Disease

Myopia

About the Disease
Myopia, also known as near-sightedness, is related to night blindness, congenital stationary, type 1a and degenerative myopia, and has symptoms including aniseikonia An important gene associated with Myopia is FBN1 (Fibrillin 1), and among its related pathways/superpathways are Extracellular matrix organization and Syndecan-1-mediated signaling events. The drugs Fluorometholone and Loteprednol etabonate have been mentioned in the context of this disorder. Affiliated tissues include eye, retina and endothelial.

Common Targets
AHI1 | MICAL3 | C2 | CA4 | PYROXD1 | TCF7L2 | GRB2 | OPA3 | PRKACB | TJP2 | SLC39A8 | DIAPH2 | OFD1 | PLCB4 | ZNRF3 | TMEM98 | G7422 | FBXW11 | SHISA6 | PRDX1 | SPAG17 | B4GALNT2 | TNKS | ZBTB38 | OTX2 | AP1B1 | COL8A1 | PSEN1 | WNT7B | COL18A1 | MROH2A | AKAP12 | FAM161A | CFB | ACAN | SOCS1 | ALDH1A2 | OSBPL3 | RBFOX1 | GUCY2D | Vascular endothelial growth factors (VEGF) (nonspecified subtype) | RBMXL3 | CEP128 | TGIF1 | FBN1 | ZMAT4 | LUM | SRF | DUOX2 | SNRNP200 | PROSER2 | PAX2 | LRFN5 | Gamma-Aminobutyric acid type B receptor | ITM2B | ZNF644 | PRPH2 | RASGRF1 | COL1A1 | CFD | HS3ST4 | XRCC2 | ADCY3 | TRMT44 | PRDX5 | MGRN1 | FZD4 | UPK2 | BMP3 | ROCK1 | G3725 | ZEB2 | MYOC | TIMM50 | SKP1 | CHRM1 | RHO | G3479 | COL9A1 | TMPO | SORBS3 | BTRC | CRX | ROM1 | MIR548H4 | MIR2277 | EXOC7 | CPSF1 | NEXMIF | MIR100HG | BICC1 | SYN3 | MIR548G | PPP3CC | TOPORS | MICU2 | ANGPTL2 | LOC105374009 | LRPAP1 | DLG2 | PDE6C | PRPF8 | OPN1LW | CTNNBIP1 | MIR328 | RDH5 | MIR423 | PRPF6 | CEP290 | TMEM187 | ABCA1 | SNTB1 | TBL1XR1 | GUCA1B | CMSS1 | CTSH | P3H2 | KRT12 | ELAPOR1 | NLK | BLOC1S1-RDH5 | EFEMP1 | LRIT2 | SLC16A2 | ALDH1A1 | IBTK | OXT | MFN2 | JAG1 | TSPAN12 | DNAH12 | FGB | MAGT1 | RGS5 | HOXA2 | IMPG1 | CAPN8 | FGF10 | SEMA4A | VIPR2 | SAGE1 | MAML2 | CPD | ARMS2 | SOD3 | MIR636 | RBP3 | RP2 | KCNQ5 | PPFIA2 | RIMS1 | G2475 | KMT2A | G3480 | PPP1R3B | LAMA2 | ARFGEF2 | CR1 | RPGR | LAMA1 | CSNK2B | FBXO31 | BEST1 | RSPO1 | KCNMA1 | USH2A | LINC02456 | OPN1SW | PDE11A | SLC39A5 | LOC105369944 | Adenosine receptor (nonspecified subtype) | CAPN5 | IL31RA | VCX | FARP2 | PAX6 | RB1 | ATL3 | USPL1 | AKR1B10 | RBX1 | RGR | PRSS56 | G7157 | GJD2 | Muscarinic Acetylcholine Receptor (mAChR) (nonspecified subtype) | LOXL3 | Complement Complex | LRRC4C | COL11A1 | OPA1 | ACTC1 | NR3C1 | MSRA | SCO2 | TREX1 | C3 | NDUFAF7 | G3082 | SFRP1 | CFH | OPN1MW | CPTP | KLHDC8B | ODF2L | NYX | MMP2 | SLC66A2 | SLITRK6 | MIR6737 | LOC642846 | COL2A1 | NT5DC1 | VDR | CC2D2A | G4233 | KATNIP | ANPEP | CTNND2 | ALDH1A3 | GNAT1 | P4HA2 | CACNA1F | RAB3C | PEX13 | OPTC | APOE | CLDN23 | CSAG1 | PDGFRA | RWDD4 | CYB5B | PRIMPOL | MIR7704

