Disease

Vascular Dementia

About the Disease
Vascular Dementia, also known as dementia, vascular, is related to binswanger's disease and dementia. An important gene associated with Vascular Dementia is NOTCH3 (Notch Receptor 3), and among its related pathways/superpathways are Alzheimer's disease and miRNA effects and Neuroscience. The drugs Acetaminophen and Hydrocodone have been mentioned in the context of this disorder. Affiliated tissues include brain, kidney and heart, and related phenotypes are nervous system and homeostasis/metabolism

Common Targets
HDAC3 | HDAC8 | SAR1B | MAP3K5 | PDE8A | ADIPOQ | Phosphodiesterase 1 (PDE1) (nonspecified subtype) | G7157 | CHRNA7 | GSK3B | BCHE | Neurotrophic Factor (nonspecified subtype) | Acetylcholine Receptors (Nicotinic) (nAChR) (nonspecified subtype) | IL6-AS1 | NMDA receptor | PDE9A | PDE5A | KCNK2 | G4137 | MIR138-1 | CLU | Alcohol Dehydrogenase (nonspecified subtype) | IL1A | ANK1 | DRD1 | TF | CRBN | LOC100287329 | Amyloid beta A4 precursor protein-binding family (APP-BP) (nonspecified subtype) | TGFB1 | APOE | L-Type calcium channel (nonspecified subtype) | MIR328 | FGB | BACE1 | PON1 | APP | PDE1B | DRD3 | MAOB | GABRA5 | TMEM97 | SLC40A1 | ACE | CHRM5 | HDAC6 | Soluble guanylyl cyclase | G7124 | MTHFR | CLDN1 | PLA2G7 | Phosphodiesterase 8 (nonspecified subtype) | PDE4D | G5743 | G3569 | CNR1 | HRH3 | ACHE | HDAC1 | HTR1A | SELE | SCN10A | KDR | GABA(A) receptor | MAOA | L-type voltage-dependent calcium channel complex | PDE4B | HFE | KAT2B | SIGMAR1 | IL10 | WWC1 | LTA | HAMP

