Disease

Pigment Dispersion Syndrome

About the Disease
Ocular Pigment Dispersion with or Without Glaucoma, also known as pigment dispersion syndrome, is related to megalocornea and primary angle-closure glaucoma. An important gene associated with Ocular Pigment Dispersion with or Without Glaucoma is GPDS1 (Glaucoma-Related Pigment Dispersion Syndrome 1). The drugs Loteprednol etabonate and Tobramycin have been mentioned in the context of this disorder. Affiliated tissues include eye, endothelial and brain, and related phenotypes are optic atrophy and myopia

Common Targets
PMEL

疾病靶点研报
Pigment Dispersion Syndrome

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

Other Diseases

Aarskog-Scott Syndrome | Hydrops Fetalis | Menkes Disease | Cabezas Syndrome | Nicotine Addiction | Intermittent Explosive Disorder | Spermatocele | Spinocerebellar Ataxia Type 27 | Ectopia Lentis, Isolated, Autosomal Recessive | Persistent Fetal Circulation | Osteonecrosis Of The Jaw | Spinocerebellar Ataxia Type 13 | Abetalipoproteinemia | Early Infantile Epileptic Encephalopathy 1 | Necrobiosis Lipoidica | Congenital Dysfibrinogenemia | Cardiac Arrest | Neurodevelopmental Disorders | Glioblastoma | Leber Congenital Amaurosis | Nevus | Duane Retraction Syndrome | Chiari Malformation Type I | Myelitis, Transverse | Cheilitis | DiGeorge Syndrome | Gastritis, Atrophic | Hemolytic Anemia | Adenosine Deaminase Deficiency | Arts Syndrome | Rubinstein-Taybi Syndrome | Aneurysm, Abdominal Aortic | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Thrombotic Microangiopathy | Pathological Gambling | Osteogenesis Imperfecta Type VI | Peroxisomal Disorder | Hepatitis, Alcoholic | Hyperekplexia | Neonatal Progeroid Syndrome | Neuroblastoma | Nager Acrofacial Dysostosis | Heart Failure | Antisocial Personality Disorder | Apparent Mineralocorticoid Excess Syndrome | Eating Disorder | Hyperinsulinism-hyperammonemia Syndrome | REM Sleep Behavior Disorder | Stargardt Disease | Angioedema, Acquired | Cornelia De Lange Syndrome | Takayasu's Arteritis | Learning Disability | Adrenoleukodystrophy, X-linked | Cantu Syndrome | Parkinsonism | Ectrodactyly | Cryptococcal Meningitis | Vascular Calcification | Acromesomelic Dysplasia | Goiter | Urticaria | Haim-Munk Syndrome | Cranioectodermal Dysplasia | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Spinocerebellar Ataxia Type 12 | IgA Deficiency | Hypophosphatasia | Fibromyalgia | Centronuclear Myopathy | Melanocytic Nevus | Pontocerebellar Hypoplasia Type 7 | Castleman Disease | Endocarditis | Bernard-Soulier Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Congenital Mirror Movements | Hemoglobinopathies | Myoclonus | Turner's Syndrome | Molybdenum Cofactor Deficiency | Hereditary Folate Malabsorption | Goiter, Nodular | Measles | Cerebrotendinous Xanthomatosis | Angiosarcoma Of The Breast | Porencephaly | Cysticercosis | Pemphigoid | Leigh Syndrome | Combined Deficiency Of Factor V And Factor VIII | Cerebellar Ataxia, Cayman Type | Posterior Polar Cataract | Charcot-Marie-Tooth Disease Type 2E | Vitamin A Deficiency | Palmoplantar Keratoderma | Wieacker-Wolff Syndrome | Steel Syndrome | Alpers Syndrome | Glutaric Aciduria Type 2 | Blepharoconjunctivitis | Pure Autonomic Failure | Adult Polyglucosan Body Disease | Charcot-Marie-Tooth Disease, Type 2A | Blepharo-cheilo-odontic Syndrome | Poretti-Boltshauser Syndrome | Long QT Syndrome Type 2 | Meniere's Disease | Endophthalmitis | Spinocerebellar Ataxia Type 14 | Platelet Disorders | Odonto-onycho-dermal Dysplasia | Adenoma, Pleomorphic | Borjeson-Forssman-Lehmann Syndrome | Hemochromatosis Type 1 | Oculodentodigital Dysplasia | Specific Granule Deficiency | Cri-du-chat Syndrome | Uveitis | Urolithiasis | Erythrokeratodermia Variabilis | Polyneuropathy | Scleroderma | Adrenomyeloneuropathy | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Familial Exudative Vitreoretinopathy | Anterior Segment Dysgenesis | Usher Syndrome Type III | Carney Triad | Venous Insufficiency | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Guillain-Barre Syndrome | Hyperandrogenemia | Retinopathy Of Prematurity | Schistosomiasis | Rolandic Epilepsy | Peeling Skin Syndrome, Acral Type | HELLP Syndrome | Spondyloarthritis | Mitochondrial Cytopathy | Cancer, Brain | Congenital Heart Block | DOCK8 Immunodeficiency Syndrome | Intestinal Hypomagnesemia 1 | 3-hydroxy-3-methylglutaric Aciduria | Guanidinoacetate Methyltransferase Deficiency | Kindler Syndrome | Spinal Muscular Atrophy | Malaria, Cerebral | Spitzoid Melanoma | Iron Metabolism Disorders | Hypospadias | Ehlers-Danlos Syndrome | Neurotoxicity | Basal Ganglia Disease, Biotin-responsive | Cutis Laxa | Adenocarcinoma | Tracheal Disorders | Autism Spectrum Disorders | Spinocerebellar Ataxia Type 17 | Anorchia | Keratocystic Odontogenic Tumor | Episodic Ataxia Type 1 | Restless Legs Syndrome | Progressive Encephalopathy-optic Atrophy Syndrome | Neuronal Ceroid Lipofuscinosis | Tylosis With Esophageal Cancer | Pulverulent Zonular Cataract | VEXAS Syndrome | Headache | Hepatitis E | Xeroderma Pigmentosum Variant Type | Open-angle Glaucoma | Seizures-scoliosis-macrocephaly Syndrome | Hemorrhagic Disorders | Nephropathy | Hepatitis D | Campomelic Dysplasia | Pseudo-pseudohypoparathyroidism | Hypervalinemia | Aphasia | Ependymoma | Conjunctivitis | Stomatitis | Oligospermia | Allergic Contact Dermatitis | Angioimmunoblastic T-cell Lymphoma | Crigler-Najjar Syndrome | Geleophysic Dysplasia | Intestinal Tuberculosis | Brenner Tumor | Corneal Edema | Hamartoma | Myasthenia | 3-methylglutaconic Aciduria Type IV | Glaucomatocyclitic Crisis | Brugada Syndrome 1 | Placenta Previa | Sarcoma, Alveolar Soft Part | LMNA-related Congenital Muscular Dystrophy | Ileitis | Congenital Primary Aphakia | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Craniopharyngioma | Paget's Disease Of The Breast | Mountain Sickness | Vulvovaginitis | Papilloma | Myopathy | Spinocerebellar Ataxia Type 40 | Ganglioneuroma | Hypertensive Retinopathy | Acute Kidney Injury | Coloboma | Synovitis | Autosomal Recessive Spastic Paraplegia Type 75 | Paternal Uniparental Disomy Of Chromosome 14 | Mitochondrial Disease | Congenital Bile Acid Synthesis Defect | Cerebral Cavernous Malformations | Polyarteritis Nodosa | Fowler's Syndrome | Familial Male-limited Precocious Puberty | Hyperprolactinemia | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Rhabdoid Tumor | Osteosclerosis | Thromboembolism | Dyslipidemia | Vaginitis | Omenn Syndrome | Bursitis | Coronary Restenosis | Familial Hypobetalipoproteinemia | Inflammatory Myopathy | Cold-induced Sweating Syndrome | Hyperparathyroidism, Secondary | Familial Partial Lipodystrophy | Megalencephaly | Myocarditis | HANAC Syndrome | Metabolic Syndrome | Acrodermatitis | Alagille Syndrome | Smith-Magenis Syndrome | Kearns-Sayre Syndrome | Hypothalamic Obesity | Pseudoachondroplasia | Spinocerebellar Ataxia Type 42 | Cervical Dystonia | Myelomeningocele | Acrodermatitis Enteropathica | Juvenile Hyaline Fibromatosis | Spinocerebellar Ataxia Type 38 | Ichthyosis Bullosa Of Siemens | Gyrate Atrophy Of The Choroid And Retina | Rothmund-Thomson Syndrome | Neutrophilia | Basal