Disease

Anterior Uveitis

About the Disease
Anterior Uveitis, also known as iridocyclitis, is related to infectious anterior uveitis and glaucomatocyclitic crisis. An important gene associated with Anterior Uveitis is TLR4 (Toll Like Receptor 4), and among its related pathways/superpathways are Innate Immune System and MIF Mediated Glucocorticoid Regulation. The drugs Ganciclovir and Dexamethasone acetate have been mentioned in the context of this disorder. Affiliated tissues include eye, retina and endothelial, and related phenotypes are no effect and no effect

Common Targets
G7099 | GPR137 | OS9 | CFB | IL2RA | FKBP1A | HLA-B | LTA | HLA-DRB1 | ANXA11 | HLA-DQA1 | TRAF5 | MROH3P | PPP3R2 | PPP3CC | NOTCH4 | CCDC88B | G7124 | BTNL2 | HLA-A | BAD | NR3C1 | HLA-DRA | TLR2 | HERC2 | TGFB2 | HSPA1A | ERAP1 | RAB23 | PPP3CB | CCR5 | PPP3R1 | CFH | HLA-C | HSPA1L | TGFB3 | HLA-DQB1 | IL23R | C2 | Protein Phosphatase 2B

疾病靶点研报
Anterior Uveitis

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

Other Diseases

Retinal Diseases | Hyperlipidemia Type V | Astrocytoma, Anaplastic | Spinocerebellar Ataxia Type 42 | Benign Familial Infantile Seizures | L-2-Hydroxyglutaric Aciduria | Vascular Cognitive Impairment | Hyperinsulinemic Hypoglycemia | Intestinal Pseudo-obstruction | Leprosy | Familial Isolated Hyperparathyroidism | Ehlers-Danlos Syndrome | Supravalvular Aortic Stenosis | Majeed Syndrome | Malaria, Cerebral | Keratosis | Atelosteogenesis Type 2 | Thrombosis | Thrombophilia | Hypocalcemia | Takayasu's Arteritis | Hypercalciuria | Diarrhea | Platelet Disorders | Osteomalacia | Hypersomnia | Hyperbilirubinemia, Neonatal | Polymyositis | Retinal Vasculitis | Dermatitis Herpetiformis | Contact Dermatitis | Epilepsy Of Infancy With Migrating Focal Seizures | Diabetes Type 1 | Aldosterone Deficiency | Glanzmann Thrombasthenia | Acute Tubular Necrosis | Thrombotic Microangiopathy | Angiosarcoma | Dysferlinopathy | Pycnodysostosis | Bardet-Biedl Syndrome | Epithelioid Hemangioma | Pemphigoid | Mitochondrial DNA Depletion Syndrome | Wiedemann-Steiner Syndrome | Dyggve-Melchior-Clausen Disease | Hepatopulmonary Syndrome | Thrombocythemia, Essential | Pouchitis | Cardiomyopathy, Dilated, 1L | Impetigo | Cousin Syndrome | Cysticercosis | Agoraphobia | Multicentric Carpotarsal Osteolysis Syndrome | Toxoplasmosis | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Jacobsen Syndrome | Intermittent Claudication | Allergic Contact Dermatitis | Congenital Torticollis | Congenital Heart Defects | Thrombocytopenia | Ophthalmoplegia | Cardiomyopathy, Restrictive | Cystitis, Interstitial | Chronic Enteropathy Associated With SLCO2A1 Gene | Carney Triad | Gingivitis | Open-angle Glaucoma | Autoimmune Autonomic Ganglionopathy | Sulfite Oxidase Deficiency | Lateral Meningocele Syndrome | Dystonia-parkinsonism, X-linked | Crimean-Congo Hemorrhagic Fever | Periodic Limb Movement Disorder | Biotinidase Deficiency | Inflammatory Joint Disease | Camptocormia | Early Infantile Epileptic Encephalopathy | Hypertension, Portal | Acute Chest Syndrome | Brugada Syndrome 1 | Niemann-Pick Disease, Type B | Hypertension, Renal | Charcot-Marie-Tooth Disease Type 4 | Abetalipoproteinemia | Cri-du-chat Syndrome | Ependymoma | Carcinoma, Merkel Cell | B-cell Prolymphocytic Leukemia | Vitiligo | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Polyomavirus Nephropathy | Myoclonus-dystonia Syndrome | Mucolipidosis Type III | Peritonitis | Incontinentia Pigmenti | Kohlschutter-Tonz Syndrome | Pierpont Syndrome | Hidradenitis | Hepatitis B, Chronic | Hypersensitivity Pneumonitis | Hydrops Fetalis | Cerebrovascular Disorders | Familial