疾病靶点研报
Vascular Dementia

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

Other Diseases

Adenoid Cystic Carcinoma | Hyperlipidemia Type V | Menetrier Disease | Waardenburg Syndrome Type 2 | Hydrocephalus | Meesmann Corneal Dystrophy | Agnathia-Otocephaly Complex | Carbohydrate Metabolism Disorders | Blepharitis | Juvenile Hyaline Fibromatosis | Congenital Adrenal Hyperplasia 1 | Phosphoglycerate Dehydrogenase Deficiency | Chronic Inflammatory Demyelinating Polyneuropathy | Encephalopathy, Ethylmalonic | Thanatophoric Dysplasia Type 1 | Fraser Syndrome | Microphthalmia, Syndromic 7 | Neurofibromatosis | Precocious Puberty | Adenomatoid Tumor | Osteogenesis Imperfecta Type VI | Benign Familial Neonatal Convulsions | Leukoplakia | Vitelliform Macular Dystrophy | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Cat Eye Syndrome | Pseudo-pseudohypoparathyroidism | Cartilage Disorders | Juvenile Myelomonocytic Leukemia | Antenatal Bartter Syndrome Type 1 | Kaposiform Hemangioendothelioma | Preaxial Polydactyly | Osteoporosis | Periventricular Nodular Heterotopia | Vaginitis | Stomatitis | Phenylketonuria II | Agranulocytosis | Restrictive Dermopathy | Progressive Osseous Heteroplasia | Fibromyalgia | Pancreatitis, Chronic | Vertigo | Scleroderma | Idiopathic Pulmonary Fibrosis | Chronic Kidney Disease | Fukuyama Congenital Muscular Dystrophy | Autosomal Recessive Bestrophinopathy | Congenital Hereditary Endothelial Dystrophy Type II | Sweet Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Hereditary Spherocytosis | Gynecomastia | Fatty Aldehyde Dehydrogenase Deficiency | Chronic Thromboembolic Pulmonary Hypertension | Erythema Nodosum | Sporadic Hemiplegic Migraine | McCune-Albright Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Major Depression | Cardiomyopathy, Hypertrophic | Kernicterus | Cyst | Measles | Necrobiosis Lipoidica | Oligoasthenoteratozoospermia | Oculocutaneous Albinism Type 2 | Vertebrobasilar Insufficiency | Congenital Absence Of Vas Deferens | Gastric Atrophy | Nephritis, Interstitial | X-linked Sideroblastic Anemia | Polydactyly | Silicosis | Keloid | Hyperinsulinemic Hypoglycemia | Eating Disorder | Klinefelter Syndrome | Oculocutaneous Albinism | Alpha-mannosidosis | Geleophysic Dysplasia | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Disseminated Intravascular Coagulation | Spinocerebellar Ataxia Type 2 | Senior-Loken Syndrome | Eosinophilia | Prostatitis | Benign Familial Infantile Seizures | Skin Papilloma | Jacobsen Syndrome | Neurofibromatosis Type 1 | Congenital Myopathy | Cholera | Cabezas Syndrome | C3 Glomerulonephritis | Cluster Headache | Pulmonary Tuberculosis | GLUT1 Deficiency Syndrome | Aicardi-Goutieres Syndrome | Periodic Limb Movement Disorder | Saethre-Chotzen Syndrome | Myositis | Tinea Versicolor | Charcot-Marie-Tooth Disease, Type 2 | Schaaf-Yang Syndrome | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Antisocial Personality Disorder | Hypertensive Nephropathy | Christianson Syndrome | Hyperoxaluria | Ureteropelvic Junction Obstruction | Vitamin A Deficiency | Polycystic Liver | Hemolytic Uremic Syndrome | Knobloch Syndrome | Tic Disorder | Hyperinsulinism-hyperammonemia Syndrome | 3C Syndrome | Shwachman-Bodian-Diamond Syndrome | Skin Carcinoma | Lennox-Gastaut Syndrome | Myoclonus-dystonia Syndrome | Hyperandrogenemia | Metabolic Diseases | Dyggve-Melchior-Clausen Disease | Endometriosis | Sarcoidosis, Pulmonary | Acromesomelic Dysplasia | Heavy Chain Disease | Brachydactyly | Neurofibroma | Graves Disease | Fanconi Syndrome | Primary Ovarian Insufficiency | Hereditary Hemorrhagic Telangiectasia Type 2 | Adams-Oliver Syndrome | Osmotic Demyelination Syndrome | Pseudohypoparathyroidism Type 1B | Neurocysticercosis | Leukodystrophies | Camurati-Engelmann Disease | Peters-plus Syndrome | Glycogen Storage Disease Type 0 | Asphyxia Neonatorum | Primary Lateral Sclerosis | Waldenstrom Macroglobulinemia | Palsy, Cerebral | Van Der Knaap Disease | Chronic Lymphocytic Leukemia | Chronic Beryllium Disease | Roberts Syndrome | Neurodegeneration With Brain Iron Accumulation | Graft-versus-host Disease | Desbuquois Syndrome | Myofibromatosis | Noonan Syndrome-like Disorder With Loose Anagen Hair | GATA2 Deficiency | Mitochondrial Cytopathy | Uveitis, Anterior | Large Granular Lymphocytic Leukemia | Pituitary Stalk Interruption Syndrome | Tumoral Calcinosis | Gallstones | Congenital Hereditary Endothelial Dystrophy Type I | Double Outlet Right Ventricle | Waardenburg Syndrome Type 4 | Renal Hypomagnesemia 3 | Sclerosing Cholangitis | Centronuclear Myopathy | Communication Disorders | IgA Deficiency | Von Hippel-Lindau Disease | Spinal Muscular Atrophy | Waardenburg Syndrome | Lichen Sclerosus | Auriculocondylar Syndrome | Congenital Primary Aphakia | Burn-McKeown Syndrome | Necrotizing Autoimmune Myopathy | Niemann-Pick Disease, Type A | Non-bullous Congenital Ichthyosiform Erythroderma | Schnitzler Syndrome | Early Infantile Epileptic Encephalopathy 4 | Contact Dermatitis | Schamberg Disease | Bare Lymphocyte Syndrome | Wolfram Syndrome | Creatine Deficiency Syndrome | Liddle Syndrome | Hemochromatosis Type 2 | Autosomal Recessive