Exostoses
Exostoses
About the Disease
Exostosis, also known as osteophyte, is related to exostoses, multiple, type i and hereditary multiple osteochondromas. An important gene associated with Exostosis is EXT2 (Exostosin Glycosyltransferase 2), and among its related pathways/superpathways are Phospholipase-C Pathway and Glycosaminoglycan metabolism. The drugs Clonidine and Adrenergic alpha-Agonists have been mentioned in the context of this disorder. Affiliated tissues include bone, eye and spinal cord, and related phenotypes are growth/size/body region and limbs/digits/tail
Common Targets
EXT2

Note: If you'd like to get a target analysis report for Exostoses, 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 Exostoses at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Trichomegaly | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Aplasia Cutis Congenita | Neuroleptic Malignant Syndrome | Apparent Mineralocorticoid Excess Syndrome | Periodontitis | Situs Inversus | Esophageal Motility Disorders | Rotor Syndrome | Erectile Dysfunction | Macrophage Activation Syndrome | Kaposi Sarcoma | Corneal Edema | Specific Granule Deficiency | Gastroenteritis, Eosinophilic | Leukocyte Adhesion Deficiency Type 1 | Leukocyte Adhesion Deficiency | Restrictive Dermopathy | Seizures | Glomerulonephritis, Membranoproliferative | Hydrocephalus, Normal Pressure | Renal Hypouricemia | Asthma, Exercise-induced | Postpartum Depression | Sick Sinus Syndrome 1 | Leukemia | Waardenburg Syndrome | Ehlers-Danlos Syndrome | Tracheal Disorders | Kallmann Syndrome | Spinocerebellar Ataxia Type 16 | Erysipelas | Erythema Nodosum | Persistent Truncus Arteriosus | Leber Hereditary Optic Neuropathy | Histiocytosis | Sarcosinemia | Creatine Deficiency Syndrome Due To AGAT Deficiency | Contact Dermatitis | Mitochondrial Disease | Encephalopathy, Hepatic | Alopecia Totalis | Thrombocythemia, Essential | Endometriosis | Arrhythmogenic Right Ventricular Cardiomyopathy | Japanese Encephalitis | Personality Disorders | Epidermolysis Bullosa Dystrophica | Adenylosuccinate Lyase Deficiency | Lichen Planus | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Distal Myopathy 2 | Congenital Bilateral Absence Of Vas Deferens | Neurocysticercosis | McKusick Type Metaphyseal Chondrodysplasia | Osteogenesis Imperfecta Type I | Adrenal Insufficiency | Osteogenesis Imperfecta Type VI | Pyruvate Decarboxylase Deficiency | Mandibuloacral Dysplasia With Type A Lipodystrophy | Hepatic Adenomatosis | Prurigo Nodularis | Sleep Apnea | Encephalopathy, Ethylmalonic | Norrie Disease | Non-Langerhans Cell Histiocytosis | IMAGe Syndrome | Chronic Mucocutaneous Candidiasis | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Vertebrobasilar Insufficiency | PHARC Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Snyder-Robinson Syndrome | Herpes Genitalis | Leukemia-lymphoma, Adult T-cell | Spinocerebellar Ataxia Type 23 | Iron Metabolism Disorders | Early Infantile Epileptic Encephalopathy 13 | Cryptosporidiosis | 3-methylglutaconic Aciduria Type I | Chronic Periodontitis | Intermittent Explosive Disorder | Melanoma | Adams-Oliver Syndrome | Leukodystrophies | Spinocerebellar Ataxia Type 5 | Polyarteritis Nodosa | Optic Neuropathy | Antiphospholipid Syndrome | Heterotaxy | Glaucoma | Cardiospondylocarpofacial Syndrome | Pneumonia, Mycoplasma | Bruck Syndrome | Dystonia | Hyperoxaluria | Hepatitis, Autoimmune | Spitzoid Melanoma | Idiopathic Pulmonary Fibrosis | Ichthyosis, X-linked | Renal Tubular Dysgenesis | Myelitis | Pneumothorax | Chronic Myelomonocytic Leukemia | Diabetes Insipidus | Sporadic Inclusion Body Myositis | Basal Ganglia Cerebrovascular Disease | Bursitis | Metachondromatosis | Hypodontia | Dermatomyositis | Leigh Syndrome | Atrial Septal Defect | Calcium Pyrophosphate Deposition Disease | Thin Basement Membrane Disease | T-cell Lymphoma, Subcutaneous Panniculitis-like | Compartment Syndrome | Keratocystic Odontogenic Tumor | Spinocerebellar Ataxia Type 27 | Pregnancy, Ectopic | Ectodermal Dysplasia | Chondrodysplasia Punctata 2, X-linked Dominant | Antisocial Personality Disorder | Colon Adenoma | Leprosy | Epithelioid Hemangioma | Spinocerebellar Ataxia Type 14 | Learning Disability | Cervicitis | Lymphopenia | Hyperparathyroidism-jaw Tumor Syndrome | Fatty Aldehyde Dehydrogenase Deficiency | Neurofibromatosis Type 1 | Campomelic Dysplasia | Danon Disease | Niemann-Pick Disease | Vestibular Disease | Bronchiectasis | Gastritis, Atrophic | Neuroma | Polyneuropathy | Stuve-Wiedemann Syndrome | Ellis-Van Creveld Syndrome | Incontinentia Pigmenti | Patent Ductus Arteriosus | X-linked Myotubular Myopathy | Tic Disorder | T-cell Prolymphocytic Leukemia | Extramammary Paget's Disease | Treacher Collins Syndrome | Cirrhosis | Trichuriasis | Low Phospholipid Associated Cholelithiasis | Waardenburg Syndrome Type 2E | Dysplastic Nevus | Spinocerebellar Ataxia Type 38 | Primary Sclerosing Cholangitis | Wiedemann-Steiner Syndrome | Spondylolisthesis | Colitis, Microscopic | Scleroderma | Neuromuscular Disorders | Gastroenteritis | Esthesioneuroblastoma | Spondylometaphyseal Dysplasia | Tyrosinemia Type 1 | Intestinal Tuberculosis | Retinal Degeneration | Schindler Disease | Generalized Epilepsy And Paroxysmal Dyskinesia | Corneal Dystrophy | Carcinoma In Situ | Focal Cortical Dysplasia Type 2 | Familial Isolated Hyperparathyroidism | Heterotopic Ossification | Pancreatitis | Prolymphocytic Leukemia | Sensory Neuropathy | Pancreatitis, Chronic | Diabetes Type 1 | Lymphoproliferative Disorders | Paroxysmal Nocturnal Hemoglobinuria | Pseudoachondroplasia | Trimethylaminuria | Nail-Patella Syndrome | Astrocytoma | Metabolic Syndrome | Thyroiditis, Autoimmune | Polycystic Kidney, Autosomal Recessive | Lattice Corneal Dystrophy Type 1 | Fibrillation, Atrial | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Fragile X Syndrome | Camptocormia | Wolman Disease | Traboulsi Syndrome | Pyruvate Carboxylase Deficiency Disease | Myasthenia | Birt-Hogg-Dube Syndrome | Sitosterolemia | Pneumococcal Meningitis | Gingivitis | Fukuyama Congenital Muscular Dystrophy | Familial Digital Arthropathy-brachydactyly | Retinitis | Hemochromatosis Type 1 | Diabetes Insipidus, Neurogenic | Reticular Dysgenesis | Woodhouse-Sakati Syndrome | Knobloch Syndrome | Diverticulitis | Congenital Lipoid Adrenal Hyperplasia | Bartsocas-Papas Syndrome | Glycogen Storage Disease Type 5 | Fundus Albipunctatus | Hyperammonemia | Arthritis, Gouty | Babesiosis | Early Infantile Epileptic Encephalopathy 1 | Mountain Sickness | Paronychia | McCune-Albright Syndrome | Sotos Syndrome | Hypoplastic Left Heart Syndrome | Inborn Errors Of Metabolism | Ocular Surface Squamous Neoplasia | Pituitary Disorders | Tinea Versicolor | Amyotrophic Lateral Sclerosis, Juvenile | Juvenile Myelomonocytic Leukemia | Pseudomyxoma Peritonei | Prolidase Deficiency | Non-epidermolytic Palmoplantar Keratoderma | Pendred Syndrome | Conn Syndrome | Carcinoma, Merkel Cell | Acromegaly | Infantile Liver Failure Syndrome 1 | Charcot-Marie-Tooth Disease, Type 2 | Oligodendroglioma | Chondrodysplasia Punctata | Paget's Disease Of The Breast | Raynaud Phenomenon | Angelman Syndrome | Lymphoma, AIDS-related | Spondyloperipheral Dysplasia | Astigmatism | Metaphyseal Chondrodysplasia, Schmid Type | Pituitary Dwarfism | Weill-Marchesani Syndrome | Fibrosarcoma | Metatropic Dysplasia | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Amelogenesis Imperfecta | Dystonia Musculorum Deformans | Osteogenesis Imperfecta Type IV | Thrombotic Microangiopathy | Oral Lichen Planus | Encephalitis | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Megaloblastic Anemia | Schnitzler Syndrome | Speech Disorders | Hereditary Hemorrhagic Telangiectasia | Combined Deficiency Of Factor V And Factor VIII | Pulverulent Zonular Cataract | Hennekam Lymphangiectasia-lymphedema Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Prader-Willi Syndrome | Necrotizing Autoimmune Myopathy | Adenoma, Villous | Eccrine Porocarcinoma | Crimean-Congo Hemorrhagic Fever | Vogt-Koyanagi-Harada Syndrome | Neuromyotonia | Cancer, Breast | Otitis Media | Long QT Syndrome Type 2 | Fibromuscular Dysplasia | Hepatic Steatosis | Wiskott-Aldrich Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Agranulocytosis | SAPHO Syndrome | Localized Scleroderma | Osteogenesis Imperfecta | Pompe Disease | Citrullinemia | Polymyalgia Rheumatica | Hypotrichosis Simplex | Cardiac Arrest | Gastritis | Actinomycetoma | Progressive Osseous Heteroplasia | Constipation | Pleomorphic Xanthoastrocytoma | Acute Leukemia | Endometrial Hyperplasia | NGLY1 Deficiency | Hypermetropia | Fucosidosis | Hemangioblastoma | Cold-induced Sweating Syndrome | Desbuquois Syndrome | Craniopharyngioma | Glaucoma, Congenital | Primary Biliary Cholangitis | 3C Syndrome | Dysthymia | Hypoalbuminemia | Cryopyrin-associated Periodic Syndromes | Optic Nerve Diseases | Schwannoma | Micropenis | Klinefelter Syndrome | Robinow Syndrome | Herpes Simplex Dermatitis | Conduct Disorder | Charcot-Marie-Tooth Disease Type 4D | Myelitis, Transverse | Zygomycosis | Primary Torsion Dystonia | Ophthalmia, Sympathetic | Pierre Robin Syndrome | Cancer, Kidney | Hemolytic Anemia | Insulin Resistance | Ileitis | Nanophthalmos | Lung Diseases | Vitamin K Deficiency | Common Cold | Neutropenia | Cerebral Cavernous Malformations | Overactive Bladder | Chronic Myeloid Leukemia | Facioscapulohumeral Muscular Dystrophy | Hereditary Inclusion Body Myopathy | Harlequin Ichthyosis | Pulmonary Vein Stenosis | Olmsted Syndrome | Ataxia-ocular Apraxia 2 | Chronic Idiopathic Myelofibrosis | Paroxysmal Kinesigenic Dyskinesia | Lassa Fever | Cranial Nerve Disease | Epidermolysis Bullosa Acquisita | Pituitary Stalk Interruption Syndrome | Asperger Syndrome | Achondrogenesis | Diastrophic Dysplasia | Sleep Disorder | Androgenic Alopecia | Vertigo | Glioma | Peripheral T-cell Lymphoma | Acute Chest Syndrome | Sickle Cell Anemia | Connective Tissue Disorders | Meningeal Melanocytoma | Lymphedema | Molybdenum Cofactor Deficiency | 3-methylglutaconic Aciduria | Histoplasmosis | Opisthorchiasis | Keratopathy | Osteogenesis Imperfecta Type V | Rash | Cryptococcal Meningitis | Holoprosencephaly | Mucolipidosis | Prostatitis | Oculocutaneous Albinism | Aneurysm, Abdominal Aortic | Thrombosis | Progressive Familial Intrahepatic Cholestasis | Open-angle Glaucoma | Erdheim-Chester Disease | Spinocerebellar Ataxia Type 28 | Micro Syndrome | Epidermolytic Palmoplantar Keratoderma | Congenital Dysfibrinogenemia | Inflammatory Bowel Disease | Chondroma | Dengue Hemorrhagic Fever | Congenital Adrenal Hyperplasia | Multiple System Atrophy | X-linked Acrogigantism | Charcot-Marie-Tooth Disease Axonal Type 2N | Niemann-Pick Disease, Type A | Hydrolethalus Syndrome | Globozoospermia | Fibronectin Glomerulopathy | Dysmorphophobia | Behavioral Variant Of Frontotemporal Dementia | Obsessive-compulsive Disorder | Chitayat Syndrome | Adenosine Deaminase Deficiency | Bipolar Disorder | Anterior Segment Dysgenesis