Disease

Pleomorphic Xanthoastrocytoma

About the Disease
Pleomorphic Xanthoastrocytoma, also known as pxa, is related to glioma susceptibility 1 and malignant astrocytoma, and has symptoms including seizures An important gene associated with Pleomorphic Xanthoastrocytoma is TP53 (Tumor Protein P53), and among its related pathways/superpathways are "Cell Cycle, Mitotic" and Prolactin Signaling. The drugs Dabrafenib and Trametinib have been mentioned in the context of this disorder. Affiliated tissues include brain, eye and temporal lobe, and related phenotypes are neoplasm and normal

Common Targets
RPTOR | NOTCH3 | FANCD2 | ETV4 | CSF1R | RARA | RAD52 | CHEK1 | NUP93 | CDK4 | G673 | CDKN2B | TRRAP | PPP2R1A | G1029 | G4851 | PDGFRB | ARID2 | NOTCH4 | ROS1 | XPO1 | TBX3 | FLT4 | G7157 | GATA2 | G999 | SMARCA4 | MRE11 | GSK3B | MEN1 | FANCI | RAF1 | G2033 | FGFR4 | FGF19 | FGF23 | CCNE1 | G4233 | DOT1L | VCP | PBRM1 | NF1 | FANCA | RUNX1 | MGMT | LRP1B | NOTCH2 | PARP4 | ARID1A | G2146 | G3845 | MSH6 | PIK3CG | RNF43 | G472 | KDM5A | FANCM | MED12

