Causes of Learning disability

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Conditions listing medical complications: Learning disability:

The following list of medical conditions have 'Learning disability' or similar listed as a medical complication in our database. This computer-generated list of complications may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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More Information About Learning disability

• Learning disability: Introduction
• Medical Textbooks Online for Learning disability
• Symptom combinations for Learning disability

List of 392 causes of Learning disability

This section shows a full list of all the diseases and conditions listed as a possible cause of Learning disability in our database from various sources.

• 22q11.2 deletion syndrome - Learning disability
• 3-Methylglutaconic aciduria type 1
• 3-Methylglutaconic aciduria type 3
• 3-Methylglutaconic aciduria type 4
• 47, XYY syndrome - learning disability
• 47,XXX syndrome - learning disability
• 48,XXXY syndrome
• 49,XXXXX syndrome
• 6-Pyruvoyl tetrahydropterin synthase deficiency
• Adenylosuccinate lyase deficiency
• Aicardi Goutieres syndrome
• Aicardi's syndrome
• Akesson syndrome
• Alexander disease
• Allan-Herndon-Dudley syndrome
• Alpha thalassaemia X-linked mental retardation syndrome
• Alpha-L-iduronidase deficiency
• Alpha-mannosidase deficiency
• Alpha-thalassemia/mental retardation syndrome, deletion type
• Amelo-cerebro-hypohidrotic syndrome - learning disability
• Aminomethyltransferase deficiency
• Andermann syndrome
• Angelman's syndrome
• Apert syndrome
• Arginase deficiency
• Arginosuccinate synthetase deficiency
• Arginosuccinic aciduria
• Arkless-Graham syndrome
• Arterial occlusive disease, progressive - hypertension - heart defects - bone fragility - brachysyndactyly - learning disability
• Aspartoacylase deficiency
• Aspartylglucosaminuria
• Athabaskan brain stem dysgenesis
• Atkin-Flaitz-Patil syndrome
• Autism - learning disability
• Baller-Gerold syndrome
• Baraitser-Winter syndrome
• Bardet-Biedl syndrome
• Behr syndrome
• Berardinelli lipodystrophy syndrome
• Bertini syndrome
• Bilateral frontoparietal polymicrogyria
• Birth hypoxia
• Black locks, oculocutaneous albinism, and deafness of the sensorineural type
• Blepharonasofacial syndrome
• Blepharophimosis syndrome
• Borjeson-Forssman-Lehmann syndrome
• Branchial arch syndrome X-linked - learning disability
• BRESHECK syndrome
• Bruch-de Lange syndrome
• CAMFAK syndrome
• Carbamoylphosphate synthetase 1 deficiency disease
• Carbamoylphosphate synthetase deficiency
• Carbohydrate deficient glycoprotein syndrome type 1a
• Carbonic anhydrase type 2 deficiency
• Cardiofaciocutaneous syndrome
• Carnosinaemia
• Cerebral palsy, spastic, diplegic - learning disability
• Cerebrocostomandibular syndrome
• Ceroid lipofuscinosis neuronal 2 late infantile
• Ceroid lipofuscinosis neuronal type 8
• Ceroid lipofuscinosis, neuronal 1, infantile
• Ceroid lipofuscinosis, neuronal 3, juvenile
• Ceroid lipofuscinosis, neuronal 5
• Charcot-Marie-Tooth-Hoffmann syndrome, X-linked type 2
• CHARGE syndrome
• Child abuse
• Childhood disintegrative disorder
• Cholestanol storage disease
• Christian syndrome 1
• Chromosome 12p tetrasomy syndrome
• Chromosome 13 trisomy syndrome
• Chromosome 18 trisomy syndrome
• Chromosome 1q21.1 Duplication Syndrome - learning disability
• Chromosome 21 ring syndrome
• Chromosome 22 ring syndrome
• Chromosome 22, microdeletion 22q11 - learning disability
• Chromosome 22q deletion - learning disability
