766870005", "description": "Epiphyseal dysplasia, hearing loss, dysmorphism syndrome", "attributes": null }, { "code": "766871009", "description": "Diencephalic mesencephalic junction dysplasia", "attributes": null }, { "code": "768473009", "description": "Purine rich element binding protein A syndrome", "attributes": null }, { "code": "768677000", "description": "Protein phosphatase 2 regulatory subunit b (b56) delta-related intellectual disability", "attributes": null }, { "code": "76880004", "description": "Angelman syndrome", "attributes": null }, { "code": "768843007", "description": "Tall stature, intellectual disability, facial dysmorphism syndrome", "attributes": null }, { "code": "770404004", "description": "Autosomal recessive chorioretinopathy and microcephaly syndrome", "attributes": null }, { "code": "770431001", "description": "Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation", "attributes": null }, { "code": "770564004", "description": "Microcephalic primordial dwarfism Alazami type", "attributes": null }, { "code": "770565003", "description": "Microcephalic primordial dwarfism Dauber type", "attributes": null }, { "code": "770604006", "description": "X-linked cerebral, cerebellar, coloboma syndrome", "attributes": null }, { "code": "770679002", "description": "Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome", "attributes": null }, { "code": "770719004", "description": "3q27.3 microdeletion syndrome", "attributes": null }, { "code": "770721009", "description": "Microcephaly, thin corpus callosum, intellectual disability syndrome", "attributes": null }, { "code": "770723007", "description": "Optic atrophy, intellectual disability syndrome", "attributes": null }, { "code": "770725000", "description": "Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly", "attributes": null }, { "code": "770750002", "description": "Intellectual disability, seizures, macrocephaly, obesity syndrome", "attributes": null }, { "code": "770751003", "description": "Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome", "attributes": null }, { "code": "770755007", "description": "Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome", "attributes": null }, { "code": "770756008", "description": "2p13.2 microdeletion syndrome", "attributes": null }, { "code": "770790004", "description": "Developmental delay with autism spectrum disorder and gait instability", "attributes": null }, { "code": "770793002", "description": "5p13 microduplication syndrome", "attributes": null }, { "code": "770794008", "description": "11p15.4 microduplication syndrome", "attributes": null }, { "code": "770898002", "description": "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency", "attributes": null }, { "code": "770901001", "description": "Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome", "attributes": null }, { "code": "770907002", "description": "Kagami Ogata syndrome", "attributes": null }, { "code": "770941005", "description": "Alopecia, progressive neurological defect, endocrinopathy syndrome", "attributes": null }, { "code": "771074000", "description": "Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome", "attributes": null }, { "code": "771077007", "description": "Intellectual disability, short stature, hypertelorism syndrome", "attributes": null }, { "code": "771148008", "description": "X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome", "attributes": null }, { "code": "771149000", "description": "Hepatic fibrosis, renal cyst, intellectual disability syndrome", "attributes": null }, { "code": "771179007", "description": "Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome", "attributes": null }, { "code": "771262009", "description": "Pseudoleprechaunism syndrome Patterson type", "attributes": null }, { "code": "771336003", "description": "Polymicrogyria with optic nerve hypoplasia", "attributes": null }, { "code": "771448004", "description": "Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency", "attributes": null }, { "code": "771470001", "description": "Jawad syndrome", "attributes": null }, { "code": "771472009", "description": "Developmental and speech delay due to SRY-box 5 deficiency", "attributes": null }, { "code": "771476007", "description": "Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome", "attributes": null }, { "code": "771477003", "description": "15q overgrowth syndrome", "attributes": null }, { "code": "771512003", "description": "Autism spectrum disorder due to AUTS2 activator of transcription and developmental regulator deficiency", "attributes": null }, { "code": "772127009", "description": "White Sutton syndrome", "attributes": null }, { "code": "772224009", "description": "Warburg micro syndrome", "attributes": null }, { "code": "772225005", "description": "RAB18, member RAS oncogene family deficiency", "attributes": null }, { "code": "77287004", "description": "Borderline intellectual