Fibronectin Glomerulopathy

About the Disease
Glomerulopathy with Fibronectin Deposits 2, also known as fibronectin glomerulopathy, is related to nephrotic syndrome and glomerulopathy with fibronectin deposits 1. An important gene associated with Glomerulopathy with Fibronectin Deposits 2 is FN1 (Fibronectin 1), and among its related pathways/superpathways is Signaling by ALK in cancer. Affiliated tissues include kidney and endothelial, and related phenotypes are hypertension and proteinuria

Common Targets
G2335 | C3

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

Other Diseases

Obsessive-compulsive Disorder | Crisponi Syndrome | Sepiapterin Reductase Deficiency | Pituitary Disorders | Aromatic L-amino Acid Decarboxylase Deficiency | Hemorrhagic Disorders | Craniofacial Dysostosis | Demyelinating Diseases | Alexander Disease | Cannabis Abuse | Macrodactyly | T-cell Leukemia | Generalized Epilepsy And Paroxysmal Dyskinesia | Lipodystrophy | Arthrogryposis | Christianson Syndrome | Apert Syndrome | Asphyxia Neonatorum | Eosinophilia | Spinocerebellar Ataxia Type 6 | Cerebrovascular Disorders | Glomerulonephritis, Membranoproliferative | Coloboma | Aldosteronism | Double Outlet Right Ventricle | Benign Recurrent Intrahepatic Cholestasis 1 | Still Disease | DNA Ligase IV Deficiency | Osteosarcoma | Compartment Syndrome | Pyruvate Dehydrogenase Deficiency | Pseudoachondroplasia | Meningioma, Benign | Walker-Warburg Syndrome | Holt-Oram Syndrome | Waardenburg Syndrome Type 1 | Glutaric Aciduria Type 2 | Congenital Myopathy | Renal Dysplasia | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Cystitis, Interstitial | Vaginitis | Tularemia | Gaucher Disease | Hyperlipidemia | Galactosialidosis | Transcobalamin Deficiency | Liver Failure | Infantile Liver Failure Syndrome 1 | Usher Syndrome Type I | Sporadic Hemiplegic Migraine | Androgenic Alopecia | Antenatal Bartter Syndrome Type 1 | Anemia | Pycnodysostosis | Proopiomelanocortin Deficiency | Patent Ductus Arteriosus | Rubinstein-Taybi Syndrome | Myotonia | Craniofrontonasal Syndrome | Adams-Oliver Syndrome | Erythrokeratodermia Variabilis | Whipple's Disease | Chondrodysplasia Punctata 2, X-linked Dominant | Bruck Syndrome | Lymphoma | Gastric Atrophy | McKusick Type Metaphyseal Chondrodysplasia | Cramp Fasciculation Syndrome | Panniculitis | Crigler-Najjar Syndrome | Congenital Mirror Movements | Diverticulitis | Ileitis | Microvillus Inclusion Disease | Myocarditis | Basal Ganglia Disease, Biotin-responsive | Cerebellar Ataxia, Cayman Type | Aarskog-Scott Syndrome | Nephrosclerosis | Speech Disorders | Preaxial Polydactyly | Primary Hyperoxaluria Type 1 | Personality Disorders | Pericarditis | Reticular Dysgenesis | Synovitis | Osteoporosis | Bartter Syndrome | Tracheal Disorders | Esthesioneuroblastoma | Celiac Disease | Sezary Syndrome | Chylothorax, Congenital | Sarcoidosis, Pulmonary | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Facioscapulohumeral Muscular Dystrophy Type 2 | Multiple Myeloma | Transient Bullous Dermolysis Of The Newborn | Calcium Pyrophosphate Deposition Disease | Malignant Fibrous Histiocytoma | Zollinger-Ellison Syndrome | Kaposi Sarcoma | Goiter, Nodular | Progressive Familial Intrahepatic Cholestasis | Vitamin B12 Deficiency | Scleritis | Primary Hyperoxaluria Type 3 | Alcoholism | Chronic Granulomatous Disease | Basan Syndrome | Fibromuscular Dysplasia | Odonto-onycho-dermal Dysplasia | Spinocerebellar Ataxia Type 42 | Panic Disorder | Trismus-pseudocamptodactyly Syndrome | Cocaine-Related Disorders | Prolidase