• Chromosome 22q11.2 deletion syndrome - learning disability
• Chromosome 4 ring syndrome
• Chromosome 6 ring syndrome
• Chromosome 7 deletion p21-p22.1 - learning disability
• Chromosome 7q deletion syndrome
• Chromosome 8 recombinant syndrome
• Chromosome 8 trisomy syndrome
• Chromosome 8, mosaic trisomy - Learning disability
• Chromosome 8, trisomy - learning disability
• Chromosome 9 inversion or duplication - learning disability
• Chromosome 9 ring syndrome
• Chromosome 9 trisomy syndrome
• Chromosome 9, partial trisomy 9p - learning disability
• Chromosome 9p duplication syndrome
• Chronic illness
• Chylomicron retention disease
• CINCA syndrome
• Cockayne syndrome
• CODAS (cerebral, ocular, dental, auricular, skeletal) syndrome
• Coenzyme Q 10 (CoQ10), deficiency - learning disability
• Coenzyme Q10 deficiency
• Coffin syndrome 1
• Coffin-Lowry syndrome
• Coffin-Siris syndrome
• Cohen syndrome
• Coloboma uveal with cleft lip palate and mental retardation - learning disability
• Coloboma, cleft lip/palate and mental retardation syndrome - learning disability
• Congenital disorder of glycosylation type 2a
• Congenital muscular dystrophy, autosomal recessive
• Congenital myotonic dystrophy
• Cornelia de Lange syndrome
• Corpus callosum agenesis type 2
• Costello syndrome
• Craniofacial dysmorphism-polysyndactyly syndrome
• Cri du chat syndrome 5p−
• Crome syndrome
• Cross-McKusick-Breen syndrome
• Cumming syndrome
• Cystathionine beta-synthase deficiency
• Cytomegalovirus, congenital
• D-glycerate kinase deficiency
• De Barsy syndrome
• Deletion 22q11 - learning disability
• Deletion 5p - learning disability
• Desbuquois syndrome
• Dibasic aminoaciduria type 1
• Dibasic aminoaciduria type 2
• Diffuse sclerosis of Schilder
• DiGeorge syndrome - learning disability
• Dihydropteridine reductase deficiency
• Dihydropyrimidine dehydrogenase deficiency
• Down syndrome
• Dubowitz syndrome
• Duplication 9p partial - learning disability
• Dyggve-Melchior-Clausen dysplasia
• Dyke-Davidoff-Masson syndrome
• Dysosteosclerosis
• Emery-Dreifuss muscular dystrophy, X-linked
• Epidermal naevus syndrome
• Ethylmalonic encephalopathy
• Faciocardiorenal syndrome
• Familial histiocytic reticulosis
• Fanconi anaemia
• Farber's disease
• Feingold syndrome
• Fetal aminopterin-like syndrome
• Filippi syndrome
• Fitzsimmons syndrome
• Floating-Harbor syndrome
• Focal dermal hypoplasia
• Four X syndrome
• Fragile X syndrome
• Frontometaphyseal dysplasia
• Fryns syndrome 2
• Fryns-van den Berghe syndrome
• Fucosidosis
• Fukuyama congenital muscular dystrophy
• Fumarase deficiency
• Galactose epimerase deficiency
• Galactosemia type 1
• Galactosialidosis
• Galloway-Mowat syndrome
• Gamma-aminobutyrate transaminase deficiency
• Gangliosidosis GM1, type 3
• Gangliosidosis GM3
• Gareis-Mason syndrome
• Gaucher's disease
• Generalized gangliosidosis GM1
• Gerhardt syndrome
• Giant axonal neuropathy
• Gillespie syndrome
• Glucose phosphate isomerase deficiency
• Glucose transport defect, blood-brain barrier - learning disability
• Glucose transporter type 1 deficiency
• Glutamate formiminotransferase deficiency
• Glutaric aciduria type 1
• Glutathione synthase deficiency
• Glycerol kinase deficiency
• Glycine decarboxylase deficiency
• GM1 gangliosidosis, type 2
• GM2 gangliosidosis type AB
• Golabi-Ito-Hall syndrome
• GOMBO syndrome
• Grubben syndrome
• Hair-brain syndrome
• Hartnup's disease
• Hearing impairment
• Hennekam syndrome
• Hereditary orotic aciduria
• Hereditary sensory and autonomic neuropathy type 4
