Disease

Galloway-Mowat Syndrome

About the Disease
Galloway-Mowat Syndrome, also known as galloway mowat syndrome, is related to galloway-mowat syndrome 1 and galloway-mowat syndrome 2. An important gene associated with Galloway-Mowat Syndrome is OSGEP (O-Sialoglycoprotein Endopeptidase), and among its related pathways/superpathways are Processing of Capped Intron-Containing Pre-mRNA and Gene Silencing by RNA. Affiliated tissues include brain, kidney and eye, and related phenotypes are global developmental delay and microcephaly

Common Targets
YRDC | WDR73 | PRDM15 | TPRKB | LAGE3 | OSGEP | GON7 | TP53RK | NUP107

疾病靶点研报
Galloway-Mowat Syndrome

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

Other Diseases

Nephrotic Syndrome Type 1 | Chondrodysplasia Punctata 2, X-linked Dominant | Pneumonia, Bacterial | Hydrolethalus Syndrome | Bloom Syndrome | Angiomyolipoma | Combined Pituitary Hormone Deficiency | Vertigo | Fibrosarcoma | Carney Triad | Cranial Nerve Disease | Osteogenesis Imperfecta Type V | Addison Disease | Hodgkin Lymphoma | Chylomicron Retention Disease | Obesity | Prostatitis | Sporadic Inclusion Body Myositis | Congenital Nephrotic Syndrome | Riboflavin Transporter Deficiency Neuronopathy | Chondrodysplasia Punctata | Cryptorchidism | Corneal Neovascularization | Glycogen Storage Disease Type 4 | Clouston Hidrotic Ectodermal Dysplasia | Primary Sclerosing Cholangitis | Autism | Skin Fragility-woolly Hair Syndrome | McCune-Albright Syndrome | Nephritis, Interstitial | Eosinophilia | Geleophysic Dysplasia | Crisponi Syndrome | Menetrier Disease | Whipple's Disease | Hermansky-Pudlak Syndrome | Thyroiditis | Pyruvate Kinase Deficiency | Hoyeraal-Hreidarsson Syndrome | Gardner Syndrome | Kaposiform Hemangioendothelioma | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Choroiditis | Adult Polyglucosan Body Disease | Amyloidosis | Postpoliomyelitis Syndrome | Inflammatory Linear Verrucous Epidermal Nevus | Botulism | LEOPARD Syndrome | Optic Nerve Hypoplasia, Bilateral | Esophageal Adenocarcinoma | Rolandic Epilepsy | Amyotrophic Lateral Sclerosis, Juvenile | Evans Syndrome | Non-small Cell Lung Cancer | Neutrophilia | Neurocutaneous Melanocytosis | Agnathia-Otocephaly Complex | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Marinesco-Sjogren Syndrome | Recurrent Respiratory Papillomatosis | Peeling Skin Syndrome Type B | Prolymphocytic Leukemia | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Tyrosinemia Type 2 | Fabry's Disease | Pure Red Cell Aplasia | Pyruvate Carboxylase Deficiency Disease | Diabetic Neuropathy | Spinal And Bulbar Muscular Atrophy | Otopalatodigital Syndrome Type 2 | Lung Diseases | Congenital Dyserythropoietic Anemia | Imerslund-Grasbeck Syndrome | Juvenile Myelomonocytic Leukemia | Congenital Absence Of Vas Deferens | Glomerulonephritis, Membranoproliferative | Dentinogenesis Imperfecta | Galactosialidosis | Mevalonate Kinase Deficiency | Desbuquois Syndrome | Meckel-Gruber Syndrome | Dysfibrinogenemia | Gangliosidosis | Facioscapulohumeral Muscular Dystrophy | Takayasu's Arteritis | Neurofibromatosis Type 1 | Myopia | Congenital Disorders Of Glycosylation Type II | Metatropic Dysplasia | Schwannomatosis | Autonomic Nervous System Disorders | Autonomic Neuropathy | Optic Neuritis | Congenital Myopathy | Multisystemic Smooth Muscle Dysfunction Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Marshall-Smith Syndrome | Schizencephaly | Cirrhosis | Platelet Disorders | Distal Spinal Muscular Atrophy | Hepatoblastoma | Polycythemia | Greig Cephalopolysyndactyly Syndrome | Spinal Muscular Atrophy | Apparent Mineralocorticoid Excess Syndrome | Urea Cycle Disorder | Saul-Wilson Syndrome | Scleroderma | Chromosome 17q21.31 Deletion Syndrome | Carcinoid Tumor | Posterior Polar Cataract | Leukemia-lymphoma, Adult T-cell | Familial Pheochromocytoma-paraganglioma | Homocystinuria | Congenital Hereditary Endothelial Dystrophy Type I | Cryptococcal Meningitis | Macular Degeneration | MELAS Syndrome | Brachial Plexus Neuropathy | Motor Neuron Diseases | Aneurysm, Thoracic Aortic | Oral Lichen Planus | Gastric Atrophy | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Colitis, Lymphocytic | PHARC Syndrome | Acute Tubular Necrosis | Pityriasis Rubra Pilaris | Perivascular Epithelioid Cell Tumor | Kashin-Beck Disease | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Gastroschisis | Withdrawal Syndrome | Bullous Pemphigoid | Retinal Detachment | Polycystic Kidney, Autosomal Recessive | Alopecia | Gilbert Syndrome | Anosmia, Congenital | Glioblastoma | Congenital Aniridia | Farber Disease | Spermatocele | Spinocerebellar Ataxia Type 2 | Photosensitivity | Cabezas Syndrome | Anorectal Fistula | Spinocerebellar Ataxia Type 10 | Acute Lymphocytic Leukemia | Acute Kidney Injury | Granuloma Annulare | Behcet's Disease | Learning Disability | Sickle Cell Anemia | Hepatitis | Harlequin Ichthyosis | Renal Hypomagnesemia 3 | Chronic Neutrophilic Leukemia | Acute Lung Injury | Benign Familial Pemphigus | Glutaric Aciduria Type 3 | Pituitary Stalk Interruption Syndrome | Giant Cell Arteritis | Seborrheic Dermatitis | Anovulation | Craniosynostosis | Pernicious Anemia | Burn-McKeown Syndrome | Osteomyelitis | Fibromuscular Dysplasia | Heimler Syndrome | Spondylosis | Autoimmune Polyendocrinopathy Syndrome Type I | Congenital Tufting Enteropathy | Bladder Exstrophy | Lymphangiomatosis | Guanidinoacetate Methyltransferase Deficiency | Benign Recurrent Intrahepatic Cholestasis 1 | Endometriosis | Endocarditis | Hypothyroidism | Bone Giant Cell Tumor | Facioscapulohumeral Muscular Dystrophy Type 1 | Rotor Syndrome | Acne | Rheumatoid Arthritis | Hemochromatosis Type 1 | Cushing Syndrome | Early Infantile Epileptic Encephalopathy 1 | Spinocerebellar Ataxia Type 17 | Hypolipoproteinemia | Gastroenteritis, Eosinophilic | Gigantism | Central Pain Syndrome | Paracoccidioidomycosis | Synovitis | Relapsing Polychondritis | Onchocerciasis | Neurocutaneous Syndromes | Epidermolysis Bullosa Dystrophica | Proopiomelanocortin Deficiency | Opisthorchiasis | Hyperkeratosis | Glaucoma, Congenital | HANAC Syndrome | Peters-plus Syndrome | Keratopathy | Graft-versus-host Disease | Anemia | Lesch-Nyhan Syndrome | Milk Allergy | Spinocerebellar Ataxia Type 16 | Pyruvate Dehydrogenase Deficiency | Gestational Trophoblastic Disease | Hemangioblastoma | Multiple Myeloma | Wolfram Syndrome | Usher Syndrome Type III | Neonatal Progeroid Syndrome | Neuromuscular Disorders | Cerebral Amyloid Angiopathy | Specific Granule Deficiency | Goiter, Nodular | Hypophosphatasia | Uremia | Pulmonary Stenosis | Hennekam Lymphangiectasia-lymphedema Syndrome | Congenital Primary Aphakia | Pouchitis | Teratozoospermia | Bacterial Meningitis | Carcinoma, Signet Ring Cell | Viral Meningitis | Antisocial Personality Disorder | Epidermolytic Hyperkeratosis | Alcoholism | Richter's Syndrome | Osteogenesis Imperfecta | Pemphigus | Spinocerebellar Ataxia Type 31 | Conjunctivitis, Allergic | Cardiomyopathy, Dilated, 1L | Uremic Pruritus | Epidermal Nevus Syndrome | Gerodermia