Conjunctivitis
Conjunctivitis
About the Disease
Acute Contagious Conjunctivitis, also known as pink eye, is related to albinism, oculocutaneous, type ii and conjunctivitis, and has symptoms including bloodshot eye, conjunctival congestion and redness of eye. An important gene associated with Acute Contagious Conjunctivitis is OCA2 (OCA2 Melanosomal Transmembrane Protein), and among its related pathways/superpathways are Regulation of expression of SLITs and ROBOs and Prader-Willi and Angelman syndrome. The drugs Pheniramine and Tacrolimus have been mentioned in the context of this disorder. Affiliated tissues include eye, salivary gland and skin, and related phenotypes are homeostasis/metabolism and pigmentation
Common Targets
LDLR | DNA-Directed DNA Polymerase Complex | AMP-activated protein kinase (AMPK) | G3569 | HDC | ESR2 | CCR2 | PLG | SYK | PTPN1 | ACHE | PTGDR2 | Immunoglobulin E (IgE) | FAAH | NR3C1 | HRH1 | HTR2C | HTR2A | ALB | Potassium Channels (nonspecified subtype) | HRH4 | TRPM3 | CYP19A1
![疾病靶点研报](../img/disease-target-analysis-report.jpg)
Note: If you'd like to get a target analysis report for Conjunctivitis, 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 Conjunctivitis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.
Other Diseases
Hyperkeratosis | Rubinstein-Taybi Syndrome | Spinocerebellar Ataxia Type 23 | Hemimegalencephaly | Epidermolytic Palmoplantar Keratoderma | Acrodermatitis | Malignant Peripheral Nerve Sheath Tumor | Acute Tubular Necrosis | Hereditary Spherocytosis | Vitamin B12 Deficiency | Filariasis | Ovarian Hyperstimulation Syndrome | Cataract | Ileitis | Constipation | Renal Failure | Focal Segmental Glomerulosclerosis | Cancer, Bladder | Hereditary Pyropoikilocytosis | Hypothalamic Obesity | Vertebrobasilar Insufficiency | Bronchiolitis | Varices | Nephrotic Syndrome | Toxic Epidermal Necrolysis | Limb Girdle Muscular Dystrophy | Orotic Aciduria | Occipital Neuralgia | Spastic Paraplegia Type 7 | Atopy | Epidermolysis Bullosa Simplex With Mottled Pigmentation | 3-M Syndrome | Hereditary Mixed Polyposis Syndrome | Farber Disease | Cardiac Sarcoidosis | Cabezas Syndrome | Osteogenesis Imperfecta Type III | Takotsubo Cardiomyopathy | Fowler's Syndrome | Eczema | Long QT Syndrome Type 1 | Fibronectin Glomerulopathy | Cancer, Lung | Osteomyelitis | Osteoarthritis | Parkinsonism | Idiopathic Multicentric Castleman Disease | Amish Infantile Epilepsy Syndrome | Usher Syndrome Type I | Encephalopathy, Glycine | Gastritis, Atrophic | Paronychia | Dystrophy, Cone-rod | Pituitary Stalk Interruption Syndrome | Dysequilibrium Syndrome | Oculocutaneous Albinism Type 2 | Dyslipidemia | Spinocerebellar Ataxia Type 10 | Endophthalmitis | Osteoporosis | Ectodermal Dysplasia | Sandhoff Disease | Basal Ganglia Disease | Giant Axonal Neuropathy | Smith-Magenis Syndrome | Colitis | Persistent Fetal Circulation | Beta-Propeller Protein-associated Neurodegeneration | Retinoblastoma | Chronic Granulomatous Disease | Spondyloarthritis | Reye Syndrome | Retinal Telangiectasia | Diarrhea | Congenital Adrenal Hyperplasia 1 | Cenani-Lenz Syndactyly Syndrome | Xeroderma Pigmentosum | C3 Glomerulonephritis | Amelogenesis Imperfecta | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Nephroblastoma | Sitosterolemia | Sorsby Fundus Dystrophy | Juvenile Polyposis | Multiple Sulfatase Deficiency | Oculocutaneous Albinism Type 4 | Episodic Ataxia Type 1 | Intracerebral Hemorrhage | Jalili Syndrome | Goiter | Dementia, Vascular | Retinal Degeneration | Vasculitis | Exfoliative Dermatitis | Scleroderma, Diffuse | Chronic Thromboembolic Pulmonary Hypertension | Urticaria | Non-Hodgkin Lymphoma | Spinocerebellar Ataxia Type 5 | Sporadic Hemiplegic Migraine | Blepharophimosis Syndrome | Osteonecrosis Of The Jaw | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Senior-Loken Syndrome | Gynecomastia | Panic Disorder | Congenital Disorders Of Glycosylation | Sensory Neuropathy | Cystitis, Interstitial | Lymphoma | Hemangioendothelioma | Liver Failure, Acute Infantile | Infantile Spasm | Malonyl-CoA Decarboxylase Deficiency | Skin Papilloma | Chronic Neutrophilic Leukemia | Epilepsy, Generalized | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Ophthalmia, Sympathetic | Myoclonic Epilepsy With Ragged Red Fibers | Photosensitivity | Prolactinoma | Thyroid Hormone Resistance | Tyrosine Hydroxylase Deficiency | Ependymoma | Parkinson Disease 6, Autosomal Recessive Early-onset | Speech Disorders | Glycogen Storage Disease Type 1a | Lymphoma Lymphoblastic | Cramp Fasciculation Syndrome | Crigler-Najjar Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | POEMS Syndrome | Inflammatory Bowel Disease | Acanthosis Nigricans | Polyneuropathy | Cushing Syndrome | Thrombocythemia, Essential | Hydrocephalus, Normal Pressure | Thrombasthenia | Nephronophthisis | T-cell Lymphoma, Subcutaneous Panniculitis-like | Dysplastic Nevus | Epidermolytic Ichthyosis, Annular | Dominant Optic Atrophy | Retinitis | Acne | Kaposi Sarcoma | Spinocerebellar Ataxia Type 2 | Mevalonate Kinase Deficiency | Cherubism | Hepatitis, Chronic | Meniere's Disease | Cancer, Breast | Carcinoma, Small Cell | Diamond-Blackfan Anemia | Osteomalacia | Agammaglobulinemia | Amelanotic Melanoma | Hypotension, Orthostatic | Thalassemia | Anti-NMDA Receptor Encephalitis | Focal Facial Dermal Dysplasia | T-cell Leukemia | Ligneous Conjunctivitis | Usher Syndrome Type II | Thyroiditis | Hypogonadism | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Pheochromocytoma | Pleomorphic Xanthoastrocytoma | Hyperammonemia | C3 Glomerulopathy | Spondylo-ocular Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Neurodermatitis | Mosaic Variegated Aneuploidy Syndrome 2 | Beare-Stevenson Syndrome | Alkaptonuria | Panniculitis | Congenital Bile Acid Synthesis Defect | Sweet Syndrome | Epidermolysis Bullosa Simplex, Generalized | Hypertension, Portal | Leri Pleonosteosis | T-cell Chronic Lymphocytic Leukemia | Lymphedema | Congenital Torticollis | Osteogenesis Imperfecta Type I | Okihiro Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Syphilis | Micro Syndrome | Meningococcal Meningitis | Isovaleric Acidemia | Gastroenteritis, Eosinophilic | Urethritis | Auriculocondylar Syndrome | Chediak-Higashi Syndrome | Retinopathy, Diabetic | Conduct Disorder | Ellis-Van Creveld Syndrome | DEND Syndrome | Lennox-Gastaut Syndrome | Sporadic Inclusion Body Myositis | Wiedemann-Steiner Syndrome | Intermittent Explosive Disorder | Nemaline Myopathy 8 | Lattice Corneal Dystrophy Type 1 | Corneal Dystrophy And Perceptive Deafness | Dubin-Johnson Syndrome | Hypertension | Melanoma, Malignant | Schizotypal Personality Disorder | Crimean-Congo Hemorrhagic Fever | Fanconi Syndrome | Diabetes Gestational | Urolithiasis | Neurofibromatosis-Noonan Syndrome | Congenital Hereditary Endothelial Dystrophy Type I | Hypospadias | Schnyder Crystalline Corneal Dystrophy | Diffuse Palmoplantar Keratoderma | Bursitis | Congenital Adrenal Hyperplasia | Colitis, Lymphocytic | Diastrophic Dysplasia | Wolfram Syndrome 2 | Hepatitis, Alcoholic | Vestibular Disease | Pilomatrix Carcinoma | Familial Isolated Hyperparathyroidism | Carpal Tunnel Syndrome | Pneumothorax | Swine Influenza | Macrophage Activation Syndrome | Leber Hereditary Optic Neuropathy | Primary Lateral Sclerosis | Megaloblastic Anemia | Muscular Dystrophy | Small Lymphocytic Lymphoma | Pityriasis Rubra Pilaris | Adrenomyeloneuropathy | Mixed