疾病靶点研报
Pleomorphic xanthoastrocytoma

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

Other Diseases

Congenital Tufting Enteropathy | Congenital Bilateral Absence Of Vas Deferens | Loeys-Dietz Syndrome | Delayed Sleep Phase Syndrome | Peritonitis | Abetalipoproteinemia | Adrenomyeloneuropathy | Aarskog-Scott Syndrome | Arteriosclerosis | Glycogen Storage Disease Type 4 | Major Depression | Posterior Polar Cataract | Adenomyosis | Multicentric Carpotarsal Osteolysis Syndrome | Aldosterone Synthase Deficiency | Spondylometaphyseal Dysplasia | Klinefelter Syndrome | Teratozoospermia | Alzheimer Disease, Late Onset | Delirium | Gyrate Atrophy Of The Choroid And Retina | CHOPS Syndrome | Persistent Hyperplastic Primary Vitreous | Familial Episodic Pain Syndrome | Hyperthermia, Malignant | Dementia, Vascular | Glomerulonephritis, Membranoproliferative | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Diabetes Gestational | Polymicrogyria | Osteopathia Striata With Cranial Sclerosis | Fibrillation, Atrial | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Combined Deficiency Of Factor V And Factor VIII | Hepatopulmonary Syndrome | Shprintzen-Goldberg Syndrome | X-linked Charcot-Marie-Tooth Disease | Neurodermatitis | Salla Disease | Lymphedema | Seizures-scoliosis-macrocephaly Syndrome | Orotic Aciduria | Spermatocele | Multisystemic Smooth Muscle Dysfunction Syndrome | Leukocyte Adhesion Deficiency | Gestational Trophoblastic Disease | Pearson Syndrome | Charcot-Marie-Tooth Disease Type 4 | Cerebrotendinous Xanthomatosis | Marfan Syndrome | Ebstein Anomaly | Whipple's Disease | Cancer, Skin | Dwarfism | Supravalvular Aortic Stenosis | WAGR Syndrome | Triphalangeal Thumb-polysyndactyly Syndrome | Fundus Albipunctatus | Trichomegaly | Phenylketonuria | Lafora Disease | Vascular Cognitive Impairment | Lipoma | Epidermolysis Bullosa Simplex | Antisynthetase Syndrome | Inflammatory Joint Disease | Ovarian Sex Cord-stromal Tumor | Hypoglycemia | Inflammatory Myofibroblastic Tumor | Sick Sinus Syndrome 1 | Sjogren Syndrome | Goiter, Nodular | Macrophage Activation Syndrome | Vitamin B12 Deficiency | Cheilitis | Roberts Syndrome | Hypertelorism | Interstitial Lung Diseases | Agranulocytosis | Hemorrhoids | Kawasaki Disease | Facioscapulohumeral Muscular Dystrophy Type 1 | Alopecia | Charcot-Marie-Tooth Disease Type 2T | Nager Acrofacial Dysostosis | Language Disorders | Charcot-Marie-Tooth Disease, Type 2C | Congenital Lipoid Adrenal Hyperplasia | Acute Lung Injury | Schindler Disease | Erysipelas | Glycogen Storage Disease Type 0, Muscle | Hypoalbuminemia | Pneumonia, Bacterial | Dupuytren Disease | Fontaine Progeroid Syndrome | Spinocerebellar Ataxia Type 42 | Impetigo | Walker-Warburg Syndrome | NDH Syndrome | Sturge-Weber Syndrome | Waardenburg Syndrome Type 2 | Hemimegalencephaly | Hemorrhagic Disorders | Mucolipidosis | Hypotonia-cystinuria Syndrome | Carcinoma In Situ | Arthritis, Gouty | Pantothenate Kinase-associated Neurodegeneration | Gigantism | Niemann-Pick Disease, Type C | Cardiofaciocutaneous Syndrome | Superficial Spreading Melanoma | Hemangioma | Charcot-Marie-Tooth Disease Type 4E | Esophagitis | Pseudohypoparathyroidism Type 1A | Glycogen Storage Disease Type 0 | Neuromyotonia | Richter's Syndrome | Ehlers-Danlos Syndrome | Prediabetes | Aplastic Anemia | Jawad Syndrome | Osteonecrosis | Encephalitis, Tick-borne | Peripheral Neuropathy | Leukoplakia, Oral | Amyloidosis | Familial Advanced Sleep Phase Syndrome | Charcot-Marie-Tooth Disease Axonal Type 2N | Avian Influenza | Inflammatory Myopathy | GLUT1 Deficiency Syndrome | Herpes Genitalis | Congenital Afibrinogenemia | Chronic Enteropathy Associated With SLCO2A1 Gene | Pelizaeus-Merzbacher Disease | Photosensitivity | Vitreoretinal Degeneration, Snowflake Type | Multiple Hamartoma Syndrome | Cutis Laxa | Paget's Disease Of The Breast | Wieacker-Wolff Syndrome | Johanson-Blizzard Syndrome | Papillorenal Syndrome | Charcot-Marie-Tooth Disease Type 4D | Renal Dysplasia | Pulmonary Sclerosing Hemangioma | Eczema | Ovarian Hyperstimulation Syndrome | Erythrokeratodermia Variabilis | DEND Syndrome | Hemolytic Uremic Syndrome | VEXAS Syndrome | Spondylocostal Dysostosis | Communication Disorders | Syphilis | Osteogenesis Imperfecta Type I | Alstrom Syndrome | Hypoproteinemia, Hypercatabolic | Seizures | Cousin Syndrome | Thyroid Dysgenesis | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Varicocele | Cancer, Bladder | Pneumothorax | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Bullous Pemphigoid | Adenylosuccinate Lyase Deficiency | Antithrombin III Deficiency | Chronic Thromboembolic Pulmonary Hypertension | Neuropathy | Transcobalamin Deficiency | Bacterial Meningitis | Withdrawal Syndrome | Usher Syndrome | Seborrheic Dermatitis | Insulinoma | Endometritis | Parkinson's Disease | Focal Facial Dermal Dysplasia | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Neurofibrosarcoma | Genee-Wiedemann Syndrome | Miyoshi Myopathy | Epidermolytic Palmoplantar Keratoderma | Takayasu's Arteritis | Polycystic Kidney, Autosomal Recessive | Paracoccidioidomycosis | Geleophysic Dysplasia | Smoldering Myeloma | Neovascular Glaucoma | Cutaneous Mastocytosis | Usher Syndrome Type III | Epidermolysis Bullosa | Granular Corneal Dystrophy | B-cell Chronic Lymphocytic Leukemia | Myopia | Otitis Media | Hypertrophy | Lupus Erythematosus | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Alazami Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Graves Disease | Arts Syndrome | Cutaneous Angiosarcoma | Short-chain Acyl-CoA Dehydrogenase Deficiency | Cryptococcal Meningitis | Thrombosis | Wagner Disease | Retinal Diseases | Beta-Propeller Protein-associated Neurodegeneration | Epithelial-myoepithelial Carcinoma | Renal Failure | Dystonia Musculorum Deformans | Hyperparathyroidism-jaw Tumor Syndrome | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Glycogen Storage Disease Type 1b | Myelofibrosis | Hyperinsulinemic Hypoglycemia | Retinal Dystrophy | Reticular Dysgenesis | Congenital Ichthyosiform Erythroderma | Goiter | Thrombocytopenia | Lymphangioleiomyomatosis | Infantile Liver Failure Syndrome 1 | Borderline Personality Disorder | Multiple Myeloma | Carcinoid Tumor | Acute Chest Syndrome | Essential Fructosuria | Usher Syndrome Type IIC | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Lassa Fever | Low Tension Glaucoma | Chromosome 5q Deletion Syndrome | Hepatitis, Alcoholic | Traboulsi Syndrome | Tularemia | Jalili Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Necrobiosis Lipoidica | Spinocerebellar Ataxia Type 28 | Non-bullous Congenital Ichthyosiform Erythroderma | Coronary Heart Disease | Ileitis | Heroin Dependence | Antley-Bixler Syndrome | Trichuriasis | Monilethrix | Thyroid Dyshormonogenesis | Transthyretin-related Amyloidosis | Tenosynovial Giant Cell Tumor | Autoimmune Hemolytic Anemia | Neuroectodermal Tumors, Primitive | Fibrosarcoma | Amblyopia | L-2-Hydroxyglutaric Aciduria | Von Willebrand Disease | Epilepsy | Waardenburg Syndrome Type 4 | Leri-Weill Dyschondrosteosis | Tuberculous Meningitis | Otosclerosis | Hypermethioninemia | Sepiapterin Reductase Deficiency | Botulism | Leukemia-lymphoma, Adult T-cell | Diabetes Type 1 | Hypotrichosis | Achromatopsia | Hypertension, Renovascular | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Seminoma | Arthritis | Anti-NMDA Receptor Encephalitis | Hartsfield Syndrome | Cushing Syndrome | Acne | Pseudohermaphroditism | Neutropenia | Hypospadias | Polyarteritis Nodosa | Arrhythmogenic Right Ventricular Cardiomyopathy | Hypermetropia | Bipolar Disorder | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Cardiomyopathy, Dilated, 1L | Deafness, Dystonia, And Cerebral Hypomyelination | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Wilson's Disease | Metachondromatosis | Congenital Heart Defects | Renal Hypouricemia | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Encephalocele | Hyperlipidemia Type V | Epidermolysis Bullosa Simplex, Generalized | Erythropoietic Protoporphyria | Stickler Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Peyronie's Disease | Hydrocephalus | Liebenberg Syndrome | B-cell Prolymphocytic Leukemia | Neuronal Ceroid Lipofuscinosis | Batten Disease | Li-Fraumeni Syndrome | Placenta Previa | Imerslund-Grasbeck Syndrome | Sleep Apnea, Obstructive | T-cell Chronic Lymphocytic Leukemia | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Rickets | Diabetes | Fetal Alcohol Syndrome | Schizophrenia, Paranoid | Spinocerebellar Ataxia Type 23 | Early Infantile Epileptic Encephalopathy 1 | Micro Syndrome | Leber Hereditary Optic Neuropathy | Tietze Syndrome | Ophthalmoplegia | Primary Carnitine Deficiency | Spinocerebellar Ataxia Type 8 | Polycystic Ovary Syndrome | Desmosterolosis | Subacute Sclerosing Panencephalitis | Schamberg Disease | Spondylo-ocular Syndrome | Schaaf-Yang Syndrome | Colon Adenoma | Fibromuscular Dysplasia | Spondyloepiphyseal Dysplasia Tarda, X-linked | Chondrodysplasia Punctata 2, X-linked Dominant | Disseminated Intravascular Coagulation | Diabetes Insipidus, Neurogenic | Pycnodysostosis | Lipid Storage Myopathy | Familial Male-limited Precocious Puberty | Thanatophoric Dysplasia | Familial Pheochromocytoma-paraganglioma | Urofacial Syndrome | Basal Ganglia Cerebrovascular Disease | Osmotic Demyelination Syndrome | Thyroiditis, Autoimmune | Palmoplantar Keratoderma | Vulvovaginitis | Chronic Neutrophilic Leukemia | Erythema Nodosum | Hepatic Steatosis | Cholelithiasis | Diabetic Macular Edema | Treacher Collins Syndrome | Meier-Gorlin Syndrome | Saul-Wilson Syndrome | MIRAGE Syndrome | Meniere's Disease | Hypertension, Pulmonary | Metachromatic Leukodystrophy | Periodontitis | Glucagonoma | Nemaline Myopathy 10 | Hyperprolactinemia | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Dermatomyositis | Nephrocalcinosis | Joubert Syndrome | X-linked Creatine Transporter Deficiency | Rift Valley Fever | Nephrotic Syndrome Type 1 | Acute Anterior Uveitis | Sulfite Oxidase Deficiency | Mitochondrial Myopathy | Cyclic Vomiting Syndrome | Epiphyseal Chondrodysplasia, Miura Type | Chloridorrhea, Congenital | Nasodigitoacoustic Syndrome | Pierson Syndrome | Cellulitis | Acanthosis Nigricans | Mandibuloacral Dysplasia With Type A Lipodystrophy | Tylosis With Esophageal Cancer | Meningococcal Meningitis | Tyrosinemia Type 2 | Carpal Tunnel Syndrome | Biotinidase Deficiency | Congenital Disorders Of Glycosylation Type II | Panuveitis | Hereditary Folate Malabsorption | Swine Influenza | Gaucher Disease | Epithelioid Hemangioma | Alpha-thalassemia Myelodysplasia Syndrome | Chronic Beryllium Disease | Hyperinsulinemia