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

Photosensitivity | Takotsubo Cardiomyopathy | Multiple Sclerosis, Relapsing-remitting | Rothmund-Thomson Syndrome | Chitayat Syndrome | Dermatofibrosarcoma | Malnutrition | Charcot-Marie-Tooth Disease Type 2D | Hereditary Folate Malabsorption | Primary Ovarian Insufficiency | Epidermolysis Bullosa | Posterior Polar Cataract | Allan-Herndon-Dudley Syndrome | Intermittent Explosive Disorder | Carotid Artery Disease | Cardiomyopathy, Restrictive | Heart Failure | Ehlers-Danlos Syndrome | Granular Corneal Dystrophy | Protein S Deficiency | SAPHO Syndrome | Narcolepsy | Pulverulent Zonular Cataract | Cohen Syndrome | Esophageal Motility Disorders | Micro Syndrome | Antley-Bixler Syndrome | Smoldering Myeloma | Familial Retinal Arterial Macroaneurysm | Filariasis | Wolfram Syndrome | Wolff-Parkinson-White Syndrome | IgA Nephropathy | LRBA Deficiency | Isobutyryl-CoA Dehydrogenase Deficiency | Pneumonia, Viral | Pontocerebellar Hypoplasia Type 2 | Congenital Nephrotic Syndrome | Hemorrhage | Fetal Akinesia Deformation Sequence | Cardiofaciocutaneous Syndrome | Riboflavin Transporter Deficiency Neuronopathy | Platelet Disorders | Peroxisomal Disorder | Leukocyte Adhesion Deficiency Type 1 | Congenital Ichthyosiform Erythroderma | Mucormycosis | Spinal Muscular Atrophy | Intestinal Hypomagnesemia 1 | Keratopathy | Absence Epilepsy | Lafora Disease | Pseudoachondroplasia | Tetraplegia | Pyruvate Dehydrogenase Deficiency | Wolfram Syndrome 2 | Coffin-Siris Syndrome | Patent Ductus Arteriosus | Osteogenesis Imperfecta Type III | MELAS Syndrome | Blepharo-cheilo-odontic Syndrome | Rhizomelic Chondrodysplasia Punctata | Progressive Encephalopathy-optic Atrophy Syndrome | Lipid Metabolism Disorders | 3-methylcrotonyl-CoA Carboxylase Deficiency | Congenital Sodium Diarrhea | Pemphigus Foliaceus | Ocular Surface Squamous Neoplasia | Sarcoma, Alveolar Soft Part | Acrodysostosis | Epidermolysis Bullosa Dystrophica | Cushing Syndrome | Leiomyosarcoma | Trigonocephaly | Lymphangioma | Dysequilibrium Syndrome | Perivascular Epithelioid Cell Tumor | Charcot-Marie-Tooth Disease Type 4B1 | Congenital Adrenal Hyperplasia 1 | Osteogenesis Imperfecta | Carcinoid Tumor | Renal Dysplasia | Nephrotic Syndrome | Congenital Stationary Night Blindness | Acute Kidney Injury | Hyperthyroidism | Juvenile Myoclonic Epilepsy | Citrullinemia | Ischemia | Fucosidosis | Glycogen Storage Disease Type 5 | Juvenile Hyaline Fibromatosis | Retinoblastoma | Dementia, Vascular | Obesity | Congenital Myasthenic Syndrome | Esophageal Carcinoma | Hyperphenylalaninemia | Odonto-onycho-dermal Dysplasia | Glutathione Synthetase Deficiency | Leiomyoma | Fuchs Heterochromic Iridocyclitis | Sweet Syndrome | Pearson Syndrome | Senior-Loken Syndrome | Palsy, Cerebral | Congenital Fiber-type Disproportion Myopathy | Joubert Syndrome | Cholelithiasis | Ebstein Anomaly | Osteonecrosis Of The Jaw | Cholestasis | Methemoglobinemia | Peeling Skin Syndrome Type B | Paternal Uniparental Disomy Of Chromosome 14 | Vitreoretinopathy, Proliferative | Anosmia, Congenital | Hereditary Mixed Polyposis Syndrome | Panniculitis | Chediak-Higashi Syndrome | DRESS Syndrome | Palmoplantar Keratoderma | Niemann-Pick Disease, Type A | Primary Pigmented Nodular Adrenocortical Disease | Glutaric Aciduria Type 3 | Giant Axonal Neuropathy | Spinocerebellar Ataxia Type 28 | Hashimoto Thyroiditis | ACTH-independent Macronodular Adrenal Hyperplasia | Angioedema, Acquired | Ectrodactyly | Bloom Syndrome | Essential Fructosuria | Neurofibromatosis-Noonan Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Metaphyseal Chondrodysplasia, Schmid Type | Canavan Disease | Malaria | Dyggve-Melchior-Clausen Disease | Macular Corneal Dystrophy Type 1 | Erythema Nodosum | Usher Syndrome Type IIC | Congenital Dyserythropoietic Anemia Type 4 | Congenital Myopathy | Analgesia | Pantothenate Kinase-associated Neurodegeneration | Oligospermia | Kawasaki Disease | Stargardt Disease | Diabetes Type 2 | Conjunctivitis, Allergic | Primary Torsion Dystonia | Vitamin A Deficiency | Inflammatory Joint Disease | Cirrhosis | Leukoplakia, Oral | Synpolydactyly | Orotic Aciduria | Anorectal Fistula | Acral Lentiginous Melanoma | Glioblastoma Multiforme | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Glycogen Storage Disease Type 6 | Dent Disease | Chanarin-Dorfman Syndrome | Echinococcosis | Pendred Syndrome | Pleural Tuberculosis | Choroideremia | Snyder-Robinson Syndrome | Lyme Disease | Cheilitis | Bone Marrow Necrosis | Spinocerebellar Ataxia Type 7 | Growth Hormone Excess | Brenner Tumor | Saul-Wilson Syndrome | Stuve-Wiedemann Syndrome | Alcoholism | Sarcoidosis, Pulmonary | Hyperinsulinism-hyperammonemia Syndrome | Stuttering | Addison Disease | Primary Sclerosing Cholangitis | Congenital Afibrinogenemia | Wolman Disease | Presbyopia | Hemophilia | Cerebellar Ataxia, Cayman Type | Microcephaly | Acute Chest Syndrome | Cholangitis | Urea Cycle Disorder | Noonan Syndrome | Mucolipidosis Type III | Dysgerminoma | Exfoliative Dermatitis | Arthritis, Reactive | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Jalili Syndrome | Hyperparathyroidism, Primary | Benign Familial Infantile Seizures | Charcot-Marie-Tooth Disease, Type 1A | Non-Langerhans Cell Histiocytosis | Smith-Magenis Syndrome | Exostoses | X-linked Myotubular Myopathy | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Tietze Syndrome | Rhabdomyosarcoma, Alveolar | Hepatitis | Mastitis | Autoimmune Polyendocrine Syndrome | Cherubism | Blastomycosis | Histiocytic Sarcoma | Leri Pleonosteosis | Pulmonary Tuberculosis | Cutaneous Lupus Erythematosus | Schuurs-Hoeijmakers Syndrome | Acute Anterior Uveitis | Urolithiasis | Early Infantile Epileptic Encephalopathy 1 | Microphthalmia | Proximal Symphalangism | Anterior Segment Dysgenesis | Moyamoya Disease | Pure Autonomic Failure | Spasticity | Usher Syndrome | Early Infantile Epileptic Encephalopathy 28 | Hepatitis A | Blepharoconjunctivitis | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Primary Hyperoxaluria Type 3 | Muir-Torre Syndrome | Polyneuropathy | Neurofibromatosis | Aplasia Cutis Congenita | Corneal Edema | Pierre Robin Syndrome | Aneurysm, Thoracic Aortic | Double Outlet Right Ventricle | Cryoglobulinemia | Dystonia | Sensory Neuropathy | Polycystic Kidney, Autosomal Dominant | Cole-Carpenter Syndrome | ADNP Syndrome | Lymphangiomatosis | Epilepsy Of Infancy With Migrating Focal Seizures | Von Willebrand Disease | Schnitzler Syndrome | Pneumonia, Bacterial | Spinocerebellar Ataxia Type 5 | Vaginitis | Von Hippel-Lindau Disease | Familial Exudative Vitreoretinopathy | Lung Diseases | Micropenis | Osteomyelitis | Infectious Diarrhea | Diabetes | Chronic Thromboembolic Pulmonary Hypertension | Autosomal Recessive Bestrophinopathy | Reye