Connective Tissue Disease | Hepatitis E | Maple Syrup Urine Disease | Zygomycosis | Ocular Hypertension | Apparent Mineralocorticoid Excess Syndrome | Mumps | Cardiospondylocarpofacial Syndrome | Methemoglobinemia Type IV | Thrombophlebitis | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Insulin Resistance | Porphyria Cutanea Tarda | Blepharoconjunctivitis | Kawasaki Disease | Lentigo | Tay-Sachs Disease | Dementia | Citrullinemia | Glioma | Niemann-Pick Disease, Type C | Neuronal Ceroid Lipofuscinosis | Lissencephaly 2 | Infertility | Empyema | Pemphigus | Dystonia | Palsy, Cerebral | Mitochondrial Myopathy | Ichthyosis | Intermittent Claudication | Netherton Syndrome | Opisthorchiasis | Bartter Syndrome | Clouston Hidrotic Ectodermal Dysplasia | Arrhythmogenic Right Ventricular Cardiomyopathy | Rubeosis Iridis | Kabuki Syndrome 2 | Potocki-Shaffer Syndrome | Colitis, Collagenous | Light Chain Amyloidosis | Tricho-hepato-enteric Syndrome | Erysipelas | Charcot-Marie-Tooth Disease, Type 2 | Lung Diseases | Infantile Liver Failure Syndrome 1 | Sarcomatoid Carcinoma Of The Lung | Urofacial Syndrome | Systemic Mastocytosis | Cranioectodermal Dysplasia | Neuroleptic Malignant Syndrome | Cirrhosis | Cousin Syndrome | Angelman Syndrome | Optic Neuropathy | Acquired Partial Lipodystrophy | Neurotoxicity | Gliosarcoma | Schizophrenia, Paranoid | Split Hand-foot Malformation | Lymphopenia | Achromatopsia | Mitochondrial Cytopathy | Hypertriglyceridemia | Spinocerebellar Ataxia Type 28 | Joubert Syndrome 2 | Thyrotoxic Periodic Paralysis | Sialidosis Type I | 3C Syndrome | Hartsfield Syndrome | Vascular Calcification | Fibrillation, Atrial | Lipodystrophy | Peters-plus Syndrome | Lipoma | Alexander Disease | Anal Fissure | Pituitary Dwarfism | Hyperprolactinemia | Fibrosarcoma | Menkes Disease | Aneurysm, Abdominal Aortic | Gray Platelet Syndrome | Rheumatoid Arthritis | Van Der Knaap Disease | Fetal Akinesia Deformation Sequence | Oculodentodigital Dysplasia | Tendinopathy | Osteonecrosis | Non-small Cell Lung Cancer | Generalized Epilepsy And Paroxysmal Dyskinesia | Congenital Ichthyosiform Erythroderma | Vitreoretinopathy, Proliferative | Agnathia-Otocephaly Complex | Prolidase Deficiency | Myelomeningocele | Neovascular Glaucoma | Abetalipoproteinemia | Adenosine Deaminase 2 Deficiency | Chronic Granulomatous Disease, X-linked | Cutis Laxa | Esthesioneuroblastoma | Polycystic Kidney, Autosomal Recessive | Periodontitis | Pyruvate Decarboxylase Deficiency | Tietze Syndrome | Papillon-Lefevre Syndrome | Colon Adenoma | Oculocutaneous Albinism | Seminoma | Asthma, Exercise-induced | Tuberculosis | Sarcosinemia | Cohen Syndrome | Dysfibrinogenemia | Cerebellofaciodental Syndrome | Methylmalonic Aciduria And Homocystinuria, CblC Type | Fabry's Disease | Sepiapterin Reductase Deficiency | Partington Syndrome | Angina Pectoris | Bietti Crystalline Dystrophy | Leukemia-lymphoma, Adult T-cell | Spinocerebellar Ataxia Type 1 | Pancreatitis, Chronic | Aceruloplasminemia | Keratocystic Odontogenic Tumor | Coffin-Siris Syndrome | Schwannoma | Angioimmunoblastic T-cell Lymphoma | Carotid Artery Disease | Otitis Externa | Fahr Disease | Gastritis | Multiple Sclerosis, Chronic Progressive | Vitamin K Deficiency | Carcinoma, Signet Ring Cell | Plasma Cell Dyscrasia | Tinea | Li-Fraumeni Syndrome | Histiocytic Sarcoma | Juvenile Myelomonocytic Leukemia | Myhre Syndrome | Meningitis | Bone Marrow Necrosis | Hepatitis D | Gastric Atrophy | Stuttering | Brooke-Spiegler Syndrome | Rhabdomyosarcoma, Embryonal | Protein C Deficiency | Disseminated Intravascular Coagulation | Chronic Idiopathic Myelofibrosis | Hyperparathyroidism | Plasmacytoma | Leukoplakia, Oral | Neurofibromatosis