疾病靶点研报
Myopia

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

Other Diseases

Leber Congenital Amaurosis | Pericarditis | Succinic Semialdehyde Dehydrogenase Deficiency | Warsaw Breakage Syndrome | Persistent Truncus Arteriosus | Cole-Carpenter Syndrome | Pleural Tuberculosis | Polymicrogyria | Spinocerebellar Ataxia Type 5 | Coronary Heart Disease | Chronic Thromboembolic Pulmonary Hypertension | Peters-plus Syndrome | Atherosclerosis | Congenital Primary Aphakia | Anterior Segment Dysgenesis | Mucolipidosis Type IV | Becker Muscular Dystrophy | Hypertriglyceridemia | Atrioventricular Septal Defect | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Lewy Body Dementia | Pyruvate Decarboxylase Deficiency | Chediak-Higashi Syndrome | Idiopathic Pulmonary Fibrosis | Familial Isolated Hyperparathyroidism | Tangier Disease | Vasculitis | Epidermolytic Hyperkeratosis | Infertility, Male | Disseminated Superficial Actinic Porokeratosis | Neurodevelopmental Disorders | Vitiligo | Frank-ter Haar Syndrome | Azoospermia | Leri Pleonosteosis | Leiomyoma | Limb Girdle Muscular Dystrophy | Pseudohermaphroditism | Chromosome 5q Deletion Syndrome | Epicondylitis | Primary Pigmented Nodular Adrenocortical Disease | Cryptococcal Meningitis | Conjunctivitis, Allergic | Hypoalbuminemia | Postpoliomyelitis Syndrome | AIDS | Osteochondrosis | Hereditary Mixed Polyposis Syndrome | Glycogen Storage Disease Type 1a | Microcephaly, Seizures, And Developmental Delay | Cri-du-chat Syndrome | Non-Langerhans Cell Histiocytosis | Sjogren Syndrome | Pituitary Dwarfism | Vitamin D Deficiency | Borjeson-Forssman-Lehmann Syndrome | Lymphangioma | Chronic Inflammatory Demyelinating Polyneuropathy | DNA Ligase IV Deficiency | Papilledema | Glycogen Storage Disease Type 4 | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Smoldering Myeloma | Syncope | Angiodysplasia | T-cell Chronic Lymphocytic Leukemia | Woodhouse-Sakati Syndrome | Familial Hypertrophic Cardiomyopathy | Acral Lentiginous Melanoma | Craniosynostosis | Metabolic Diseases | Schizophrenia, Paranoid | PASLI Disease | Keloid | Osteochondroma | Dystonia-parkinsonism, X-linked | Hypokalemia | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Split Hand-foot Malformation | LMNA-related Congenital Muscular Dystrophy | Primary Hyperoxaluria Type 3 | Cancer, Bladder | Autoimmune Disease | Erythromelalgia | Hemorrhagic Disorders | Hereditary Neuropathy With Liability To Pressure Palsies | Vulvovaginitis | 3-methylcrotonyl-CoA Carboxylase Deficiency | Hypobetalipoproteinemias | Paracoccidioidomycosis | Epidermolytic Ichthyosis, Annular | Nail-Patella Syndrome | Pemphigus | Riboflavin Transporter Deficiency Neuronopathy | Restrictive Dermopathy | Low Tension Glaucoma | VACTERL/VATER Association | Encephalopathy, Hepatic | Congenital Afibrinogenemia | Nephrotic Syndrome Type 1 | Sclerosing Cholangitis | Vertigo | Diarrhea | Silicosis | Hyperlipidemia | Cystinosis | Diabetes Mellitus, Transient Neonatal | Exocrine Pancreatic Insufficiency | Knobloch Syndrome | Hyperinsulinemia | Spinocerebellar Ataxia Type 27 | Perry Syndrome | Cenani-Lenz Syndactyly Syndrome | Charcot-Marie-Tooth Disease Axonal Type 2N | Optic Neuritis | Rickets | Jalili Syndrome | Fucosidosis | Nail Disorder, Nonsyndromic Congenital | Nephritis, Interstitial | Galactosialidosis | Myosin Storage Myopathy | Werner's Syndrome | Acute Coronary Syndrome | Holt-Oram Syndrome | Viral Meningitis | Sick