Disease

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)

疾病靶点研报
Learning Disability

Note: If you'd like to get a target analysis report for Learning Disability, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Learning Disability at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Dementia, Vascular | Anodontia | Inborn Errors Of Metabolism | Hemorrhoids | Congenital Dyserythropoietic Anemia | Microphthalmia, Syndromic 7 | Polycythemia Vera | Rubinstein-Taybi Syndrome | Early Infantile Epileptic Encephalopathy 13 | Oculodentodigital Dysplasia | Autonomic Neuropathy | Nephrosclerosis | Intestinal Hypomagnesemia 1 | Hypervalinemia | Hemochromatosis Type 2 | Seizures-scoliosis-macrocephaly Syndrome | Traboulsi Syndrome | Pseudomyxoma Peritonei | Combined Deficiency Of Factor V And Factor VIII | Nemaline Myopathy 8 | Diastrophic Dysplasia | Androgenic Alopecia | Optic Neuritis | Eclampsia | Primary Pigmented Nodular Adrenocortical Disease | Jalili Syndrome | Cole-Carpenter Syndrome | Alazami Syndrome | Carotid Artery Disease | Palmoplantar Keratoderma | Pelizaeus-Merzbacher Disease | Burn-McKeown Syndrome | Ichthyosis Hystrix, Curth-Macklin Type | Nemaline Myopathy | Dysgerminoma | Splenomegaly | Diabetes Gestational | Toxic Epidermal Necrolysis | Johanson-Blizzard Syndrome | Stomatitis | Malignant Fibrous Histiocytoma | Coffin-Lowry Syndrome | Cervical Dystonia | Endocarditis | Familial Thoracic Aortic Aneurysm | Paronychia | Meningeal Melanocytoma | Myosin Storage Myopathy | Liver Failure, Acute Infantile | Mumps | Antiphospholipid Syndrome | Spinocerebellar Ataxia Type 40 | Progressive Familial Intrahepatic Cholestasis Type 2 | Polydactyly | Blastoma, Pleuropulmonary | Speech Disorders | Reye Syndrome | Paget's Disease Of The Breast | Kaposi Sarcoma | Hyperinsulinism-hyperammonemia Syndrome | Hypogammaglobulinemia | Lipoma | Posterior Polar Cataract | Erythrokeratodermia Variabilis | Myositis, Focal | Interstitial Lung Diseases | Charcot-Marie-Tooth Disease, Type 2 | Wolfram Syndrome 2 | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Carcinoma, Transitional Cell | Glutaric Aciduria Type 2 | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Chondrodysplasia Punctata | Camptocormia | Charcot-Marie-Tooth Disease Axonal Type 2N | Nager Acrofacial Dysostosis | Retinal Dystrophy | Kidney Stones | Mixed Connective Tissue Disease | Angiomyolipoma | Lymphoma, AIDS-related | Metachromatic Leukodystrophy | Primary Lateral Sclerosis | Subcortical Band Heterotopia | Facioscapulohumeral Muscular Dystrophy Type 2 | Spinocerebellar Ataxia Type 16 | Greig Cephalopolysyndactyly Syndrome | Primary Ovarian Insufficiency | Scoliosis | Spondylolisthesis | Pseudohypoparathyroidism Type 1B | Distal Spinal Muscular Atrophy | Polyarteritis Nodosa | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Alopecia Totalis | Erythromelalgia | Systemic Lupus Erythematosus | Plasma Cell Dyscrasia | Antisocial Personality Disorder | Bethlem Myopathy | Triple A Syndrome | Familial Hypertrophic Cardiomyopathy | DNA Ligase IV Deficiency | Enhanced S-cone Syndrome | Conjunctivitis | Gastritis, Atrophic | Mandibuloacral Dysplasia With Type A Lipodystrophy | Multiple Myeloma | Cardiac Sarcoidosis | Huntington's Disease | Anorexia Nervosa | Erythropoietic Protoporphyria | Tularemia | Lichen Planus | Gynecomastia | Dyggve-Melchior-Clausen Disease | Usher Syndrome Type III | Cohen Syndrome | Hyperlipidemia Type V | Spondyloarthritis | Early Infantile Epileptic