Syndrome | Ichthyosis Hystrix, Curth-Macklin Type | Autoimmune Disease | Pseudohypoaldosteronism | Epithelioid Hemangioma | Achromatopsia | Prediabetes | Vitelliform Macular Dystrophy | Mucolipidosis | Schnyder Crystalline Corneal Dystrophy | Charcot-Marie-Tooth Disease Type 4E | Pathological Gambling | Hypospadias | Polymyositis | Sarcoma, Endometrial Stromal | Williams Syndrome | Polyradiculopathy | Pituitary Stalk Interruption Syndrome | Basal Ganglia Disease | Erythematotelangiectatic Rosacea | Haim-Munk Syndrome | Otitis Externa | Spondyloarthritis | Cervicitis | Impulse Control Disorder | Calcium Pyrophosphate Deposition Disease | Scleroderma | Wiskott-Aldrich Syndrome | Acrodermatitis | X-linked Acrogigantism | Disseminated Superficial Actinic Porokeratosis | Steel Syndrome | Metatropic Dysplasia | C3 Glomerulonephritis | Tyrosinemia Type 2 | Temporal Lobe Epilepsy | Galactosemia | Neurodevelopmental Disorders | Mitochondrial Disease | Prolymphocytic Leukemia | Depression | Hypotension, Orthostatic | Creutzfeldt-Jakob Disease | Coronary Artery Disease | Neuromuscular Disorders | Glutaric Aciduria Type 1 | Hyperlipidemia Type V | Krabbe Disease | Mandibuloacral Dysplasia With Type A Lipodystrophy | Methylmalonic Acidemia | Gardner Syndrome | Christianson Syndrome | Yellow Fever | GLUT1 Deficiency Syndrome | Avellino Corneal Dystrophy | Bicuspid Aortic Valve | Muckle-Wells Syndrome | Recurrent Respiratory Papillomatosis | 5-oxoprolinase Deficiency | Congenital Tufting Enteropathy | Optic Nerve Hypoplasia, Bilateral | Ophthalmoplegia | D-2-Hydroxyglutaric Aciduria | Angiosarcoma | Knobloch Syndrome | CDKL5 Deficiency Disorder | Porphyria | Skin Carcinoma | C3 Glomerulopathy | N-acetylglutamate Synthase Deficiency | Seizures | Episodic Ataxia Type 2 | Cerebrovascular Disorders | Hyperekplexia | Hernia, Inguinal | Succinic Semialdehyde Dehydrogenase Deficiency | Waardenburg Syndrome Type 2 | Cryopyrin-associated Periodic Syndromes | Argininosuccinic Aciduria | Brugada Syndrome 1 | Heart Block | Hemochromatosis | Hyperprolactinemia | Nephrocalcinosis | Familial Cerebral Amyloid Angiopathy | Farber Disease | Major Depression | Brachial Plexus Neuropathy | Epiphyseal Chondrodysplasia, Miura Type | GATA2 Deficiency | Twin-to-twin Transfusion Syndrome | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Hypercalciuria | Neuroectodermal Tumors, Primitive | Gallstones | Keratosis, Actinic | Galactosialidosis | Prostatitis | Fontaine Progeroid Syndrome | Homocystinuria | Keloid | Delayed Sleep Phase Syndrome | Keratitis-ichthyosis-deafness Syndrome | Conn Syndrome | Wiedemann-Steiner Syndrome | Hemorrhoids | Rash | Behcet's Disease | Dysthymia | Spondylocarpotarsal Synostosis Syndrome | Early Infantile Epileptic Encephalopathy 4 | Cataract | Neurofibromatosis Type 2 | Persistent Fetal Circulation | Retinopathy, Diabetic | Congenital Muscular Dystrophy | Cryptococcal Meningitis | Hereditary Sensory And Autonomic Neuropathy | Hypotrichosis | Amyotrophic Lateral Sclerosis | Pulmonary Veno-occlusive Disease | Cousin Syndrome | Multiple Myeloma | Sturge-Weber Syndrome | Pituitary Disorders | Diffuse Mesangial Sclerosis | Papulopustular Rosacea | Dowling-Degos Disease | Hemangioendothelioma | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Small Lymphocytic Lymphoma | Enlarged Vestibular Aqueduct | Carcinoma, Merkel Cell | Waardenburg Syndrome Type 4 | Otitis Media