Disease

Vaginitis

About the Disease
Vaginitis, also known as inflammation of vagina, is related to postmenopausal atrophic vaginitis and vulvovaginitis, and has symptoms including leukorrhea, vaginal pruritus and vaginal odor. An important gene associated with Vaginitis is ESR1 (Estrogen Receptor 1), and among its related pathways/superpathways are Innate Immune System and Signal Transduction. The drugs Cranberry and Hyaluronic acid have been mentioned in the context of this disorder. Affiliated tissues include breast, skin and cervix, and related phenotypes are no effect and no effect

Common Targets
PPARG

疾病靶点研报
Vaginitis

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

Other Diseases

Inflammatory Myofibroblastic Tumor | Spondylosis | Hypotension, Orthostatic | Learning Disability | Relapsing Polychondritis | Cataplexy | Smith-Magenis Syndrome | Zollinger-Ellison Syndrome | Budd-Chiari Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Lentigo | Spinocerebellar Ataxia Type 16 | Pierson Syndrome | Choriocarcinoma | Personality Disorders | Multicystic Renal Dysplasia | Kabuki Syndrome 2 | Cold-induced Sweating Syndrome | Chromosome 9q34.3 Deletion Syndrome | Hyperhomocysteinemia | Cardiofaciocutaneous Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Glycogen Storage Disease Type 3 | Bulimia Nervosa | Familial Dysautonomia | Retinitis Pigmentosa | Neural Tube Defect | Prurigo Nodularis | Alpha-mannosidosis | Sick Sinus Syndrome 1 | Hemochromatosis Type 2 | Diabetes Insipidus, Neurogenic | Spinal Muscular Atrophy Type 2 | Ellis-Van Creveld Syndrome | Spinocerebellar Ataxia Type 6 | Schizotypal Personality Disorder | Osteogenesis Imperfecta Type II | Adenosine Deaminase Deficiency | Lyme Disease | Nephroblastoma | Noonan Syndrome | Christianson Syndrome | Stuttering | Stroke, Ischemic | DRESS Syndrome | Hyperandrogenemia | Erysipelas | Apert Syndrome | Allan-Herndon-Dudley Syndrome | Chudley-McCullough Syndrome | Neuromyotonia | Congenital Stationary Night Blindness | Subcortical Band Heterotopia | Acromesomelic Dysplasia | Hyperacusis | Heroin Dependence | Milk Allergy | Fetal Akinesia Deformation Sequence | Pulmonary Vein Stenosis | Silver-Russell Syndrome | Chondrodysplasia Punctata 2, X-linked Dominant | Pseudo-pseudohypoparathyroidism | Prediabetes | Paroxysmal Nocturnal Hemoglobinuria | Rift Valley Fever | Hyperthermia, Malignant | Melanoma, Uveal | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Carcinoma, Small Cell | Amenorrhea | Blepharo-cheilo-odontic Syndrome | Obsessive-compulsive Disorder | Phenylketonuria II | Renal Hypomagnesemia 3 | Macular Corneal Dystrophy | Pseudohypoparathyroidism Type 1B | Iron Deficiency Anemia | Growth Hormone Excess | Lesch-Nyhan Syndrome | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Thrombocythemia, Essential | Hemorrhagic Disorders | Neurodermatitis | Atrioventricular Septal Defect | Corneal Neovascularization | Peritonitis | Hypotrichosis Simplex | Aneurysm, Abdominal Aortic | Pontocerebellar Hypoplasia Type 2 | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Rothmund-Thomson Syndrome | Feingold Syndrome | Acrodermatitis Enteropathica | Craniometaphyseal Dysplasia | Pityriasis Rubra Pilaris | Fanconi Anemia | Asperger Syndrome | Glycogen Storage Disease Type 5 | Primary Sclerosing Cholangitis | Axenfeld-Rieger Syndrome | Polyneuropathy | Conjunctivitis, Allergic | Impetigo | Chordoid Glioma | Nephrotic Syndrome | Multicentric Carpotarsal Osteolysis Syndrome | Hyperlipidemia Type V | Metatropic Dysplasia | Paternal Uniparental Disomy Of Chromosome 14 | Chronic Mucocutaneous Candidiasis | Hyperinsulinism-hyperammonemia