Disease

Varices

About the Disease
Varicose Veins, also known as varices, is related to klippel-trenaunay-weber syndrome and telangiectasis, and has symptoms including angina pectoris, chest pain and edema. An important gene associated with Varicose Veins is VV (Varicose Veins), and among its related pathways/superpathways are Innate Immune System and Signal Transduction. The drugs Hesperidin and Ibuprofen have been mentioned in the context of this disorder. Affiliated tissues include liver, skin and heart, and related phenotypes are varicose veins and homeostasis/metabolism

Common Targets
JAK2 | G196 | MTHFR | G4318 | CAND1.11 | EFEMP1 | TIMP2 | KCNH8 | ANGPT1 | MTR | LOC107985270 | LOC107985892 | SOX18 | SKAP2 | CASZ1

疾病靶点研报
Varices

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

Other Diseases

Riboflavin Transporter Deficiency Neuronopathy | Treacher Collins Syndrome | Bartsocas-Papas Syndrome | Combined Pituitary Hormone Deficiency | Encephalopathy | Nemaline Myopathy | Retinal Detachment | Fascioliasis | Barakat Syndrome | Shprintzen-Goldberg Syndrome | TARP Syndrome | HELLP Syndrome | Platelet Disorders | Metachromatic Leukodystrophy | Leiomyoma | Schizoaffective Disorder | Familial Digital Arthropathy-brachydactyly | Thrombocytopenia | Lymphedema | Lathosterolosis | Zygomycosis | Spitz Nevus | Infectious Diarrhea | Acute Leukemia | Congenital Heart Defects | Cutaneous Angiosarcoma | Angiomyolipoma | Benign Familial Pemphigus | Multiple Sclerosis | Methylmalonic Acidemia | Otopalatodigital Syndrome Type 2 | Progressive Familial Intrahepatic Cholestasis Type 1 | Primary Progressive Nonfluent Aphasia | Moyamoya Disease | Greenberg Dysplasia | Neuronal Ceroid Lipofuscinosis | D-2-Hydroxyglutaric Aciduria | Dyskeratosis Congenita | Presbycusis | Neurocysticercosis | Neuroectodermal Tumors, Primitive | Dermatofibrosarcoma | Autism | Microcephalic Primordial Dwarfism | Leukemia | Bare Lymphocyte Syndrome | Allan-Herndon-Dudley Syndrome | Aplasia Cutis Congenita | Melanoma, Uveal | Hypotrichosis | Cold-induced Sweating Syndrome | Obesity, Morbid | Infertility, Male | Congenital Generalized Lipodystrophy | Ellis-Van Creveld Syndrome | Adenoid Cystic Carcinoma | Roberts Syndrome | Sweet Syndrome | Kaposi Sarcoma | Genitopatellar Syndrome | Amyloidosis | Thromboembolism | Rash | Nephrotic Syndrome Type 1 | Mosaic Variegated Aneuploidy Syndrome 2 | Autosomal Recessive Congenital Ichthyosis | Pneumonia, Viral | Anti-glomerular Basement Membrane Disease | GAPO Syndrome | Cartilage Disorders | Hepatitis C, Chronic | Esotropia | Insulin Resistance | Congenital Myopathy | Cerebellar Ataxia, Cayman Type | Lysosomal Acid Lipase Deficiency | Cholangiocarcinoma | Alpha-thalassemia Myelodysplasia Syndrome | Angiosarcoma | Oculocutaneous Albinism Type 1 | Hemoglobinopathies | Cabezas Syndrome | Tietze Syndrome | Albinism | Hyperekplexia | Myopathy | Crohn's Disease | Hereditary Mixed Polyposis Syndrome | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Acanthosis Nigricans | Prader-Willi Syndrome | C3 Glomerulopathy | Glomerulonephritis, Membranoproliferative | Primary Carnitine Deficiency | Glomerulonephritis | Hereditary Hemorrhagic Telangiectasia | Von Hippel-Lindau Disease | Congenital Hypofibrinogenemia | Neurofibrosarcoma | Borderline Personality Disorder | Nager Acrofacial Dysostosis | Hyperlipidemia Type V | Pemphigus Foliaceus | AIDS Dementia Complex | Dental Caries | Tardive Dyskinesia | Meesmann Corneal Dystrophy | Isovaleric Acidemia | Congenital Lipoid Adrenal Hyperplasia | Prolactinoma | Hyperoxaluria | Astrocytoma | Spinal Muscular Atrophy | Wolff-Parkinson-White Syndrome | Mucolipidosis