Adenomatoid Tumor

About the Disease
Benign Mesothelioma, also known as mesothelioma, is related to malignant pleural mesothelioma and asbestosis, and has symptoms including coughing and snoring. An important gene associated with Benign Mesothelioma is CALB2 (Calbindin 2), and among its related pathways/superpathways are Keratinization and Cytoskeletal Signaling. The drugs Dexamethasone acetate and Dexamethasone have been mentioned in the context of this disorder. Affiliated tissues include lung, t cells and liver, and related phenotypes are growth/size/body region and digestive/alimentary

Common Targets
G3845 | SPTA1 | DICER1 | FOXP1 | NUTM1 | POLQ | RAD50 | TRAF7 | PTPRB | LRP1B | MED12 | SPEN

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

Other Diseases

Rolandic Epilepsy | Klippel-Feil Syndrome | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Intestinal Pseudo-obstruction | Cleidocranial Dysplasia | Pulmonary Sclerosing Hemangioma | Niemann-Pick Disease, Type C | Blepharophimosis Syndrome | Fibromyalgia | Ichthyosis | Bethlem Myopathy | Prader-Willi Syndrome | Chronic Lymphocytic Leukemia | Dermatomyositis | Gastroenteritis, Eosinophilic | Adenoid Cystic Carcinoma | Lipoma | X-linked Sideroblastic Anemia | Systemic Mastocytosis | Primary Pigmented Nodular Adrenocortical Disease | Cholestasis | Goiter | Adrenal Insufficiency | Glycogen Storage Disease Type 3 | Charcot-Marie-Tooth Disease Type 4B1 | Glioblastoma | Isobutyryl-CoA Dehydrogenase Deficiency | Keratoacanthoma | Hyperhomocysteinemia | Dental Caries | Hyperinsulinism-hyperammonemia Syndrome | Nicotine Dependence | Sarcoma, Endometrial Stromal | Congenital Mirror Movements | Charcot-Marie-Tooth Disease Type 4E | Hypercholesterolemia, Familial | Vestibular Disease | Osteogenesis Imperfecta Type III | Behcet's Disease | Porphyria, Acute Intermittent | Diastrophic Dysplasia | Progressive Encephalopathy-optic Atrophy Syndrome | Hypertriglyceridemia | Generalized Epilepsy With Febrile Seizures Plus | Gaucher Disease | Basal Ganglia Cerebrovascular Disease | Dupuytren Disease | Genitopatellar Syndrome | Aicardi-Goutieres Syndrome | Leukemia-lymphoma, Adult T-cell | Anorectal Malformations | Charcot-Marie-Tooth Disease Type 3 | Menetrier Disease | Restrictive Dermopathy | Trichomegaly | Polydactyly | Hypertrophy | Phenylketonuria | Cardiomyopathy, Hypertrophic | Acute Chest Syndrome | Postaxial Polydactyly | 3-methylglutaconic Aciduria | Familial Partial Lipodystrophy | Kernicterus | Rickets | Cardiomyopathy, Restrictive | Cardiospondylocarpofacial Syndrome | Primary Torsion Dystonia | Cantu Syndrome | Cerebrotendinous Xanthomatosis | Cranial Nerve Disease | Aldosterone Deficiency | Primary Progressive Aphasia | Spinocerebellar Ataxia Type 31 | Hyperostosis | Glioblastoma Multiforme | Intracerebral Hemorrhage | Congestive Heart Failure | Hypertension | Lymphangioma | Cholera | Glycogen Storage Disease Type 1a | Cryptosporidiosis | Lymphedema-distichiasis Syndrome | Cohen Syndrome | Juvenile Myoclonic Epilepsy | Lichen Sclerosus | Proopiomelanocortin Deficiency | Fibrosarcoma | Meier-Gorlin Syndrome | Hyperparathyroidism-jaw Tumor Syndrome | Niemann-Pick Disease, Type B | Spinocerebellar Ataxia Type 2 | Sarcosinemia | Tularemia | Opisthorchiasis | Carcinoid Syndrome | Pfeiffer Syndrome | Glutathione Synthetase Deficiency | Bainbridge-Ropers Syndrome | Familial Male-limited Precocious Puberty | Ulcerative Colitis | Congenital Tufting Enteropathy | Calcium Pyrophosphate Deposition Disease | Hereditary Hemorrhagic Telangiectasia | Basal Ganglia Disease | Platelet Disorders | Intermittent Explosive Disorder | Vogt-Koyanagi-Harada