Disease

Macular Corneal Dystrophy Type 1

About the Disease
Macular Dystrophy, Corneal, also known as macular corneal dystrophy, is related to corneal dystrophy, meesmann, 1 and keratitis, hereditary. An important gene associated with Macular Dystrophy, Corneal is CHST6 (Carbohydrate Sulfotransferase 6), and among its related pathways/superpathways are Metabolism and Disease. The drugs Fomepizole and Antidotes have been mentioned in the context of this disorder. Affiliated tissues include eye, endothelial and skin, and related phenotypes are corneal crystals and punctate opacification of the cornea

Common Targets
CHST6

疾病靶点研报
Macular Corneal Dystrophy Type 1

Note: If you'd like to get a target analysis report for Macular Corneal Dystrophy Type 1, 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 Macular Corneal Dystrophy Type 1 at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Goiter, Nodular | Primrose Syndrome | Congenital Ichthyosiform Erythroderma | Neuronal Ceroid Lipofuscinosis | Polymicrogyria | Thrombasthenia | Long QT Syndrome Type 3 | Myasthenia | Blepharitis | Kabuki Syndrome | Parapsoriasis | Progressive Encephalopathy-optic Atrophy Syndrome | Muckle-Wells Syndrome | Hypercholesterolemia, Familial | Nasodigitoacoustic Syndrome | Congenital Poikiloderma | Dysfibrinogenemia | Neurodermatitis | Schistosomiasis | Pearson Syndrome | Charcot-Marie-Tooth Disease Type 2E | Protein S Deficiency | Carotid Artery Disease | Chediak-Higashi Syndrome | Corneal Neovascularization | Ligneous Conjunctivitis | Osteonecrosis | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Zellweger Syndrome | VACTERL Association | Schistosomiasis Mansoni | Ellis-Van Creveld Syndrome | Bullous Pemphigoid | Parkinson Disease 6, Autosomal Recessive Early-onset | Infectious Diarrhea | Spinocerebellar Ataxia Type 2 | Lymphoproliferative Disease, X-linked | Cholesteryl Ester Storage Disease | Mitochondrial Cytopathy | Creutzfeldt-Jakob Disease | Eiken Syndrome | Hypotrichosis Simplex | Polycystic Kidney, Autosomal Recessive | Alstrom Syndrome | Gingivitis | PHARC Syndrome | Hypercalciuria | Bardet-Biedl Syndrome | Hepatitis A | Situs Inversus | Carpal Tunnel Syndrome | Maple Syrup Urine Disease | Wilson's Disease | Juvenile Myelomonocytic Leukemia | Kleine-Levin Syndrome | Gastric Atrophy | Majeed Syndrome | Holt-Oram Syndrome | Fabry's Disease | Diastrophic Dysplasia | Light Chain Amyloidosis | Trichomegaly | Retinal Vasculitis | Vitreoretinal Degeneration, Snowflake Type | Pleurisy | Cancer, Skin | Myelitis, Transverse | Congenital Dyserythropoietic Anemia Type 1 | Hemochromatosis Type 2 | Ameloblastic Carcinoma | Myoclonus-dystonia Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Optic Neuropathy, Anterior Ischemic | Hepatitis | Familial Male-limited Precocious Puberty | Raine Syndrome | Neuromyelitis Optica | Pupil Disorders | Dwarfism | Spinocerebellar Ataxia | Cancer, Bladder | Sulfite Oxidase Deficiency | Cystitis, Interstitial | Schindler Disease | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Shwachman-Bodian-Diamond Syndrome | Fetal Alcohol Syndrome | Duodenal Atresia | Congenital Lipoid Adrenal Hyperplasia | Lesch-Nyhan Syndrome | Pfeiffer Syndrome | Myositis | Pseudohypoparathyroidism Type 2 | Babesiosis | Myofibrillar Myopathy | Muscular Dystrophy | Schuurs-Hoeijmakers Syndrome | Blepharo-cheilo-odontic Syndrome | Galactosialidosis | T-cell Prolymphocytic Leukemia | Rubinstein-Taybi Syndrome | Hypertension | Distal Spinal Muscular Atrophy | Inflammatory Myopathy | Lymphoproliferative Disorders | Osteogenesis Imperfecta Type IV | Motor