Type II | Inflammatory Myopathy | Pierson Syndrome | Choroideremia | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Basal Ganglia Disease, Biotin-responsive | Yellow Fever | Stromal Corneal Dystrophy | Polycystic Liver | Hyperinsulinemia | Cole-Carpenter Syndrome | Marinesco-Sjogren Syndrome | Neovascular Glaucoma | Dengue Hemorrhagic Fever | Coffin-Lowry Syndrome | Lipid Storage Diseases | Epidermolysis Bullosa Dystrophica | Hypocalcemia | Glioblastoma | Bone Giant Cell Tumor | Lattice Corneal Dystrophy Type 1 | Postpoliomyelitis Syndrome | Stargardt Disease | Waldenstrom Macroglobulinemia | Pseudoexfoliation Syndrome | Charcot-Marie-Tooth Disease | Hydrocephalus, Normal Pressure | Leishmaniasis, Cutaneous | Melanoma | Menetrier Disease | Cryopyrin-associated Periodic Syndromes | Polydactyly | Interstitial Lung Diseases | Mast Cell Leukemia | Sickle Cell Disease | Liver Failure, Acute Infantile | Endometritis | Myositis, Focal | Peeling Skin Syndrome Type B | Neuromyelitis Optica | Antiphospholipid Syndrome | Renal Hypomagnesemia 3 | Esthesioneuroblastoma | Carcinoma, Merkel Cell | Spinocerebellar Ataxia Type 21 | Spondyloarthritis | Restless Legs Syndrome | Optic Neuropathy | Hypoproteinemia, Hypercatabolic | Parvovirus B19 Infection | Cardiospondylocarpofacial Syndrome | Crisponi Syndrome | Down Syndrome | DOCK8 Immunodeficiency Syndrome | Chondrosarcoma | Cervicitis | Colon Adenoma | Renal Tubular Dysgenesis | Proctitis | Metatropic Dysplasia | Waardenburg Syndrome | Hemorrhagic Disorders | Costello Syndrome | Coffin-Siris Syndrome | Pilomatrix Carcinoma | Retinal Vasculitis | Encephalopathy, Hepatic | Hennekam Lymphangiectasia-lymphedema Syndrome | T-cell Chronic Lymphocytic Leukemia | Pituitary Stalk Interruption Syndrome | Haim-Munk Syndrome | Lymphangiomatosis | Gastroschisis | Intracerebral Hemorrhage | Chorea-acanthocytosis | Trismus-pseudocamptodactyly Syndrome | Prolymphocytic Leukemia | Dent Disease | Vertigo | Supravalvular Aortic Stenosis | Amish Infantile Epilepsy Syndrome | Agammaglobulinemia | Charcot-Marie-Tooth Disease Type 4B1 | Generalized Epilepsy And Paroxysmal Dyskinesia | B-cell Prolymphocytic Leukemia | Mountain Sickness | Gastroenteritis, Eosinophilic | Renal Medullary Carcinoma | Sarcoma, Endometrial Stromal | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Acne | Omenn Syndrome | Hypotonia-cystinuria Syndrome | Benign Familial Infantile Seizures | Hypereosinophilic Syndrome | Ganglioglioma | Microcephaly | Scleroderma | Postaxial Polydactyly | Congenital Stromal Corneal Dystrophy | Ollier Disease | Cardiomyopathy, Hypertrophic | Charcot-Marie-Tooth Disease Type 4E | Chronic Neutrophilic Leukemia | Nephritis, Interstitial | Nail-Patella Syndrome | Holt-Oram Syndrome | Pseudohypoparathyroidism Type 1C | Myoclonic Epilepsy With Ragged Red Fibers | Vitreoretinopathy, Proliferative | Avellino Corneal Dystrophy | Polymyositis | Eccrine Porocarcinoma | Lymphedema-distichiasis Syndrome | Episodic Ataxia Type 1 | Phenylketonuria | Congenital Primary Aphakia | Neuroma | Charcot-Marie-Tooth Disease, Type 2 | Juvenile Myelomonocytic Leukemia | Galactosemia | Osteopathia Striata With Cranial Sclerosis | Focal Facial Dermal Dysplasia | Hermansky-Pudlak Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Toxic Epidermal Necrolysis | Gastric Atrophy | Disseminated Intravascular Coagulation | Charcot-Marie-Tooth Disease Type 2T | Atelosteogenesis Type 1 | Juvenile Polyposis | Myoclonic Atonic Epilepsy | Esophageal Carcinoma | Pyloric Stenosis, Infantile Hypertrophic | Alopecia Areata | Perivascular Epithelioid Cell Tumor | Botulism | Hereditary Sensory Neuropathy