Encephalopathy 28 | Carcinoid Tumor | GAPO Syndrome | Gerstmann-Straussler-Scheinker Syndrome | Hypodontia | Myelitis, Transverse | Ameloblastoma | Lymphangioleiomyomatosis | Neurofibromatosis Type 2 | Giant Axonal Neuropathy | Diabetes Insipidus, Neurogenic | Vulvovaginitis | Metanephric Adenoma | Dysplastic Nevus | Li-Fraumeni Syndrome | Osteopetrosis | Panuveitis | Polycystic Kidney, Autosomal Recessive | Obsessive-compulsive Disorder | Loeys-Dietz Syndrome | Syndactyly | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Juvenile Hyaline Fibromatosis | Rolandic Epilepsy | Cutaneous T-cell Lymphoma | Lymphedema | Hartsfield Syndrome | Acute Coronary Syndrome | Lipid Storage Myopathy | Chorea-acanthocytosis | DRESS Syndrome | Arthritis | Brooke-Spiegler Syndrome | Niemann-Pick Disease | Hemorrhagic Disorders | Prune Belly Syndrome | Hypopituitarism | Behcet's Disease | Fowler's Syndrome | Fundus Albipunctatus | Immunoproliferative Disorders | Gilbert Syndrome | Alveolar Capillary Dysplasia | Chondromyxoid Fibroma | Danon Disease | Antley-Bixler Syndrome | Ellis-Van Creveld Syndrome | Smith-Magenis Syndrome | Hypophosphatasia | Desmosterolosis | Acromegaly | Cornelia De Lange Syndrome | Mosaic Variegated Aneuploidy Syndrome 2 | Ophthalmoplegia | Congenital Lipoid Adrenal Hyperplasia | Zygomycosis | Facioscapulohumeral Muscular Dystrophy Type 1 | Apert Syndrome | Seasonal Mood Disorder | Sickle Cell Disease | Primary Biliary Cholangitis | Exocrine Pancreatic Insufficiency | Hypereosinophilic Syndrome | SAPHO Syndrome | Hemolytic Anemia | Leukoplakia | Chorea | Schwartz-Jampel-Aberfeld Syndrome | Keloid | Frank-ter Haar Syndrome | Pathological Gambling | Angiodysplasia | Neurofibromatosis | Emery-Dreifuss Muscular Dystrophy | Large Granular Lymphocytic Leukemia | Spinocerebellar Ataxia | MELAS Syndrome | Pulmonary Alveolar Microlithiasis | Tyrosinemia | Precocious Puberty | Distal Myopathy 2 | Sotos Syndrome | Carbonic Anhydrase VA Deficiency | T-cell Prolymphocytic Leukemia | Narcolepsy | Ichthyosis Bullosa Of Siemens | Raine Syndrome | Shock, Cardiogenic | Myopia | Pituitary Stalk Interruption Syndrome | Primary Familial Brain Calcification | Lymphomatoid Granulomatosis | Japanese Encephalitis | Cancer, Brain | Methylmalonic Acidemia | Arthritis, Gouty | Lymphoma | Benign Recurrent Intrahepatic Cholestasis 1 | Kleine-Levin Syndrome | Central Retinal Artery Occlusion | Renal Medullary Carcinoma | VEXAS Syndrome | Peyronie's Disease | Williams Syndrome | Ligneous Conjunctivitis | Exfoliative Dermatitis | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Autism | Kindler Syndrome | Currarino Syndrome | Meesmann Corneal Dystrophy | Cutaneous Angiosarcoma | Polycystic Liver | Hydrops Fetalis | Retinitis | Skin Carcinoma | Urea Cycle Disorder | NDH Syndrome | Sulfite Oxidase Deficiency | Stiff-man Syndrome | Fragile X Syndrome | Cardiomyopathy, Peripartum | Senior-Loken Syndrome | Pseudohypoparathyroidism Type 2 | Alkaptonuria | Rhabdomyosarcoma, Alveolar | Botulism | Intracranial Hypertension | Pulmonary Alveolar Proteinosis | Dysfibrinogenemia | Galloway-Mowat Syndrome | Diabetes | Chronic Enteropathy Associated With SLCO2A1 Gene | DiGeorge Syndrome | Hereditary Neuropathy With Liability To Pressure Palsies | Pseudoexfoliation Syndrome | Lateral Meningocele Syndrome | Esophageal Adenocarcinoma | Pyruvate Carboxylase Deficiency Disease | Hypermethioninemia | Epithelial-myoepithelial Carcinoma | CHOPS Syndrome | Facioscapulohumeral