Fraser Syndrome
Fraser Syndrome
About the Disease
Fraser Syndrome 1, also known as fraser syndrome, is related to branchiootorenal syndrome and branchiootorenal syndrome 1. An important gene associated with Fraser Syndrome 1 is FRAS1 (Fraser Extracellular Matrix Complex Subunit 1), and among its related pathways/superpathways are Phospholipase-C Pathway and Primary focal segmental glomerulosclerosis (FSGS). Affiliated tissues include eye, kidney and skin, and related phenotypes are blindness and renal hypoplasia
Common Targets
FRAS1 | GRIP1 | FREM2
Note: If you'd like to get a target analysis report for Fraser 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 Fraser Syndrome at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.
Other Diseases
Kaposiform Hemangioendothelioma | Pulmonary Tuberculosis | Adenosine Deaminase Deficiency | Colitis | Twin-to-twin Transfusion Syndrome | Hydrocephalus, Normal Pressure | Cavitary Optic Disc Anomalies | Kindler Syndrome | Pachyonychia Congenita | Sick Sinus Syndrome 1 | Renal Tubular Acidosis | Nicotine Addiction | Gallstones | Familial Mediterranean Fever | Gerstmann-Straussler-Scheinker Syndrome | Insulin Resistance | Scapuloperoneal Spinal Muscular Atrophy | Encephalopathy, Glycine | Waardenburg Syndrome Type 2E | Wiedemann-Steiner Syndrome | Osteoporosis | Intracerebral Hemorrhage | Cocaine-Related Disorders | Abetalipoproteinemia | Rosacea | Keratitis | Seizures-scoliosis-macrocephaly Syndrome | Holt-Oram Syndrome | Albinism | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | X-linked Creatine Transporter Deficiency | Central Core Disease | Necrobiosis Lipoidica | Blomstrand Osteochondrodysplasia | Oligodendroglioma | Hernia, Inguinal | Distal Myopathy 2 | Anthrax | Gingivitis | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Meningioma | Corneal Dystrophies, Hereditary | Language Disorders | Acute Generalized Exanthematous Pustulosis | Dysequilibrium Syndrome | Muir-Torre Syndrome | Pyelonephritis | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Primary Progressive Aphasia | Hypermethioninemia | Interstitial Lung Diseases | Lymphoproliferative Disorders | Raynaud Phenomenon | Uveitis, Anterior | Dermatitis | Infantile Refsum Disease | Nephritis, Interstitial | Citrullinemia | Papillon-Lefevre Syndrome | Neuromuscular Disorders | Nemaline Myopathy 10 | Panniculitis | Thyroiditis, Autoimmune | Mesothelioma, Malignant | Neurodevelopmental Disorders | Sorsby Fundus Dystrophy | Cutaneous Angiosarcoma | Rothmund-Thomson Syndrome | Lyme Disease | Purpura | Aneurysm, Abdominal Aortic | Microcephalic Primordial Dwarfism | Erythematotelangiectatic Rosacea | Sulfite Oxidase Deficiency | T-cell Lymphoma, Subcutaneous Panniculitis-like | Delayed Sleep Phase Syndrome | Diabetic Neuropathy | Barakat Syndrome | McCune-Albright Syndrome | Mitochondrial Cytopathy | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Vasculitis | Pseudomyxoma Peritonei | X-linked Charcot-Marie-Tooth Disease | Oligospermia | Lassa Fever | Vitamin D Deficiency | Hepatic Steatosis | Rift Valley Fever | Blepharitis | Diabetic Encephalopathy | Antley-Bixler Syndrome | Liebenberg Syndrome | Thalassemia, Beta | Pierre Robin Syndrome | Congenital Hereditary Endothelial Dystrophy Type II | Hairy Cell Leukemia | Emery-Dreifuss Muscular Dystrophy | Heavy Chain Disease | Fibromuscular Dysplasia | Posterior Polar Cataract | Hennekam Lymphangiectasia-lymphedema Syndrome | Enlarged Vestibular Aqueduct | Encephalitis, Tick-borne | Bernard-Soulier Syndrome | Retinitis Pigmentosa | Chronic Mucocutaneous Candidiasis | Ventricular Septal Defect | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Tylosis With Esophageal Cancer | Vulvovaginitis | Progressive Encephalopathy-optic Atrophy Syndrome | Woodhouse-Sakati Syndrome | Asthma | Scleroderma, Diffuse | Optic Atrophy 2 | Glycogen Storage Disease Type 3 | Diabetes Type 1 | Thrombosis | Prolidase Deficiency | Cardiomyopathy, Dilated, 1L | Chronic Inflammatory Demyelinating Polyneuropathy | Vaginitis | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Long QT Syndrome Type 2 | Epidermolysis Bullosa | Usher Syndrome Type I | Hereditary Sensory Neuropathy Type 1 | Anosmia, Congenital | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Splenomegaly | Malignant Peripheral Nerve Sheath Tumor | Portal Vein Thrombosis | Sleep Disorder | Porokeratosis | Hypertrophy | Renal Failure | Pleural Tuberculosis | Dyslexia | Wolfram Syndrome 2 | Focal Dermal Hypoplasia | Mast Cell Leukemia | Brugada Syndrome 1 | Purpura, Thrombotic Thrombocytopenic | Retinoschisis | Bronchitis | Sarcosinemia | Fibrillation, Atrial | Lafora Disease | Herpes Simplex Dermatitis | Giant Cell Arteritis | Congenital Heart Block | Snyder-Robinson Syndrome | Coenzyme Q10 Deficiency | Phenylketonuria | Hemophilia | Spondylometaphyseal Dysplasia | Infectious Diarrhea | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Cole-Carpenter Syndrome | Sialoadenitis | Hypobetalipoproteinemias | Coffin-Siris Syndrome | Neuroblastoma | Cryptococcal Meningitis | Hemorrhagic Disorders | Otitis Externa | Macular Corneal Dystrophy Type 1 | Klippel-Feil Syndrome | Autosomal Recessive Congenital Ichthyosis | Liver Diseases | Trigonocephaly | Atrioventricular Septal Defect | Uterine Leiomyoma | Alkaptonuria | Periodontitis | Apparent Mineralocorticoid Excess Syndrome | Polycystic Ovary Syndrome | Oculocutaneous Albinism Type 2 | Bronchitis, Chronic | Loeys-Dietz Syndrome Type 4 | Currarino Syndrome | Nasodigitoacoustic Syndrome | Duchenne Muscular Dystrophy | Noonan Syndrome-like Disorder With Loose Anagen Hair | Cardiac Arrest | Non-Hodgkin Lymphoma | Geleophysic Dysplasia | Sickle Cell Disease | Gout | Cutaneous Lupus Erythematosus | Pseudoexfoliation Syndrome | Neurodegeneration With Brain Iron Accumulation | Meningitis | Methemoglobinemia Type IV | Tangier Disease | Odonto-onycho-dermal Dysplasia | Glomerulonephritis, Membranous | Cystinuria | Alcoholism | Tatton-Brown-Rahman Syndrome | Glycogen Storage Disease Type 1b | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Sengers Syndrome | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Sarcoidosis | Anuria | Cranioectodermal Dysplasia | Venous Insufficiency | Carcinoma, Signet Ring Cell | Osteomalacia | Colitis, Lymphocytic | Multifocal Motor Neuropathy | Optic Nerve Hypoplasia, Bilateral | Hypopituitarism | Lichen Planus | Glycogen Storage Disease Type 0 | Polymicrogyria | Myelofibrosis | AIDS Dementia Complex | Frank-ter Haar Syndrome | Dyskeratosis Congenita | Hyperinsulinemic Hypoglycemia | Primary Progressive Nonfluent Aphasia | Acromicric Dysplasia | Erythrokeratodermia Variabilis | DRESS Syndrome | Autonomic Neuropathy | Cirrhosis | Xeroderma Pigmentosum | GAPO Syndrome | Neutrophilia | Intestinal Tuberculosis | Becker Muscular Dystrophy | Primary Biliary Cholangitis | Chronic Granulomatous Disease | Corneal Ulcer | Congenital Nephrotic Syndrome | Binge Eating Disorder | Congenital Adrenal Hyperplasia 1 | Sponastrime Dysplasia | Papulopustular Rosacea | Autonomic Nervous System Disorders | Cataplexy | Paronychia | Pneumonia, Viral | ICF Syndrome | Retinopathy Of Prematurity | Limb Girdle Muscular Dystrophy | Neuroendocrine Cancer | Retinal