Deficiency | Diabetes Gestational | Batten Disease | Osteosclerosis | Teratozoospermia | Mumps | Polycystic Liver | Hyperuricemic Nephropathy, Familial Juvenile | Dominant Optic Atrophy | Hypertension, Renovascular | Triphalangeal Thumb-polysyndactyly Syndrome | Bursitis | Occipital Neuralgia | Ectrodactyly | Constipation | Pancreatitis, Chronic | Retinoschisis | Neurofibromatosis | Pseudoexfoliation Syndrome | Anthrax | Nasodigitoacoustic Syndrome | Hyperoxaluria | Retinal Coloboma | Encephalopathy | Iron Metabolism Disorders | Hypercalciuria | Tietze Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Saul-Wilson Syndrome | Cabezas Syndrome | Porphyria, Acute Intermittent | Melanoma, Uveal | Lymphoma, B-cell | Long QT Syndrome Type 3 | Acrodermatitis | Neurofibrosarcoma | Persistent Fetal Circulation | Schistosomiasis | Hypohidrotic Ectodermal Dysplasia | Glutaric Aciduria Type 3 | Congenital Dyserythropoietic Anemia Type 1 | ADNP Syndrome | Partington Syndrome | Histoplasmosis | Hydrops Fetalis | Rhabdomyosarcoma, Alveolar | Chediak-Higashi Syndrome | Medulloblastoma | Coffin-Siris Syndrome | Achromatopsia | Retinitis Pigmentosa 3 | Sotos Syndrome | Splenomegaly | Conn Syndrome | Wiedemann-Steiner Syndrome | Vertigo | Gingivitis | Headache | Heart Septal Defects | Mixed Connective Tissue Disease | Epidermodysplasia Verruciformis | Hemangioblastoma | Stromal Corneal Dystrophy | Steel Syndrome | Branchiootorenal Syndrome | Lyme Disease | Cockayne Syndrome | Hypodontia | Craniolenticulosutural Dysplasia | 3-M Syndrome | Myofibromatosis | Sensory Neuropathy | Hypotension, Orthostatic | Uveitis, Anterior | Seizures-scoliosis-macrocephaly Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Borderline Personality Disorder | Graft-versus-host Disease | Hyperostosis | Systemic Mastocytosis | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Pigment Dispersion Syndrome | Angiosarcoma | Prediabetes | Antithrombin III Deficiency | Hypertensive Retinopathy | Currarino Syndrome | Brachial Plexus Neuropathy | Erythema Multiforme | Dysthymia | Focal Facial Dermal Dysplasia | Schnyder Crystalline Corneal Dystrophy | Pseudohypoaldosteronism | Nicotine Addiction | Agranulocytosis | Congenital Adrenal Hyperplasia 1 | Dyggve-Melchior-Clausen Disease | Auriculocondylar Syndrome | Hyperthermia, Malignant | Spinocerebellar Ataxia Type 40 | Asperger Syndrome | Pulmonary Capillary Hemangiomatosis | Norrie Disease | Macular Corneal Dystrophy Type 1 | Noonan Syndrome | Hyperkeratosis | Kidney Stones | Giant Cell Glioblastoma | Diabetic Encephalopathy | Benign Familial Pemphigus | Pontocerebellar Hypoplasia Type 7 | Peripheral T-cell Lymphoma | Autosomal Recessive Spastic Paraplegia Type 54 | Meningioma | Thrombotic Microangiopathy | Acral Lentiginous Melanoma | Stroke | Apparent Mineralocorticoid Excess Syndrome | Reye Syndrome | Early Infantile Epileptic Encephalopathy 13 | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Cardiomyopathy, Hypertrophic | Lymphopenia | Cancer, Breast | Creatine Deficiency Syndrome Due To AGAT Deficiency | Dermatofibrosarcoma | Binge Eating Disorder | Acute Lung Injury | Gangliosidosis | Chronic Granulomatous Disease, X-linked | Cushing Syndrome | Pityriasis Rubra Pilaris | Muir-Torre Syndrome | Hypolipoproteinemia | Isovaleric Acidemia | Urofacial Syndrome | Cystinosis | Hydrocephalus, Normal Pressure | Schizencephaly | Carbohydrate Metabolism Disorders | Dystonia-parkinsonism, X-linked | Paraplegia | Borjeson-Forssman-Lehmann Syndrome | Chiari Malformation Type I | Spondylo-ocular