Osteodysplastica | Heroin Dependence | LRBA Deficiency | Centronuclear Myopathy | Sulfite Oxidase Deficiency | Hypoalbuminemia | Bronchiectasis | Distal Myopathy | Renal Tubular Acidosis | Microtia | Mabry Syndrome | Hypercholesterolemia, Familial | Bethlem Myopathy | Glycogen Storage Disease Type 1a | Hypotrichosis Simplex | Perry Syndrome | Erectile Dysfunction | Familial Partial Lipodystrophy | Hypertension | Esotropia | Sarcosinemia | Benign Familial Infantile Seizures | AIDS | Dent Disease | Epidermolysis Bullosa Simplex, Localized | Primary Pigmented Nodular Adrenocortical Disease | Fragile X Syndrome | Sarcoma, Endometrial Stromal | Acrocallosal Syndrome | Spinocerebellar Ataxia Type 15 | Granular Corneal Dystrophy Type 1 | Insulin Resistance | Leber Hereditary Optic Neuropathy | Meningococcal Meningitis | Pneumonia, Mycoplasma | Hyperoxaluria | Adrenoleukodystrophy, X-linked | Exotropia | Aspartylglycosaminuria | Hyperekplexia | Necrotizing Autoimmune Myopathy | Postaxial Polydactyly | Infantile Spasm | Cervicitis | Myelitis, Transverse | DiGeorge Syndrome | Double Outlet Right Ventricle | Major Depression | Carpal Tunnel Syndrome | Emery-Dreifuss Muscular Dystrophy | Myelitis | Systemic Mastocytosis | Canavan Disease | Headache | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Spinocerebellar Ataxia Type 21 | Infertility, Male | Fraser Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Chloridorrhea, Congenital | Pierre Robin Syndrome | Nevus | Blue Nevus | Panniculitis | Myasthenia | Skin Papilloma | Schizophrenia | Mumps | Bardet-Biedl Syndrome | Pneumococcal Meningitis | Autoimmune Hemolytic Anemia | Tendinitis | Torticollis | Kernicterus | Thrombotic Microangiopathy | Hypoplastic Left Heart Syndrome | Neurofibroma | Porphyria, Variegate | Blastoma, Pleuropulmonary | Congenital Adrenal Hyperplasia 1 | Carpenter Syndrome | Keratosis, Actinic | Hemoglobinopathies | Exocrine Pancreatic Insufficiency | McLeod Syndrome | Methemoglobinemia Type IV | Osteochondrosis | Neuroleptic Malignant Syndrome | Kidney Stones | Babesiosis | Bernard-Soulier Syndrome | Goiter | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Pulverulent Zonular Cataract | Dementia | Hyperlipidemia, Familial Combined | Discoid Lupus Erythematosus | Sclerosteosis 2 | Cold Agglutinin Disease | Congenital Torticollis | Vogt-Koyanagi-Harada Syndrome | Chronic Granulomatous Disease, X-linked | Pneumoconiosis | Angioedema, Acquired | Marfan Syndrome | Ganglioglioma | Avian Influenza | Amelanotic Melanoma | Pompe Disease | Strabismus | Spinocerebellar Ataxia Type 8 | Epidermolysis Bullosa Simplex, Generalized | Acute Chest Syndrome | Eczema | Basan Syndrome | Scoliosis | Vaginitis | Gynecomastia | Hypobetalipoproteinemias | Johanson-Blizzard Syndrome | Heavy Chain Disease | Hydrocephalus | Ichthyosis | Myopathy | Pleural Tuberculosis | Glutathione Synthetase Deficiency | Palmoplantar Keratoderma | Rickets | Aphasia | Rhinitis | Waardenburg Syndrome Type 4A | Hemolytic Uremic Syndrome | Chitayat Syndrome | Myositis | Meningioma | Familial Hypobetalipoproteinemia | Charcot-Marie-Tooth Disease, Type 6 | Cancer, Lung | Lipid Metabolism Disorders | Vitamin D Deficiency | Hyperkalemic Periodic Paralysis | Woodhouse-Sakati Syndrome | Prolactinoma | Thyrotoxic Periodic Paralysis | Hypertension, Portal | Cancer, Colon | Fatty Aldehyde Dehydrogenase Deficiency | Proteasome-associated Autoinflammatory Syndrome 2 | NGLY1 Deficiency | Cellulitis | MIRAGE Syndrome | Retinoblastoma | Angelman Syndrome | Acrodermatitis