Disease

Spondylolisthesis

About the Disease
Spondylolisthesis, also known as acquired spondylolisthesis, is related to back pain and spondylolysis, and has symptoms including back pain An important gene associated with Spondylolisthesis is MMP3 (Matrix Metallopeptidase 3), and among its related pathways/superpathways are ERK Signaling and Phospholipase-C Pathway. The drugs Pregabalin and Oxycodone have been mentioned in the context of this disorder. Affiliated tissues include set of vertebrae, bone and spinal cord, and related phenotypes are spondylolysis and spondylolisthesis at l5-s1

Common Targets
WNT3A | VDR

疾病靶点研报
Spondylolisthesis

Note: If you'd like to get a target analysis report for Spondylolisthesis, 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 Spondylolisthesis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

GNE Myopathy | Meconium Ileus | Iron Overload | Oculocutaneous Albinism Type 4 | Gastric Atrophy | Glioblastoma Multiforme | Yellow Fever | Klippel-Feil Syndrome | Alstrom Syndrome | Macrodactyly | Tangier Disease | Congenital Lipoid Adrenal Hyperplasia | Ischemia | Centronuclear Myopathy | Crimean-Congo Hemorrhagic Fever | Primary Biliary Cholangitis | Congenital Hereditary Endothelial Dystrophy Type II | Presbycusis | Polymyalgia Rheumatica | Cornelia De Lange Syndrome | Cutaneous T-cell Lymphoma | Poikiloderma With Neutropenia | Common Variable Immunodeficiency | Scleroderma, Diffuse | Atherosclerosis | Heterotopic Ossification | Milk Allergy | Jawad Syndrome | Stroke | Bartter Syndrome | Hypertriglyceridemia | Dermatofibrosarcoma | Hypertension, Portal | Periodontitis | Tinea Versicolor | Angelman Syndrome | Prurigo Nodularis | Myocardial Infarction | Spinocerebellar Ataxia Type 6 | Pelizaeus-Merzbacher Disease | Goiter | Diabetic Macular Edema | Camptocormia | Focal Dermal Hypoplasia | Polyradiculopathy | Glutaric Aciduria Type 1 | Calcium Pyrophosphate Deposition Disease | Diabetes Type 2 | Epidermolysis Bullosa Acquisita | Glaucoma, Congenital | Oculocutaneous Albinism | IgA Deficiency | Leber Congenital Amaurosis | Acromesomelic Dysplasia | Neutropenia | Arthritis, Reactive | Menkes Disease | Duane Retraction Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Methylmalonic Aciduria And Homocystinuria, CblC Type | Fetal Akinesia Deformation Sequence | Danon Disease | Progressive Encephalopathy-optic Atrophy Syndrome | Encephalopathy, Glycine | Pneumothorax | Hamartoma | Specific Granule Deficiency | Neurofibroma, Plexiform | Cenani-Lenz Syndactyly Syndrome | Smith-Kingsmore Syndrome | Charcot-Marie-Tooth Disease Type 4E | Poirier-Bienvenu Neurodevelopmental Syndrome | Achondrogenesis | Schamberg Disease | Bardet-Biedl Syndrome | ADNP Syndrome | Hepatitis E | Congenital Bilateral Absence Of Vas Deferens | Mandibuloacral Dysplasia With Type A Lipodystrophy | Colorectal Adenoma | Ocular Albinism Type 1 | Larsen Syndrome | Basal Cell Nevus Syndrome | Micro Syndrome | Ghosal Syndrome | Biotinidase Deficiency | Oculocutaneous Albinism Type 2 | Hereditary Inclusion Body Myopathy | Waardenburg Syndrome Type 2 | Tardive Dyskinesia | Norrie Disease | Retinal Vasculitis | Monilethrix | Myosin Storage Myopathy | Hepatic Steatosis | Amenorrhea | Adrenal Insufficiency | Heterotaxy | Pituitary Disorders | Osteogenesis Imperfecta | Ocular Surface Squamous Neoplasia | Alopecia Areata | Restrictive Dermopathy | Heart Septal Defects | Meningeal Melanocytoma | Esophagitis, Eosinophilic | Sarcosinemia | Arthritis, Gouty | Constipation | Nevus | Fukuyama Congenital Muscular Dystrophy | Lissencephaly 2 | Gray Platelet Syndrome | Limb Girdle Muscular Dystrophy | Ophthalmia, Sympathetic | Primary Torsion Dystonia | HELLP Syndrome | Paroxysmal Nocturnal Hemoglobinuria | Teratozoospermia | Leukoplakia | Antisynthetase Syndrome | Hypertension, Pulmonary | Primary Lateral Sclerosis | Esophageal Adenocarcinoma | Sarcoma | Pseudohermaphroditism | Congenital Ichthyosiform Erythroderma | Fabry's Disease | Chondroma | Optic Nerve Hypoplasia, Bilateral | Arrhythmogenic Right Ventricular Cardiomyopathy | Congenital Heart Defects | Chronic Inflammatory Demyelinating Polyneuropathy | Meningococcal Meningitis | Hepatitis C, Chronic | Usher Syndrome | Sarcoma, Endometrial Stromal | Craniosynostosis | Dysmorphophobia | Essential Fructosuria | Blepharoconjunctivitis | Hyperthyroidism | Asthma | Sleep Apnea, Obstructive | Spinocerebellar Ataxia Type 17 | Melanoma, Uveal | Mesothelioma, Malignant | Multiple Sclerosis, Chronic Progressive | Adenomyosis | Histoplasmosis | Cancer, Prostate | Epidermolysis Bullosa Simplex, Localized | Acute Anterior Uveitis | Amyloidosis | Asthma, Nocturnal | Localized Scleroderma | Pseudohypoparathyroidism Type 1C | Alveolar Capillary Dysplasia | Intellectual Disability, Autosomal Dominant 5 | Botulism | Autism Spectrum Disorders | Hernia, Inguinal | Chronic Beryllium Disease | Diffuse Mesangial Sclerosis | Episodic Ataxia Type 1 | Facioscapulohumeral Muscular Dystrophy Type 2 | Wolfram Syndrome | Pancreatitis | Spitzoid Melanoma | Clouston Hidrotic Ectodermal Dysplasia | Leprosy | Synpolydactyly | Cranial Nerve Disease | Erythematotelangiectatic Rosacea | Aneurysm, Thoracic Aortic | Nephrotic Syndrome Type 1 | Skin Carcinoma | Conduct Disorder | Lateral Meningocele Syndrome | Hypotrichosis Simplex | Gastritis, Atrophic | Osteitis | Renal Failure | Tic Disorder | Motion Sickness | Ichthyosis Hystrix, Curth-Macklin Type | Melanocytic Nevus | Sclerosteosis | LEOPARD Syndrome | Spondylocostal Dysostosis | Li-Fraumeni Syndrome | Netherton Syndrome | Neurodevelopmental Disorders | Kearns-Sayre Syndrome | Hartsfield Syndrome | 5-oxoprolinase Deficiency | Alexander Disease | Pyelonephritis | Salla Disease | Hemorrhage | Sarcoidosis, Pulmonary | Thalassemia, Beta | Fibromuscular Dysplasia | Tuberculosis | Charcot-Marie-Tooth Disease Type 2E | Osteoarthritis | Miyoshi Myopathy | Gynecomastia | Adrenoleukodystrophy, X-linked | Corneal Dystrophy | Congenital Hypofibrinogenemia | Pituitary Stalk Interruption Syndrome | Cushing Syndrome | Benign Hereditary Chorea | Prostatitis | Guillain-Barre Syndrome | Thymoma, Malignant | Neutrophilia | Dengue Shock Syndrome | Otitis Media | Achromatopsia | Pseudohypoparathyroidism Type 1A | Delirium | Cramp Fasciculation Syndrome | Pleomorphic Xanthoastrocytoma | Congenital Disorders Of Glycosylation Type II | Charcot-Marie-Tooth Disease Axonal Type 2N | Primary Pigmented Nodular Adrenocortical Disease | Postpoliomyelitis Syndrome | Isobutyryl-CoA Dehydrogenase Deficiency | Lattice Corneal Dystrophy | Disseminated Superficial Actinic Porokeratosis | Oligospermia | Carbohydrate Metabolism Disorders | Cardiomyopathy, Hypertrophic | Polyomavirus Nephropathy | Restless Legs Syndrome | Shwachman-Bodian-Diamond Syndrome | Anuria | Xeroderma Pigmentosum Variant Type | Peutz-Jeghers Syndrome | Chronic Mucocutaneous Candidiasis | Atelosteogenesis Type 1 | Myoclonic Epilepsy With Ragged Red Fibers | Leukoplakia, Oral | Heart Failure | DOCK8 Immunodeficiency Syndrome | Rubinstein-Taybi Syndrome | Anovulation | Potocki-Shaffer Syndrome | Axenfeld-Rieger Syndrome | Coloboma | Hemorrhoids | Stargardt Disease | Dyggve-Melchior-Clausen Disease | Split