Sinus Syndrome 1 | Hyperparathyroidism, Primary | Early Infantile Epileptic Encephalopathy 4 | Krabbe Disease | Essential Fructosuria | Skin Carcinoma | Fuchs Heterochromic Iridocyclitis | Sclerosteosis | Mountain Sickness | Farber Disease | Gastric Atrophy | Thrombosis | Autonomic Nervous System Disorders | Polymyositis | Papulopustular Rosacea | Spinocerebellar Ataxia Type 1 | Poirier-Bienvenu Neurodevelopmental Syndrome | Hyperparathyroidism, Secondary | Lipid Metabolism Disorders | Sleep Disorder | Bone Marrow Necrosis | Autoimmune Hemolytic Anemia | Paraganglioma | Bronchiolitis | Mitochondrial DNA Depletion Syndrome | Cavitary Optic Disc Anomalies | Purpura | Stromal Corneal Dystrophy | Hemochromatosis | Glomerulonephritis, Membranous | Otitis Media | Glycogen Storage Disease Type 6 | Progressive Familial Intrahepatic Cholestasis Type 3 | Lymphedema-distichiasis Syndrome | Acute Motor Axonal Neuropathy | McLeod Syndrome | Myopia | Pneumonia, Mycoplasma | Genitopatellar Syndrome | Diabetic Encephalopathy | Usher Syndrome | Porphyria, Variegate | Oculocutaneous Albinism Type 4 | Mevalonate Kinase Deficiency | Hereditary Sensory Neuropathy Type 1 | Charcot-Marie-Tooth Disease Type 4B1 | Acrocallosal Syndrome | Leri-Weill Dyschondrosteosis | Dysmorphophobia | Glutaric Aciduria Type 1 | Hemophagocytic Lymphohistiocytosis | Cerebrovascular Disorders | Hypermetropia | Cyst | Insulin Resistance | Fontaine Progeroid Syndrome | Obesity | Branchiootorenal Syndrome | Retinal Telangiectasia | Renal Tubular Acidosis | Esophageal Adenocarcinoma | Speech Disorders | Creatine Deficiency Syndrome Due To AGAT Deficiency | Loeys-Dietz Syndrome Type 4 | Cutaneous T-cell Lymphoma | Idiopathic Multicentric Castleman Disease | Alagille Syndrome | Spondylolisthesis | Neuronal Ceroid Lipofuscinosis | Polyomavirus Nephropathy | Gnathodiaphyseal Dysplasia | Familial Advanced Sleep Phase Syndrome | Chronic Neutrophilic Leukemia | Spondylosis | Basal Ganglia Disease, Biotin-responsive | Myotonic Disorders | Usher Syndrome Type III | Keratosis, Actinic | Arts Syndrome | Non-small Cell Lung Cancer | Nijmegen Breakage Syndrome | Glioma | Blepharoconjunctivitis | Tendinitis | Congenital Adrenal Hyperplasia 1 | Blepharo-cheilo-odontic Syndrome | Hereditary Hemorrhagic Telangiectasia Type 2 | Dysequilibrium Syndrome | Hyperlipidemia Type V | Blepharitis | Hypotrichosis | Hermansky-Pudlak Syndrome | Oculocutaneous Albinism | Thrombotic Microangiopathy | Vascular Cognitive Impairment | Heimler Syndrome | Fetal Akinesia Deformation Sequence | Currarino Syndrome | Macular Corneal Dystrophy | Amelogenesis Imperfecta | Kidney Stones | Polycythemia | Nicotine Addiction | Prediabetes | Spinocerebellar Ataxia Type 3 | Motion Sickness | Granular Corneal Dystrophy | C3 Glomerulopathy | Antenatal Bartter Syndrome Type 1 | Schizophrenia | Hemolytic Anemia | Lymphoma, Mantle Cell | Congenital Absence Of Vas Deferens | Wiedemann-Steiner Syndrome | Carney Triad | Growth Hormone Excess | Bipolar Disorder | Dermatomyositis | Diabetic Macular Edema | Best Macular Dystrophy | Allan-Herndon-Dudley Syndrome | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Keratoacanthoma | Arthritis, Gouty | Congenital Fiber-type Disproportion Myopathy | Basal Cell Nevus Syndrome | Adrenomyeloneuropathy | Facioscapulohumeral Muscular Dystrophy Type 1 | Beckwith-Wiedemann Syndrome | Poretti-Boltshauser Syndrome | Greenberg Dysplasia | Basal Ganglia Disease | Generalized Epilepsy With Febrile Seizures Plus | High Molecular Weight Kininogen Deficiency | COACH Syndrome | Intracerebral Hemorrhage | Skin Papilloma | Oguchi Disease-2 | Episodic Ataxia Type 1 | Hypopigmentation | Jacobsen Syndrome | Glioblastoma | Micropenis | Spinocerebellar Ataxia Type 23 | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Chronic Beryllium Disease | Mucolipidosis Type III | Hepatitis, Alcoholic | Osteoglophonic Dysplasia | Lamellar Ichthyosis | Schamberg Disease | Heart Failure | Costello Syndrome | Acromegaly | Nephroblastoma | Melanoma, Uveal | Corneal Ulcer | DRESS Syndrome | Pupil Disorders | Sporadic Inclusion Body Myositis | Cornelia De Lange Syndrome | Meleda Disease | Transient Bullous Dermolysis Of The Newborn | Myoclonus | Richter's Syndrome | Keratosis | Beta-Propeller Protein-associated Neurodegeneration | Waardenburg Syndrome Type 4 | GATA2 Deficiency | Fragile X Syndrome | Primary Cutaneous Amyloidosis | Loeys-Dietz Syndrome | Crisponi Syndrome | Astigmatism | Dermatitis Herpetiformis | Congenital Dyserythropoietic Anemia Type 4 | Ehlers-Danlos Syndrome | Micro Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Megalencephaly | Lupus Erythematosus | Charcot-Marie-Tooth Disease Type 2E | Cutaneous Mastocytosis | Oculopharyngeal Muscular Dystrophy | Juvenile Hyaline Fibromatosis | Asthma, Exercise-induced | Carney-Stratakis Syndrome | Infertility | Goldenhar Syndrome | Carpenter Syndrome | X-linked Acrogigantism | Endometrial Hyperplasia | Conn Syndrome | Autosomal Recessive Spastic Paraplegia Type 54 | Thromboembolism | Hepatorenal Syndrome | Sialidosis | Cocaine-Related Disorders | Cardiomyopathy, Peripartum | Cancer, Kidney | Kashin-Beck Disease | Neurofibromatosis Type 1 | Melanocytic Nevus | Eosinophilia | Bare Lymphocyte Syndrome | Prader-Willi Syndrome | Hepatitis | Seizures-scoliosis-macrocephaly Syndrome | Perivascular Epithelioid Cell Tumor | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Dysplastic Nevus | Dystonia | Camptocormia | Osteomalacia | Waardenburg Syndrome Type 2 | Actinomycetoma | Bone Giant Cell Tumor | Fraser Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Autism | Pulmonary Veno-occlusive Disease | Pyruvate Kinase Deficiency | GLUT1 Deficiency Syndrome | B-cell Prolymphocytic Leukemia | Discoid Lupus Erythematosus | Diabetes Type 1 | Leukoplakia, Oral | Distal Spinal Muscular Atrophy | Stargardt Disease | Progressive External Ophthalmoplegia | Cheilitis | Neutrophilia | Craniopharyngioma | Renal Hypomagnesemia 3 | Apraxia | Unverricht-Lundborg Syndrome | Encephalopathy | Sclerocornea | Smith-Magenis Syndrome | Splenomegaly | Androgen Insensitivity | Compartment Syndrome | Wilson's Disease | Microphthalmia | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Ectrodactyly | Celiac Disease | Microtia | Nicolaides-Baraitser Syndrome | Coronary Artery Disease | Achromatopsia | Infantile Liver Failure Syndrome 1 | Hereditary Pyropoikilocytosis | Panic Disorder | Dental Caries | Fabry's Disease | Endometritis | Congenital Myasthenic Syndrome | Sandhoff Disease | Myeloid Leukemia | Anorectal Malformations | Pseudohypoparathyroidism Type 2 | Behcet's Disease | Acquired Partial Lipodystrophy | Erythema Multiforme | Paget's Disease Of The Breast | Li-Fraumeni Syndrome | Hidradenitis | Ependymoma | Cerebral Cavernous Malformations | Tinea Versicolor | Hereditary Spastic Paraplegia | Otitis Externa | Glycogen Storage Disease Type 0