Learning Disability
Learning Disability
About the Disease
Learning Disability, also known as learning disabilities, is related to sotos syndrome and dysgraphia. An important gene associated with Learning Disability is FIBP (FGF1 Intracellular Binding Protein), and among its related pathways/superpathways are Neuroscience and Fragile X syndrome. The drugs Dopamine and Aripiprazole have been mentioned in the context of this disorder. Affiliated tissues include brain, temporal lobe and eye.
Common Targets
ATXN7 | MED23 | SRGAP2C | DNAAF4-CCPG1 | OPHN1 | TAF1 | ADORA1 | ADORA2A-AS1 | GPT2 | SPECC1L-ADORA2A | G1385 | TBC1D7 | ADORA2A | FOXP2 | NOS3 | PLA2G6 | PURA | MROH6 | LRP2BP | ZIC1 | TELO2 | DEAF1 | PARK7 | DDX3X | HCFC1 | DNAAF4 | ARHGEF2 | PRKCE | ADAT3 | IL1RAPL2 | GRIN2B | cAMP Responsive Element Binding Protein (CREB) (nonspecified subtype)

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Other Diseases
Trichomegaly | Bone Giant Cell Tumor | Diabetes Type 1 | Dysequilibrium Syndrome | Thrombocythemia, Essential | Wilson's Disease | Craniolenticulosutural Dysplasia | Episodic Ataxia Type 2 | Best Macular Dystrophy | Retinitis Pigmentosa | Bare Lymphocyte Syndrome | Microvillus Inclusion Disease | Avellino Corneal Dystrophy | N-acetylglutamate Synthase Deficiency | Progressive Familial Intrahepatic Cholestasis Type 1 | Spinal Cord Diseases | Long QT Syndrome Type 1 | Diabetic Encephalopathy | Pseudohypoparathyroidism Type 2 | Cholestasis, Intrahepatic | Insulin Resistance | Adenoma, Villous | Sitosterolemia | Globozoospermia | Seizures | Campomelic Dysplasia | Language Disorders | Dystonia-parkinsonism, X-linked | Ocular Albinism Type 1 | Hydrops Fetalis | ACTH-independent Macronodular Adrenal Hyperplasia | Batten Disease | Tyrosinemia | Familial Advanced Sleep Phase Syndrome | Sick Sinus Syndrome | Cerebrovascular Disorders | Neuromyelitis Optica | Polymicrogyria | Eating Disorder | Poretti-Boltshauser Syndrome | Cancer, Prostate | Scoliosis | Agnathia-Otocephaly Complex | Common Variable Immunodeficiency | Diabetic Neuropathy | Sepiapterin Reductase Deficiency | GATA2 Deficiency | Cerebellofaciodental Syndrome | Bursitis | Crisponi Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Congenital Dyserythropoietic Anemia Type 1 | Retinopathy, Diabetic | Seminoma | Ocular Surface Squamous Neoplasia | Liddle Syndrome | Leukemia-lymphoma, Adult T-cell | T-cell Chronic Lymphocytic Leukemia | Mitochondrial DNA Depletion Syndrome | Dowling-Degos Disease | Adenosine Deaminase 2 Deficiency | Hypertriglyceridemia | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Nance-Horan Syndrome | Corneal Dystrophies, Hereditary | Juvenile Xanthogranuloma | Congenital Hereditary Endothelial Dystrophy Type II | Zimmermann-Laband Syndrome | Hashimoto Thyroiditis | Hairy Cell Leukemia | Chanarin-Dorfman Syndrome | Postaxial Polydactyly | Lymphomatoid Granulomatosis | Dysthymia | Hemochromatosis | Thymoma, Malignant | Erysipelas | Neurofibromatosis Type 2 | Pendred Syndrome | Dystonia | Mitochondrial Encephalomyopathy | Lichen Sclerosus | Bernard-Soulier Syndrome | Neurocysticercosis | Alpha-1 Antitrypsin Deficiency | Sickle Cell Anemia | Treacher Collins Syndrome | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Acquired Partial Lipodystrophy | Olmsted Syndrome | Otosclerosis | Osteomalacia | Familial Digital Arthropathy-brachydactyly | Biotinidase Deficiency | Wolman Disease | Tyrosinemia Type 1 | Spinocerebellar Ataxia Type 17 | Microphthalmia | Peroxisomal Disorder | Pompe Disease | Long QT Syndrome Type 3 | Endophthalmitis | Li-Fraumeni Syndrome | Premature Ejaculation | Binge Eating Disorder | Castleman Disease | Gastroschisis | Tietze Syndrome | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Leishmaniasis, Visceral | Fanconi Anemia | Melanocytic Nevus | Dengue Hemorrhagic Fever | Apraxia | Superficial Spreading Melanoma | Monilethrix | Open-angle Glaucoma | Joubert Syndrome 2 | Chondrodysplasia Punctata 2, X-linked Dominant | Oligoasthenoteratozoospermia | Endometrial Hyperplasia | Schwannoma | Peripheral T-cell Lymphoma | Hemophagocytic Lymphohistiocytosis | Rash | Benign Hereditary Chorea | Pneumonia, Mycoplasma | Kernicterus | Glutaric Aciduria Type 1 | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Thyroid Dyshormonogenesis | GM2-gangliosidosis AB Variant | Hyperparathyroidism-jaw Tumor Syndrome | Wolff-Parkinson-White Syndrome | Optic Neuropathy | Sarcoma, Endometrial Stromal | Gyrate Atrophy Of The Choroid And Retina | Erythema Multiforme | Congenital Tufting Enteropathy | Membranous Nephropathy | Myositis, Focal | Carcinoid Syndrome | Transient Bullous Dermolysis Of The Newborn | Cardiac Arrest | Pfeiffer Syndrome | Tendinitis | Lathosterolosis | Hereditary Folate Malabsorption | Epidermal Nevus Syndrome | Early Infantile Epileptic Encephalopathy 28 | Necrobiosis Lipoidica | Rheumatic Heart Disease | Cystinosis | X-linked Acrogigantism | Peutz-Jeghers Syndrome | Molybdenum Cofactor Deficiency | Ileitis | Hemolytic Uremic Syndrome, Atypical | Intermittent Explosive Disorder | Cholera | Muckle-Wells Syndrome | Cone Dystrophy | Erectile Dysfunction | Multiple Epiphyseal Dysplasia | Noonan Syndrome-like Disorder With Loose Anagen Hair | Xeroderma Pigmentosum Variant Type | Lymphoma, B-cell | Hyper IgE Syndrome | Diverticulitis | Duchenne Muscular Dystrophy | Hyperuricemia | Retinal Diseases | Babesiosis | B-cell Chronic Lymphocytic Leukemia | Proteus Syndrome | Usher Syndrome | Schuurs-Hoeijmakers Syndrome | Polycystic Liver | Mood Disorder | Pancytopenia | Protein S Deficiency | Stevens-Johnson Syndrome | D-2-Hydroxyglutaric Aciduria | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Heimler Syndrome | 3-methylglutaconic Aciduria Type IV | Vitreoretinal Degeneration, Snowflake Type | Myopathy | Blau Syndrome | Tibial Muscular Dystrophy | Narcolepsy | Discoid Lupus Erythematosus | Tylosis With Esophageal Cancer | Hyperinsulinemic Hypoglycemia | Ganglioneuroma | Herpes Simplex Dermatitis | Infertility, Male | Primary Progressive Aphasia | Cardiofaciocutaneous Syndrome | Alveolar Capillary Dysplasia | Vitiligo | Hepatitis, Autoimmune | Hemosiderosis | Angioedema, Hereditary | Hypertension, Pulmonary | Macrodactyly | Sertoli Cell-only Syndrome | Milk Allergy | Oculocutaneous Albinism Type 1 | Osteogenesis Imperfecta Type VI | Succinic Semialdehyde Dehydrogenase Deficiency | Hyperinsulinemia | Greig Cephalopolysyndactyly Syndrome | Thrombophilia | Dementia, Vascular | Thyroid Hormone Resistance | Pleurisy | Netherton Syndrome | Renal Dysplasia | Pyoderma Gangrenosum | Blepharo-cheilo-odontic Syndrome | Mycosis Fungoides | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Sclerosteosis 2 | Rosacea | Blomstrand Osteochondrodysplasia | Hemochromatosis Type 2 | Pseudohypoparathyroidism Type 1B | Tonsillitis | Multiple Sclerosis, Secondary Progressive | Axenfeld-Rieger Syndrome | Eiken Syndrome | Silicosis | Osteogenesis Imperfecta | Chronic Idiopathic Myelofibrosis | Schizoaffective Disorder | Congenital Adrenal Hyperplasia | Pseudoachondroplasia | Lymphoproliferative Disease, X-linked | Thanatophoric Dysplasia Type 1 | Multiple System Atrophy | Hypohidrotic Ectodermal Dysplasia | Anti-NMDA Receptor Encephalitis | Fontaine Progeroid Syndrome | Hypermetropia | Congenital Dyserythropoietic Anemia | Tangier Disease | Hypercholesterolemia | Pontocerebellar Hypoplasia Type 7 | Hypolipoproteinemia | Hyperbilirubinemia, Neonatal | Usher Syndrome Type II | Gnathodiaphyseal Dysplasia | Bronchitis, Chronic | Synpolydactyly | Cohen Syndrome | Fragile X Syndrome | Pseudomyxoma Peritonei | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Congenital Absence Of Vas Deferens | Hyperparathyroidism, Secondary | Huntington's Disease | Patent Foramen Ovale | Spinocerebellar Ataxia Type 15 | Otopalatodigital Syndrome Type 2 | Chronic Myeloid Leukemia | Headache | Dystrophy, Cone-rod | CEDNIK Syndrome | Osteosarcoma | Phenylketonuria | Retinitis | Optic Neuritis | Hyperphenylalaninemia | Cholelithiasis | Angelman Syndrome | Neuroleptic Malignant Syndrome | Glutathione Synthetase Deficiency | Periventricular Nodular Heterotopia | Eccrine Porocarcinoma | Follicular Dendritic Cell Sarcoma | Neuroectodermal Tumors, Primitive | Spinocerebellar Ataxia Type 27 | Tic Disorder | Oral Lichen Planus | Kohlschutter-Tonz Syndrome | Leukodystrophies | Oguchi Disease-2 | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Blood Protein Disorders | Salla Disease | Pernicious Anemia | Gestational Trophoblastic Disease | Rhabdomyosarcoma, Embryonal | McLeod Syndrome | Diffuse Intrinsic Pontine Glioma | Miyoshi Myopathy | Hypotrichosis Simplex | Non-Langerhans Cell Histiocytosis | Goldenhar Syndrome | Keratitis | Wiskott-Aldrich Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Hepatitis D | Amelanotic Melanoma | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Polyradiculopathy | Limb Girdle Muscular Dystrophy | Lipid Storage Myopathy | Teratozoospermia | Infantile Spasm | Hepatorenal Syndrome | Cutis Laxa | Congenital Ichthyosiform Erythroderma | Premenstrual Syndrome | Spasticity | Lymphoma, Mantle Cell | Thyrotoxic Periodic Paralysis | Brugada Syndrome 1 | Anthrax | Early Infantile Epileptic Encephalopathy | Glycogen Storage Disease Type 0, Muscle | Rheumatoid Arthritis | Coloboma | Kashin-Beck Disease | Uterine Leiomyoma | Stroke, Hemorrhagic | Renal Tubular Acidosis | Alopecia | Retinal Degeneration | Lipodystrophy | Juvenile Hyaline Fibromatosis | Guillain-Barre Syndrome | Retinal Vasculitis | Celiac Disease | Hepatic Adenomatosis | Ureteropelvic Junction Obstruction | Cantu Syndrome | Optic Atrophy 2 | Primary Progressive Nonfluent Aphasia | Crouzon Syndrome With Acanthosis Nigricans | Prediabetes | Congenital Hemolytic Anemia | Canavan Disease | Diabetes | Osteoglophonic Dysplasia | Pelizaeus-Merzbacher Disease | Hyperbilirubinemia | Woodhouse-Sakati Syndrome | Progressive Familial Intrahepatic Cholestasis | Sclerosing Cholangitis | Pierson Syndrome | Reticular Dysgenesis | Orthostatic Intolerance | Long QT Syndrome Type 2 | Acute Coronary Syndrome | Heavy Chain Disease | Moyamoya Disease | Inborn Errors Of Metabolism | Megaloblastic Anemia | Primary Hyperoxaluria | Proximal Symphalangism | Sleep Apnea | Hemolytic Uremic Syndrome | Coronary Heart Disease | Neurofibromatosis | Leri Pleonosteosis | Familial Isolated Hyperparathyroidism | Unverricht-Lundborg Syndrome | Toxoplasmosis | Acromegaly | Choriocarcinoma | Autosomal Recessive Spastic Paraplegia Type 75 | Nevus | Exostoses | Niemann-Pick Disease, Type B | Vestibular Disease | Optic Nerve Hypoplasia, Bilateral | Anterior Segment Dysgenesis | Familial Pheochromocytoma-paraganglioma | Hyperacusis | Lyme Disease | Cousin Syndrome | Fibrosarcoma | Myelitis, Transverse | Conduct Disorder | Chordoid Glioma | Leukoplakia | Fetal And Neonatal Alloimmune Thrombocytopenia | Angina Pectoris | Retinal Telangiectasia | Craniometaphyseal Dysplasia | Pontocerebellar Hypoplasia | Cavitary Optic Disc Anomalies | Prostatitis | Bacterial Meningitis | Costello Syndrome | Pemphigus Foliaceus | Pulmonary Stenosis