Ganglia Cerebrovascular Disease | Dysfibrinogenemia | Mevalonate Kinase Deficiency | Congenital Absence Of Vas Deferens | Creatine Deficiency Syndrome Due To AGAT Deficiency | Kawasaki Disease | Angina Pectoris | Meier-Gorlin Syndrome | Rickets | Diabetes Type 2 | Cerebellofaciodental Syndrome | Marshall-Smith Syndrome | Paronychia | Weill-Marchesani Syndrome | Agnathia-Otocephaly Complex | Kabuki Syndrome 2 | Glycogen Storage Disease Type 4 | Cryptosporidiosis | Pneumoconiosis | Congenital Disorders Of Glycosylation | Sertoli Cell-only Syndrome | Lipid Storage Diseases | Smith-Kingsmore Syndrome | Sensory Neuropathy | Vogt-Koyanagi-Harada Syndrome | Congenital Sodium Diarrhea | Proteasome-associated Autoinflammatory Syndrome 2 | Heart Block | Giant Cell Glioblastoma | Adenomatoid Tumor | Chronic Granulomatous Disease, X-linked | Amish Infantile Epilepsy Syndrome | Chitayat Syndrome | Niemann-Pick Disease, Type B | MIRAGE Syndrome | Gallstones | Sclerosteosis | Wolfram Syndrome 2 | Congenital Fiber-type Disproportion Myopathy | Choriocarcinoma | Botulism | Spinocerebellar Ataxia Type 20 | Coffin-Lowry Syndrome | Antiphospholipid Syndrome | Myoclonus-dystonia Syndrome | Greig Cephalopolysyndactyly Syndrome | Oculopharyngeal Muscular Dystrophy | Constipation | Infantile Nephropathic Cystinosis | Hyperparathyroidism, Primary | Supravalvular Aortic Stenosis | Hereditary Hemorrhagic Telangiectasia | Epidermolysis Bullosa | Congenital Muscular Dystrophy | Hypermetropia | Exotropia | Language Disorders | Hypertension | Hoyeraal-Hreidarsson Syndrome | Dysplastic Nevus | Otosclerosis | Glycogen Storage Disease Type 5 | Neuropathy | Sporadic Inclusion Body Myositis | Marfan Syndrome | IMAGe Syndrome | AIDS | Pyruvate Carboxylase Deficiency Disease | Chediak-Higashi Syndrome | Hyperlipidemia | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Osteochondrosis | Sotos Syndrome | Major Depression | Persistent Mullerian Duct Syndrome | Cramp Fasciculation Syndrome | Pancreatitis, Chronic | Renal Hypomagnesemia 3 | Delayed Sleep Phase Syndrome | Birt-Hogg-Dube Syndrome | Rhabdomyosarcoma, Embryonal | Retinal Detachment | Oculocutaneous Albinism Type 4 | Polymicrogyria | Anemia | Pulmonary Stenosis | Lupus Erythematosus | COACH Syndrome | Osteomyelitis | Werner's Syndrome | Mucolipidosis | Pulmonary Veno-occlusive Disease | Retinal Dystrophy | Idiopathic Multicentric Castleman Disease | Osteogenesis Imperfecta Type IV | Cerebrovascular Disorders | Osteochondroma | Malignant Fibrous Histiocytoma | Arteriovenous Malformations | Phosphoglycerate Dehydrogenase Deficiency | Dysgerminoma | Pyloric Stenosis, Infantile Hypertrophic | Scleritis | Multiple Sulfatase Deficiency | Oguchi Disease-2 | Pendred Syndrome | Yellow Fever | Diffuse Palmoplantar Keratoderma | Waardenburg Syndrome Type 2E | Myopia | Conn Syndrome | Toxic Epidermal Necrolysis | Early Infantile Epileptic Encephalopathy 28 | Rheumatoid Arthritis | Left Ventricular Noncompaction | Lichen Sclerosus | Schwannomatosis | Esophagitis | Bardet-Biedl Syndrome | Oculocutaneous Albinism Type 1 | Ischemia | Dwarfism | Situs Inversus | Pulmonary Capillary Hemangiomatosis | Nephrotic Syndrome | Impulse Control Disorder | Pouchitis | Fuchs Dystrophy | Spinocerebellar Ataxia | Smith-Lemli-Opitz Syndrome | Hepatic Veno-occlusive Disease | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Lymphopenia | Alpha-mannosidosis | Thalassemia, Beta | Meningococcal Infections | X-linked Acrogigantism | Oral Lichen Planus | Syphilis | B-cell Prolymphocytic Leukemia | Sporadic Hemiplegic Migraine | Stevens-Johnson Syndrome