Pheochromocytoma-paraganglioma | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Usher Syndrome Type IIC | Hyperferritinemia-cataract Syndrome | Spinocerebellar Ataxia Type 5 | Lymphoma Lymphoblastic | Genee-Wiedemann Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Central Retinal Artery Occlusion | Spinocerebellar Ataxia Type 16 | Ghosal Syndrome | Mastitis | Usher Syndrome Type III | Megaloblastic Anemia | Sitosterolemia | Purpura | Saul-Wilson Syndrome | Leukocyte Adhesion Deficiency | Fibronectin Glomerulopathy | Pyruvate Carboxylase Deficiency Disease | Meckel-Gruber Syndrome | Progressive Encephalopathy-optic Atrophy Syndrome | Synpolydactyly | Leukoplakia | Localized Scleroderma | Heavy Chain Disease | Amyloidosis | Myositis, Focal | Pyloric Stenosis, Infantile Hypertrophic | Marfan Syndrome | Vasculitis | Spasticity | Plasma Cell Dyscrasia | Thrombophlebitis | Focal Cortical Dysplasia Type 2 | Ganglioneuroma | Johanson-Blizzard Syndrome | Corticobasal Syndrome | GATA2 Deficiency | Leber Congenital Amaurosis | Trimethylaminuria | Autoimmune Polyendocrine Syndrome | Crigler-Najjar Syndrome | Headache | Proximal Symphalangism | Erythromelalgia | 3-methylglutaconic Aciduria Type I | Congenital Nystagmus | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Metatropic Dysplasia | Ebstein Anomaly | Bacterial Meningitis | Wieacker-Wolff Syndrome | Oculocutaneous Albinism | Centronuclear Myopathy | ADNP Syndrome | Sclerosteosis | Li-Fraumeni Syndrome | Neurotoxicity | Williams Syndrome | Eiken Syndrome | Huntington's Disease | Methylmalonic Acidemia | Vici Syndrome | Chromosome 17q21.31 Deletion Syndrome | Myelitis | Bronchitis | Familial Exudative Vitreoretinopathy | Tylosis With Esophageal Cancer | Histoplasmosis | Infantile Refsum Disease | Ovarian Sex Cord-stromal Tumor | Charcot-Marie-Tooth Disease Type 4E | Cutaneous Mastocytosis | 3-M Syndrome | Cardiospondylocarpofacial Syndrome | Mucolipidosis Type IV | Bursitis | Dermatofibrosarcoma | B-cell Chronic Lymphocytic Leukemia | Sarcoma, Endometrial Stromal | Hereditary Multiple Exostoses | Restrictive Dermopathy | Anorectal Fistula | Scapuloperoneal Myopathy, X-linked Dominant | Renpenning Syndrome | Adenoma, Pituitary | Pigment Dispersion Syndrome | Canavan Disease | Benign Familial Pemphigus | Acromicric Dysplasia | Odonto-onycho-dermal Dysplasia | Craniometaphyseal Dysplasia | Eating Disorder | Gaucher Disease | Familial Glucocorticoid Deficiency | Galactosialidosis | Hepatitis D | Congenital Central Hypoventilation Syndrome | Spinocerebellar Ataxia Type 28 | Spondylometaphyseal Dysplasia | Adrenomyeloneuropathy | Okihiro Syndrome | Chanarin-Dorfman Syndrome | Glycogen Storage Disease Type 1 | Hernia, Inguinal | Analgesia | Ovarian Hyperstimulation Syndrome | Diabetic Neuropathy | Malignant Fibrous Histiocytoma | Evans Syndrome | Progressive Familial Intrahepatic Cholestasis Type 2 | Hereditary Inclusion Body Myopathy | Encephalopathy | HANAC Syndrome | Multiple Sulfatase Deficiency | Neurocutaneous Syndromes | Vaginitis | Mucormycosis | Acne | Non-bullous Congenital Ichthyosiform Erythroderma | Hyperparathyroidism, Secondary | Camurati-Engelmann Disease | Avian Influenza | IgA Nephropathy | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Myelomeningocele | Toxic Epidermal Necrolysis | Raine Syndrome | Neurodevelopmental Disorders | CREST Syndrome | Autism Spectrum Disorders | Hypertension, Essential | Dental Caries | Cartilage Disorders | Protein S Deficiency | Gastric Atrophy | Blepharitis | Guttate Psoriasis | Personality Disorders | Blastoma, Pleuropulmonary | Prune Belly Syndrome | Coffin-Lowry Syndrome | Juvenile Hyaline