Epicondylitis
Epicondylitis
About the Disease
Epicondylitis, also known as tennis elbow, is related to tendinopathy and frozen shoulder. An important gene associated with Epicondylitis is PRR4 (Proline Rich 4), and among its related pathways/superpathways are Signal Transduction and Integrin Pathway. The drugs Levobupivacaine and Naproxen have been mentioned in the context of this disorder. Affiliated tissues include epicondyle, bone and liver, and related phenotypes are cardiovascular system and normal
Common Targets
PDGFB

Note: If you'd like to get a target analysis report for Epicondylitis, 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 Epicondylitis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Sturge-Weber Syndrome | Perry Syndrome | Hereditary Elliptocytosis | Lymphoma, Primary Cutaneous Anaplastic Large Cell | WAGR Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Left Ventricular Noncompaction | Tricho-hepato-enteric Syndrome | Pilomatrix Carcinoma | Schizophrenia | Hypercholesterolemia, Familial | Schizoaffective Disorder | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Sialoadenitis | Acute Leukemia | 3C Syndrome | Pheochromocytoma | Pleurisy | Blau Syndrome | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Lymphedema | Crohn's Disease | Congenital Afibrinogenemia | Familial Cerebral Amyloid Angiopathy | Von Willebrand Disease | Leiomyosarcoma | Zollinger-Ellison Syndrome | Depression | Primary Torsion Dystonia | Charcot-Marie-Tooth Disease Type 4E | Botulism | Carcinoma, Squamous Cell | Vasculitis | Vitelliform Macular Dystrophy | Fukuyama Congenital Muscular Dystrophy | Retinitis Pigmentosa 3 | Glycogen Storage Disease Type 4 | Axenfeld-Rieger Syndrome | Intellectual Disability, Autosomal Dominant 5 | Maple Syrup Urine Disease | AIDS | Nanophthalmos | Myhre Syndrome | Alopecia Totalis | Keratitis | Aphasia | Nance-Horan Syndrome | Osteoglophonic Dysplasia | Macular Corneal Dystrophy | Ectodermal Dysplasia | Angina Pectoris | Osmotic Demyelination Syndrome | Hypotonia-cystinuria Syndrome | Transcobalamin Deficiency | Behavioral Variant Of Frontotemporal Dementia | Gestational Trophoblastic Disease | Benign Familial Infantile Seizures | Leishmaniasis, Visceral | Hereditary Pyropoikilocytosis | Hypokalemia | Paroxysmal Nocturnal Hemoglobinuria | Basal Ganglia Disease | Postaxial Polydactyly | Pancreatitis | Cousin Syndrome | Avian Influenza | Carey-Fineman-Ziter Syndrome | Cataplexy | Arthritis, Gouty | Premature Ejaculation | Isobutyryl-CoA Dehydrogenase Deficiency | Budd-Chiari Syndrome | Hypertension | Calcium Pyrophosphate Deposition Disease | Pontocerebellar Hypoplasia Type 2 | Fibrillation, Atrial | Wolff-Parkinson-White Syndrome | Vitreoretinopathy, Proliferative | Primary Aldosteronism | Ollier Disease | Polycystic Kidney, Autosomal Dominant | Astigmatism | Trichorhinophalangeal Syndrome | Contact Dermatitis | Eclampsia | Epidermodysplasia Verruciformis | Carcinoma In Situ | Addison Disease | Schaaf-Yang Syndrome | Schuurs-Hoeijmakers Syndrome | Ophthalmoplegia | Niemann-Pick Disease | Lymphoma Lymphoblastic | Renal Medullary Carcinoma | Hypokalemic Periodic Paralysis | Homocystinuria | Liddle Syndrome | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Familial Digital Arthropathy-brachydactyly | Hypertriglyceridemia | Hepatic Veno-occlusive Disease | Sick Sinus Syndrome 1 | Cryptosporidiosis | Uremic Pruritus | Renal Oncocytoma | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Gynecomastia | Amyotrophic Lateral Sclerosis | Brenner Tumor | Hyperparathyroidism-jaw Tumor Syndrome | Myelitis, Transverse | Sclerosteosis | Fibrosarcoma | Epidermolysis Bullosa Dystrophica | Leprosy | Cancer, Lung | Congenital Bile Acid Synthesis Defect | Long QT Syndrome Type 3 | Plasmacytoma | Glutaric Aciduria Type 1 | Paternal Uniparental Disomy Of Chromosome 14 | Hypervalinemia | Aarskog-Scott Syndrome | Hereditary Xerocytosis | Bone Marrow Necrosis | Pseudohypoparathyroidism Type 1B | Peyronie's Disease | Japanese Encephalitis | Atopic Dermatitis | Rolandic Epilepsy | Spinocerebellar Ataxia Type 8 | Micropenis | Priapism | Keratosis, Actinic | Echinococcosis | Ganglioneuroma | Dominant Optic Atrophy | Transthyretin-related Amyloidosis | Schamberg Disease | Disseminated Superficial Actinic Porokeratosis | Pearson Syndrome | Multicentric Carpotarsal Osteolysis Syndrome | 5-oxoprolinase Deficiency | Chondrosarcoma | Alpha-1 Antitrypsin Deficiency | Combined Malonic And Methylmalonic Acidemia | Spinocerebellar Ataxia Type 3 | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Burn-McKeown Syndrome | Progressive Familial Intrahepatic Cholestasis Type 3 | Neuronal Ceroid Lipofuscinosis | Giant Cell Glioblastoma | Papulopustular Rosacea | Pulmonary Tuberculosis | Wagner Disease | Erectile Dysfunction | Carbohydrate Metabolism Disorders | Mycosis Fungoides | Gastric Atrophy | Encephalopathy, Hepatic | Nevus | Charcot-Marie-Tooth Disease Type 2D | Hereditary Sensory Neuropathy Type 1 | Molybdenum Cofactor Deficiency | Camptocormia | Hypophosphatasia | Alkaptonuria | Christianson Syndrome | Biotinidase Deficiency | Cervicitis | Osteogenesis Imperfecta Type I | Rheumatic Heart Disease | Meier-Gorlin Syndrome | Idiopathic Pulmonary Fibrosis | Hypercalcemia | Retinitis | Hypotrichosis | Erythrokeratodermia Variabilis | Congenital Absence Of Vas Deferens | Acute Lymphocytic Leukemia | Eating Disorder | Retinal Degeneration | Aldosterone Deficiency | Spinocerebellar Ataxia Type 12 | Alopecia | Epidermolysis Bullosa Acquisita | Interstitial Lung Diseases | VACTERL/VATER Association | Incontinentia Pigmenti | Congestive Heart Failure | Adenoid Cystic Carcinoma | Extramammary Paget's Disease | Waardenburg Syndrome | Giant Cell Arteritis | Oculocutaneous Albinism Type 2 | Impetigo | Bronchiolitis | Turner's Syndrome | Erythropoietic Protoporphyria | Tardive Dyskinesia | Sandhoff Disease | Citrullinemia | Abetalipoproteinemia | Arthritis, Psoriatic | Tularemia | Precocious Puberty | Microvillus Inclusion Disease | ADNP Syndrome | Megalencephaly | Long QT Syndrome Type 1 | Keratoconus | Methemoglobinemia Type IV | Papillon-Lefevre Syndrome | Double Outlet Right Ventricle | Noonan Syndrome | Hypersomnia | Paget's Disease Of The Breast | Schwartz-Jampel-Aberfeld Syndrome | Endometriosis | Osteogenesis Imperfecta | Congenital Ichthyosiform Erythroderma | Hidradenitis Suppurativa | Menetrier Disease | Adrenal Insufficiency | Hyperuricemic Nephropathy, Familial Juvenile | LMNA-related Congenital Muscular Dystrophy | Intracranial Hypertension | Achondrogenesis | X-linked Charcot-Marie-Tooth Disease | Spinal Muscular Atrophy | Glanzmann Thrombasthenia | Persistent Fetal Circulation | Occipital Neuralgia | Osteochondroma | Leri-Weill Dyschondrosteosis | Leukemia | Platelet Disorders | Mitochondrial Encephalomyopathy | Personality Disorders | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Meningococcal Infections | Viral Meningitis | Pemphigus Foliaceus | Malignant Fibrous Histiocytoma | Hyperphenylalaninemia | Pantothenate Kinase-associated Neurodegeneration | Smith-Kingsmore Syndrome | Imerslund-Grasbeck Syndrome | Best Macular Dystrophy | Cockayne Syndrome | Familial Exudative Vitreoretinopathy | Hereditary Folate Malabsorption | Brugada Syndrome 1 | Mitochondrial DNA Depletion Syndrome | Tangier Disease | Epilepsy Of Infancy With Migrating Focal Seizures | Myosin