Spastic Paraplegia Type 54 | Craniopharyngioma | NDH Syndrome | Axenfeld-Rieger Syndrome | Demyelinating Diseases | Cole-Carpenter Syndrome | Intermittent Claudication | Hepatitis | Pemphigoid | Beare-Stevenson Syndrome | Actinomycetoma | Cancer, Colon | Distal Myopathy | Pterygium | Presbyopia | Aldosterone Synthase Deficiency | Exfoliative Dermatitis | Basan Syndrome | LMNA-related Congenital Muscular Dystrophy | Hemorrhagic Disorders | Chronic Granulomatous Disease, X-linked | Amebiasis | Primary Pigmented Nodular Adrenocortical Disease | Combined Malonic And Methylmalonic Acidemia | Erythematotelangiectatic Rosacea | Scabies | Corneal Ulcer | Thrombotic Microangiopathy | Non-small Cell Lung Cancer | Isovaleric Acidemia | Ghosal Syndrome | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Fascioliasis | GAPO Syndrome | Dengue Hemorrhagic Fever | Chondrodysplasia Punctata | Wiedemann-Steiner Syndrome | Idiopathic Multicentric Castleman Disease | Progressive Familial Intrahepatic Cholestasis Type 1 | Primary Familial Brain Calcification | Sialidosis | Cone Dystrophy | Cryopyrin-associated Periodic Syndromes | Osteochondroma | Hypophosphatasia | Melanoma | Gilbert Syndrome | Amyotrophic Lateral Sclerosis, Juvenile | Bursitis | VEXAS Syndrome | Bone Marrow Necrosis | Papulopustular Rosacea | Autism | Arteriosclerosis | Retinopathy Of Prematurity | Polyneuropathy | Hypersensitivity | Periodontitis | Hypogonadism | Fragile X Syndrome | Astrocytoma, Anaplastic | Acute Kidney Injury | Ichthyosis Hystrix, Curth-Macklin Type | Glomerulonephritis, Membranoproliferative | Behcet's Disease | Noonan Syndrome | Pityriasis Rubra Pilaris | Personality Disorders | Temtamy Preaxial Brachydactyly Syndrome | Bartsocas-Papas Syndrome | Jalili Syndrome | Myotonia | Spinocerebellar Ataxia Type 40 | Multiple Sclerosis, Chronic Progressive | Apraxia | Hypereosinophilic Syndrome | Atrioventricular Septal Defect | Cannabis Abuse | Choroiditis | Primary Progressive Aphasia | Hepatic Veno-occlusive Disease | Oral Lichen Planus | Endometrial Hyperplasia | Adenoma, Villous | Peeling Skin Syndrome, Acral Type | Weill-Marchesani Syndrome | Xeroderma Pigmentosum | Jaundice, Obstructive | Bone Giant Cell Tumor | Pycnodysostosis | Mabry Syndrome | Otitis Media | Creatine Deficiency Syndrome Due To AGAT Deficiency | Charcot-Marie-Tooth Disease Axonal Type 2N | Congenital Aniridia | Dementia, Vascular | Coenzyme Q10 Deficiency | Zellweger Syndrome | Familial Retinal Arterial Macroaneurysm | Liver Failure, Acute Infantile | Pheochromocytoma | Chronic Idiopathic Myelofibrosis | Infertility | Microtia | Thin Basement Membrane Disease | Hypercalciuria | Mycosis Fungoides | Sclerosteosis | FG Syndrome | Urethritis | VACTERL Association | Lymphoma | ADNP Syndrome | Gerstmann-Straussler-Scheinker Syndrome | Adenocarcinoma | Tremor | Galactosemia | Thrombosis | Epidermolytic Palmoplantar Keratoderma | Proopiomelanocortin Deficiency | Mesothelioma, Malignant | Dubin-Johnson Syndrome | Becker Muscular Dystrophy | Heart Block | Proctitis | Polycythemia | Diabetic Neuropathy | Chorea | Hepatic Steatosis | Encephalopathy, Hepatic | Diffuse Intrinsic Pontine Glioma | Hyperammonemia | Niemann-Pick Disease | Sarcomatoid Carcinoma Of The Lung | Ellis-Van Creveld Syndrome | Myelitis | Meningioma, Benign | Craniosynostosis | Guttate Psoriasis | Richter's Syndrome | Cutis Laxa | Nephrosclerosis | Ophthalmoplegia | Keratosis, Actinic | Teratozoospermia | Renal Tubular Acidosis | Fetal Alcohol Syndrome | Best Macular Dystrophy | Kleine-Levin Syndrome | DRESS Syndrome | Tendinopathy | Osteogenesis Imperfecta Type IV | Diabetes Type 1 | Costello Syndrome | CHOPS Syndrome | Hereditary Sensory And Autonomic Neuropathy | Hereditary Hemorrhagic Telangiectasia | AIDS Dementia Complex | Conjunctivitis, Allergic | Progressive Familial Intrahepatic Cholestasis Type 3 | Conduct Disorder | Lymphoproliferative Disease, X-linked | Acute Lung Injury | Empyema | Dystrophy, Cone-rod | Microcephalic Primordial Dwarfism | Nail Disorder, Nonsyndromic Congenital | Crohn's Disease | Chondroma | Nephrotic Syndrome | Sponastrime Dysplasia | Walker-Warburg Syndrome | Hypertension, Pulmonary | Dental Caries | Cardiomyopathy, Dilated, 1L | Pulmonary Stenosis | Methemoglobinemia | Cancer, Breast | Polymicrogyria | Asthma | Neutrophilia | Frontotemporal Dementia | Prune Belly Syndrome | Spinocerebellar Ataxia Type 12 | Retinoblastoma | Osteonecrosis Of The Jaw | Fowler's Syndrome | Hyperkalemic Periodic Paralysis | Non-Hodgkin Lymphoma | Sitosterolemia | Mountain Sickness | Oculocutaneous Albinism Type 4 | Pelizaeus-Merzbacher Disease | Growth Hormone Excess | Carbonic Anhydrase VA Deficiency | Cervicitis | Macular Corneal Dystrophy | Hemophagocytic Lymphohistiocytosis | Takenouchi-Kosaki Syndrome | Blue Rubber Bleb Nevus Syndrome | Diabetic Encephalopathy | Adult Polyglucosan Body Disease | Renal Medullary Carcinoma | Optic Atrophy 2 | Pyruvate Decarboxylase Deficiency | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Gitelman Syndrome | Hypohidrotic Ectodermal Dysplasia, X-linked | Mandibuloacral Dysplasia With Type A Lipodystrophy | Hepatopulmonary Syndrome