Gastric Atrophy

About the Disease
Atrophic Gastritis, also known as gastritis, atrophic, is related to pernicious anemia and carcinoid tumors, intestinal, and has symptoms including dyspepsia An important gene associated with Atrophic Gastritis is GAST (Gastrin), and among its related pathways/superpathways are IL-1 Family Signaling Pathways and Bacterial infections in CF airways. The drugs Mecobalamin and Hydroxocobalamin have been mentioned in the context of this disorder. Affiliated tissues include spleen, liver and bone marrow, and related phenotypes are neoplasm and digestive/alimentary

Common Targets
TENM2 | MAFK | IGFBP7-AS1 | HRH2 | CCDC92B | PSCA | COL13A1 | IL10 | NAV3 | ST8SIA6 | SPSB1 | ATG16L1 | MEX3A | TET3 | ADCY2 | CELF4 | DNMT3B | RYR2 | ATG12 | SLC66A1L | OSTM1-AS1 | FSTL5 | TTTY14 | STIM1 | LINC01607 | MGC27382 | RGS6 | G1786 | GAK | DNAJA1P5 | PHF21B | G238 | LANCL1 | PPFIA1 | EDN3 | RAP1GAP2 | GPR83 | GHRHR | OLFM3 | ACSS3 | SLCO1B3 | FABP2 | PITPNB | LHPP | NKAIN2 | STRAP | CPOX