• Herpes, Neonatal - learning disability
• Herpes, Neonatal - Central Nervous System Infection - learning disability
• Herpes, Neonatal - Disseminated - learning disability
• Hidrotic ectodermal dysplasia
• Hischsprung disease-microcephaly-mental retardation syndrome
• Histidinaemia
• Holoprosencephaly
• Homocarnosinase deficiency
• Hoyeraal-Hreidarsson syndrome
• Human HOXA1 Syndromes - learning disability
• Hydrocephalus
• Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome
• Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome - learning disability
• Hypochondroplasia
• Hypothyroidism, congenital
• I-cell disease
• Iduronate sulphatase deficiency
• Iminodipeptiduria
• Inborn amino acid metabolism disorder - learning disability
• Incontinentia pigmenti
• Intraventricular haemorrhage
• Jackson-Weiss syndrome
• Jacobsen syndrome
• Jaffe-Campanacci syndrome
• Johanson-Blizzard syndrome
• Joubert syndrome
• Kabuki make-up syndrome
• Klinefelter syndrome
• Klinefelter variant
• Kohlschutter syndrome
• Krause-van Schooneveld-Kivlin syndrome
• Langer-Giedion syndrome
• Lathosterolosis
• Laurence-Moon syndrome
• Lennox-Gastaut syndrome
• Lenz microphthalmia syndrome
• Lenz-Majewski hyperostosis syndrome
• Leprechaunism
• Lesch-Nyhan syndrome
• Leucinosis - learning disability
• Lowe syndrome
• Lowry-MacLean syndrome
• Lowry-Wood syndrome
• Lujan-Fryns syndrome
• Lysine: alpha-ketoglutarate reductase deficiency
• Malonyl-CoA decarboxylase deficiency
• Maple syrup urine disease
• Marinesco-Sjogren-Garland syndrome
• Marshall-Smith-Weaver syndrome
• Martsolf syndrome
• Meckel-Gruber syndrome
• Megalencephalic leukoencephalopathy with subcortical cysts - learning disability
• MELAS
• Menke disease
• Methionine malabsorption
• Methionine synthase deficiency
• Methylenetetrahydrofolate reductase deficiency
• Methylmalonic aciduria type 2
• Mevalonate kinase deficiency
• Michels syndrome
• Microcephaly - oculo-digito-esophageal-duodenal syndrome (MODED) - learning disability
• Microphthalmia-dermal aplasia-sclerocornea syndrome
• Miller-Dieker syndrome
• Mirhosseini-Holmes-Walton syndrome
• Mohr-Tranebjaerg syndrome
• Molybdenum cofactor deficiency
• Monoamine oxidase A (MAOA) deficiency
• Mowat-Wilson syndrome - learning disability
• Mucolipidosis III
• Mucolipidosis IV
• Mucopolysaccharidosis VII
• Mucosulfatidosis
• Multiple pterygium syndrome
• Muscle-eye-brain disease
• Myhre syndrome
• Myotonic dystrophy
• NADH-dependent methemoglobin reductase deficiency
• Neuhauser syndrome
• Neural tube defects
• Neurofibromatosis type 1
• Neuropathy - ataxia - retinitis pigmentosa - learning disability
• Neuropathy ataxia and retinis pigmentosa - learning disability
• Nijmegen chromosome breakage syndrome
• NOMID syndrome - learning disability
• Non-ketotic hyperglycinemia L protein deficiency
• Non-ketotic hyperglycinemia type 3
• Nonbullous congenital ichthyosiform erythroderma
• Noonan's syndrome
• Norrie's disease
• Occipital horn syndrome
• Oculocerebrocutaneous syndrome
• Oculodigitoesophagoduodenal syndrome - learning disability
• Ohdo blepharophimosis syndrome
• Ohtahara syndrome
• Opitz trigonocephaly syndrome
• Opitz-Frias syndrome
• Opitz-Kaveggia syndrome
• Oral-facial-digital syndrome type 3
• Ornithine carbamyltransferase deficiency
• Orofaciodigital syndrome type 1
• Osteopathia striata with cranial sclerosis
• Osteoporosis-pseudoglioma syndrome
• Otopalatodigital syndrome type 2
• Paraplegia - brachydactyly - cone-shaped epiphysis - learning disability
• Periodic hyperlysinemia
• Peroxisomal acyl-CoA oxidase deficiency
• Pettigrew syndrome