Type 1 | Sengers Syndrome | Chronic Beryllium Disease | Hemangioma | Kallmann Syndrome | Pulmonary Tuberculosis | Dystonia | Infertility | Esophagitis, Eosinophilic | Rubeosis Iridis | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Hyperostosis | Pyruvate Decarboxylase Deficiency | Pre-eclampsia | Babesiosis | Tyrosinemia Type 2 | Coloboma | Microvillus Inclusion Disease | Peutz-Jeghers Syndrome | Familial Isolated Hyperparathyroidism | Primary Pigmented Nodular Adrenocortical Disease | Neurofibroma | Carcinoid Syndrome | Spitzoid Melanoma | Blastomycosis | Schizotypal Personality Disorder | Cholera | Stomatitis | Neurofibromatosis Type 2 | Urolithiasis | CREST Syndrome | Danon Disease | Pulmonary Sclerosing Hemangioma | Colitis, Microscopic | Mucolipidosis | Asthma, Exercise-induced | Tenosynovial Giant Cell Tumor | Iron Overload | Heroin Dependence | Dwarfism | Heterotopic Ossification | Liver Failure | Salla Disease | Microtia | Usher Syndrome | Vitamin K Deficiency | Non-proliferative Diabetic Retinopathy | Tangier Disease | Personality Disorders | Smith-Magenis Syndrome | Conn Syndrome | Ichthyosis Bullosa Of Siemens | Osteoporosis-pseudoglioma Syndrome | Retinal Dystrophy | Long QT Syndrome Type 2 | Peritonitis | Lennox-Gastaut Syndrome | 3-methylglutaconic Aciduria | Hyperammonemia | Smith-Lemli-Opitz Syndrome | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Epiphyseal Chondrodysplasia, Miura Type | Phenylketonuria II | Avian Influenza | Hydrocephalus | Macular Corneal Dystrophy Type 1 | Tay-Sachs Disease | Congenital Muscular Dystrophy | Priapism | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Cystinosis | Uremic Pruritus | Carcinoma, Squamous Cell | Corneal Dystrophy | Wolfram Syndrome | Cardiomyopathy, Restrictive | Glioblastoma Multiforme | Compartment Syndrome | Split Hand-foot Malformation | Hamartoma | Cancer, Prostate | Osteomyelitis | Crigler-Najjar Syndrome | Spinocerebellar Ataxia Type 10 | Coenzyme Q10 Deficiency | Epithelial-myoepithelial Carcinoma | Alstrom Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Myelomeningocele | Myoclonus-dystonia Syndrome | Adenosine Deaminase 2 Deficiency | Premenstrual Syndrome | Stevens-Johnson Syndrome | Hypoparathyroidism | Familial Glucocorticoid Deficiency | Papillon-Lefevre Syndrome | Thalassemia | Juvenile Xanthogranuloma | Peeling Skin Syndrome, Acral Type | Keratosis | Carcinoma, Signet Ring Cell | Prolidase Deficiency | Carcinoma, Transitional Cell | Hemangioblastoma | Chronic Periodontitis | Delayed Sleep Phase Syndrome | Polymyalgia Rheumatica | Beare-Stevenson Syndrome | Chondroma | Kaposiform Hemangioendothelioma | Torticollis | Polycythemia | Facioscapulohumeral Muscular Dystrophy | Pelizaeus-Merzbacher Disease | Thrombasthenia | Thyroiditis, Autoimmune | Multiple Sclerosis, Primary Progressive | Rosacea | X-linked Sideroblastic Anemia | Tricho-hepato-enteric Syndrome | Encephalopathy, Glycine | Primary Hyperoxaluria Type 1 | Nance-Horan Syndrome | Pigment Dispersion Syndrome | DICER1 Syndrome | Keratoconjunctivitis | Myasthenia | HIBCH Deficiency | Postpartum Depression | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | KBG Syndrome | Wieacker-Wolff Syndrome | Nephrocalcinosis | Adenocarcinoma | Corneal Dystrophy And Perceptive Deafness | Palmoplantar Keratoderma | Argininosuccinic Aciduria | Anorectal Fistula | Pancreatitis | Glutaric Aciduria Type 3 | Rothmund-Thomson Syndrome | Fabry's Disease | Aromatic L-amino Acid Decarboxylase Deficiency | Fukuyama Congenital Muscular Dystrophy | Chitayat Syndrome | Hemophilia | Carbamoyl Phosphate Synthetase I Deficiency | Primary Hyperoxaluria | Carcinoma In Situ