Disease

Hypertensive Retinopathy

About the Disease
Hypertensive Retinopathy is related to retinal vascular disease and microvascular complications of diabetes 5. An important gene associated with Hypertensive Retinopathy is VWF (Von Willebrand Factor), and among its related pathways/superpathways is "Agents Acting on the Renin-Angiotensin System Pathway, Pharmacodynamics". Affiliated tissues include retina, eye and kidney, and related phenotypes are homeostasis/metabolism and cardiovascular system

Common Targets
FECH

疾病靶点研报
Hypertensive Retinopathy

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

Other Diseases

Scabies | Deafness, Dystonia, And Cerebral Hypomyelination | Retinal Vasculitis | Myocarditis | Encephalopathy, Glycine | Hypercalcemia | Macrophage Activation Syndrome | Hidradenitis | Combined Deficiency Of Factor V And Factor VIII | Sarcoidosis | Cirrhosis | Schnitzler Syndrome | Renal Dysplasia | Basal Cell Nevus Syndrome | Ocular Hypertension | Woodhouse-Sakati Syndrome | Saethre-Chotzen Syndrome | Spitzoid Melanoma | Alstrom Syndrome | Addison Disease | Alpha-1 Antitrypsin Deficiency | Glycogen Storage Disease Type 0, Muscle | Hepatic Adenomatosis | Double Outlet Right Ventricle | Focal Cortical Dysplasia Type 2 | Constipation | Fibrosis | Niemann-Pick Disease, Type B | Neutrophilia | 3-methylcrotonyl-CoA Carboxylase Deficiency | Long QT Syndrome Type 3 | Primary Erythromelalgia | Generalized Epilepsy And Paroxysmal Dyskinesia | Myoclonus | Cholesteryl Ester Storage Disease | Hypersensitivity | Thyrotoxic Periodic Paralysis | Phenylketonuria | Gastritis | Myelomeningocele | Amish Infantile Epilepsy Syndrome | Adams-Oliver Syndrome | Haim-Munk Syndrome | Hepatitis, Autoimmune | Renal Medullary Carcinoma | GM2-gangliosidosis AB Variant | Emery-Dreifuss Muscular Dystrophy | Mabry Syndrome | Fraser Syndrome | Endometriosis | Scleroderma | Noonan Syndrome | Gitelman Syndrome | Polyomavirus Nephropathy | Cardiac Arrest | Patent Ductus Arteriosus | Osteosarcoma | Spinocerebellar Ataxia Type 16 | Wagner Disease | Osteonecrosis Of The Jaw | Coenzyme Q10 Deficiency | Congenital Heart Block | Thyroid Dysgenesis | Spinal And Bulbar Muscular Atrophy | Pierson Syndrome | Hepatitis, Alcoholic | Giant Cell Glioblastoma | Congenital Hypofibrinogenemia | Non-Hodgkin Lymphoma | Bicuspid Aortic Valve | Epidermal Nevus Syndrome | Fibrodysplasia Ossificans Progressiva | Hemoglobinopathies | Synpolydactyly | Tremor | Antithrombin III Deficiency | Amenorrhea | Axenfeld-Rieger Syndrome | Leukocyte Adhesion Deficiency Type 1 | Congenital Dyserythropoietic Anemia Type 1 | Hepatitis A | Microcephaly, Seizures, And Developmental Delay | Familial Mediterranean Fever | Hereditary Xerocytosis | Nephrotic Syndrome | Chondrosarcoma | Melanocytic Nevus | Hydronephrosis | Hodgkin Lymphoma | Chorea-acanthocytosis | Fontaine Progeroid Syndrome | Feingold Syndrome | Antley-Bixler Syndrome | Malignant Peripheral Nerve Sheath Tumor | Neuronal Ceroid Lipofuscinosis | Hypothyroidism | Antiphospholipid Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Carpenter Syndrome | Tuberculosis | Intellectual Disability, Autosomal Dominant 5 | Histoplasmosis | Mood Disorder | Primary Familial Brain Calcification | Congenital Ichthyosiform Erythroderma | Cancer, Colon | Sickle Cell Disease | Polycystic Liver | Frank-ter Haar Syndrome | Spinocerebellar Ataxia Type 20 | Hypoplastic Left Heart Syndrome | Endometritis | Meconium Ileus | Usher Syndrome Type IIC | 5-oxoprolinase Deficiency | Cone Dystrophy | Familial Partial Lipodystrophy | Chanarin-Dorfman Syndrome | Ventricular Septal Defect | NDH Syndrome | Corneal Edema | Pierpont Syndrome | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Hyperuricemic Nephropathy, Familial Juvenile | Pulmonary Alveolar Microlithiasis | Urofacial Syndrome | Myhre Syndrome | Melanoma, Uveal | Spondylocarpotarsal Synostosis Syndrome | Osteoarthritis | Achromatopsia | Multiple Sclerosis, Primary Progressive | Hypermetropia | Apparent Mineralocorticoid Excess Syndrome | Asthma, Exercise-induced | Lung Diseases | Congenital Nystagmus | Myofibromatosis | Progressive Familial Intrahepatic Cholestasis Type 2 | Niemann-Pick Disease, Type C | Hyperlipidemia | Atelosteogenesis Type 1 | Chordoma | Ligneous Conjunctivitis | Harlequin Ichthyosis | Glycogen Storage Disease Type 3 | Carcinoma, Small Cell | Optic Atrophy 2 | Vasculitis | Papilledema | Micropenis | Fanconi Syndrome | Pilomatrix Carcinoma | Familial Episodic Pain Syndrome | Martsolf Syndrome | Autism Spectrum Disorders | Kidney Stones | Argininosuccinic Aciduria | Leprosy | Lewy Body Dementia | Chronic Lymphocytic Leukemia | Autoimmune Polyendocrinopathy Syndrome Type I | PASLI Disease | Brachydactyly | Hypopituitarism | Mast Cell Leukemia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Bipolar Disorder | Congenital Disorders Of Glycosylation Type II | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Anorchia | McKusick Type Metaphyseal Chondrodysplasia | Anxiety Disorders | Meier-Gorlin Syndrome | Encephalopathy, Ethylmalonic | Smoldering Myeloma | Pityriasis Rubra Pilaris | Thrombotic Microangiopathy | AIDS | Epidermolysis Bullosa | Episodic Ataxia Type 2 | Meningitis | Psoriasis | Split Hand-foot Malformation | Pneumonia, Mycoplasma | Encephalopathy | Primary Lateral Sclerosis | Presbyopia | Omenn Syndrome | Spina Bifida | Bietti Crystalline Dystrophy | Pseudohypoparathyroidism Type 1C | Periventricular Leukomalacia | Meningioma | Congenital Myopathy | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Sjogren Syndrome | Muckle-Wells Syndrome | Farber Disease | Diabetes Type 1 | Iron Metabolism Disorders | Glaucoma, Congenital | Conduct Disorder | Hemophagocytic Lymphohistiocytosis | Blastomycosis | Twin-to-twin Transfusion Syndrome | Schizophrenia, Paranoid | Acrodysostosis | Pure Autonomic Failure | Osteoglophonic Dysplasia | X-linked Sideroblastic Anemia | Lymphoma, B-cell | Vascular Calcification | Malonyl-CoA Decarboxylase Deficiency | Sarcoidosis, Pulmonary | Mucormycosis | Cleidocranial Dysplasia | Leukemia | Crigler-Najjar Syndrome | Aneurysm, Abdominal Aortic | Chordoid Glioma | Aceruloplasminemia | Majeed Syndrome | Protein C Deficiency | Charcot-Marie-Tooth Disease, Type 2A | Fukuyama Congenital Muscular Dystrophy | Myelitis, Transverse | Van Der Knaap Disease | Spinocerebellar Ataxia Type 14 | Polycystic Kidney, Autosomal Recessive | Menkes Disease | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Alagille Syndrome | Scapuloperoneal Myopathy, X-linked Dominant | Bartsocas-Papas Syndrome | Xeroderma Pigmentosum | Aldosteronism | Congenital Hemolytic Anemia | Inflammatory Myopathy | Asperger Syndrome | Peroxisomal Disorder | Colon Adenoma | Ellis-Van Creveld Syndrome | Amebiasis | Sensory Neuropathy | Astigmatism | X-linked Creatine Transporter Deficiency | Behcet's Disease | Senior-Loken Syndrome | Opisthorchiasis | Hereditary Spherocytosis | Osteomalacia | Urea Cycle Disorder | Infantile Liver Failure Syndrome 1 | Li-Fraumeni