Papilledema

About the Disease
Optic Papillitis, also known as papilledema, is related to intracranial hypertension, idiopathic and abducens palsy, and has symptoms including edema An important gene associated with Optic Papillitis is MOG (Myelin Oligodendrocyte Glycoprotein), and among its related pathways/superpathways is Overview of nanoparticle effects. The drugs Minocycline and Lymecycline have been mentioned in the context of this disorder. Affiliated tissues include tongue, eye and endothelial, and related phenotype is immune system.

Common Targets
CTSK | G6774

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

Other Diseases

Cataract | Combined Pituitary Hormone Deficiency | Tuberculous Meningitis | Primary Hyperoxaluria Type 1 | Cluster Headache | Thanatophoric Dysplasia | Polyarteritis Nodosa | Atherosclerosis | Spinocerebellar Ataxia Type 1 | Glomerulonephritis | Leukocyte Adhesion Deficiency Type 1 | Hemoglobinopathies | Eosinophilia | Epilepsy | Myhre Syndrome | Dyslexia | Atopic Dermatitis | Cardiomyopathy, Hypertrophic | Mosaic Variegated Aneuploidy Syndrome 2 | Chorea | Danon Disease | Cystitis, Interstitial | Aneurysm, Abdominal Aortic | Chondrosarcoma | Spinocerebellar Ataxia Type 42 | Borjeson-Forssman-Lehmann Syndrome | Dementia, Vascular | Autosomal Recessive Spastic Paraplegia Type 54 | Klippel-Feil Syndrome | Takotsubo Cardiomyopathy | Aphasia | Charcot-Marie-Tooth Disease Type 4 | Retinal Dystrophy, Early-onset Severe | Pompe Disease | Neurofibroma, Plexiform | Dysferlinopathy | Cranial Nerve Disease | Diabetic Nephropathy | Carbonic Anhydrase VA Deficiency | Parkinson's Disease | Hepatopulmonary Syndrome | Gangliosidosis, GM1 | Acral Lentiginous Melanoma | Arts Syndrome | Endocarditis | Heavy Chain Disease | Cushing Syndrome | Macular Corneal Dystrophy Type 1 | Conn Syndrome | Metachromatic Leukodystrophy | Glioblastoma Multiforme | Ghosal Syndrome | Emery-Dreifuss Muscular Dystrophy | Schwartz-Jampel-Aberfeld Syndrome | Dermatomyositis | Lathosterolosis | Nanophthalmos | Growth Hormone Excess | Temporal Lobe Epilepsy | Amyotrophic Lateral Sclerosis | Erythropoietic Protoporphyria | Congenital Myopathy | Anencephaly | Lyme Disease | Congenital Primary Aphakia | Microcephaly, Seizures, And Developmental Delay | Trigonocephaly | Pseudomyxoma Peritonei | Goiter | Empyema | Cryptococcal Meningitis | Currarino Syndrome | Spondylocarpotarsal Synostosis Syndrome | Rotor Syndrome | Skin Carcinoma | Endometriosis | T-cell Lymphoma, Subcutaneous Panniculitis-like | Mumps | Eating Disorder | Lymphoma Lymphoblastic | Osteomyelitis | Cousin Syndrome | Central Core Disease | Meningioma, Benign | Lupus Erythematosus | Tylosis With Esophageal Cancer | Rift Valley Fever | Infertility, Male | Cancer, Kidney | Hypogonadism | Myoclonic Epilepsy With Ragged Red Fibers | Histoplasmosis | Saethre-Chotzen Syndrome | Cutaneous Mastocytosis | Schnitzler Syndrome | Gastroenteritis, Eosinophilic | Hereditary Inclusion Body Myopathy | Progressive Osseous Heteroplasia | Hemosiderosis | Hypotension, Orthostatic | Vitreoretinal Degeneration, Snowflake Type | Guillain-Barre Syndrome | Bicuspid Aortic Valve | LEOPARD Syndrome | Ichthyosis | Hyperparathyroidism, Primary | Keratocystic Odontogenic Tumor | Scleroderma, Diffuse | Dystonia-parkinsonism, X-linked | Spondyloarthritis | Dystonia | Allergic Contact Dermatitis | Lymphoproliferative Disease, X-linked | Retinal Vasculitis | Cyclic Vomiting Syndrome | Hypertension, Renovascular | Malonyl-CoA