Benign Meningioma

About the Disease
Benign Meningioma, also known as meningioma, benign, is related to spinal meningioma and neurofibromatosis, type ii. An important gene associated with Benign Meningioma is NF2 (NF2, Moesin-Ezrin-Radixin Like (MERLIN) Tumor Suppressor), and among its related pathways/superpathways are Regulation of TP53 Activity and Neuroscience. Affiliated tissues include brain, lung and bone, and related phenotypes are Increased cell death in HCT116 cells and homeostasis/metabolism

Common Targets
BRCA2 | CDKN2B | G2099 | TP73 | CASP8 | CD44 | CHFR | FHIT | RARB | DAPK1 | HIC1 | GSTP1 | APC | G672 | CDKN1B | VHL | G472 | MLH1 | CADM1 | RASSF1 | G5728 | TIMP3 | G1029 | CDH13

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

Other Diseases

Pneumococcal Meningitis | AIDS Dementia Complex | Anorchia | Still Disease | Cutaneous Mastocytosis | Spinocerebellar Ataxia Type 13 | Arthritis, Reactive | Non-Hodgkin Lymphoma | Cervical Dystonia | Cardiospondylocarpofacial Syndrome | Otopalatodigital Syndrome Type 2 | Craniofacial Dysostosis | Tay-Sachs Disease | Anti-NMDA Receptor Encephalitis | Ectrodactyly | Seasonal Mood Disorder | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Myelitis | Microphthalmia, Syndromic 7 | Hypoproteinemia, Hypercatabolic | 3-methylglutaconic Aciduria Type I | Cancer, Colon | Dysthymia | Lafora Disease | Myocardial Infarction | Peters-plus Syndrome | Progressive Encephalopathy-optic Atrophy Syndrome | Histoplasmosis | Congenital Torticollis | Charcot-Marie-Tooth Disease Type 2E | Urea Cycle Disorder | Melnick-Needles Syndrome | Succinic Semialdehyde Dehydrogenase Deficiency | Anterior Segment Dysgenesis | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Congenital Central Hypoventilation Syndrome | Paternal Uniparental Disomy Of Chromosome 14 | Rosacea | Cranial Nerve Disease | Facioscapulohumeral Muscular Dystrophy Type 2 | Ganglioneuroma | Citrullinemia | Exotropia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Amish Infantile Epilepsy Syndrome | Fahr Disease | Myopia | Senior-Loken Syndrome | Nephrotic Syndrome | Cousin Syndrome | Liver Diseases | Hereditary Sensory And Autonomic Neuropathy | Congenital Lipoid Adrenal Hyperplasia | Campomelic Dysplasia | Infertility, Male | Retinal Degeneration | Hepatitis E | Myotonia | Rhabdomyosarcoma | Juvenile Hyaline Fibromatosis | Endometritis | Aceruloplasminemia | Coronary Restenosis | Relapsing Polychondritis | Marinesco-Sjogren Syndrome | Psoriasis | Methylmalonic Aciduria And Homocystinuria, CblC Type | Mitochondrial Cytopathy | Xeroderma Pigmentosum Variant Type | Warsaw Breakage Syndrome | Primary Aldosteronism | Urofacial Syndrome | Fibronectin Glomerulopathy | Ganglioglioma | Pompe Disease | Poirier-Bienvenu Neurodevelopmental Syndrome | Pneumonia, Bacterial | Glutaric Aciduria Type 2 | Prune Belly Syndrome | Hemangioendothelioma | Mumps | Nephronophthisis | Spinal Cord Diseases | Arteriosclerosis | Lentigo | Iron Overload | Pterygium | Prostatitis | Molybdenum Cofactor Deficiency | Huntington's Disease-like 2 | Atelosteogenesis Type 2 | Spinocerebellar Ataxia Type 15 | Metanephric Adenoma | Contact Dermatitis | Heavy Chain Disease | Lymphoma | Esotropia | Systemic Lupus Erythematosus | Schwannoma | Congenital Generalized Lipodystrophy | Metachondromatosis | Nestor-Guillermo Progeria Syndrome | Cherubism | Congenital Heart Block | Pulmonary Veno-occlusive Disease | Oculopharyngeal Muscular Dystrophy | Turner's Syndrome | Adams-Oliver Syndrome | Hyperbilirubinemia | Monilethrix | Hemorrhage | Schaaf-Yang