Syndrome | Tracheal Disorders | Neuromyotonia | Nephroblastoma | Empyema | Sweet Syndrome | Diamond-Blackfan Anemia | Cerebellar Ataxia, Cayman Type | Hypertension | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Genitopatellar Syndrome | Cryptorchidism | Synovitis | Norrie Disease | Gilbert Syndrome | Stomatitis | Multisystemic Smooth Muscle Dysfunction Syndrome | Arthritis, Gouty | Renal Tubular Dysgenesis | Paronychia | Demyelinating Diseases | Treacher Collins Syndrome | Sengers Syndrome | Mycosis Fungoides | Optic Neuropathy, Anterior Ischemic | Exfoliative Dermatitis | Lipoma | Ganglioneuroma | Porphyria Cutanea Tarda | Hypopigmentation | Microphthalmia, Syndromic 7 | Primary Biliary Cholangitis | Lyme Disease | Angiosarcoma Of The Breast | Cystinuria | Malaria | Gangliosidosis, GM1 | Epidermolytic Ichthyosis, Annular | Crisponi Syndrome | Congenital Aniridia | Sturge-Weber Syndrome | Limb Girdle Muscular Dystrophy | Glomerulonephritis, Membranoproliferative | McLeod Syndrome | Stiff-man Syndrome | Keratosis, Actinic | Scleroderma, Diffuse | Motor Neuron Diseases | Withdrawal Syndrome | Pulmonary Stenosis | Nance-Horan Syndrome | Bare Lymphocyte Syndrome | Isobutyryl-CoA Dehydrogenase Deficiency | Renal-hepatic-pancreatic Dysplasia | Central Pain Syndrome | Seborrheic Dermatitis | Tinea | Cholangiocarcinoma | Spondylocostal Dysostosis | Schistosomiasis | Anorectal Fistula | Polymicrogyria | Primary Progressive Nonfluent Aphasia | Headache | Adenomatoid Tumor | Angiosarcoma | Aromatic L-amino Acid Decarboxylase Deficiency | Purpura | Polyneuropathy | Poretti-Boltshauser Syndrome | Crouzon Syndrome With Acanthosis Nigricans | Multiple Sclerosis, Chronic Progressive | Tendinitis | Distal Myopathy | Fetal Alcohol Syndrome | Hypersensitivity Pneumonitis | Light Chain Amyloidosis | Rheumatic Heart Disease | Papillorenal Syndrome | Klinefelter Syndrome | Amelanotic Melanoma | Growth Hormone Excess | Macular Corneal Dystrophy Type 1 | Ornithine Transcarbamylase Deficiency | Osteoporosis | Autosomal Recessive Spastic Paraplegia Type 35 | Rotor Syndrome | Basal Ganglia Cerebrovascular Disease | Partington Syndrome | Diabetes Mellitus, Transient Neonatal | Epicondylitis | Bardet-Biedl Syndrome | Conjunctivitis, Allergic | Acute Anterior Uveitis | Hemangioblastoma | Bulimia Nervosa | Autonomic Neuropathy | Still Disease | Retinoschisis | Adenylosuccinate Lyase Deficiency | Pemphigus | Alpha-mannosidosis | Pyruvate Carboxylase Deficiency Disease | Vitiligo | Amyotrophic Lateral Sclerosis | Guanidinoacetate Methyltransferase Deficiency | Pyruvate Decarboxylase Deficiency | Polymyositis | Schamberg Disease | Gastroenteritis, Eosinophilic | Congenital Torticollis | Parvovirus B19 Infection | Onchocerciasis | Hyperbilirubinemia, Neonatal | Oculopharyngeal Muscular Dystrophy | Acute Leukemia | Primary Aldosteronism | Angioedema, Acquired | Waardenburg Syndrome | TARP Syndrome | Galactosemia | Leiomyoma | Acute Tubular Necrosis | Evans Syndrome | Panuveitis | Multifocal Motor Neuropathy | Perivascular Epithelioid Cell Tumor | Glomerulonephritis | WAGR Syndrome | Cramp Fasciculation Syndrome | Hepatitis D | Liver Failure | GATA2 Deficiency | Thrombosis | Ichthyosis, X-linked | Primary Progressive Aphasia | Pelizaeus-Merzbacher Disease | Amyotrophic Lateral Sclerosis, Juvenile | Wiedemann-Steiner Syndrome | Nestor-Guillermo Progeria Syndrome | Dystrophy, Cone-rod | Trachoma | Erythropoietic Protoporphyria | Wolfram Syndrome 2 | Acrocallosal Syndrome | Hyperbilirubinemia