Disease

Retinoschisis

About the Disease
Retinoschisis 1, X-Linked, Juvenile, also known as retinoschisis, is related to juvenile retinoschisis and nicolaides-baraitser syndrome. An important gene associated with Retinoschisis 1, X-Linked, Juvenile is RS1 (Retinoschisin 1), and among its related pathways/superpathways are Visual phototransduction and Visual Cycle in Retinal Rods. The drugs Bupivacaine and Triamcinolone have been mentioned in the context of this disorder. Affiliated tissues include retina, eye and pineal, and related phenotypes are abnormality of eye movement and cataract

Common Targets
RS1 | CRB1

疾病靶点研报
Retinoschisis

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

Other Diseases

Canavan Disease | Walker-Warburg Syndrome | WAGR Syndrome | Emery-Dreifuss Muscular Dystrophy | Donnai-Barrow Syndrome | Nasodigitoacoustic Syndrome | Megalencephaly | Familial Pheochromocytoma-paraganglioma | Tatton-Brown-Rahman Syndrome | Pleomorphic Xanthoastrocytoma | Cellulitis | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | ACTH-independent Macronodular Adrenal Hyperplasia | Spinal Cord Diseases | Analgesia | Osteopetrosis | Chronic Granulomatous Disease, X-linked | Bladder Exstrophy | Preaxial Polydactyly | Central Core Disease | Congenital Heart Block | Intestinal Obstruction | Charcot-Marie-Tooth Disease, Type 2C | Histiocytosis | Colon Adenoma | Hyperkalemic Periodic Paralysis | Otosclerosis | Angiomyolipoma | Hemophilia | Diarrhea | Menkes Disease | Jacobsen Syndrome | Autoimmune Hemolytic Anemia | Torticollis | Non-bullous Congenital Ichthyosiform Erythroderma | Spinocerebellar Ataxia Type 13 | Leigh Syndrome | Spinal Muscular Atrophy | Dyggve-Melchior-Clausen Disease | Chromosome 17q21.31 Deletion Syndrome | Hemoglobinopathies | Congenital Ichthyosiform Erythroderma | Hereditary Pyropoikilocytosis | Stomatitis | Globozoospermia | Synovitis | Learning Disability | Atherosclerosis | Charcot-Marie-Tooth Disease Type 4B1 | Cervicitis | Frontometaphyseal Dysplasia | Neural Tube Defect | Proteasome-associated Autoinflammatory Syndrome 2 | Myelodysplasia | Keratoconus | Erdheim-Chester Disease | Pupil Disorders | Anthrax | Sporadic Hemiplegic Migraine | Hoyeraal-Hreidarsson Syndrome | Erythematotelangiectatic Rosacea | Meningococcal Meningitis | Myelitis, Transverse | KBG Syndrome | Progressive Osseous Heteroplasia | Cystinosis | Carcinoma, Squamous Cell | Diffuse Intrinsic Pontine Glioma | Aldosterone Deficiency | Bacterial Meningitis | Keratocystic Odontogenic Tumor | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Chronic Lymphocytic Leukemia | Agoraphobia | Yellow Fever | Familial Partial Lipodystrophy | Periventricular Nodular Heterotopia | Cat Eye Syndrome | Mucolipidosis Type II | Acute Coronary Syndrome | Hypersomnia | Charcot-Marie-Tooth Disease, Type 2 | Growth Hormone Excess | Li-Fraumeni Syndrome | Stroke | Nephropathy | Corticobasal Syndrome | Blepharospasm | Frank-ter Haar Syndrome | Iron Metabolism Disorders | Rickets | Riboflavin Transporter Deficiency Neuronopathy | Metaphyseal Chondrodysplasia, Schmid Type | Myhre Syndrome | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Roberts Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Facioscapulohumeral Muscular Dystrophy Type 1 | Juvenile Myelomonocytic Leukemia | Pityriasis Rubra Pilaris | Mycosis Fungoides | Pseudohypoparathyroidism Type 1A | Rhabdomyosarcoma | Beckwith-Wiedemann Syndrome | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Neovascular Glaucoma | Polymicrogyria | Chromosome 8q21.11 Deletion Syndrome | Triphalangeal Thumb-polysyndactyly Syndrome | Diabetes Insipidus | Deafness, Dystonia, And Cerebral Hypomyelination | Mood Disorder | Renal Oncocytoma | Gestational Trophoblastic Disease | Mohr-Tranebjaerg Syndrome | Antisynthetase Syndrome | Sarcoma, Ewing | Hypoalbuminemia | Hyperphenylalaninemia | Spinocerebellar Ataxia Type 38 | Woodhouse-Sakati Syndrome | Hyperinsulinemia | Gastritis, Atrophic | Schindler Disease | Corneal Edema | Macular Degeneration | Multisystemic Smooth Muscle Dysfunction Syndrome | Bainbridge-Ropers Syndrome | Dysmorphophobia | Language Disorders | Spinal Muscular Atrophy Type 2 | SAPHO Syndrome | Neuronal Ceroid Lipofuscinosis | Schizotypal Personality Disorder | Stuve-Wiedemann Syndrome | Exocrine Pancreatic Insufficiency | Congenital Dyserythropoietic Anemia Type 1 | Osteochondroma | Oculodentodigital Dysplasia | Spinocerebellar Ataxia Type 27 | Tinea Versicolor | Obsessive-compulsive Disorder | 3-methylglutaconic Aciduria | Lesch-Nyhan Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Aarskog-Scott Syndrome | Cramp Fasciculation Syndrome | VEXAS Syndrome | Charcot-Marie-Tooth Disease | Agammaglobulinemia | Glomerulonephritis, Membranous | Hypoparathyroidism | Leukodystrophies | Hyperinsulinemic Hypoglycemia | Systemic Lupus Erythematosus | DOCK8 Immunodeficiency Syndrome | Melanoma | Porencephaly | Unverricht-Lundborg Syndrome | Non-Hodgkin Lymphoma | Arrhythmogenic Right Ventricular Cardiomyopathy | Pulverulent Zonular Cataract | Van Der Knaap Disease | Dwarfism | Cancer, Lung | Pterygium | Cheilitis | Vitiligo | MIRAGE Syndrome | Hemorrhoids | Gardner Syndrome | Placenta Previa | Joubert Syndrome | Osteoporosis | Thromboembolism | Retinitis Pigmentosa 3 | Lymphangiomatosis | Hypertelorism | Eccrine Porocarcinoma | Paget's Disease Of The Breast | Megaloblastic Anemia | Lymphomatoid Granulomatosis | Inflammatory Joint Disease | Spondylometaphyseal Dysplasia | Sotos Syndrome | Congenital Dyserythropoietic Anemia Type 4 | Orthostatic Intolerance | Absence Epilepsy | Vitelliform Macular Dystrophy | Dyskeratosis Congenita | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Tay-Sachs Disease | Hyperinsulinism-hyperammonemia Syndrome | Japanese Encephalitis | Pheochromocytoma | Hypertrophy | Neurocutaneous Syndromes | Calcium Pyrophosphate Deposition Disease | 5-oxoprolinase Deficiency | GNE Myopathy | Wolfram Syndrome | Paroxysmal Kinesigenic Dyskinesia | Epidermolytic Palmoplantar Keratoderma | Granular Corneal Dystrophy | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Parkinson's Disease | Pathological Gambling | Communication Disorders | Hyperbilirubinemia, Neonatal | Neurofibromatosis Type 2 | Barrett Esophagus | X-linked Myotubular Myopathy | Hereditary Sensory Neuropathy Type 1 | Porphyria | Smith-Kingsmore Syndrome | Ameloblastic Carcinoma | X-linked Creatine Transporter Deficiency | Aldosteronism | Crimean-Congo Hemorrhagic Fever | Kabuki Syndrome | Molybdenum Cofactor Deficiency | Familial Hemiplegic Migraine | Epidermolytic Hyperkeratosis | Early Infantile Epileptic Encephalopathy | Nicolaides-Baraitser Syndrome | Acne Vulgaris | Schamberg Disease | Camptocormia | Primary Lateral Sclerosis | Syndactyly | Peeling Skin Syndrome Type B | Varices | Bipolar Disorder | Chondrosarcoma | Acute Generalized Exanthematous Pustulosis | Jaundice, Obstructive | Blepharophimosis Syndrome | Pyruvate Carboxylase Deficiency Disease | Arthropathy | Glycogen Storage Disease Type 0, Muscle | Prostatitis | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Paraganglioma, Carotid Body | Autonomic Nervous System Disorders | Premature Ejaculation | Insulin Resistance | Epilepsy, Generalized | Bone Marrow Necrosis | Myofibrillar Myopathy | Cystinuria | Brachydactyly | Myopia | Spinocerebellar Ataxia Type 5 | Cousin Syndrome | Desbuquois Syndrome | Bruck Syndrome | Glycogen Storage Disease