Syndrome | Cystinosis | Hemochromatosis Type 1 | Neuroectodermal Tumors, Primitive | Pregnancy, Ectopic | Anorexia Nervosa | Congenital Torticollis | Hidradenitis Suppurativa | Fetal Alcohol Syndrome | Glucagonoma | T-cell Chronic Lymphocytic Leukemia | Congenital Bilateral Absence Of Vas Deferens | Nephrosclerosis | Hyperostosis | Epidermolysis Bullosa Simplex, Generalized | Myasthenia | Guanidinoacetate Methyltransferase Deficiency | Glioblastoma Multiforme | Chronic Granulomatous Disease, X-linked | Myotonia | Cryoglobulinemia | Epidermolytic Ichthyosis, Annular | Hypopigmentation | Rash | Dominant Optic Atrophy | Neuronal Ceroid Lipofuscinosis | Meningioma | Peeling Skin Syndrome, Acral Type | Chronic Granulomatous Disease | Epilepsy Of Infancy With Migrating Focal Seizures | Carcinoid Tumor | Hypobetalipoproteinemias | Myelitis | Arthrogryposis | Short-chain Acyl-CoA Dehydrogenase Deficiency | Chondrodysplasia Punctata | Juvenile Polyposis | Cryopyrin-associated Periodic Syndromes | Acrocallosal Syndrome | Myelofibrosis | Lipodystrophy | Proteus Syndrome | Autonomic Nervous System Disorders | Neurocysticercosis | Fascioliasis | Hypertension | Osmotic Demyelination Syndrome | Retinopathy, Diabetic | Schizencephaly | Trachoma | Encephalopathy, Ethylmalonic | Congenital Bile Acid Synthesis Defect | DOCK8 Immunodeficiency Syndrome | Hypercalcemia | Fuchs Heterochromic Iridocyclitis | Brenner Tumor | Thrombotic Microangiopathy | GAPO Syndrome | Hepatitis B, Chronic | Pseudomyxoma Peritonei | Asthma | Esthesioneuroblastoma | Nephrocalcinosis | Epidermolysis Bullosa Acquisita | Large Granular Lymphocytic Leukemia | Nemaline Myopathy | Leishmaniasis, Visceral | Dental Caries | Carcinoma, Signet Ring Cell | Influenza | Intestinal Pseudo-obstruction | Glaucoma, Congenital | Dent Disease | Metabolic Diseases | Obesity, Morbid | Ocular Albinism Type 1 | Epidermolysis Bullosa Dystrophica | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Kindler Syndrome | Lymphoma, Follicular | Congenital Dyserythropoietic Anemia Type 4 | Skin Fragility-woolly Hair Syndrome | Wiskott-Aldrich Syndrome | Allergic Contact Dermatitis | Mucolipidosis Type III | Blue Rubber Bleb Nevus Syndrome | Autosomal Recessive Spastic Paraplegia Type 75 | Erythema Multiforme | Mohr-Tranebjaerg Syndrome | Charcot-Marie-Tooth Disease Type 4D | Ghosal Syndrome | Irritable Bowel Syndrome | Tendinopathy | Central Core Disease | Granular Corneal Dystrophy | Diabetes | Xeroderma Pigmentosum Variant Type | Sleep Disorder | Zygomycosis | Episodic Ataxia | Hydrolethalus Syndrome | Gastrointestinal Disorders | Majeed Syndrome | Mevalonate Kinase Deficiency | Heimler Syndrome | Neovascular Glaucoma | Schistosomiasis | Spitz Nevus | Medulloblastoma | ACTH-independent Macronodular Adrenal Hyperplasia | Macrophagic Myofasciitis | Spondyloperipheral Dysplasia | Myocarditis | Malaria | Goiter | Cancer, Colon | Erythropoietic Protoporphyria | Chromosome 16p11.2 Deletion Syndrome | Ovarian Sex Cord-stromal Tumor | Waardenburg Syndrome Type 4A | Sarcosinemia | Lymphoma, B-cell | Crisponi Syndrome | Combined Pituitary Hormone Deficiency | Anencephaly | Marfan Syndrome | Recurrent Respiratory Papillomatosis | Walker-Warburg Syndrome | Schizophrenia, Paranoid | Carotid Artery Disease | Peters-plus Syndrome | Hepatitis | Retinal Detachment | Pheochromocytoma | Leri-Weill Dyschondrosteosis | Thyroid Hormone Resistance | Multiple Sclerosis, Secondary Progressive | Hereditary Coproporphyria | Glomerulonephritis, Membranoproliferative | Skin Papilloma | Osteonecrosis Of The Jaw | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Shprintzen-Goldberg