Storage Myopathy | C3 Glomerulopathy | Campomelic Dysplasia | Sarcomatoid Carcinoma Of The Lung | Macrodactyly | Hoyeraal-Hreidarsson Syndrome | Oguchi Disease-2 | Superficial Spreading Melanoma | Ehlers-Danlos Syndrome | Exfoliative Dermatitis | Malonyl-CoA Decarboxylase Deficiency | MIRAGE Syndrome | Thanatophoric Dysplasia Type 1 | Charcot-Marie-Tooth Disease, Type 6 | Chromosome 9q34.3 Deletion Syndrome | Dupuytren Disease | Exotropia | 3-hydroxy-3-methylglutaric Aciduria | Persistent Mullerian Duct Syndrome | Pernicious Anemia | Poirier-Bienvenu Neurodevelopmental Syndrome | Congenital Central Hypoventilation Syndrome | Pulmonary Veno-occlusive Disease | Nail-Patella Syndrome | Angiosarcoma Of The Breast | Bipolar Disorder | Charcot-Marie-Tooth Disease Axonal Type 2N | Adams-Oliver Syndrome | Frontotemporal Dementia | Hemimegalencephaly | Hypopituitarism | Gardner Syndrome | Acute Anterior Uveitis | DNA Ligase IV Deficiency | Hyperekplexia | Wolfram Syndrome | Thrombocythemia, Essential | Agnathia-Otocephaly Complex | Arthritis | Sick Sinus Syndrome | Vici Syndrome | Congenital Disorders Of Glycosylation Type II | Hyperacusis | Hypopigmentation | Riboflavin Transporter Deficiency Neuronopathy | Thyrotoxic Periodic Paralysis | Spinocerebellar Ataxia Type 31 | Uveitis, Anterior | Hydrocephalus | Hypogammaglobulinemia | Ghosal Syndrome | Androgenic Alopecia | Porphyria | Immunoproliferative Disorders | Desmosterolosis | Myocarditis | Ocular Surface Squamous Neoplasia | Sensorineural Hearing Loss | Vitreoretinal Degeneration, Snowflake Type | Spina Bifida | Nicotine Dependence | Varicocele | Cluster Headache | Spinocerebellar Ataxia Type 5 | Hemophagocytic Lymphohistiocytosis | Pompe Disease | Reye Syndrome | Hypermethioninemia | Oculocutaneous Albinism Type 1 | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Palsy, Cerebral | Amblyopia | Hypotrichosis Simplex | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Lattice Corneal Dystrophy Type 1 | Hyperinsulinism-hyperammonemia Syndrome | Pancreatitis, Chronic | Monilethrix | Coma | LRBA Deficiency | Alcoholism | Erdheim-Chester Disease | Hypercalciuria | Hemorrhoids | Hyperammonemia | Sickle Cell Disease | Diabetes Gestational | Apert Syndrome | Primary Lateral Sclerosis | Neuroma | Galactosialidosis | Megaloblastic Anemia | Osteopetrosis | Aicardi-Goutieres Syndrome | Leukoencephalopathy, Progressive Multifocal | Lipid Storage Diseases | Keratosis, Seborrheic | Purpura | Waardenburg Syndrome Type 4 | Schizencephaly | Bainbridge-Ropers Syndrome | Split Hand-foot Malformation | Neurocutaneous Syndromes | Congenital Myasthenic Syndrome | Cerebrovascular Disorders | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Stroke, Hemorrhagic | Leukoplakia | Osteoarthritis | Intracerebral Hemorrhage | Huntington's Disease-like 2 | Neurofibromatosis | Paracoccidioidomycosis | Tuberculous Meningitis | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Anti-NMDA Receptor Encephalitis | Kawasaki Disease | Dysequilibrium Syndrome | Knobloch Syndrome | Lathosterolosis | Craniopharyngioma | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Osteogenesis Imperfecta Type II | Eczema | Protein C Deficiency | Glomerulonephritis | Sialidosis Type I | 3-methylcrotonyl-CoA Carboxylase Deficiency | Thrombocytopenia | Beta-Propeller Protein-associated Neurodegeneration | Creatine Deficiency Syndrome | Trachoma | Glioblastoma | Xeroderma Pigmentosum Variant Type | Lymphangioma | Acute Coronary Syndrome | MELAS Syndrome | Angioedema, Hereditary | Enlarged Vestibular Aqueduct | Esophageal Motility Disorders | Hyperparathyroidism, Secondary | Craniosynostosis | Neurofibrosarcoma | Anterior Segment Dysgenesis