• Phenylalanine hydroxylase deficiency
• Pitt-Rogers-Danks syndrome
• Poor self esteem
• Potocki-Shaffer syndrome
• PPM-X syndrome
• Prader-Willi syndrome
• Progressive encephalopathy-edema-hypsarrhythmia-optic atrophy syndrome
• Propionyl-CoA carboxylase deficiency
• Proteus syndrome
• Proud syndrome
• Pseudohypoparathyroidism type 1a
• Purine nucleoside phosphorylase (PNP) deficiency
• Pyruvate dehydrogenase deficiency
• Ramon syndrome
• Recessive deafness-onychodystrophy-osteodystrophy-retardation syndrome
• Renpenning syndrome 1
• Rett syndrome
• Rhizomelic chondrodysplasia punctata
• Ritscher-Schinzel syndrome
• Roberts pseudothalidomide syndrome
• Rubella, congenital
• Rubinstein-Taybi syndrome
• Rud's syndrome
• Rutherfurd syndrome
• Ruvalcaba-Reichert-Smith syndrome
• Saccharopine dehydrogenase deficiency
• Saethre-Chotzen syndrome, chromosome 7 p21.1p21.3 - learning disability
• Salaam attacks
• Salla disease
• Sanfilippo disease
• Sanjad-Sakati syndrome
• Sarcosinaemia
• Say-Meyer syndrome
• Schinzel acrocallosal syndrome
• Schizencephaly
• Schwartz-Jampel-Aberfeld syndrome
• Scott craniodigital syndrome
• Seemanova syndrome 1
• Seemanova-Lesny syndrome
• Seitelberger's disease
• Septo-Optic Dysplasia - learning disability
• Septooptic dysplasia - digital anomalies - learning disability
• Severe myoclonic epilepsy in infancy
• Shprintzen omphalocele syndrome - learning disability
• Shprintzen syndorme - learning disability
• Shprintzen-Golberg craniosynostosis - learning disability
• Shprintzen-Goldberg syndrome
• Shwachman-Diamond syndrome
• Sialidosis type 1
• Sjogren-Larsson syndrome
• Smith-Lemli-Opitz syndrome
• Smith-Magenis syndrome
• Smith-McCort dysplasia
• Sotos syndrome - learning disability
• Sphingomyelinase deficiency
• Spina bifida - learning disability
• Spondylometaphyseal dysplasia, X-linked
• Sturge-Weber syndrome
• Subependymal nodular heterotopia - learning disability
• Succinic semialdehyde dehydrogenase deficiency
• Sulfatidosis juvenile, Austin type - learning disability
• Sulphite oxidase deficiency
• Sutherland-Haan syndrome
• Syphilis, congenital
• Tay-Sachs disease
• Ter Haar syndrome
• Thyroid agenesis - learning disability
• Timothy syndrome
• Tricho-thiodystrophy
• Triosephosphate isomerase deficiency
• Trisomy 18 mosaicism - learning disability
• Trisomy 8 mosaicism - learning disability
• Trisomy X
• Tuberous sclerosis
• Turner's syndrome
• Tyrosinaemia type 2
• Urocanate hydratase deficiency
• Van der Knaap disease
• Varadi-Papp syndrome
• Velocardiofacial syndrome - learning disability
• Vision impairment
• Waardenburg syndrome type 3
• WAGR syndrome
• Waisman-Laxova syndrome
• Walker-Warburg syndrome
• Wieacker-Wolff syndrome
• Wiedemann-Rautenstrauch syndrome
• Williams syndrome
• Wolf-Hirschhorn syndrome
• Worster-Drought syndrome
• Wrinkly skin syndrome
• X-linked mental retardation 1
• X-linked mental retardation-hypotonic facies syndrome
• X-linked periventricular heterotopia
• Xylosylprotein 4-beta-galactosyltransferase deficiency
• Young-Hughes syndrome
• Yunis-Varon syndrome
• Zunich neuroectodermal syndrome

Medical Textbooks about Learning disability

Free online access to excerpts without registration is available to view excerpts from medical textbooks about the causes and diagnosis of Learning disability. Refer to our list of medical textbooks discussions about Learning disability (Free online access to book excerpts, no registration).

 » Next page: Diagnostic Guides Online for Learning disability

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