Syndrome | Reflex Epilepsy | Hyperparathyroidism | Diarrhea | Fowler's Syndrome | Macular Corneal Dystrophy Type 1 | Adult Polyglucosan Body Disease | Alpers Syndrome | Neurofibromatosis Type 1 | Restless Legs Syndrome | Babesiosis | Localized Scleroderma | Pigment Dispersion Syndrome | Agnathia-Otocephaly Complex | Gerstmann-Straussler-Scheinker Syndrome | Donnai-Barrow Syndrome | Endometrial Hyperplasia | Esotropia | Genitopatellar Syndrome | Vogt-Koyanagi-Harada Syndrome | Lipid Storage Myopathy | Hernia, Inguinal | Lymphangioleiomyomatosis | Mitochondrial DNA Depletion Syndrome | Polycystic Kidney, Autosomal Dominant | Lymphedema-distichiasis Syndrome | Hypertension, Essential | Frontometaphyseal Dysplasia | Hereditary Folate Malabsorption | Congenital Mirror Movements | Carpal Tunnel Syndrome | Malaria, Cerebral | Spondylometaphyseal Dysplasia | Sulfite Oxidase Deficiency | Corticobasal Syndrome | Keratosis, Actinic | Sleep Apnea | Bernard-Soulier Syndrome | Congenital Tufting Enteropathy | Melanoma, Malignant | Glycogen Storage Disease Type 1b | Thanatophoric Dysplasia Type 1 | Microvillus Inclusion Disease | Nutrition Disorders | Aneurysm, Thoracic Aortic | Amelogenesis Imperfecta | Fraser Syndrome | Diabetic Neuropathy | Nemaline Myopathy 10 | Premature Ejaculation | Heterotaxy | Charcot-Marie-Tooth Disease Type 4 | Keratoconjunctivitis | Spermatocele | C3 Glomerulonephritis | Filariasis | Sclerosteosis | Waardenburg Syndrome Type 2E | Clouston Hidrotic Ectodermal Dysplasia | Oligospermia | Infantile Nephropathic Cystinosis | Liddle Syndrome | Lymphomatoid Granulomatosis | Meningeal Melanocytoma | Encephalocele | Eating Disorder | ADNP Syndrome | Monilethrix | Impulse Control Disorder | Adenoma, Pituitary | Lactose Intolerance | Cardiac Sarcoidosis | Liebenberg Syndrome | Prostatitis | Hypogammaglobulinemia | Cone Dystrophy | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Coronary Heart Disease | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Xeroderma Pigmentosum | Hydrocephalus, Normal Pressure | Cartilage Disorders | Congenital Nephrotic Syndrome | Congenital Nystagmus | Anxiety Disorders | Spinocerebellar Ataxia Type 3 | Cholecystitis | Arterial Tortuosity Syndrome | Common Variable Immunodeficiency | X-linked Sideroblastic Anemia | X-linked Acrogigantism | Dermatitis | Focal Dermal Hypoplasia | Cholestasis | Wolfram Syndrome 2 | Gnathodiaphyseal Dysplasia | Common Cold | Aldosteronism | Leukoencephalopathy, Progressive Multifocal | Metaphyseal Chondrodysplasia, Schmid Type | Muscular Dystrophy | Alopecia | Hypogonadism | Currarino Syndrome | Mycosis Fungoides | Corneal Dystrophies, Hereditary | Keloid | Parapsoriasis | GM2-gangliosidosis AB Variant | Mabry Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Retinoschisis | Dengue Shock Syndrome | Sialidosis | Polymyositis | Tenosynovial Giant Cell Tumor | Malnutrition | Bartter Syndrome | Botulism | Optic Atrophy 2 | Hyperthyroidism | Sclerosing Cholangitis | Phenylketonuria | Mucolipidosis | Chronic Enteropathy Associated With SLCO2A1 Gene | Kidney Stones | Migraine | Synpolydactyly | Adenylosuccinate Lyase Deficiency | Multiple Epiphyseal Dysplasia | Periodontitis | Glycogen Storage Disease Type 6 | Kleine-Levin Syndrome | Anal Fissure | Bethlem Myopathy | Premenstrual Syndrome | Glioma | Insulin Resistance | Hypertensive Retinopathy | Familial Exudative Vitreoretinopathy | Rhabdomyosarcoma, Embryonal | Coffin-Siris Syndrome | Hypoproteinemia, Hypercatabolic | Spitzoid Melanoma | Sarcoma, Ewing | Rheumatoid Arthritis | Hepatopulmonary Syndrome | Papillon-Lefevre Syndrome