Syndrome | Spinocerebellar Ataxia Type 16 | Becker Muscular Dystrophy | Nager Acrofacial Dysostosis | Familial Isolated Hyperparathyroidism | Macrophage Activation Syndrome | Hepatitis E | Autism Spectrum Disorders | Neural Tube Defect | Multicystic Renal Dysplasia | Keratosis, Seborrheic | Acute Chest Syndrome | Meier-Gorlin Syndrome | Megaloblastic Anemia | Epilepsy, Generalized | Trichotillomania | Dysfibrinogenemia | Pyruvate Carboxylase Deficiency Disease | 3-methylglutaconic Aciduria | Pituitary Dwarfism | Spinocerebellar Ataxia Type 27 | Sjogren Syndrome | Congenital Hereditary Endothelial Dystrophy Type II | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Agoraphobia | Cystitis | Behcet's Disease | Uterine Leiomyoma | Bronchitis | Glaucoma, Congenital | Congenital Diaphragmatic Hernia | Prolactinoma | Nephritis, Interstitial | Syncope | Oculopharyngeal Muscular Dystrophy | Angiomyolipoma | Small Lymphocytic Lymphoma | Bernard-Soulier Syndrome | Hidradenitis Suppurativa | 5-oxoprolinase Deficiency | Nevus | Nephrotic Syndrome | Tumoral Calcinosis | Hemolytic Anemia | Oligospermia | Sarcoma | Shprintzen-Goldberg Syndrome | Heterotopic Ossification | Combined Pituitary Hormone Deficiency | Congenital Torticollis | Oral Lichen Planus | Thalassemia | Analgesia | Paget's Disease Of The Breast | Myoclonus | Cryptosporidiosis | Hernia, Inguinal | Dysequilibrium Syndrome | Intermittent Claudication | Keratoconjunctivitis | Chromosome 8q21.11 Deletion Syndrome | Osteogenesis Imperfecta Type I | Epilepsy Of Infancy With Migrating Focal Seizures | Withdrawal Syndrome | Lactose Intolerance | Familial Advanced Sleep Phase Syndrome | Congenital Nystagmus | Angioedema, Acquired | Spinocerebellar Ataxia Type 38 | Hyperkalemic Periodic Paralysis | Retinal Dystrophy | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Diamond-Blackfan Anemia | Acromicric Dysplasia | Jacobsen Syndrome | Usher Syndrome | Tangier Disease | Oligoastrocytoma | Milk Allergy | Hereditary Spherocytosis | Hashimoto Thyroiditis | T-cell Lymphoma, Subcutaneous Panniculitis-like | Creatine Deficiency Syndrome | Erythropoietic Protoporphyria | Oligoasthenoteratozoospermia | Congenital Stromal Corneal Dystrophy | Spinal Muscular Atrophy | Malnutrition | Nephroblastoma | Craniometaphyseal Dysplasia | Adenoma, Pleomorphic | Subacute Sclerosing Panencephalitis | Adenoma, Villous | Okihiro Syndrome | Gastritis | Large Granular Lymphocytic Leukemia | Chronic Myeloid Leukemia | Myosin Storage Myopathy | Trachoma | Nanophthalmos | Fundus Albipunctatus | Chromosome 17q21.31 Deletion Syndrome | Carney Triad | Jawad Syndrome | Inflammatory Joint Disease | Charcot-Marie-Tooth Disease, Type 2 | Paraganglioma, Carotid Body | Ichthyosis Bullosa Of Siemens | Enterocolitis, Necrotizing | Cousin Syndrome | Peters-plus Syndrome | Neurocysticercosis | Neuroectodermal Tumors, Primitive | Danon Disease | Liddle Syndrome | Crimean-Congo Hemorrhagic Fever | Exostoses | Multiple Sulfatase Deficiency | Kabuki Syndrome 2 | Ovarian Hyperstimulation Syndrome | Long QT Syndrome Type 2 | Meningococcal Infections | Hypopituitarism | Primary Biliary Cholangitis | Adenylosuccinate Lyase Deficiency | X-linked Charcot-Marie-Tooth Disease | Glycogen Storage Disease Type 1 | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Myositis, Focal | Richter's Syndrome | Esotropia | Central Retinal Artery Occlusion | Corticobasal Syndrome | Carcinoma, Merkel Cell | Schizophrenia, Paranoid | Granular Corneal Dystrophy Type 1 | Pendred Syndrome | Carpal Tunnel Syndrome | Otitis Externa