Hand-foot Malformation | Reflex Epilepsy | Usher Syndrome Type II | Carcinoid Tumor | Craniofacial Dysostosis | Microtia | Glomerulonephritis, Membranoproliferative | Purpura | Tyrosinemia Type 2 | Primary Sclerosing Cholangitis | Tyrosinemia Type 1 | Anal Fissure | Hepatitis, Chronic | Adenoma, Pituitary | B-cell Chronic Lymphocytic Leukemia | Eccrine Porocarcinoma | Glycogen Storage Disease | Light Chain Amyloidosis | Retinopathy, Diabetic | Delayed Sleep Phase Syndrome | Glanzmann Thrombasthenia | Hemimegalencephaly | Spinocerebellar Ataxia | Coronary Heart Disease | Dyskeratosis Congenita | Hypoglycemia | X-linked Myotubular Myopathy | Myeloid Leukemia | Renal Hypouricemia | Benign Familial Neonatal Convulsions | Greig Cephalopolysyndactyly Syndrome | Autosomal Recessive Congenital Ichthyosis | Alpha-mannosidosis | Anthrax | Hypobetalipoproteinemias | Distal Spinal Muscular Atrophy | Von Hippel-Lindau Disease | Goiter, Nodular | Porphyria, Variegate | Hepatorenal Syndrome | Angiosarcoma Of The Breast | Schwannomatosis | Retinal Detachment | Hidradenitis Suppurativa | Diabetic Neuropathy | Vertigo | Smith-Lemli-Opitz Syndrome | Osteomalacia | Genitopatellar Syndrome | Borderline Personality Disorder | PHARC Syndrome | Smoldering Myeloma | Arteriovenous Malformations | Cardiospondylocarpofacial Syndrome | Hypopituitarism | Pulmonary Tuberculosis | Johanson-Blizzard Syndrome | Infantile Refsum Disease | Blood Protein Disorders | Lymphangioleiomyomatosis | Esotropia | Ectrodactyly | Spinal Muscular Atrophy | Dementia | Lichen Sclerosus | Congenital Hemolytic Anemia | X-linked Acrogigantism | H Syndrome | Adenoma, Pleomorphic | Sarcoma, Ewing | Sturge-Weber Syndrome | Non-small Cell Lung Cancer | Hypophosphatasia | Cardiomyopathy, Peripartum | Low Phospholipid Associated Cholelithiasis | Hyperparathyroidism | Esophagitis | Hereditary Pyropoikilocytosis | Blau Syndrome | VEXAS Syndrome | Methylmalonic Acidemia | Omenn Syndrome | Tenosynovial Giant Cell Tumor | Microvillus Inclusion Disease | Focal Cortical Dysplasia Type 2 | Anorexia Nervosa | Hyperglycemia | Cheilitis | Birt-Hogg-Dube Syndrome | Dysplastic Nevus | Choroideremia | Retinitis Pigmentosa | Acute Generalized Exanthematous Pustulosis | Traboulsi Syndrome | Sarcoma, Alveolar Soft Part | Sickle Cell Anemia | CHOPS Syndrome | Intermittent Explosive Disorder | Chorea-acanthocytosis | Succinic Semialdehyde Dehydrogenase Deficiency | Hypercholesterolemia | Glycogen Storage Disease Type 0, Muscle | Adams-Oliver Syndrome | Impulse Control Disorder | Azoospermia | Gastroenteritis | Meningioma, Benign | Pemphigus | Becker Muscular Dystrophy | Congenital Nystagmus | Ocular Hypertension | Sotos Syndrome | Chanarin-Dorfman Syndrome | Cirrhosis | Diamond-Blackfan Anemia | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Fetal And Neonatal Alloimmune Thrombocytopenia | Hypermetropia | McLeod Syndrome | Panuveitis | Dengue Hemorrhagic Fever | Leukemia-lymphoma, Adult T-cell | Hypothalamic Obesity | Congenital Fiber-type Disproportion Myopathy | Spinocerebellar Ataxia Type 5 | Renal Medullary Carcinoma | Connective Tissue Disorders | Sertoli Cell-only Syndrome | Idiopathic Multicentric Castleman Disease | Hereditary Mixed Polyposis Syndrome | Hyperparathyroidism, Primary | Spinocerebellar Ataxia Type 38 | Lymphoma, AIDS-related | Hyperkalemic Periodic Paralysis | Erysipelas | HUPRA Syndrome | Schizoaffective Disorder | Multiple Sulfatase Deficiency | Congenital Poikiloderma | Pterygium | Leri Pleonosteosis | Inflammatory Myofibroblastic Tumor | Measles | Castleman Disease | Osteogenesis Imperfecta Type I