Decarboxylase Deficiency | Heart Septal Defects | Rhinitis | Angina Pectoris | Esotropia | Learning Disability | Viral Meningitis | Stroke | Carpenter Syndrome | Teratozoospermia | Open-angle Glaucoma | Hypereosinophilic Syndrome | Cri-du-chat Syndrome | Protein S Deficiency | Seasonal Mood Disorder | Oguchi Disease-2 | 3-hydroxy-3-methylglutaric Aciduria | Iron Overload | Crouzon Syndrome With Acanthosis Nigricans | Vestibular Disease | Zellweger Syndrome | Waardenburg Syndrome Type 2 | Pemphigus Foliaceus | Venous Insufficiency | Orotic Aciduria | Neurofibromatosis Type 1 | Coenzyme Q10 Deficiency | Raine Syndrome | Potocki-Shaffer Syndrome | Nephritis, Interstitial | Spinocerebellar Ataxia Type 10 | C3 Glomerulopathy | Persistent Fetal Circulation | Spinocerebellar Ataxia Type 3 | Dominant Optic Atrophy | Fibromuscular Dysplasia | Sorsby Fundus Dystrophy | Acromesomelic Dysplasia | Aromatic L-amino Acid Decarboxylase Deficiency | Sleep Disorder | Hypopituitarism | Osteoglophonic Dysplasia | Hepatitis B, Chronic | Toxic Epidermal Necrolysis | Oculocutaneous Albinism | Strabismus | Cancer, Colon | Prader-Willi Syndrome | Placenta Previa | Pernicious Anemia | Thyroid Dyshormonogenesis | Pyruvate Decarboxylase Deficiency | Chondrodysplasia Punctata | Spondyloepiphyseal Dysplasia Tarda, X-linked | Pemphigus Vulgaris | Kernicterus | Adult Polyglucosan Body Disease | Stomatitis | Bronchiolitis | Chromosome 8q21.11 Deletion Syndrome | Cerebral Amyloid Angiopathy | Onchocerciasis | Common Variable Immunodeficiency | Hyperinsulinemia | Spinocerebellar Ataxia Type 5 | Carbamoyl Phosphate Synthetase I Deficiency | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Aplastic Anemia | Leprosy | Obsessive-compulsive Disorder | Vascular Calcification | Hypoplastic Left Heart Syndrome | Ocular Albinism Type 1 | Chronic Myeloid Leukemia | Abetalipoproteinemia | Macrophagic Myofasciitis | Hepatoblastoma | Sponastrime Dysplasia | Oligospermia | Blue Nevus | Beta-Propeller Protein-associated Neurodegeneration | Oligoasthenoteratozoospermia | Liebenberg Syndrome | Spinocerebellar Ataxia Type 27 | Epithelioid Hemangioma | Leukocyte Adhesion Deficiency | Connective Tissue Disorders | Agnathia-Otocephaly Complex | Heroin Dependence | Spinocerebellar Ataxia Type 2 | Toxoplasmosis | Tardive Dyskinesia | Frontometaphyseal Dysplasia | Rash | Retinal Coloboma | Metabolic Syndrome | Congenital Heart Defects | Polycystic Liver | Hypertension, Renal | Pyelonephritis | Long QT Syndrome Type 1 | Fascioliasis | Amish Infantile Epilepsy Syndrome | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Nemaline Myopathy | Gastroenteritis | Congenital Absence Of Vas Deferens | Charcot-Marie-Tooth Disease, Type 2C | Noonan Syndrome | Antley-Bixler Syndrome | Intestinal Hypomagnesemia 1 | Woodhouse-Sakati Syndrome | Paracoccidioidomycosis | Beare-Stevenson Syndrome | Optic Neuropathy, Anterior Ischemic | Ileitis | Sezary Syndrome | Myocarditis | Intracranial Hypertension | Osteoarthritis | Subacute Sclerosing Panencephalitis | Hereditary Hemorrhagic Telangiectasia | Amebiasis | Chylothorax, Congenital | Antisocial Personality Disorder | Charcot-Marie-Tooth Disease Type 2E | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Keratitis-ichthyosis-deafness Syndrome | Charcot-Marie-Tooth Disease Type 2D | Thrombophilia | Graves Disease | Tetraplegia | Fukuyama Congenital Muscular Dystrophy | Cholelithiasis | Thromboembolism | Neurofibromatosis Type 2 | Smith-Lemli-Opitz Syndrome | Psoriasis | Rothmund-Thomson Syndrome | Congenital Disorders Of Glycosylation | Ischemia | Hemangioblastoma | Neurocutaneous Melanocytosis | Urea Cycle Disorder | Oculocutaneous Albinism Type 1 | 3-methylglutaconic Aciduria Type IV | Hemolytic Anemia | Esthesioneuroblastoma | Neuroendocrine Cancer | Cutaneous Lupus Erythematosus | Anodontia | Anorchia | Porencephaly | Lipid Metabolism Disorders | Pure Red Cell Aplasia | Oculocutaneous Albinism Type 4 | Molybdenum Cofactor Deficiency | Atelosteogenesis Type 1 | Premenstrual Syndrome | Hemorrhoids | Primary Progressive Aphasia | Bietti Crystalline Dystrophy | Acute Kidney Injury | CHOPS Syndrome | Pyruvate Dehydrogenase Deficiency | Gerstmann-Straussler-Scheinker Syndrome | Metabolic Diseases | Chronic Inflammatory Demyelinating Polyneuropathy | Overactive Bladder | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Early Infantile Epileptic Encephalopathy 13 | Chronic Mucocutaneous Candidiasis | Sengers Syndrome | Paraganglioma | Acute Leukemia | Lipid Storage Diseases | Vogt-Koyanagi-Harada Syndrome | Anemia | Infantile Neuroaxonal Dystrophy | Presbyopia | Keratoconus | Angiosarcoma | Papilloma | Scleroderma | Thanatophoric Dysplasia Type 1 | Okihiro Syndrome | Liver Failure, Acute Infantile | Carney Triad | Ameloblastic Carcinoma | Mabry Syndrome | Infectious Diarrhea | Heterotopic Ossification | Pulmonary Alveolar Microlithiasis | Vitiligo | Juvenile Myelomonocytic Leukemia | Myopia | Chudley-McCullough Syndrome | Arthropathy | Pituitary Dwarfism | Dentinogenesis Imperfecta | Dementia | Hyperparathyroidism | Juvenile Myoclonic Epilepsy | Milk Allergy | Charcot-Marie-Tooth Disease | DNA Ligase IV Deficiency | Vaginitis | Frank-ter Haar Syndrome | Craniometaphyseal Dysplasia | Sclerosing Cholangitis | Hyperammonemia | Gastritis | Cold-induced Sweating Syndrome | Aneurysm, Thoracic Aortic | Rhabdomyosarcoma | Monilethrix | Pycnodysostosis | Fibrosarcoma | Lesch-Nyhan Syndrome | Congenital Myasthenic Syndrome | Vitamin K Deficiency | Acromegaly | Hereditary Spherocytosis | Pneumococcal Meningitis | Cerebral Cavernous Malformations | Gallstones | Usher Syndrome Type III | Essential Fructosuria | Japanese Encephalitis | Coffin-Lowry Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Anorexia Nervosa | Cervical Dystonia | Spinal Muscular Atrophy Type 2 | Polycythemia | Zimmermann-Laband Syndrome | Charcot-Marie-Tooth Disease, Type 6 | 3C Syndrome | Primary Lateral Sclerosis | Spondylocostal Dysostosis | Epidermolytic Ichthyosis, Annular | Granular Corneal Dystrophy Type 1 | Multifocal Motor Neuropathy | Lymphangioleiomyomatosis | McCune-Albright Syndrome | Twin-to-twin Transfusion Syndrome | Usher Syndrome Type IIC | Amelogenesis Imperfecta | Fragile X Syndrome | Tyrosinemia | Azoospermia | Goiter, Nodular | Ganglioglioma | Cirrhosis | Hypersensitivity | Cystinosis | Vasculitis | Alcoholism | Pleomorphic Xanthoastrocytoma | Schwannoma | Desbuquois Syndrome | Usher Syndrome Type II | Otitis Externa | Cold Agglutinin Disease | Rhabdoid Tumor | Malnutrition | Nail-Patella Syndrome | Epidermolysis Bullosa | Sarcoma, Ewing | Uremic Pruritus | Kaposi Sarcoma | Sertoli Cell-only Syndrome | Epidermolysis Bullosa Simplex, Localized | Meier-Gorlin Syndrome | Angiodysplasia | Myelitis | Neurofibromatosis-Noonan Syndrome | Jaundice, Obstructive | Fetal Alcohol Syndrome | Enlarged Vestibular Aqueduct | Alzheimer Disease, Late Onset | Pyruvate Carboxylase Deficiency Disease | Atrial Septal Defect | Light Chain Amyloidosis