Dystrophy, Early-onset Severe | Benign Familial Infantile Seizures | Antithrombin III Deficiency | Bardet-Biedl Syndrome | Crisponi Syndrome | C3 Glomerulonephritis | Chondrodysplasia Punctata 1, X-linked Recessive | Lung Diseases | Polyarteritis Nodosa | Behcet's Disease | Osteogenesis Imperfecta Type II | Primary Familial Brain Calcification | Adenoma, Pituitary | Major Depression | Otopalatodigital Syndrome Type 2 | Spinal Muscular Atrophy Type 2 | Retinopathy, Diabetic | Histoplasmosis | Biotinidase Deficiency | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Babesiosis | Treacher Collins Syndrome | Angiosarcoma Of The Breast | Greig Cephalopolysyndactyly Syndrome | Orotic Aciduria | Alstrom Syndrome | Occipital Neuralgia | Bulimia Nervosa | Hypoglycemia | Syncope | Dyggve-Melchior-Clausen Disease | Esophagitis | Synpolydactyly | Sialidosis | Pearson Syndrome | Early Infantile Epileptic Encephalopathy 28 | Harlequin Ichthyosis | Congenital Nystagmus | Lattice Corneal Dystrophy Type 1 | Macrodactyly | Duodenal Atresia | Acrodermatitis | Acral Lentiginous Melanoma | Spinocerebellar Ataxia Type 21 | L-2-Hydroxyglutaric Aciduria | Fanconi Anemia | Fibromyalgia | Eosinophilic Asthma | Heart Failure | Leishmaniasis, Visceral | Optic Neuritis | Jalili Syndrome | Spinocerebellar Ataxia Type 5 | Obesity | Spondylolisthesis | Analgesia | Peripheral T-cell Lymphoma | Anterior Segment Dysgenesis | Renal Oncocytoma | Double Outlet Right Ventricle | Spinocerebellar Ataxia | Optic Neuropathy | Pneumoconiosis | Palmoplantar Keratoderma | Leber Hereditary Optic Neuropathy | Encephalocele | Meckel-Gruber Syndrome | Restrictive Dermopathy | Iron Metabolism Disorders | Phenylketonuria II | Choroiditis | Pemphigus Foliaceus | HIBCH Deficiency | Pontocerebellar Hypoplasia Type 2 | Congenital Adrenal Hyperplasia | Van Der Knaap Disease | Congenital Fiber-type Disproportion Myopathy | Diverticulitis | Proctitis | Angiodysplasia | Micro Syndrome | Niemann-Pick Disease, Type A | Peritonitis | Pemphigus | Diastrophic Dysplasia | Anodontia | Neurofibromatosis Type 1 | Vascular Calcification | GNE Myopathy | Castleman Disease | Birk-Barel Syndrome | Nicotine Dependence | Esophageal Carcinoma | Pelvic Inflammatory Disease | Perry Syndrome | Aarskog-Scott Syndrome | Malonyl-CoA Decarboxylase Deficiency | Carpenter Syndrome | Axenfeld-Rieger Syndrome | Patent Foramen Ovale | Osteosclerosis | Generalized Epilepsy And Paroxysmal Dyskinesia | Ichthyosis | Chloridorrhea, Congenital | McLeod Syndrome | Adenomatoid Tumor | Spondyloperipheral Dysplasia | Fucosidosis | Uremia | Stuve-Wiedemann Syndrome | Tuberculous Meningitis | Gitelman Syndrome | Non-bullous Congenital Ichthyosiform Erythroderma | Desmosterolosis | Esthesioneuroblastoma | Discoid Lupus Erythematosus | Hyperlipidemia, Familial Combined | Retinal Coloboma | MIRAGE Syndrome | Myhre Syndrome | Saethre-Chotzen Syndrome | Pernicious Anemia | Renal Hypouricemia | Persistent Mullerian Duct Syndrome | Pain | Hemoglobinopathies | Microcephaly, Seizures, And Developmental Delay | Agranulocytosis | Spinal Cord Diseases | Ganglioglioma | Scleroderma | Familial Isolated Hyperparathyroidism | Huntington's Disease-like 2 | Dupuytren Disease | Non-epidermolytic Palmoplantar Keratoderma | Cleidocranial Dysplasia | Charcot-Marie-Tooth Disease Type 4 | Chronic Thromboembolic Pulmonary Hypertension | Hereditary Sensory And Autonomic Neuropathy | VEXAS Syndrome | Juvenile Polyposis | Desbuquois Syndrome | Zygomycosis | Hepatitis, Chronic | Stroke, Ischemic | Hyperhomocysteinemia | Hepatitis D | Li-Fraumeni Syndrome | Glanzmann Thrombasthenia | Lentigo