disability", "attributes": null }, { "code": "773230003", "description": "Cyclin-dependent kinase-like 5 deficiency", "attributes": null }, { "code": "773274001", "description": "X-linked intellectual disability, craniofacioskeletal syndrome", "attributes": null }, { "code": "773303005", "description": "Spondyloepimetaphyseal dysplasia Genevieve type", "attributes": null }, { "code": "773307006", "description": "Zechi Ceide syndrome", "attributes": null }, { "code": "773329005", "description": "CK syndrome", "attributes": null }, { "code": "773400009", "description": "Severe feeding difficulties, failure to thrive, microcephaly due to ASXL transcriptional regulator 3 deficiency syndrome", "attributes": null }, { "code": "773404000", "description": "Roifman syndrome", "attributes": null }, { "code": "773405004", "description": "Intellectual disability with strabismus syndrome", "attributes": null }, { "code": "773416006", "description": "Intellectual disability, facial dysmorphism, hand anomalies syndrome", "attributes": null }, { "code": "773418007", "description": "Xylosyltransferase 1 congenital disorder of glycosylation", "attributes": null }, { "code": "773419004", "description": "Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome", "attributes": null }, { "code": "773493002", "description": "9q31.1q31.3 microdeletion syndrome", "attributes": null }, { "code": "773494008", "description": "14q24.1q24.3 microdeletion syndrome", "attributes": null }, { "code": "773498006", "description": "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency", "attributes": null }, { "code": "773547003", "description": "13q12.3 microdeletion syndrome", "attributes": null }, { "code": "773548008", "description": "Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome", "attributes": null }, { "code": "773551001", "description": "Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome", "attributes": null }, { "code": "773552008", "description": "Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome", "attributes": null }, { "code": "773553003", "description": "Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome", "attributes": null }, { "code": "773554009", "description": "THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome", "attributes": null }, { "code": "773556006", "description": "Short ulna, dysmorphism, hypotonia, intellectual disability syndrome", "attributes": null }, { "code": "773578004", "description": "Spondylocostal dysostosis, hypospadias, intellectual disability syndrome", "attributes": null }, { "code": "773581009", "description": "Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome", "attributes": null }, { "code": "773583007", "description": "Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome", "attributes": null }, { "code": "773587008", "description": "X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome", "attributes": null }, { "code": "773621003", "description": "Intellectual disability, hypotonia, brachycephaly, pyloric stenosis, cryptorchidism syndrome", "attributes": null }, { "code": "773670004", "description": "Distal Xq28 microduplication syndrome", "attributes": null }, { "code": "773692000", "description": "Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome", "attributes": null }, { "code": "773699009", "description": "Pitt Hopkins-like syndrome", "attributes": null }, { "code": "773735007", "description": "Deafness with onychodystrophy syndrome", "attributes": null }, { "code": "773769008", "description": "Ataxia, photosensitivity, short stature syndrome", "attributes": null }, { "code": "773772001", "description": "Rare non-syndromic intellectual disability", "attributes": null }, { "code": "773984007", "description": "Piebald trait with neurologic defects syndrome", "attributes": null }, { "code": "774068004", "description": "AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome", "attributes": null }, { "code": "774070008", "description": "Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome", "attributes": null }, { "code": "774102003", "description": "Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome", "attributes": null }, { "code": "774149004", "description": "Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome", "attributes": null }, { "code": "774203000", "description": "Intellectual disability, severe speech delay, mild dysmorphism syndrome", "attributes": null }, { "code": "776204008", "description": "Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome", "attributes": null }, { "code": "777998000", "description": "Temtamy preaxial brachydactyly syndrome", "attributes": null }, { "code": "778009001", "description": "Blepharophimosis, intellectual disability syndrome, Verloes type", "attributes": null }, { "code": "778011005", "description": "Severe intellectual disability and progressive spastic paraplegia", "attributes": null }, { "code": "778025006", "description": "Atypical