Disease

Giant Cell Glioblastoma

About the Disease
Giant Cell Glioblastoma, also known as monstrocellular sarcoma, is related to glioma susceptibility 1 and sarcoma, and has symptoms including headache and seizures. An important gene associated with Giant Cell Glioblastoma is MSH2 (MutS Homolog 2), and among its related pathways/superpathways are Apoptotic Pathways in Synovial Fibroblasts and ERK Signaling. The drugs Sargramostim and Molgramostim have been mentioned in the context of this disorder. Affiliated tissues include brain, eye and endothelial, and related phenotypes are Decreased viability and Decreased viability

Common Targets
G673 | MGMT

疾病靶点研报
Giant Cell Glioblastoma

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

Other Diseases

Myelitis | Sleep Disorder | Poirier-Bienvenu Neurodevelopmental Syndrome | Spondylosis | Swine Influenza | Neuroblastoma | Goiter, Nodular | Spinocerebellar Ataxia Type 3 | Meningococcal Meningitis | Hemophilia | Thrombophilia | Spinocerebellar Ataxia Type 15 | Kallmann Syndrome | Pulmonary Tuberculosis | Hypoalbuminemia | Priapism | Usher Syndrome | Macrodactyly | Larsen Syndrome | Immunoproliferative Disorders | Parkinsonism | Porphyria | Papillorenal Syndrome | Antley-Bixler Syndrome | Peeling Skin Syndrome, Acral Type | Primary Torsion Dystonia | Xeroderma Pigmentosum Variant Type | Mitochondrial Cytopathy | Frontometaphyseal Dysplasia | Sialidosis | Dwarfism | Congenital Nystagmus | Camptocormia | Hemolytic Uremic Syndrome, Atypical | Gastroenteritis | Bethlem Myopathy | Acne | Cutaneous Mastocytosis | Diarrhea | Ganglioglioma | Monilethrix | Bacterial Meningitis | Chronic Lymphocytic Leukemia | Cyclic Vomiting Syndrome | Cyst | ADNP Syndrome | Multiple Hamartoma Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Chronic Periodontitis | T-cell Prolymphocytic Leukemia | Purpura, Thrombotic Thrombocytopenic | Lennox-Gastaut Syndrome | 3C Syndrome | Congenital Diaphragmatic Hernia | Asthma | VACTERL Association | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Metachromatic Leukodystrophy | GM2-gangliosidosis AB Variant | Encephalitis | Erectile Dysfunction | Fontaine Progeroid Syndrome | Limb Girdle Muscular Dystrophy | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Fundus Albipunctatus | Lesch-Nyhan Syndrome | Hyperoxaluria | Malignant Peripheral Nerve Sheath Tumor | Marfan Syndrome | Paraganglioma | Pregnancy, Ectopic | Vertebrobasilar Insufficiency | Pycnodysostosis | Yellow Fever | Retinal Telangiectasia | Orthostatic Intolerance | Congenital Bilateral Absence Of Vas Deferens | Hyperbilirubinemia, Neonatal | Carney Triad | Charcot-Marie-Tooth Disease, Type 2A | Retinoblastoma | Congenital Dyserythropoietic Anemia Type 4 | Arthritis, Gouty | Turner's Syndrome | Leprosy | Craniosynostosis | Hypersomnia | Sporadic Inclusion Body Myositis | Glaucoma, Congenital | Gangliosidosis, GM1 | Apraxia | Basal Ganglia Disease | Epidermolytic Ichthyosis, Annular | Hydrocephalus, Normal Pressure | Hepatitis B, Chronic | Venous Insufficiency | Ichthyosis Hystrix, Curth-Macklin Type | Polyradiculopathy | Hepatitis D | Congenital Disorders Of Glycosylation | Oculocutaneous Albinism Type 2 | Charcot-Marie-Tooth Disease Type 4E | Cat Eye Syndrome | Anthrax | Persistent Fetal Circulation | Spondylocostal Dysostosis | Hyperlipidemia | Fibromyalgia | Oculocutaneous Albinism | Hypohidrotic Ectodermal Dysplasia | Nemaline Myopathy 8 | Niemann-Pick Disease, Type B | Rolandic Epilepsy | Platelet Disorders | Lipid Metabolism Disorders | Metatropic Dysplasia | Chronic Thromboembolic Pulmonary Hypertension | Marshall-Smith Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Blomstrand Osteochondrodysplasia | Prader-Willi Syndrome | Iron Deficiency Anemia | Homocystinuria | Exocrine Pancreatic Insufficiency | Multiple Sulfatase Deficiency | Sarcosinemia | Rubeosis Iridis | Lichen Planus | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Retinopathy, Diabetic | Renal Hypouricemia | Hyperferritinemia-cataract Syndrome | Avellino Corneal Dystrophy | Duane Retraction Syndrome | Keratitis-ichthyosis-deafness Syndrome | Chudley-McCullough Syndrome | Myositis, Focal | Carcinoma, Merkel Cell | Syncope | Optic Neuropathy, Anterior Ischemic | Anal Fissure | Hereditary Xerocytosis | Albinism | Congenital Tufting Enteropathy | Onchocerciasis | Peeling Skin Syndrome Type B | Hepatoblastoma | Martsolf Syndrome | Epidermolysis Bullosa Acquisita | Adenoma, Villous | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Nemaline Myopathy | Lymphoproliferative Disorders | Asthma, Nocturnal | Herpes Simplex Dermatitis | Maternally Inherited Diabetes And Deafness | Conduct Disorder | Acquired Partial Lipodystrophy | Saethre-Chotzen Syndrome | Fibrodysplasia Ossificans Progressiva | Joubert Syndrome | Mabry Syndrome | Pontocerebellar Hypoplasia | Schizotypal Personality Disorder | Hereditary Multiple Exostoses | Hypercholesterolemia | Retinitis | PHARC Syndrome | Stickler Syndrome | Hyperkeratosis | Polyomavirus Nephropathy | Bardet-Biedl Syndrome | Sponastrime Dysplasia | Blue Nevus | Sarcoma | Left Ventricular Noncompaction | Erdheim-Chester Disease | Creatine Deficiency Syndrome | Superficial Spreading Melanoma | Idiopathic Pulmonary Fibrosis | Paraplegia | Sorsby Fundus Dystrophy | Tularemia | Primary Lateral Sclerosis | Vaginitis | Neovascular Glaucoma | Hydrocephalus | Myositis | Lassa Fever | Pemphigoid | Pyruvate Decarboxylase Deficiency | Uremic Pruritus | Withdrawal Syndrome | Abetalipoproteinemia | Tetraplegia | Autoimmune Disease | Primary Cutaneous Amyloidosis | Gastroenteritis, Eosinophilic | Goldenhar Syndrome | Emery-Dreifuss Muscular Dystrophy | Dysequilibrium Syndrome | Melanoma | Fraser Syndrome | Smoldering Myeloma | Encephalopathy, Glycine | Cervicitis | Pityriasis Rubra Pilaris | Dupuytren Disease | Oculocutaneous Albinism Type 1 | Hyperuricemic Nephropathy, Familial Juvenile | Reflex Epilepsy | Congenital Afibrinogenemia | Antisocial Personality Disorder | Epidermolytic Hyperkeratosis | Cryoglobulinemia | X-linked Sideroblastic Anemia | Distal Myopathy 2 | Heart Failure | Familial Hypertrophic Cardiomyopathy | Charcot-Marie-Tooth Disease Type 2T | Von Hippel-Lindau Disease | Personality Disorders | Endometrial Hyperplasia | Paget's Disease Of The Breast | Best Macular Dystrophy | Heavy Chain Disease | Wiskott-Aldrich Syndrome | Kleine-Levin Syndrome | Duodenal Atresia | Batten Disease | Leber Hereditary Optic Neuropathy | Seminoma | Carbamoyl Phosphate Synthetase I Deficiency | Cold-induced Sweating Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Chromosome 8q21.11 Deletion Syndrome | Leukoplakia | Sleep Apnea, Obstructive | Noonan Syndrome | Hyperglycemia | Renal-hepatic-pancreatic Dysplasia | Inborn Errors Of Metabolism | Galactosialidosis | Brachydactyly | Open-angle Glaucoma | Hereditary Sensory And Autonomic Neuropathy | Empyema | Multifocal Motor Neuropathy | Nevus | Alpha-thalassemia Myelodysplasia Syndrome | Cryptosporidiosis | Heart Septal Defects | Lymphangioleiomyomatosis | Paronychia | Kohlschutter-Tonz Syndrome | TARP Syndrome | Hyperphosphatasia With Intellectual Disability Syndrome 4 | IgA Nephropathy | Nephrotic Syndrome Type 1 | Myelomeningocele | Jawad Syndrome | Autonomic Neuropathy | Chondroma | Lattice Corneal Dystrophy Type 1 | Multicystic Renal Dysplasia | Vitelliform Macular Dystrophy | Patent Ductus Arteriosus | Maple Syrup Urine Disease | Congenital Heart Block | Ischemia | Intellectual Disability, Autosomal Dominant 5 | Renal Tubular Acidosis | Tumoral Calcinosis | Malonyl-CoA Decarboxylase Deficiency | Peripheral T-cell Lymphoma | Craniometaphyseal Dysplasia | Mohr-Tranebjaerg Syndrome | Asplenia | Polymyositis | Double Outlet Right Ventricle | Cerebral Amyloid Angiopathy | Hyperinsulinism-hyperammonemia Syndrome | Cervical Dystonia | Sclerosing Cholangitis | FG Syndrome | Spinocerebellar Ataxia Type 7 | Uveitis, Anterior | Tyrosinemia Type 1 | Cranial Nerve Disease | Intestinal Hypomagnesemia 1 | Cutaneous T-cell Lymphoma | Twin-to-twin Transfusion Syndrome | Atrial Septal Defect | Bruck Syndrome | Aplasia Cutis Congenita | Familial Retinal Arterial Macroaneurysm | Ectodermal Dysplasia | Donnai-Barrow Syndrome | Senior-Loken Syndrome | Conn Syndrome | Wolman Disease | Ulcerative Colitis | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Asphyxia Neonatorum | Diffuse Mesangial Sclerosis | Glycogen Storage Disease Type 9 | Hidradenitis Suppurativa | Asperger Syndrome | Progressive Myoclonic Epilepsy | Chromosome 16p11.2 Deletion Syndrome | Stevens-Johnson Syndrome | Macular Corneal Dystrophy | Fowler's Syndrome | Facioscapulohumeral Muscular Dystrophy Type 2 | Postpoliomyelitis Syndrome | Multisystemic Smooth Muscle Dysfunction Syndrome | Hypermethioninemia | Corneal Dystrophies, Hereditary | Multiple Sclerosis, Secondary Progressive | Skin Fragility-woolly Hair Syndrome | Vitiligo | Mucolipidosis Type III | Lymphangiomatosis | Urolithiasis | Perivascular Epithelioid Cell Tumor | Hypocalcemia | Agnathia-Otocephaly Complex | Vertigo | Cutis Laxa | Spinocerebellar Ataxia Type 2 | Eiken Syndrome | Hereditary Spastic Paraplegia | Renal Oncocytoma | Meningeal Melanocytoma | Desmosterolosis | Acute Coronary Syndrome | Epithelial-myoepithelial Carcinoma | Waardenburg Syndrome Type 2 | Aceruloplasminemia | Greenberg Dysplasia | Lipodystrophy | Jaundice, Obstructive | Sepiapterin Reductase Deficiency | Aldosterone Synthase Deficiency | Nance-Horan Syndrome | HANAC Syndrome | Teratozoospermia | Mitochondrial Disease | DICER1 Syndrome | DEND Syndrome | Congenital Bile Acid Synthesis Defect | Creatine Deficiency Syndrome Due To AGAT Deficiency | Citrullinemia | Epidermolysis Bullosa | Autosomal Recessive Spastic Paraplegia Type 75 | Vascular Cognitive Impairment | Congenital Hereditary Endothelial Dystrophy Type II | Inflammatory Myofibroblastic Tumor | Neonatal Progeroid Syndrome | Hyperthyroidism | Whipple's Disease | Blepharo-cheilo-odontic Syndrome | Congenital Adrenal Hyperplasia | Traboulsi Syndrome | Splenomegaly | Osteogenesis Imperfecta Type I | Diamond-Blackfan Anemia | Pfeiffer Syndrome | Hemophagocytic Lymphohistiocytosis | Polydactyly | Hyperacusis | Leishmaniasis, Visceral | Pseudohypoparathyroidism Type 1C | Synovitis | Cancer, Lung | Intestinal Pseudo-obstruction | Preaxial Polydactyly | Compartment Syndrome | Van Der Knaap Disease | Medulloblastoma | Anodontia | Facioscapulohumeral Muscular Dystrophy Type 1 | Hemorrhage | Meningioma, Benign | Microphthalmia, Syndromic 7 | Osteopathia Striata With Cranial Sclerosis | Sporadic Hemiplegic Migraine | Delirium | Isobutyryl-CoA Dehydrogenase Deficiency | Eosinophilia | Keratopathy | Anterior Segment Dysgenesis | Giant Axonal Neuropathy | Focal Segmental Glomerulosclerosis | Osteonecrosis Of The Jaw | Ventricular Septal Defect | Von Willebrand Disease | Corneal Edema | Trichuriasis | Neurocutaneous Melanocytosis