Muscular Dystrophy | Adenoid Cystic Carcinoma | Superficial Spreading Melanoma | Achondrogenesis | Tibial Muscular Dystrophy | Goldenhar Syndrome | Delirium | Pulmonary Capillary Hemangiomatosis | Norrie Disease | Hypohidrotic Ectodermal Dysplasia | Cystinosis | T-cell Leukemia | Osteogenesis Imperfecta Type III | Pre-eclampsia | Cockayne Syndrome | Niemann-Pick Disease, Type C | Autosomal Recessive Spastic Paraplegia Type 35 | Fetal And Neonatal Alloimmune Thrombocytopenia | Trichomegaly | Cardiomyopathy, Restrictive | Pupil Disorders | Ollier Disease | Diabetes Mellitus, Transient Neonatal | Lupus Erythematosus | Periventricular Nodular Heterotopia | Restless Legs Syndrome | Prader-Willi Syndrome | Cystitis | Glycogen Storage Disease Type 0, Muscle | Acrodermatitis Enteropathica | Paracoccidioidomycosis | Bronchiectasis | Intestinal Pseudo-obstruction | Pyruvate Dehydrogenase Deficiency | Synovitis | Hyperostosis | Osteoporosis | Necrobiosis Lipoidica | Primary Carnitine Deficiency | Blepharophimosis Syndrome | Spinocerebellar Ataxia Type 8 | Distal Myopathy | Varices | Galactosialidosis | Benign Hereditary Chorea | Postaxial Polydactyly | Plasma Cell Leukemia | Peritonitis | Adenomatoid Tumor | Congenital Disorders Of Glycosylation Type II | Anosmia, Congenital | Fibrillation, Atrial | Hemochromatosis | Sleep Apnea, Central | Down Syndrome | Hepatorenal Syndrome | Arteriovenous Malformations | Rheumatic Heart Disease | Cat Eye Syndrome | Anthrax | Eccrine Porocarcinoma | Myoclonic Epilepsy With Ragged Red Fibers | Klippel-Feil Syndrome | Tremor | Charcot-Marie-Tooth Disease Type 2T | Sarcoidosis | Hypertension | Muckle-Wells Syndrome | Celiac Disease | Fascioliasis | Spinocerebellar Ataxia Type 12 | Benign Familial Neonatal Convulsions | Anorchia | Hyperoxaluria | Scapuloperoneal Spinal Muscular Atrophy | Heimler Syndrome | Inflammatory Joint Disease | Maple Syrup Urine Disease | Uveitis | 3-methylglutaconic Aciduria Type IV | Thin Basement Membrane Disease | Insulinoma | Fetal Akinesia Deformation Sequence | Cholestasis, Intrahepatic | Spondyloperipheral Dysplasia | Spinocerebellar Ataxia Type 15 | Pleural Tuberculosis | Takayasu's Arteritis | Alopecia Areata | Fatty Aldehyde Dehydrogenase Deficiency | Esophageal Carcinoma | Birk-Barel Syndrome | Lesch-Nyhan Syndrome | Poikiloderma With Neutropenia | Stroke, Hemorrhagic | Neural Tube Defect | Liebenberg Syndrome | Congenital Diaphragmatic Hernia | Chronic Myelomonocytic Leukemia | Swine Influenza | FG Syndrome | Abetalipoproteinemia | Systemic Mastocytosis | Hyperparathyroidism, Secondary | Microcephalic Primordial Dwarfism | Cryptococcal Meningitis | Knobloch Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Cirrhosis | Pneumothorax | Cardiofaciocutaneous Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Thalassemia, Beta | Smoldering Myeloma | Histiocytosis | Diabetes Insipidus, Nephrogenic | Usher Syndrome Type II | Leukemia-lymphoma, Adult T-cell | Diabetic Neuropathy | Congenital Central Hypoventilation Syndrome | Chordoma | Adenomyosis | Ocular Hypertension | Occipital Neuralgia | Hemorrhage | Chromosome 8q21.11 Deletion Syndrome | L-2-Hydroxyglutaric Aciduria | LMNA-related Congenital Muscular Dystrophy | Lissencephaly 2 | Spasticity | Thanatophoric Dysplasia | Tardive Dyskinesia | Sick Sinus Syndrome 1 | Spinocerebellar Ataxia Type 38 | Epidermolysis Bullosa Simplex, Generalized | Enlarged Vestibular Aqueduct | Waardenburg Syndrome Type 2E | Neurofibromatosis Type 1