Syndrome | Shock, Cardiogenic | Diabetes Mellitus, Transient Neonatal | Rift Valley Fever | Gilbert Syndrome | Muckle-Wells Syndrome | Dentinogenesis Imperfecta | Noonan Syndrome-like Disorder With Loose Anagen Hair | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Paroxysmal Nocturnal Hemoglobinuria | Pitt-Hopkins Syndrome | Familial Hypobetalipoproteinemia | Pulverulent Zonular Cataract | Glycogen Storage Disease Type 1b | Lafora Disease | Zollinger-Ellison Syndrome | Autosomal Recessive Spastic Paraplegia Type 35 | Cryopyrin-associated Periodic Syndromes | Corneal Neovascularization | Thrombotic Microangiopathy | Frontotemporal Dementia | Fucosidosis | Hypertensive Retinopathy | Autosomal Recessive Bestrophinopathy | HELLP Syndrome | Choroiditis | Spondylocostal Dysostosis | Urethritis | Frontometaphyseal Dysplasia | Porphyria, Variegate | Stevens-Johnson Syndrome | Adenomatoid Tumor | Protein S Deficiency | Adenoma, Pleomorphic | Gnathodiaphyseal Dysplasia | Monilethrix | Myelomeningocele | Miyoshi Myopathy | Epilepsy Of Infancy With Migrating Focal Seizures | Heterotaxy | Lymphoproliferative Disorders | Progressive Familial Intrahepatic Cholestasis | Vertebrobasilar Insufficiency | Autoimmune Polyendocrine Syndrome | Lipid Metabolism Disorders | Autonomic Neuropathy | Adenomyosis | Orotic Aciduria | Hyperlipidemia | Aceruloplasminemia | Rheumatoid Arthritis | Wiedemann-Steiner Syndrome | Niemann-Pick Disease, Type A | Hemimegalencephaly | Basal Ganglia Disease, Biotin-responsive | Blepharo-cheilo-odontic Syndrome | Esophageal Adenocarcinoma | Branchiootorenal Syndrome | Blepharospasm | Schizotypal Personality Disorder | Palsy, Cerebral | Lamellar Ichthyosis | Purpura, Thrombotic Thrombocytopenic | Neurofibromatosis | Spinocerebellar Ataxia Type 21 | Stomatitis | Lipodystrophy | Wagner Disease | IgA Deficiency | Congenital Primary Aphakia | Leiomyoma | Vitamin D Deficiency | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Granular Corneal Dystrophy | Tylosis With Esophageal Cancer | Benign Familial Infantile Seizures | Extramammary Paget's Disease | Larsen Syndrome | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Spondyloepiphyseal Dysplasia Tarda, X-linked | Hypertension, Essential | Primary Ovarian Insufficiency | Spitz Nevus | Intestinal Hypomagnesemia 1 | Atelosteogenesis Type 1 | Autosomal Recessive Spastic Paraplegia Type 54 | 3-methylcrotonyl-CoA Carboxylase Deficiency | Tendinitis | Androgen Insensitivity | NGLY1 Deficiency | Peripheral Neuropathy | Mannosidase Deficiency Diseases | Fukuyama Congenital Muscular Dystrophy | Osteomyelitis | Chondrodysplasia Punctata | Hepatitis A | Metachromatic Leukodystrophy | Tinea | Oligodendroglioma | Subcortical Band Heterotopia | Cryptococcal Meningitis | Paronychia | Dubin-Johnson Syndrome | Spinocerebellar Ataxia Type 6 | Hereditary Spastic Paraplegia | Fascioliasis | Duodenal Atresia | Poikiloderma With Neutropenia | Hyperoxaluria | Hyperthermia, Malignant | Ollier Disease | Gallstones | Colitis, Lymphocytic | Polymyositis | Esotropia | Marshall-Smith Syndrome | Primary Progressive Nonfluent Aphasia | Nijmegen Breakage Syndrome | Tinea Versicolor | Gingivitis | Congenital Aniridia | Urofacial Syndrome | Rhabdoid Tumor | DRESS Syndrome | Microtia | Asthma | Danon Disease | Cartilage Disorders | Anthrax | Hypertension, Renovascular | Tremor | Transient Bullous Dermolysis Of The Newborn | Conn Syndrome | Temporal Lobe Epilepsy | Pyruvate Dehydrogenase Deficiency | Diffuse Palmoplantar Keratoderma | Hemochromatosis Type 2 | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Sarcomatoid Carcinoma Of The Lung | Neural