Fibromatosis | Cirrhosis | Presbyopia | Pain | Behavioral Variant Of Frontotemporal Dementia | Nemaline Myopathy 10 | Subcortical Band Heterotopia | Skin Papilloma | Cutaneous T-cell Lymphoma | Hypogammaglobulinemia | Azoospermia | Cole-Carpenter Syndrome | Cabezas Syndrome | Pure Autonomic Failure | Coronary Heart Disease | Spastic Paraplegia Type 7 | Yellow Fever | Episodic Ataxia | Mitochondrial Disease | Aspartylglycosaminuria | Sick Sinus Syndrome 1 | Lymphangioleiomyomatosis | Ichthyosis Bullosa Of Siemens | Infantile Neuroaxonal Dystrophy | Stuve-Wiedemann Syndrome | Panic Disorder | Milk Allergy | Hidradenitis Suppurativa | Alstrom Syndrome | Leukocyte Adhesion Deficiency Type 1 | Costello Syndrome | Adenomatoid Tumor | Porokeratosis | Neurogenic Bladder | Acanthosis Nigricans | Knobloch Syndrome | Basal Ganglia Disease | Choroideremia | Atrioventricular Septal Defect | Avellino Corneal Dystrophy | Posterior Polar Cataract | Hereditary Coproporphyria | Hemosiderosis | Histiocytic Sarcoma | Transcobalamin Deficiency | Gastritis, Atrophic | Anuria | Pseudohypoparathyroidism Type 2 | Kaposi Sarcoma | Benign Recurrent Intrahepatic Cholestasis 1 | Waardenburg Syndrome Type 2E | Meesmann Corneal Dystrophy | Keratopathy | Brooke-Spiegler Syndrome | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Paternal Uniparental Disomy Of Chromosome 14 | Glutathione Synthetase Deficiency | Ophthalmia, Sympathetic | Hyperandrogenemia | Neurofibromatosis Type 2 | Wolcott-Rallison Syndrome | Sleep Disorder | Measles | Fragile X Syndrome | Lassa Fever | Takotsubo Cardiomyopathy | Skin Fragility-woolly Hair Syndrome | Rheumatic Heart Disease | Macular Degeneration | Pemphigus Foliaceus | Familial Cerebral Amyloid Angiopathy | Acute Lung Injury | Peroxisomal Disorder | Klinefelter Syndrome | Hypopituitarism | X-linked Creatine Transporter Deficiency | Burn-McKeown Syndrome | Congenital Hemolytic Anemia | NDH Syndrome | Porphyria, Variegate | Mucolipidosis | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Nutrition Disorders | Infantile Liver Failure Syndrome 1 | Multisystemic Smooth Muscle Dysfunction Syndrome | VEXAS Syndrome | Pontocerebellar Hypoplasia | Sertoli Cell-only Syndrome | Tendinopathy | Birk-Barel Syndrome | High Molecular Weight Kininogen Deficiency | Superficial Spreading Melanoma | Dowling-Degos Disease | Carey-Fineman-Ziter Syndrome | Stargardt Disease | Membranous Nephropathy | Tetraplegia | Astrocytoma | Alexander Disease | Infectious Diarrhea | Coffin-Siris Syndrome | C3 Glomerulopathy | Torticollis | Cockayne Syndrome | Congenital Dysfibrinogenemia | Stroke, Ischemic | Fanconi Syndrome | Spondyloarthritis | Pyruvate Dehydrogenase Deficiency | Adenomyosis | Leukemia-lymphoma, Adult T-cell | Panuveitis | Adrenal Insufficiency | Greig Cephalopolysyndactyly Syndrome | Cardiac Sarcoidosis | Kawasaki Disease | IMAGe Syndrome | Myopathy | Photosensitivity | Autism | Congenital Hereditary Endothelial Dystrophy Type II | Sarcoma, Alveolar Soft Part | Nevus | Epithelial-myoepithelial Carcinoma | Arthrogryposis | Spermatocele | Facioscapulohumeral Muscular Dystrophy Type 2 | Adenocarcinoma | Enhanced S-cone Syndrome | Tuberculosis | Shock, Cardiogenic | Optic Atrophy 2 | Hoyeraal-Hreidarsson Syndrome | Blomstrand Osteochondrodysplasia | Cold-induced Sweating Syndrome | Zygomycosis | Congenital Hypofibrinogenemia | Lissencephaly 2 | Hyperammonemia | Rosacea | Herpes Genitalis | LRBA Deficiency | Fetal Alcohol Syndrome | Cardiofaciocutaneous Syndrome | Hypertension | Orthostatic Intolerance | Otosclerosis | Exostoses | Exotropia | Blepharospasm | NGLY1 Deficiency | Charcot-Marie-Tooth Disease Type 3