Neuron Diseases | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Cenani-Lenz Syndactyly Syndrome | Blue Nevus | Agoraphobia | Vitamin K Deficiency | Jalili Syndrome | Hypogonadism | Paroxysmal Nocturnal Hemoglobinuria | Cataract | Spinal Muscular Atrophy | Renal Hypouricemia | Familial Hypertrophic Cardiomyopathy | CHOPS Syndrome | Tularemia | Paternal Uniparental Disomy Of Chromosome 14 | Pitt-Hopkins Syndrome | Hypermetropia | Neurocysticercosis | Hashimoto Thyroiditis | Meckel-Gruber Syndrome | Spinocerebellar Ataxia Type 40 | Saul-Wilson Syndrome | Epicondylitis | Hereditary Spherocytosis | Hypersensitivity Pneumonitis | Blood Protein Disorders | Spondylocarpotarsal Synostosis Syndrome | Lymphopenia | Hemophilia | Autosomal Recessive Bestrophinopathy | Oligoastrocytoma | Leukocyte Adhesion Deficiency | Pemphigus Foliaceus | Orthostatic Intolerance | Pemphigoid | Onchocerciasis | Cryoglobulinemia | Leukocyte Adhesion Deficiency Type 1 | Polycystic Ovary Syndrome | Progressive Myoclonic Epilepsy | Progressive Familial Intrahepatic Cholestasis | Spinocerebellar Ataxia Type 8 | Neurofibromatosis | Joubert Syndrome 2 | Hepatitis C, Chronic | Hypoglycemia | Heterotopic Ossification | Bone Giant Cell Tumor | ICF Syndrome | Hyperbilirubinemia, Neonatal | Depression | Pompe Disease | Schnyder Crystalline Corneal Dystrophy | Cystitis | Diabetic Encephalopathy | Chylothorax, Congenital | Robinow Syndrome | Niemann-Pick Disease, Type A | Heart Failure | Esophageal Adenocarcinoma | Cryptorchidism | Spinocerebellar Ataxia Type 28 | Hypoparathyroidism | Hemangioblastoma | Dupuytren Disease | Lymphoma | Epidermolysis Bullosa Acquisita | Sandhoff Disease | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Early Infantile Epileptic Encephalopathy 1 | Juvenile Hyaline Fibromatosis | Oligospermia | Scleroderma | Hemochromatosis Type 1 | Lennox-Gastaut Syndrome | Hyperacusis | Mitochondrial DNA Depletion Syndrome 13 | Persistent Truncus Arteriosus | Huntington's Disease | Trimethylaminuria | Corneal Edema | Ophthalmia, Sympathetic | Optic Atrophy 2 | Warsaw Breakage Syndrome | Brachial Plexus Neuropathy | Hypertension, Renal | Metaphyseal Chondrodysplasia, Schmid Type | Coronary Restenosis | Genitopatellar Syndrome | Trigonocephaly | Haim-Munk Syndrome | Non-small Cell Lung Cancer | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Conn Syndrome | Hypokalemia | McKusick Type Metaphyseal Chondrodysplasia | Sarcoidosis, Pulmonary | Fibrillation, Atrial | Presbyopia | Chronic Kidney Disease | Bloom Syndrome | Azoospermia | Hepatic Veno-occlusive Disease | Angina Pectoris | Epidermolytic Ichthyosis, Annular | Congenital Torticollis | Colitis, Microscopic | Pain | Apparent Mineralocorticoid Excess Syndrome | Meesmann Corneal Dystrophy | Retinal Coloboma | Moyamoya Disease | Mevalonate Kinase Deficiency | Oguchi Disease-2 | Pneumonia, Viral | Myasthenia Gravis | Protein C Deficiency | Enterocolitis, Necrotizing | Tay-Sachs Disease | Takayasu's Arteritis | Bethlem Myopathy | Spinocerebellar Ataxia Type 1 | IgA Deficiency | Lymphangioleiomyomatosis | Donnai-Barrow Syndrome | Spinocerebellar Ataxia Type 15 | Carcinoid Tumor | Malnutrition | Agnathia-Otocephaly Complex | Epiphyseal Chondrodysplasia, Miura Type | Transthyretin-related Amyloidosis | Exocrine Pancreatic Insufficiency | VACTERL/VATER Association | Zygomycosis | Hepatic Adenomatosis | Common Variable Immunodeficiency | Chondrodysplasia Punctata 2, X-linked Dominant | Spondylosis | Galactosemia | Transcobalamin Deficiency | Carcinoma, Merkel Cell | Craniometaphyseal Dysplasia | Lymphomatoid Granulomatosis | Retinopathy, Diabetic | Klinefelter Syndrome | Hyperammonemia | Bladder Exstrophy | Porphyria, Variegate | Miyoshi Myopathy | Poikiloderma With Neutropenia | Conduct Disorder | Hypertension, Essential | Retinitis | Congenital Stationary Night Blindness | Myocarditis | Schaaf-Yang Syndrome | Prolactinoma | Diffuse Intrinsic Pontine Glioma | Fucosidosis | Neurocutaneous Syndromes | Hypothalamic Obesity | Uveitis, Anterior | Aldosterone Deficiency | Pseudohypoparathyroidism Type 1C | Endometrial Hyperplasia | Macular Corneal Dystrophy | Thrombocythemia, Essential | Metatropic Dysplasia | Liver Failure | Menetrier Disease | Exostoses | Glaucoma | Neutrophilia | Juvenile Myoclonic Epilepsy | Osteoglophonic Dysplasia | Early Infantile Epileptic Encephalopathy 13 | Frank-ter Haar Syndrome | Anterior Segment Dysgenesis | Spondyloarthritis | Hyperphenylalaninemia | Sick Sinus Syndrome 1 | Neuroendocrine Cancer | Periodontitis | Hyperhomocysteinemia | Pseudoexfoliation Syndrome | Cold-induced Sweating Syndrome | Stiff-man Syndrome | Ehlers-Danlos Syndrome | C3 Glomerulopathy | Werner's Syndrome | Teratozoospermia | Hepatitis, Alcoholic | Syncope | Double Outlet Right Ventricle | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Keratosis, Seborrheic | Corticobasal Syndrome | Pseudohypoparathyroidism Type 1B | Gangliosidosis, GM1 | Hyperinsulinemic Hypoglycemia | Niemann-Pick Disease, Type C | Alpha-mannosidosis | Cholelithiasis | Hypertensive Retinopathy | Kashin-Beck Disease | Rift Valley Fever | Sclerosteosis 2 | Meleda Disease | Bartsocas-Papas Syndrome | Anencephaly | Leukemia | Congenital Central Hypoventilation Syndrome | Arterial Tortuosity Syndrome | Acute Lung Injury | Oculocutaneous Albinism Type 4 | Hyperuricemia | Choroiditis | Cyclic Vomiting Syndrome | Benign Familial Neonatal Convulsions | Diffuse Palmoplantar Keratoderma | Epilepsy Of Infancy With Migrating Focal Seizures | Congenital Myasthenic Syndrome | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Pancreatitis, Chronic | Argininosuccinic Aciduria | Choriocarcinoma | Niemann-Pick Disease | Sporadic Inclusion Body Myositis | Chromosome 9q34.3 Deletion Syndrome | Porphyria | Low Tension Glaucoma | Hennekam Lymphangiectasia-lymphedema Syndrome | Cherubism | Primary Familial Brain Calcification | Cold Agglutinin Disease | Homocystinuria | Tyrosinemia | Bietti Crystalline Dystrophy | Spastic Paraplegia Type 7 | Arteriovenous Malformations | Hypopituitarism | Cocaine-Related Disorders | Iron Deficiency Anemia | Dermatomyositis | Dysplastic Nevus | Stroke | Okihiro Syndrome | Lentigo | Silver-Russell Syndrome | Charcot-Marie-Tooth Disease Type 2D | Left Ventricular Noncompaction | Cholera | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Tic Disorder | Cutaneous Lupus Erythematosus | Pemphigus Vulgaris | Porphyria Cutanea Tarda | Adenomatoid Tumor | Otitis Externa | Fibromyalgia | Castleman Disease | X-linked Acrogigantism | Unverricht-Lundborg Syndrome | Colitis, Collagenous | Language Disorders | Pituitary Dwarfism | Prader-Willi Syndrome | Glanzmann Thrombasthenia | Stromal Corneal Dystrophy | Triple A Syndrome | Mannosidase Deficiency Diseases | Nephrocalcinosis | TARP Syndrome | Pleural Tuberculosis | Acanthosis Nigricans | Hyper IgE Syndrome | Paroxysmal Kinesigenic Dyskinesia | Familial Episodic Pain Syndrome | Cystinuria | Paracoccidioidomycosis | Hidradenitis | Splenomegaly | Sleep Disorder | Eclampsia | Bone Marrow Necrosis | Antley-Bixler Syndrome | Microvillus Inclusion Disease | Osteomalacia | Cockayne Syndrome | Micropenis | Retinal Degeneration | Gastritis | Apraxia