Disease

Colon Adenoma

About the Disease
Colon Adenoma, also known as adenomatous polyp of colon, is related to adenoma and adenocarcinoma. An important gene associated with Colon Adenoma is SLC26A3 (Solute Carrier Family 26 Member 3), and among its related pathways/superpathways are ERK Signaling and Disease. The drugs Simethicone and Sodium sulfate have been mentioned in the context of this disorder. Affiliated tissues include colon, lymph node and breast, and related phenotypes are Increased shRNA abundance (Z-score > 2) and Increased shRNA abundance (Z-score > 2)

Common Targets
HOXA7 | LMF1 | G673 | HOXD10 | MIR375 | NTRK3 | EVX1 | PRAC2 | PROM1 | G3845 | CDX2 | PRAC1 | OPLAH | GJB2

疾病靶点研报
Colon Adenoma

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

Other Diseases

Acrodysostosis | Cyclic Vomiting Syndrome | Cancer, Prostate | Acute Kidney Injury | Chondrodysplasia Punctata 2, X-linked Dominant | Meningococcal Meningitis | Bronchitis | Glutaric Aciduria Type 2 | Carbonic Anhydrase VA Deficiency | Ichthyosis Bullosa Of Siemens | Thrombasthenia | Myelofibrosis | Duane Retraction Syndrome | Mevalonate Kinase Deficiency | Pre-eclampsia | Epidermal Nevus Syndrome | Cystitis | Klinefelter Syndrome | Kernicterus | Lentigo | Blood Protein Disorders | Borjeson-Forssman-Lehmann Syndrome | Frontometaphyseal Dysplasia | Pseudohypoparathyroidism Type 1A | Pseudohermaphroditism | Goiter, Nodular | Asperger Syndrome | Oculopharyngeal Muscular Dystrophy | Endometriosis | Intermittent Claudication | Lafora Disease | Hereditary Spastic Paraplegia | Carotid Artery Disease | Chronic Periodontitis | Progressive Myoclonic Epilepsy | Seizures-scoliosis-macrocephaly Syndrome | Dermatofibrosarcoma | Chondrodysplasia Punctata | Pituitary Stalk Interruption Syndrome | Prolidase Deficiency | Farber Disease | Thrombophilia | Keratitis-ichthyosis-deafness Syndrome | Arthritis, Psoriatic | Thrombocythemia, Essential | Spinal Muscular Atrophy | Bietti Crystalline Dystrophy | Posterior Polar Cataract | Cancer, Bladder | Neurotoxicity | Diverticulitis | Portal Vein Thrombosis | Antenatal Bartter Syndrome Type 1 | Cholangitis | Insulin Resistance | Hepatitis D | Hyperinsulinemic Hypoglycemia | Schistosomiasis | Infectious Diarrhea | Vaginitis | Panniculitis | Esthesioneuroblastoma | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Diabetic Nephropathy | Anodontia | Corneal Dystrophies, Hereditary | Aromatic L-amino Acid Decarboxylase Deficiency | Pierre Robin Syndrome | Rash | Disseminated Intravascular Coagulation | Wilson's Disease | Papilledema | Bronchiectasis | Vertebrobasilar Insufficiency | Varices | Eating Disorder | Ocular Surface Squamous Neoplasia | AIDS Dementia Complex | Myositis | Chromosome 8q21.11 Deletion Syndrome | Guttate Psoriasis | Diabetes | Coronary Artery Disease | Hyperhomocysteinemia | Learning Disability | Cleidocranial Dysplasia | Knobloch Syndrome | Progressive Familial Intrahepatic Cholestasis Type 3 | Lymphoma Lymphoblastic | Optic Neuropathy | Tenosynovial Giant Cell Tumor | Restless Legs Syndrome | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Retinoblastoma | Waldenstrom Macroglobulinemia | Keratosis, Seborrheic | Spinal And Bulbar Muscular Atrophy | Gastroschisis | Hernia, Inguinal | Ellis-Van Creveld Syndrome | Jaundice, Obstructive | Osteochondrosis | Dominant Optic Atrophy | Stroke, Ischemic | Hyperostosis | Primary Hyperoxaluria Type 1 | Odonto-onycho-dermal Dysplasia | Mohr-Tranebjaerg Syndrome | Blue Nevus | Congestive Heart Failure | Proctitis | Fundus Albipunctatus | Congenital Dyserythropoietic Anemia | Angiodysplasia | Scleroderma | Esophageal Carcinoma | Treacher Collins Syndrome | Anal Fissure | Benign Recurrent Intrahepatic Cholestasis 1 | Benign Hereditary Chorea | Citrullinemia | Malignant Fibrous Histiocytoma | Ocular Albinism Type 1 | Giant Cell Arteritis | Tic Disorder | Epidermolysis Bullosa Simplex | Charcot-Marie-Tooth Disease | Tetanus | Jalili Syndrome | Ependymoma | Pierpont Syndrome | Anti-glomerular Basement Membrane Disease | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Long QT Syndrome Type 2 | Joubert Syndrome | Systemic Lupus Erythematosus | Follicular Dendritic Cell Sarcoma | Acrocallosal Syndrome | Pelizaeus-Merzbacher Disease | Heroin Dependence | Fukuyama Congenital Muscular Dystrophy | Lymphoma, AIDS-related | Sarcoma, Ewing | Brenner Tumor | Oculocutaneous Albinism Type 1 | Primary Familial Brain Calcification | Neutrophilia | Sleep Apnea, Obstructive | Cholesteryl Ester Storage Disease | ICF Syndrome | Fowler's Syndrome | Sialidosis | Motor Neuron Diseases | Chitayat Syndrome | Familial Hyperaldosteronism | Isovaleric Acidemia | Osteoarthritis | Malonyl-CoA Decarboxylase Deficiency | Spasticity | Leprosy | Primary Ovarian Insufficiency | Congenital Generalized Lipodystrophy | Rhabdomyosarcoma | Hypolipoproteinemia | Multiple Sclerosis, Chronic Progressive | Glycogen Storage Disease Type 6 | Epicondylitis | Congenital Torticollis | Microvillus Inclusion Disease | Sarcomatoid Carcinoma Of The Lung | Myoclonic Atonic Epilepsy | Seminoma | Juvenile Polyposis | Neurofibrosarcoma | Fontaine Progeroid Syndrome | Erythromelalgia | Epilepsy, Generalized | Atopy | Oculocutaneous Albinism Type 2 | Batten Disease | Mitochondrial DNA Depletion Syndrome 13 | Donnai-Barrow Syndrome | Retinal Degeneration | Hyperlipidemia | Cardiomyopathy, Dilated, 1L | Glaucoma, Congenital | Myelitis, Transverse | B-cell Chronic Lymphocytic Leukemia | Zygomycosis | Nephronophthisis | Central Core Disease | Glycogen Storage Disease | Macular Degeneration | Frontotemporal Dementia | Agoraphobia | Budd-Chiari Syndrome | Hypertriglyceridemia | Persistent Mullerian Duct Syndrome | Aicardi-Goutieres Syndrome | Gastritis, Atrophic | Lichen Sclerosus | C3 Glomerulonephritis | Osteopathia Striata With Cranial Sclerosis | Choroideremia | Optic Neuropathy, Anterior Ischemic | Pseudohypoaldosteronism | Amyloidosis | Dystonia Musculorum Deformans | Gastrointestinal Disorders | Renal Dysplasia | Gray Platelet Syndrome | Dermatitis Herpetiformis | Encephalitis | Familial Cerebral Amyloid Angiopathy | Spondyloarthritis | Sialidosis Type I | Sclerosteosis | Tendinitis | Ameloblastic Carcinoma | Chylomicron Retention Disease | Cavitary Optic Disc Anomalies | Glomerulonephritis, Membranoproliferative | Arrhythmogenic Right Ventricular Cardiomyopathy | Spermatocele | Spinocerebellar Ataxia Type 14 | Muckle-Wells Syndrome | Glaucomatocyclitic Crisis | Narcolepsy | Infantile Neuroaxonal Dystrophy | Holt-Oram Syndrome | Carbamoyl Phosphate Synthetase I Deficiency | Lymphomatoid Granulomatosis | Axenfeld-Rieger Syndrome | Myofibromatosis | Thrombosis | Centronuclear Myopathy | Hemangioendothelioma | Branchiootorenal Syndrome | Cirrhosis | Hypoproteinemia, Hypercatabolic | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | HANAC Syndrome | Spinocerebellar Ataxia Type 7 | Neurodevelopmental Disorders | Smoldering Myeloma | Schizotypal Personality Disorder | Retinal Detachment | Ocular Hypertension | Pure Autonomic Failure | Primary Torsion Dystonia | Optic Nerve Hypoplasia, Bilateral | Loeys-Dietz Syndrome | Hypertension, Portal | Hyperparathyroidism-jaw Tumor Syndrome | Colorectal Adenoma | Osteogenesis Imperfecta Type III | Desbuquois Syndrome | Rhabdomyosarcoma, Embryonal | Avian Influenza | Cannabis Abuse | Panuveitis | Cramp Fasciculation Syndrome | Hemochromatosis Type 1 | Charcot-Marie-Tooth Disease, Type 1A | Mandibuloacral Dysplasia With Type A Lipodystrophy | Nemaline Myopathy 8 | Retinoschisis | Diffuse Mesangial Sclerosis | Glioblastoma | Thyroid Dysgenesis | Nevus | Ichthyosis, X-linked | Conjunctivitis, Allergic | Ischemia | Neuroendocrine Cancer | Diffuse Palmoplantar Keratoderma | Jawad Syndrome | Blepharoconjunctivitis | Carcinoid Tumor | Hennekam Lymphangiectasia-lymphedema Syndrome | Aceruloplasminemia | Wolman Disease | Inflammatory Myofibroblastic Tumor | Mitochondrial Encephalomyopathy | Papulopustular Rosacea | Fetal Akinesia Deformation Sequence | Pineoblastoma | Snyder-Robinson Syndrome | PHARC Syndrome | Renal Hypomagnesemia 3 | Epidermolysis Bullosa Dystrophica | Hypobetalipoproteinemias | Myositis, Focal | Double Outlet Right Ventricle | Open-angle Glaucoma | Nanophthalmos | Kidney Stones | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Smith-Lemli-Opitz Syndrome | Ichthyosis Hystrix, Curth-Macklin Type | Raine Syndrome | 3-M Syndrome | Histiocytic Sarcoma | Lymphoproliferative Disease, X-linked | Charcot-Marie-Tooth Disease Type 3 | Congenital Muscular Dystrophy | Lymphangiomatosis | Fatty Aldehyde Dehydrogenase Deficiency | Hypotension, Orthostatic | Adenoma, Pituitary | Anuria | Mood Disorder | Hepatic Steatosis | Meniere's Disease | Hashimoto Thyroiditis | Spinocerebellar Ataxia Type 6 | Familial Mediterranean Fever | HIBCH Deficiency | Trigonocephaly | Stickler Syndrome | Thin Basement Membrane Disease | Amenorrhea | Infantile Nephropathic Cystinosis | Tinea Versicolor | Pseudoachondroplasia | Thalassemia, Beta | Gerstmann-Straussler-Scheinker Syndrome | Cold Agglutinin Disease | Asplenia | Absence Epilepsy | Glutaric Aciduria Type 3 | Acute Generalized Exanthematous Pustulosis | Obsessive-compulsive Disorder | Multiple Sclerosis | Hemorrhage | Primary Progressive Aphasia | Carbohydrate Metabolism Disorders | Niemann-Pick Disease, Type A | Angioedema | Leukemia | Optic Neuritis | Diabetes Gestational | 3-methylglutaconic Aciduria | Adenomyosis | Astrocytoma, Anaplastic | Behcet's Disease | Vasculitis | Paget's Disease Of The Breast | Hepatic Adenomatosis | Diabetic Neuropathy | Brachydactyly | POEMS Syndrome | Medulloblastoma | Cardiomyopathy, Restrictive | Platelet Disorders | Omenn Syndrome | Epithelial-myoepithelial Carcinoma | Headache | NGLY1 Deficiency | Neonatal Progeroid Syndrome | Pachyonychia Congenita | Leishmaniasis, Cutaneous | Lattice Corneal Dystrophy | Hemophilia | Whipple's Disease | Heterotaxy | Nemaline Myopathy 10 | Myotonic Disorders | Hepatitis A | Lennox-Gastaut Syndrome | Canavan Disease | Spinocerebellar Ataxia Type 5 | Neurocysticercosis | Osmotic Demyelination Syndrome | Amebiasis | Endocarditis | Chordoid Glioma | Charcot-Marie-Tooth Disease Type 4E | Schwartz-Jampel-Aberfeld Syndrome | Chorea-acanthocytosis | Vulvovaginitis | Neurofibroma | Tyrosine Hydroxylase Deficiency | Bursitis | Hyperlipidemia Type V | Otitis Media | Erythema Multiforme | Heterotopic Ossification | Cushing Syndrome | Subcortical Band Heterotopia | Bacterial Meningitis | Papilloma | Waardenburg Syndrome Type 2E | Opisthorchiasis | Neuroectodermal Tumors, Primitive | Juvenile Xanthogranuloma | Scabies | Hemosiderosis | Gingivitis | IgA Deficiency