hypotonia cystinuria syndrome", "attributes": null }, { "code": "780827006", "description": "Synaptic Ras GTPase activating protein 1- related intellectual disability", "attributes": null }, { "code": "782676009", "description": "Distal trisomy 18q", "attributes": null }, { "code": "782723007", "description": "Severe intellectual disability, progressive spastic diplegia syndrome", "attributes": null }, { "code": "782736007", "description": "Intellectual disability, facial dysmorphism syndrome due to SET domain containing 5 haploinsufficiency", "attributes": null }, { "code": "782753000", "description": "Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome", "attributes": null }, { "code": "782755007", "description": "Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome", "attributes": null }, { "code": "782757004", "description": "Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome", "attributes": null }, { "code": "782772000", "description": "Congenital muscular dystrophy with intellectual disability and severe epilepsy", "attributes": null }, { "code": "782886007", "description": "Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome", "attributes": null }, { "code": "782911008", "description": "Hereditary cryohydrocytosis with reduced stomatin", "attributes": null }, { "code": "782941005", "description": "Richieri Costa-da Silva syndrome", "attributes": null }, { "code": "782945001", "description": "Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome", "attributes": null }, { "code": "783005002", "description": "Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome", "attributes": null }, { "code": "783061008", "description": "Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion", "attributes": null }, { "code": "783089006", "description": "Macrocephaly, intellectual disability, autism syndrome", "attributes": null }, { "code": "783174004", "description": "Congenital muscular dystrophy with intellectual disability", "attributes": null }, { "code": "783619003", "description": "Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion", "attributes": null }, { "code": "783702009", "description": "X-linked intellectual disability due to glutamate ionotropic receptor AMPA type subunit 3 mutations", "attributes": null }, { "code": "783703004", "description": "White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome", "attributes": null }, { "code": "785298001", "description": "Muscle eye brain disease with bilateral multicystic leukodystrophy", "attributes": null }, { "code": "785726009", "description": "Hyperekplexia epilepsy syndrome", "attributes": null }, { "code": "787093004", "description": "Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency", "attributes": null }, { "code": "787171006", "description": "21q22.11q22.12 microdeletion syndrome", "attributes": null }, { "code": "787174003", "description": "Intellectual disability, hyperkinetic movement, truncal ataxia syndrome", "attributes": null }, { "code": "787175002", "description": "Ankyrin 3 related intellectual disability, sleep disturbance syndrome", "attributes": null }, { "code": "788417006", "description": "Alopecia, epilepsy, intellectual disability syndrome Moynahan type", "attributes": null }, { "code": "788584007", "description": "Blepharophimosis and mental retardation syndrome", "attributes": null }, { "code": "79385002", "description": "Lowe syndrome", "attributes": null }, { "code": "816067005", "description": "Diabetes, hypogonadism, deafness, intellectual disability syndrome", "attributes": null }, { "code": "838441009", "description": "Mental retardation, adducted thumbs, shuffling gait, aphasia syndrome", "attributes": null }, { "code": "840505007", "description": "Down syndrome co-occurrent with leukemoid reaction associated transient neonatal pustulosis", "attributes": null }, { "code": "86765009", "description": "Mild intellectual disability", "attributes": null }, { "code": "889211000000104", "description": "Specific learning disability", "attributes": null }, { "code": "984661000000105", "description": "Mild learning disability", "attributes": null }, { "code": "984671000000103", "description": "Moderate learning disability", "attributes": null }, { "code": "984681000000101", "description": "Profound learning disability", "attributes": null } ] } ], "coding_system_release": "", "open_codelist_version_id": "33997b8e", "open_codelist_version_tag": "v1", "status": 1, "doi": "https://doi.org/10.48533/wvav-km76", "is_deleted": false, "publish_status": 2, "owner": "ieuan.scanlon", "template": { "id": 3, "name": "OpenCodelists Phenotype", "description": "OpenSafely's OpenCodelist Phenotype, visit https://www.opencodelists.org/ to learn more", "version_id": 1 }, "versions": [ { "version_id": 9043, "version_name": "Wider Learning Disability", "version_date": "2026-01-26T23:38:16.064077Z", "is_published": true, "is_latest": true } ] } ]