Tube Defect | Polycythemia Vera | Esophageal Carcinoma | Situs Inversus | Dementia | Ichthyosis Hystrix, Curth-Macklin Type | Cole-Carpenter Syndrome | Craniofacial Dysostosis | Spina Bifida | Histoplasmosis | Spinocerebellar Ataxia Type 8 | Mucolipidosis Type III | Dystonia-parkinsonism, X-linked | Kindler Syndrome | Sertoli Cell-only Syndrome | Congenital Sodium Diarrhea | Peutz-Jeghers Syndrome | Primary Cutaneous Amyloidosis | Rhinitis | Eating Disorder | Blue Rubber Bleb Nevus Syndrome | Retinitis | Congenital Central Hypoventilation Syndrome | Metanephric Adenoma | Alexander Disease | Adenoma, Villous | Hypogammaglobulinemia | Hypohidrotic Ectodermal Dysplasia, X-linked | Ornithine Transcarbamylase Deficiency | Huntington's Disease | Keratosis, Seborrheic | Chanarin-Dorfman Syndrome | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Hyperuricemic Nephropathy, Familial Juvenile | Inborn Errors Of Metabolism | Amblyopia | Primrose Syndrome | Granuloma Annulare | Lymphoma, Follicular | Camurati-Engelmann Disease | Glycogen Storage Disease Type 4 | Osteochondrosis | Leukoplakia | Familial Retinal Arterial Macroaneurysm | Hyperkalemic Periodic Paralysis | Spinocerebellar Ataxia Type 20 | Progressive Osseous Heteroplasia | Bronchitis | Epicondylitis | Chordoid Glioma | Sorsby Fundus Dystrophy | Alveolar Capillary Dysplasia | Obesity, Morbid | Thromboembolism | Treacher Collins Syndrome | Kaposi Sarcoma | Peeling Skin Syndrome, Acral Type | Spinal And Bulbar Muscular Atrophy | Mohr-Tranebjaerg Syndrome | Amenorrhea | Otosclerosis | Palmoplantar Keratoderma | DiGeorge Syndrome | Venous Insufficiency | Herpes Simplex Dermatitis | Malonyl-CoA Decarboxylase Deficiency | Sponastrime Dysplasia | Avian Influenza | Vitreoretinal Degeneration, Snowflake Type | Osteoporosis | Hypercalciuria | Dysferlinopathy | Chronic Thromboembolic Pulmonary Hypertension | Iron Metabolism Disorders | Epidermodysplasia Verruciformis | Epidermolysis Bullosa | Keratoconjunctivitis | Chondroma | Mast Cell Leukemia | Tetanus | Hemorrhage | Prolactinoma | Ophthalmoplegia | Optic Nerve Diseases | Trichorhinophalangeal Syndrome | Myelodysplasia | Cerebral Cavernous Malformations | Paraplegia | Polymicrogyria | Barakat Syndrome | Pycnodysostosis | Thrombocytopenia | Charcot-Marie-Tooth Disease Type 2T | Migraine | X-linked Myotubular Myopathy | Wolcott-Rallison Syndrome | Osteosarcoma | Congenital Myasthenic Syndrome | Meconium Ileus | Erysipelas | Congenital Adrenal Hyperplasia | Lyme Disease | Growth Hormone Excess | Kidney Stones | Blepharoconjunctivitis | Retinal Coloboma | Fuchs Heterochromic Iridocyclitis | Esophagitis, Eosinophilic | Angioedema | Hyperammonemia | Postpartum Depression | Cardiomyopathy, Dilated, 1L | Common Variable Immunodeficiency | Coffin-Siris Syndrome | Antisynthetase Syndrome | Mumps | Neuropathy | Usher Syndrome Type II | Dengue Hemorrhagic Fever | Neuroma | Spondyloperipheral Dysplasia | Megalencephaly | Multiple Epiphyseal Dysplasia | PHARC Syndrome | Fibrillation, Atrial | Botulism | Ileitis | Bietti Crystalline Dystrophy | Oculopharyngeal Muscular Dystrophy | Multiple Myeloma | Bruck Syndrome | Fabry's Disease | Osteogenesis Imperfecta Type V | Hypoparathyroidism | Amebiasis | Intellectual Disability, Autosomal Dominant 5 | Spinocerebellar Ataxia | Pigment Dispersion Syndrome | Cutaneous Mastocytosis | Relapsing Polychondritis | Brugada Syndrome 1 | Steel Syndrome | 3-methylglutaconic Aciduria Type IV | Snyder-Robinson Syndrome | Von Willebrand Disease | Synpolydactyly | Acanthosis Nigricans | Usher Syndrome | Cutaneous Angiosarcoma | Cataract | Nager Acrofacial Dysostosis | Nanophthalmos