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

Other Diseases

Fibrosarcoma | Vitamin K Deficiency | Hypercholesterolemia | Pyruvate Kinase Deficiency | Mitochondrial Disease | Tremor | Renal Failure | Coronary Artery Disease | Oligoastrocytoma | Autonomic Nervous System Disorders | Carpal Tunnel Syndrome | Cannabis Abuse | Non-Langerhans Cell Histiocytosis | Scoliosis | Ocular Albinism Type 1 | Neonatal Progeroid Syndrome | Pulmonary Stenosis | Retinopathy Of Prematurity | Familial Hypobetalipoproteinemia | Cancer, Brain | Renal Tubular Dysgenesis | Tyrosine Hydroxylase Deficiency | Optic Neuropathy, Anterior Ischemic | Chitayat Syndrome | Cancer, Lung | Periodontitis | 3-hydroxy-3-methylglutaric Aciduria | Enhanced S-cone Syndrome | Whipple's Disease | Supravalvular Aortic Stenosis | Congenital Lipoid Adrenal Hyperplasia | Coronary Restenosis | Periventricular Nodular Heterotopia | Pulmonary Alveolar Proteinosis | Presbyopia | Focal Segmental Glomerulosclerosis | Chediak-Higashi Syndrome | Lipodystrophy | Infantile Nephropathic Cystinosis | Walker-Warburg Syndrome | Papulopustular Rosacea | Retinal Vasculitis | Pompe Disease | Citrullinemia | Ellis-Van Creveld Syndrome | Scleritis | Rickets | Congenital Nephrotic Syndrome | Primary Aldosteronism | Specific Granule Deficiency | Dwarfism | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Corticobasal Syndrome | Ocular Hypertension | Leukoencephalopathy, Progressive Multifocal | Polyarteritis Nodosa | Pseudo-pseudohypoparathyroidism | Chondroma | Metaphyseal Chondrodysplasia, Schmid Type | B-cell Chronic Lymphocytic Leukemia | Spinocerebellar Ataxia Type 15 | Raine Syndrome | Crigler-Najjar Syndrome | Myocardial Infarction | Rhabdomyosarcoma, Alveolar | Hypertension, Essential | VEXAS Syndrome | Bicuspid Aortic Valve | X-linked Charcot-Marie-Tooth Disease | Generalized Epilepsy With Febrile Seizures Plus | Hyperthermia, Malignant | Leprosy | Pathological Gambling | Vitreoretinopathy, Proliferative | Myosin Storage Myopathy | Hypogonadism | Basal Ganglia Disease | Carpenter Syndrome | Proximal Symphalangism | Major Depression | Dementia | Congenital Bile Acid Synthesis Defect | Proctitis | Cataplexy | Nevus | Familial Episodic Pain Syndrome | Hidradenitis | Pilomatrix Carcinoma | Blood Protein Disorders | LRBA Deficiency | Fraser Syndrome | Paraganglioma | Myelomeningocele | Cancer, Colon | Hereditary Folate Malabsorption | Pemphigus | Neurotoxicity | Pseudomyxoma Peritonei | Diabetes Type 2 | Rotor Syndrome | Acne Vulgaris | Epidermolysis Bullosa Simplex | Skin Papilloma | Vascular Calcification | Autism Spectrum Disorders | Waardenburg Syndrome Type 2 | Swine Influenza | Ophthalmoplegia | Thanatophoric Dysplasia Type 1 | Diamond-Blackfan Anemia | Familial Partial Lipodystrophy | Nephrotic Syndrome Type 1 | Esophagitis | Oculocutaneous Albinism Type 2 | Postpoliomyelitis Syndrome | Vestibular Disease | Encephalopathy, Hepatic | Central Pain Syndrome | Craniopharyngioma | Thyroiditis, Autoimmune | Gastrointestinal Disorders | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Chromosome 9q34.3 Deletion Syndrome | Babesiosis | Schizophrenia | Menkes Disease | Apraxia | Phenylketonuria | Aspartylglycosaminuria | Nestor-Guillermo Progeria Syndrome | Lupus Erythematosus | Neutropenia | Hemosiderosis | Gangliosidosis, GM1 | Albinism | Granular Corneal Dystrophy Type 1 | Thanatophoric Dysplasia | Leigh Syndrome | Primary Torsion Dystonia | Juvenile Xanthogranuloma | Alveolar Capillary Dysplasia | Meningococcal Infections | Oculopharyngeal Muscular Dystrophy | Acromegaly | Meconium Ileus | Neuroma | Niemann-Pick Disease | Cerebellofaciodental Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Hyperphenylalaninemia | Alstrom Syndrome | Thrombocythemia, Essential | Renal Dysplasia | Dystonia Musculorum Deformans | Pituitary Stalk Interruption Syndrome | Aneurysm, Thoracic Aortic | Vitamin A Deficiency | Syndactyly | Cerebrotendinous Xanthomatosis | Weill-Marchesani Syndrome | Distal Spinal Muscular Atrophy | Nephrosclerosis | Lipid Storage Diseases | Pneumoconiosis | Light Chain Amyloidosis | Hepatitis C, Chronic | Chronic Kidney Disease | Behcet's Disease | Insulin Resistance | Renal-hepatic-pancreatic Dysplasia | Neuronal Ceroid Lipofuscinosis | Globozoospermia | Familial Hypertrophic Cardiomyopathy | Myasthenia Gravis | Sclerocornea | Osteogenesis Imperfecta Type V | Congenital Hereditary Endothelial Dystrophy Type II | GM2-gangliosidosis AB Variant | Hypokalemic Periodic Paralysis | Pyelonephritis | Polycystic Ovary Syndrome | Sialidosis | Schamberg Disease | Thalassemia | Schistosomiasis | Pre-eclampsia | Cyst | Congenital Hypofibrinogenemia | HIBCH Deficiency | Histoplasmosis | Malnutrition | Schizencephaly | Craniolenticulosutural Dysplasia | Small Lymphocytic Lymphoma | Atopic Dermatitis | Renal Hypouricemia | Open-angle Glaucoma | Hodgkin Lymphoma | Smoldering Myeloma | Angioedema | Trichothiodystrophy | Cervicitis | Cold Agglutinin Disease | Cushing Syndrome | Neuroblastoma | Lyme Disease | Peyronie's Disease | Guanidinoacetate Methyltransferase Deficiency | Polyomavirus Nephropathy | Primary Progressive Nonfluent Aphasia | Goiter | Hypohidrotic Ectodermal Dysplasia, X-linked | Idiopathic Pulmonary Fibrosis | Loeys-Dietz Syndrome Type 4 | Myoclonic Epilepsy With Ragged Red Fibers | Basal Ganglia Cerebrovascular Disease | Early Infantile Epileptic Encephalopathy | Leukocyte Adhesion Deficiency Type 1 | Congenital Torticollis | Cystitis, Interstitial | Primary Hyperoxaluria Type 1 | Harlequin Ichthyosis | Thyroid Hormone Resistance | Hyperinsulinemia | Cystinosis | Ameloblastoma | Cenani-Lenz Syndactyly Syndrome | Transient Bullous Dermolysis Of The Newborn | Polymicrogyria | ICF Syndrome | Mucormycosis | Hereditary Hemorrhagic Telangiectasia | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Iron Overload | High Molecular Weight Kininogen Deficiency | Short-chain Acyl-CoA Dehydrogenase Deficiency | Reflex Epilepsy | Anorexia Nervosa | Peeling Skin Syndrome, Acral Type | Glycogen Storage Disease Type 1 | Carney Triad | Cardiac Arrest | Loeys-Dietz Syndrome | POEMS Syndrome | Pulmonary Alveolar Microlithiasis | Reye Syndrome | McLeod Syndrome | Anovulation | Lathosterolosis | Ependymoma | Seminoma | Congenital Generalized Lipodystrophy | Neovascular Glaucoma | Cholestasis | Neurofibromatosis Type 1 | Down Syndrome | Senior-Loken Syndrome | Sclerosing Cholangitis | Holoprosencephaly | Osteonecrosis | Hyperandrogenemia | Hypotrichosis | Learning Disability | Fontaine Progeroid Syndrome | Corneal Dystrophies, Hereditary | Agnathia-Otocephaly Complex | Fahr Disease | Carey-Fineman-Ziter Syndrome | Giant Cell Glioblastoma | Dentinogenesis Imperfecta | Autosomal Recessive Congenital Ichthyosis | Cole-Carpenter Syndrome | Antithrombin III Deficiency | Sponastrime Dysplasia | Chondromyxoid Fibroma | Progressive Osseous Heteroplasia | Sjogren Syndrome | Hemorrhage | Colitis, Lymphocytic | Sick Sinus Syndrome 1 | Twin-to-twin Transfusion Syndrome | Corneal Ulcer | Cornelia De Lange Syndrome | Fuchs Heterochromic Iridocyclitis | Arteriovenous Malformations | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Sepiapterin Reductase Deficiency | Congenital Diaphragmatic Hernia | Sickle Cell Disease | Creatine Deficiency Syndrome Due To AGAT Deficiency | 3-methylglutaconic Aciduria Type I | Eosinophilia | Distal Myopathy | Cardiac Sarcoidosis | Congenital Absence Of Vas Deferens | Kallmann Syndrome | Juvenile Hyaline Fibromatosis | Chromosome 8q21.11 Deletion Syndrome | C3 Glomerulonephritis | Keratoconjunctivitis | Heart Block | Cat Eye Syndrome | Transcobalamin Deficiency | Keratoacanthoma | Histiocytosis | Exotropia | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Menetrier Disease | Dermatofibrosarcoma | Sporadic Hemiplegic Migraine | ACTH-independent Macronodular Adrenal Hyperplasia | Pachyonychia Congenita | Persistent Hyperplastic Primary Vitreous | Congestive Heart Failure | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Pelvic Inflammatory Disease | Best Macular Dystrophy | Myeloid Leukemia | Brenner Tumor | Intracranial Hypertension | Hypopigmentation | Erdheim-Chester Disease | Carcinoma, Transitional Cell | Endophthalmitis | Hydrops Fetalis | Chorea | Non-epidermolytic Palmoplantar Keratoderma | Familial Isolated Hyperparathyroidism | Melanoma | Alagille Syndrome | Epidermolysis Bullosa Acquisita | Hashimoto Thyroiditis | Primary Progressive Aphasia | Angiosarcoma | Antisocial Personality Disorder | Amyloidosis | Tyrosinemia | Joubert Syndrome 2 | Esthesioneuroblastoma | Osteomalacia | Trigonocephaly | Dominant Optic Atrophy | Retinitis Pigmentosa 3 | Stuttering | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Infertility, Male | Erythropoietic Protoporphyria | Intermittent Claudication | Phosphoglycerate Dehydrogenase Deficiency | Veno-occlusive Disease | Charcot-Marie-Tooth Disease, Type 2A | Schizotypal Personality Disorder | Sleep Apnea, Central | Glycogen Storage Disease | Glaucoma, Congenital | Glutaric Aciduria Type 1 | Wolfram Syndrome 2 | Progressive Familial Intrahepatic Cholestasis Type 1 | Necrotizing Autoimmune Myopathy | Niemann-Pick Disease, Type A | Pseudohypoparathyroidism Type 1B | Infantile Neuroaxonal Dystrophy | Hereditary Multiple Exostoses | Delayed Sleep Phase Syndrome | VACTERL/VATER Association | DiGeorge Syndrome | Acrodysostosis | Synpolydactyly | Familial Exudative Vitreoretinopathy | Spinocerebellar Ataxia Type 8 | Nemaline Myopathy 8 | Pneumonia, Bacterial | Subacute Sclerosing Panencephalitis | Meesmann Corneal Dystrophy | Carcinoid Syndrome | T-cell Chronic Lymphocytic Leukemia | Canavan Disease | Thymoma, Malignant | Congenital Disorders Of Glycosylation Type II | Glutaric Aciduria Type 3 | Leri Pleonosteosis | Neurocutaneous Melanocytosis | Polydactyly | Diffuse Mesangial Sclerosis | Long QT Syndrome Type 2 | Prurigo Nodularis | Facioscapulohumeral Muscular Dystrophy Type 2 | Botulism | Multicystic Renal Dysplasia | Adenylosuccinate Lyase Deficiency | Epidermolysis Bullosa Simplex, Localized | Tic Disorder | Prostatitis | Epidermolytic Hyperkeratosis | Facioscapulohumeral Muscular Dystrophy | Klippel-Feil Syndrome | Cystinuria | Metatropic Dysplasia | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Autosomal Recessive Spastic Paraplegia Type 75