Type 5 | Overactive Bladder | Seasonal Mood Disorder | Retinoschisis | Scleritis | Ichthyosis Hystrix, Curth-Macklin Type | Pseudoachondroplasia | Fuchs Dystrophy | Prune Belly Syndrome | Long QT Syndrome Type 3 | McKusick Type Metaphyseal Chondrodysplasia | Lateral Meningocele Syndrome | Fuchs Heterochromic Iridocyclitis | Cardiomyopathy, Dilated, 1L | Dystonia-parkinsonism, X-linked | Papillorenal Syndrome | Nephrosclerosis | Diabetic Macular Edema | Dermatomyositis | Maple Syrup Urine Disease | Leprosy | Glaucomatocyclitic Crisis | Anti-glomerular Basement Membrane Disease | Xeroderma Pigmentosum Variant Type | Zellweger Syndrome | Lipid Metabolism Disorders | Colitis, Lymphocytic | Encephalopathy, Ethylmalonic | Acute Leukemia | Camurati-Engelmann Disease | Ectrodactyly | Seizures | Polymyalgia Rheumatica | Binge Eating Disorder | Pneumonia, Mycoplasma | Hereditary Mixed Polyposis Syndrome | Acute Lymphocytic Leukemia | Coloboma | Bone Giant Cell Tumor | Polycystic Kidney, Autosomal Recessive | Microphthalmia, Syndromic 7 | Pericarditis | Multiple Hamartoma Syndrome | Coronary Artery Disease | Hemosiderosis | Eczema | Apraxia | Leishmaniasis, Visceral | Brooke-Spiegler Syndrome | Hennekam Lymphangiectasia-lymphedema Syndrome | Neurofibroma | Restrictive Dermopathy | Erythromelalgia | Congenital Aniridia | Heimler Syndrome | Alexander Disease | Spinocerebellar Ataxia Type 2 | Hereditary Folate Malabsorption | Alstrom Syndrome | Dominant Optic Atrophy | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Fatty Aldehyde Dehydrogenase Deficiency | Chondrodysplasia Punctata 2, X-linked Dominant | Atrial Septal Defect | Granular Corneal Dystrophy Type 1 | Malaria, Cerebral | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Mucolipidosis Type IV | Leiomyosarcoma | Myocarditis | Retinopathy, Diabetic | Myeloid Leukemia | Nail Disorder, Nonsyndromic Congenital | Cutaneous T-cell Lymphoma | Multiple Myeloma | Periventricular Leukomalacia | Arterial Tortuosity Syndrome | Hermansky-Pudlak Syndrome | Steel Syndrome | Aldosterone Synthase Deficiency | Microphthalmia | Botulism | Familial Dysautonomia | Coronary Heart Disease | Pituitary Dwarfism | Bronchiectasis | Sarcomatoid Carcinoma Of The Lung | Sick Sinus Syndrome 1 | Nemaline Myopathy 10 | Sialidosis | Congenital Diaphragmatic Hernia | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Proopiomelanocortin Deficiency | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Lamellar Ichthyosis | Aromatic L-amino Acid Decarboxylase Deficiency | Richter's Syndrome | Clouston Hidrotic Ectodermal Dysplasia | Pendred Syndrome | Superficial Spreading Melanoma | Subacute Sclerosing Panencephalitis | Epidermolysis Bullosa Simplex, Generalized | Follicular Dendritic Cell Sarcoma | Lymphoma, AIDS-related | Kallmann Syndrome | Kohlschutter-Tonz Syndrome | Cutaneous Lupus Erythematosus | Reflex Epilepsy | Nephritis, Interstitial | Hemochromatosis | Loeys-Dietz Syndrome Type 4 | Diffuse Mesangial Sclerosis | Congenital Dysfibrinogenemia | Aceruloplasminemia | Hypodontia | Early Infantile Epileptic Encephalopathy 28 | Neutropenia | Chondromyxoid Fibroma | Dermatitis Herpetiformis | Charcot-Marie-Tooth Disease, Type 6 | Diastrophic Dysplasia | Meningitis | Trichothiodystrophy | Fibrosis | Pontocerebellar Hypoplasia Type 7 | Hemorrhage | Hyperprolactinemia | Neuropathy | Spinocerebellar Ataxia Type 21 | Hyperekplexia | Babesiosis | Gout | Lipoma | Ichthyosis, X-linked | Oculocutaneous Albinism | Osteosarcoma | Sjogren Syndrome | Thyroiditis | Congenital Stationary Night Blindness | Charcot-Marie-Tooth Disease, Type 1A | Chromosome 9q34.3 Deletion Syndrome | Kabuki Syndrome 2 | Nance-Horan Syndrome | Autoimmune Polyendocrine Syndrome