Syndrome | Hypokalemia | Wagner Disease | Schizophrenia, Paranoid | Japanese Encephalitis | Nanophthalmos | Erythema Multiforme | Lewy Body Dementia | Tetanus | Lipid Metabolism Disorders | Opisthorchiasis | Smoldering Myeloma | Blepharo-cheilo-odontic Syndrome | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Encephalopathy | Hereditary Spastic Paraplegia | Meningioma | Intermittent Claudication | Hennekam Lymphangiectasia-lymphedema Syndrome | Oculocutaneous Albinism Type 2 | Smith-Magenis Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Familial Hypobetalipoproteinemia | Filariasis | Compartment Syndrome | 3-M Syndrome | Pneumonia, Viral | Nijmegen Breakage Syndrome | Pernicious Anemia | Kernicterus | Tangier Disease | Nicotine Dependence | Spinocerebellar Ataxia Type 5 | Intermittent Explosive Disorder | Neurofibromatosis Type 1 | Thalassemia, Beta | Emery-Dreifuss Muscular Dystrophy | Autonomic Nervous System Disorders | Autonomic Neuropathy | Pemphigus | Ollier Disease | Pituitary Disorders | Renal Tubular Dysgenesis | Inborn Errors Of Metabolism | Cleidocranial Dysplasia | Cystitis | Pemphigus Vulgaris | Unverricht-Lundborg Syndrome | Eosinophilia | Malaria | Silver-Russell Syndrome | Progressive Myoclonic Epilepsy | Feingold Syndrome | Keloid | Encephalocele | Carcinoma, Small Cell | Cardiac Arrest | Haim-Munk Syndrome | Corneal Ulcer | Wilson's Disease | Double Outlet Right Ventricle | Ovarian Sex Cord-stromal Tumor | Posterior Polar Cataract | Lysosomal Acid Lipase Deficiency | Leber Hereditary Optic Neuropathy | Canavan Disease | Autosomal Recessive Congenital Ichthyosis | Neurofibroma | Leiomyoma | Snyder-Robinson Syndrome | Astrocytoma, Anaplastic | KBG Syndrome | Focal Facial Dermal Dysplasia | Spinocerebellar Ataxia Type 20 | Hypercholesterolemia, Familial | Spondylometaphyseal Dysplasia | Neurofibroma, Plexiform | Megaloblastic Anemia | Eczema | Chloridorrhea, Congenital | Hyperinsulinemia | Thrombocytopenia | Short-chain Acyl-CoA Dehydrogenase Deficiency | Hyperandrogenemia | Eclampsia | Amenorrhea | Hypersensitivity Pneumonitis | Cavitary Optic Disc Anomalies | Werner's Syndrome | Kabuki Syndrome | Familial Male-limited Precocious Puberty | Glycogen Storage Disease Type 4 | Pneumonia, Mycoplasma | Pulmonary Vein Stenosis | Hypopigmentation | Erythematotelangiectatic Rosacea | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Subacute Sclerosing Panencephalitis | Birk-Barel Syndrome | Chondrodysplasia Punctata 2, X-linked Dominant | Noonan Syndrome | Anti-glomerular Basement Membrane Disease | Conn Syndrome | Narcolepsy | Reye Syndrome | Hypersensitivity | Epidermolysis Bullosa Acquisita | Netherton Syndrome | Hemosiderosis | Mesothelioma, Malignant | Pseudoexfoliation Syndrome | Parvovirus B19 Infection | CREST Syndrome | Fibrosarcoma | Vitiligo | Myositis | Venous Insufficiency | Perivascular Epithelioid Cell Tumor | Sensory Neuropathy | Blepharospasm | Enhanced S-cone Syndrome | Polyomavirus Nephropathy | Dermatomyositis | Androgenic Alopecia | Sorsby Fundus Dystrophy | Aspergillosis | Down Syndrome | Hypoparathyroidism | Cantu Syndrome | Brooke-Spiegler Syndrome | Chronic Myeloid Leukemia | Lipid Storage Diseases | Sotos Syndrome | Intellectual Disability, Autosomal Dominant 5 | Prader-Willi Syndrome | Osteoporosis-pseudoglioma Syndrome | Kidney Stones | Apraxia | Angioimmunoblastic T-cell Lymphoma | Polymicrogyria | Nephropathy | Platelet Disorders | Acute Leukemia | Usher Syndrome Type II | Gastroschisis | Cryptosporidiosis | Gangliosidosis | Familial Mediterranean Fever | Trigonocephaly | Zygomycosis | Axenfeld-Rieger Syndrome | Hypercholesterolemia | Babesiosis | Wolff-Parkinson-White Syndrome | Chondromyxoid Fibroma | Triple A Syndrome | Pure Red Cell Aplasia | Superficial Spreading Melanoma | Sleep Apnea | Trimethylaminuria | Proopiomelanocortin Deficiency | Polycythemia | Portal Vein Thrombosis | Basal Cell Nevus Syndrome | Hyperferritinemia-cataract Syndrome | Alcoholism | Aarskog-Scott Syndrome | Paroxysmal Nocturnal Hemoglobinuria | Angelman Syndrome | Renal Medullary Carcinoma | Spinal Muscular Atrophy | Medulloblastoma | Prolymphocytic Leukemia | Hypohidrotic Ectodermal Dysplasia | Hyperprolactinemia | Acrodermatitis | Autoimmune Polyendocrinopathy Syndrome Type I | Pituitary Dwarfism | Bruck Syndrome | Porphyria, Acute Intermittent | Osteogenesis Imperfecta Type III | Skin Carcinoma | DRESS Syndrome | Primary Progressive Nonfluent Aphasia | Conjunctivitis, Allergic | Cramp Fasciculation Syndrome | Keratosis | Keratoconjunctivitis | Colitis, Lymphocytic | Azoospermia | Spondyloepiphyseal Dysplasia Tarda, X-linked | Hypertension, Renal | N-acetylglutamate Synthase Deficiency | Hyperostosis | Barakat Syndrome | Gray Platelet Syndrome | Pelvic Inflammatory Disease | Oculocutaneous Albinism Type 1 | Zollinger-Ellison Syndrome | Angiosarcoma | Long QT Syndrome Type 3 | Diabetes Type 2 | Spinal And Bulbar Muscular Atrophy | Bainbridge-Ropers Syndrome | Muscle Wasting | Connective Tissue Disorders | Olmsted Syndrome | Osteonecrosis | Dermatofibrosarcoma | Myofibromatosis | Synovitis | Glutaric Aciduria Type 3 | Epicondylitis | Lymphoma, Mantle Cell | Osteoporosis | Esophageal Motility Disorders | Rotor Syndrome | Malaria, Cerebral | Jalili Syndrome | Carcinoma, Signet Ring Cell | Takotsubo Cardiomyopathy | Myoclonus | Charcot-Marie-Tooth Disease, Type 2 | Cyclic Vomiting Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Congenital Absence Of Vas Deferens | Loeys-Dietz Syndrome Type 4 | Microcephaly, Seizures, And Developmental Delay | Mitochondrial Encephalomyopathy | Hypocalcemia | Waardenburg Syndrome Type 2A | Pre-eclampsia | Learning Disability | Costello Syndrome | Retinopathy Of Prematurity | Behcet's Disease | Carbohydrate Metabolism Disorders | Ghosal Syndrome | Hereditary Mixed Polyposis Syndrome | Pearson Syndrome | Protein C Deficiency | Poretti-Boltshauser Syndrome | Myelomeningocele | Anemia | Pyruvate Decarboxylase Deficiency | LRBA Deficiency | Carpal Tunnel Syndrome | Nicolaides-Baraitser Syndrome | Myosin Storage Myopathy | Charcot-Marie-Tooth Disease Type 2D | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Weill-Marchesani Syndrome | Acrodysostosis | Disseminated Intravascular Coagulation | Cardiomyopathy, Dilated, 1L | McCune-Albright Syndrome | Methylmalonic Acidemia | Knobloch Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Cancer, Skin | Sengers Syndrome | Primrose Syndrome | Bronchiectasis | Hashimoto Thyroiditis | Galloway-Mowat Syndrome | Acute Motor Axonal Neuropathy | Charcot-Marie-Tooth Disease Type 4D | Shwachman-Bodian-Diamond Syndrome | GLUT1 Deficiency Syndrome | Syphilis | Ophthalmia, Sympathetic | Hemochromatosis Type 2 | 3-methylcrotonyl-CoA Carboxylase Deficiency | Yellow Fever | Otitis Media | Diabetes Insipidus | Primary Erythromelalgia | Graves Disease | Ameloblastic Carcinoma | Hypertension, Essential | PASLI Disease | Noonan Syndrome-like Disorder With Loose Anagen Hair | Occipital Neuralgia | Primary Familial Brain Calcification | Fragile X Syndrome | Osteogenesis Imperfecta Type II | Dwarfism | Chanarin-Dorfman Syndrome | Bare Lymphocyte Syndrome