Disease

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

疾病靶点研报
Epicondylitis

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.ai.

Other Diseases

Pneumonia, Viral | Aldosterone Synthase Deficiency | Spinocerebellar Ataxia Type 5 | Cirrhosis | Multiple Epiphyseal Dysplasia | Lymphangiomatosis | Carcinoma In Situ | Creatine Deficiency Syndrome | Polycythemia | Holoprosencephaly | Nemaline Myopathy | Angina Pectoris | Papilloma | Cardiac Sarcoidosis | Colitis, Lymphocytic | Poirier-Bienvenu Neurodevelopmental Syndrome | Achondrogenesis | Melnick-Needles Syndrome | Bullous Pemphigoid | Common Cold | Twin-to-twin Transfusion Syndrome | Nail Disorder, Nonsyndromic Congenital | Otosclerosis | Charcot-Marie-Tooth Disease Type 2T | Smith-Kingsmore Syndrome | Schuurs-Hoeijmakers Syndrome | Sensory Neuropathy | Analgesia | Sleep Apnea, Central | Graves Disease | Dengue Shock Syndrome | Primary Ovarian Insufficiency | Sickle Cell Disease | Gastritis, Atrophic | Pigment Dispersion Syndrome | Albinism | Heavy Chain Disease | Cancer, Breast | Major Depression | Down Syndrome | Urticaria | Multiple Myeloma | Tyrosine Hydroxylase Deficiency | Amenorrhea | Castleman Disease | Withdrawal Syndrome | Nephrocalcinosis | Meier-Gorlin Syndrome | Waardenburg Syndrome | Impetigo | Osteoporosis | Cryptosporidiosis | Rolandic Epilepsy | Acute Generalized Exanthematous Pustulosis | Benign Familial Pemphigus | Perry Syndrome | Cleidocranial Dysplasia | Traboulsi Syndrome | Stromal Corneal Dystrophy | Angioedema, Acquired | Hypersensitivity | Idiopathic Multicentric Castleman Disease | Atopic Dermatitis | Hartsfield Syndrome | Inflammatory Linear Verrucous Epidermal Nevus | Spinocerebellar Ataxia Type 23 | Astigmatism | Fahr Disease | CEDNIK Syndrome | Chronic Beryllium Disease | Japanese Encephalitis | Familial Partial Lipodystrophy | Congenital Nystagmus | Sweet Syndrome | Joubert Syndrome | Hydronephrosis | Hypopituitarism | Hepatic Veno-occlusive Disease | Moyamoya Disease | 3-methylglutaconic Aciduria Type IV | Borjeson-Forssman-Lehmann Syndrome | Congenital Tufting Enteropathy | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Atopy | Bicuspid Aortic Valve | CREST Syndrome | Congenital Poikiloderma | Turner's Syndrome | Meesmann Corneal Dystrophy | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Cardiomyopathy, Hypertrophic | 3-M Syndrome | Chorea | Botulism | Pure Autonomic Failure | Hyperammonemia | Venous Insufficiency | Amyloidosis | Hemangioma | Anti-NMDA Receptor Encephalitis | Hepatitis, Chronic | Erythema Nodosum | Hypohidrotic Ectodermal Dysplasia | Cancer, Colon | Dystonia-parkinsonism, X-linked | Cancer, Lung | Glaucoma | Mycosis Fungoides | Non-proliferative Diabetic Retinopathy | Wolman Disease | McKusick Type Metaphyseal Chondrodysplasia | Basal Ganglia Cerebrovascular Disease | Ectodermal Dysplasia | Neurofibrosarcoma | Smoldering Myeloma | Facioscapulohumeral Muscular Dystrophy | Peeling Skin Syndrome Type B | Aplasia Cutis Congenita | Macrophage Activation Syndrome | Stroke, Hemorrhagic | Congenital Heart Block | Mitochondrial DNA Depletion Syndrome 13 | Hypoplastic Left Heart Syndrome | Microcephaly | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Burn-McKeown Syndrome | Dyggve-Melchior-Clausen Disease | Apraxia | Alazami Syndrome | Acute Lung Injury | Blau Syndrome | Eating Disorder | Primary Erythromelalgia | Goldenhar Syndrome | Glycogen Storage Disease | Carcinoid Tumor | Dysequilibrium Syndrome | Oguchi Disease-2 | Tetanus | Oligoastrocytoma | Dermatitis | Pseudohermaphroditism | Myotonia | Hypereosinophilic Syndrome | Reticular Dysgenesis | Keratitis | Acral Lentiginous Melanoma | Epidermal Nevus Syndrome | Congenital Adrenal Hyperplasia 1 | Pituitary Stalk Interruption Syndrome | Bartsocas-Papas Syndrome | Autosomal Recessive Bestrophinopathy | Oculocutaneous Albinism Type 2 | Cholestasis | Myelodysplasia | Hypoproteinemia, Hypercatabolic | Hemochromatosis Type 1 | Shprintzen-Goldberg Syndrome | Renal Dysplasia | Methemoglobinemia Type IV | Diverticulitis | Peritonitis | Brenner Tumor | 3-methylcrotonyl-CoA Carboxylase Deficiency | Arthrogryposis | Genee-Wiedemann Syndrome | Retinal Dystrophy, Early-onset Severe | Hepatitis, Autoimmune | Mast Cell Leukemia | Osteoporosis-pseudoglioma Syndrome | Congenital Hemolytic Anemia | Episodic Ataxia Type 2 | Allan-Herndon-Dudley Syndrome | Arteriosclerosis | Hypotonia-cystinuria Syndrome | ICF Syndrome | Kallmann Syndrome | Kernicterus | T-cell Chronic Lymphocytic Leukemia | Polycystic Ovary Syndrome | Binge Eating Disorder | Harlequin Ichthyosis | Chronic Myelomonocytic Leukemia | Peutz-Jeghers Syndrome | Cerebrovascular Disorders | Congenital Lipoid Adrenal Hyperplasia | Kashin-Beck Disease | Wiedemann-Steiner Syndrome | Deafness, Dystonia, And Cerebral Hypomyelination | Primary Hyperoxaluria | Acute Motor Axonal Neuropathy | Agnathia-Otocephaly Complex | Glutaric Aciduria Type 3 | Hemolytic Uremic Syndrome, Atypical | Epilepsy Of Infancy With Migrating Focal Seizures | Pyruvate Carboxylase Deficiency Disease | Autoimmune Autonomic Ganglionopathy | Neurofibromatosis-Noonan Syndrome | Focal Facial Dermal Dysplasia | Sporadic Hemiplegic Migraine | Antithrombin III Deficiency | Pain | Adenoma, Villous | Gaucher Disease | Seminoma | Giant Axonal Neuropathy | Presbycusis | Osteopathia Striata With Cranial Sclerosis | Heroin Dependence | Cholangitis | B-cell Prolymphocytic Leukemia | Tangier Disease | Uveitis | Apparent Mineralocorticoid Excess Syndrome | Adenomyosis | Myelofibrosis | Myositis, Focal | Glycogen Storage Disease Type 0, Muscle | NGLY1 Deficiency | Addison Disease | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Diabetes Insipidus | Osmotic Demyelination Syndrome | Chronic Myeloid Leukemia | Systemic Lupus Erythematosus | Cenani-Lenz Syndactyly Syndrome | Hyperlipidemia, Familial Combined | Rhabdomyosarcoma, Embryonal | Familial Advanced Sleep Phase Syndrome | Liver Failure | Carpenter Syndrome | Erythropoietic Protoporphyria | Congenital Dyserythropoietic Anemia Type 4 | Disseminated Superficial Actinic Porokeratosis | Nephrotic Syndrome Type 1 | Osteitis | Torticollis | Low Phospholipid Associated Cholelithiasis | Hyperostosis | Graft-versus-host Disease | HUPRA Syndrome | Low Tension Glaucoma | Lymphangioleiomyomatosis | Treacher Collins Syndrome | Papillon-Lefevre Syndrome | Congenital Hereditary Endothelial Dystrophy Type I | Juvenile Myoclonic Epilepsy | Mountain Sickness | Mitochondrial DNA Depletion Syndrome | Rhabdomyosarcoma, Alveolar | Hypertriglyceridemia | Rhabdoid Tumor | Neuromyotonia | Erysipelas | Aspergillosis | Cancer, Kidney | Pontocerebellar Hypoplasia Type 2 | Camurati-Engelmann Disease | Kindler Syndrome | Schaaf-Yang Syndrome | Veno-occlusive Disease | Epiphyseal Chondrodysplasia, Miura Type | Diffuse Mesangial Sclerosis | Polyradiculopathy | Keratoconus | Pleural Tuberculosis | Proteus Syndrome | Language Disorders | Seborrheic Dermatitis | Xeroderma Pigmentosum Variant Type | Fascioliasis | Pulmonary Sclerosing Hemangioma | Vasculitis | Epidermolysis Bullosa Dystrophica | Dominant Optic Atrophy | Nicotine Addiction | Zellweger Syndrome | Scoliosis | Seizures-scoliosis-macrocephaly Syndrome | Non-small Cell Lung Cancer | Impulse Control Disorder | Persistent Fetal Circulation | Enlarged Vestibular Aqueduct | Autonomic Nervous System Disorders | Gray Platelet Syndrome | Ameloblastic Carcinoma | Partington Syndrome | Intracranial Hypertension | Endometrial Hyperplasia | Lentigo | Scleritis | Choriocarcinoma | Barrett Esophagus | Pontocerebellar Hypoplasia | Acute Chest Syndrome | Beta-Propeller Protein-associated Neurodegeneration | Nemaline Myopathy 10 | Hypertensive Nephropathy | Diamond-Blackfan Anemia | WAGR Syndrome | Early Infantile Epileptic Encephalopathy 4 | Blood Protein Disorders | Glioma | Pemphigus | Thyroiditis, Autoimmune | Osteochondrosis | Focal Segmental Glomerulosclerosis | 3C Syndrome | Pseudohypoaldosteronism | Thalassemia, Beta | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Neuroendocrine Cancer | Osteochondroma | Rhizomelic Chondrodysplasia Punctata | Rotor Syndrome | Spondyloarthritis | Hyperphenylalaninemia | Eccrine Porocarcinoma | Priapism | Pulmonary Capillary Hemangiomatosis | Hypogammaglobulinemia | Craniofacial Dysostosis | Whipple's Disease | Double Outlet Right Ventricle | Takotsubo Cardiomyopathy | T-cell Lymphoma, Subcutaneous Panniculitis-like | Takayasu's Arteritis | Pneumonia, Mycoplasma | Perivascular Epithelioid Cell Tumor | Eiken Syndrome | Kawasaki Disease | Bainbridge-Ropers Syndrome | Trichotillomania | Gastritis | Hypopigmentation | Myelomeningocele | Osteosarcoma | Acne Vulgaris | Hepatitis B, Chronic | Purpura, Thrombotic Thrombocytopenic | Generalized Epilepsy With Febrile Seizures Plus | Keratitis-ichthyosis-deafness Syndrome | Esthesioneuroblastoma | Paraganglioma, Carotid Body | Charcot-Marie-Tooth Disease Type 2E | Nephritis, Interstitial | Lymphoproliferative Disease, X-linked | Jaundice, Obstructive | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Chondrodysplasia Punctata 2, X-linked Dominant | Congenital Dysfibrinogenemia | Frontometaphyseal Dysplasia | Combined Pituitary Hormone Deficiency | Cardiospondylocarpofacial Syndrome | Renal-hepatic-pancreatic Dysplasia | Multiple Sclerosis, Primary Progressive | Scapuloperoneal Myopathy, X-linked Dominant | Pleurisy | Charcot-Marie-Tooth Disease | Keratosis, Seborrheic | Chorioretinitis | Macular Degeneration | Hyperparathyroidism, Secondary | Myoclonus-dystonia Syndrome | Congenital Bile Acid Synthesis Defect | Alpha-mannosidosis | Hydrocephalus | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Primary Pigmented Nodular Adrenocortical Disease | Endometritis | Glycogen Storage Disease Type 1b | Amelogenesis Imperfecta | Hereditary Multiple Exostoses | Waardenburg Syndrome Type 4 | Neurofibroma | Li-Fraumeni Syndrome | Gallstones | REM Sleep Behavior Disorder | Erythromelalgia | McLeod Syndrome | Osteoarthritis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Hepatitis D | Chondrosarcoma | Alpha-1 Antitrypsin Deficiency | Epidermolysis Bullosa Simplex, Generalized | Amyotrophic Lateral Sclerosis, Juvenile | Malaria | Hyperuricemic Nephropathy, Familial Juvenile | Neuronal Ceroid Lipofuscinosis | Leukoplakia | Hypersomnia | Amebiasis | Polycystic Kidney, Autosomal Dominant | Noonan Syndrome | Esophageal Motility Disorders | Angelman Syndrome | Congestive Heart Failure | Insulinoma | Chanarin-Dorfman Syndrome