Alveolar Rhabdomyosarcoma

About the Disease
Rhabdomyosarcoma 2, also known as alveolar rhabdomyosarcoma, is related to embryonal rhabdomyosarcoma and sarcoma. An important gene associated with Rhabdomyosarcoma 2 is PAX7 (Paired Box 7), and among its related pathways/superpathways are Malignant pleural mesothelioma and Endometrial cancer. The drugs Lenograstim and Topotecan have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle, breast and lung, and related phenotypes are alveolar rhabdomyosarcoma and muscle

Common Targets
G2064 | MGMT

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

Other Diseases

Carpenter Syndrome | Otitis Externa | Lymphedema | Deafness, Dystonia, And Cerebral Hypomyelination | Basal Ganglia Cerebrovascular Disease | Pulmonary Tuberculosis | Brenner Tumor | Pontocerebellar Hypoplasia | Jaundice, Obstructive | Ligneous Conjunctivitis | Waldenstrom Macroglobulinemia | Idiopathic Multicentric Castleman Disease | Measles | Niemann-Pick Disease, Type A | Prolactinoma | Dysequilibrium Syndrome | Christianson Syndrome | Gigantism | Leukoencephalopathy, Progressive Multifocal | Leukocyte Adhesion Deficiency | Multisystemic Smooth Muscle Dysfunction Syndrome | Hemoglobinopathies | Pontocerebellar Hypoplasia Type 2 | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Pulmonary Veno-occlusive Disease | Charcot-Marie-Tooth Disease, Type 2C | Bernard-Soulier Syndrome | Thrombosis | Neuroectodermal Tumors, Primitive | Retinal Coloboma | Epidermolysis Bullosa Dystrophica | DiGeorge Syndrome | Colitis | Neurofibromatosis | Opisthorchiasis | Nanophthalmos | Charcot-Marie-Tooth Disease, Type 2 | HANAC Syndrome | Cerebellar Ataxia, Cayman Type | Leigh Syndrome | Bronchitis | Acrodermatitis Enteropathica | Richter's Syndrome | Smith-Lemli-Opitz Syndrome | Goiter, Nodular | Progressive Familial Intrahepatic Cholestasis Type 2 | Tendinopathy | Pneumothorax | Osteomalacia | Vitamin A Deficiency | Stargardt Disease | Postpoliomyelitis Syndrome | Cenani-Lenz Syndactyly Syndrome | Usher Syndrome Type III | Lymphoma Lymphoblastic | Urolithiasis | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Hypohidrotic Ectodermal Dysplasia | B-cell Chronic Lymphocytic Leukemia | Anti-glomerular Basement Membrane Disease | N-acetylglutamate Synthase Deficiency | Cone Dystrophy | Dermatitis | Esthesioneuroblastoma | Hartnup Disease | Traboulsi Syndrome | Intracerebral Hemorrhage | Hemangioendothelioma | Vascular Cognitive Impairment | Takayasu's Arteritis | Optic Neuropathy | Schizencephaly | Charcot-Marie-Tooth Disease Axonal Type 2N | Melanocytic Nevus | Porphyria, Variegate | Huntington's Disease | Anorexia Nervosa | Microphthalmia | Anorchia | Congenital Bilateral Absence Of Vas Deferens | Nephrotic Syndrome Type 1 | Walker-Warburg Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Anencephaly | Ameloblastic Carcinoma | Conduct Disorder | Cerebrotendinous Xanthomatosis | Pontocerebellar Hypoplasia Type 7 | Acute Lymphocytic Leukemia | Cutaneous Lupus Erythematosus | Cardiomyopathy, Restrictive | Cholestasis | Meconium Ileus | Spinocerebellar Ataxia Type 31 | Carcinoma, Transitional Cell | Sarcoma, Alveolar Soft Part | Papulopustular Rosacea | Spinocerebellar Ataxia Type 3 | Duane Retraction Syndrome | Diabetes Gestational | Benign Familial Pemphigus | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Gastritis, Atrophic | Constipation | Pyruvate Kinase Deficiency | Kallmann Syndrome | Von Hippel-Lindau Disease | Benign Familial Infantile Seizures | Spitz Nevus | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Chronic Neutrophilic Leukemia | Otosclerosis | Spondylolisthesis | Apert Syndrome | Metabolic Syndrome | Keratosis | Pulmonary Stenosis | Juvenile Myelomonocytic Leukemia | Aicardi-Goutieres Syndrome | Behcet's Disease | Erdheim-Chester Disease | Rhabdomyosarcoma, Alveolar | Porphyria Cutanea Tarda | Onchocerciasis | Angelman Syndrome | Sarcomatoid Carcinoma Of The Lung | Lymphoma, AIDS-related | Mohr-Tranebjaerg Syndrome | Apparent Mineralocorticoid Excess Syndrome | Cherubism | Twin-to-twin Transfusion Syndrome | Transient Bullous Dermolysis Of The Newborn | Aldosteronism | Mitochondrial Myopathy | Avian Influenza | Gastroenteritis | Periodic Limb Movement Disorder | Arteriosclerosis | Paraganglioma | Autosomal Recessive Spastic Paraplegia Type 35 | Blue Rubber Bleb Nevus Syndrome | Combined Deficiency Of Factor V And Factor VIII | Atrioventricular Septal Defect | Purpura, Thrombotic Thrombocytopenic | Hypotension, Orthostatic | Peters-plus Syndrome | Trimethylaminuria | Genee-Wiedemann Syndrome | Bruck Syndrome | Myotonic Disorders | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Pemphigus Foliaceus | Gnathodiaphyseal Dysplasia | Anal Fissure | Pseudomyxoma Peritonei | Hypoalbuminemia | Hereditary Pyropoikilocytosis | Renal Oncocytoma | Fascioliasis | Charcot-Marie-Tooth Disease Type 4D | Pre-eclampsia | Phenylketonuria | Premature Ejaculation | Delirium | Pancreatitis, Chronic | Urticaria | Spinocerebellar Ataxia Type 21 | Hyperhomocysteinemia | Multiple Sclerosis, Chronic Progressive | Cold-induced Sweating Syndrome | Pierson Syndrome | Depression | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Barrett Esophagus | Neuromyotonia | Hemolytic Anemia | Norrie Disease | Cystinosis | Non-small Cell Lung Cancer | Tendinitis | Long QT Syndrome Type 2 | Hypospadias | Postpartum Depression | Multicystic Renal Dysplasia | Autonomic Neuropathy | Cannabis Abuse | Carpal Tunnel Syndrome | Wilson's Disease | Eosinophilia | Syncope | Myosin Storage Myopathy | Kohlschutter-Tonz Syndrome | Plasma Cell Leukemia | Usher Syndrome | Graft-versus-host Disease | Panuveitis | Microcephalic Primordial Dwarfism | Oculocutaneous Albinism Type 2 | Glycogen Storage Disease Type 1 | Cerebrovascular Disorders | Hodgkin Lymphoma | Presbyopia | Fuchs Dystrophy | Exocrine Pancreatic Insufficiency | Metaphyseal Chondrodysplasia, Schmid Type | Tonsillitis | Sialidosis Type I | Dystrophy, Cone-rod | Arthrogryposis | Bardet-Biedl Syndrome | Hidradenitis Suppurativa | Proctitis | Corneal Neovascularization | Esophageal Motility Disorders | Cardiomyopathy, Hypertrophic | Vertebrobasilar Insufficiency | Fibronectin Glomerulopathy | Loeys-Dietz Syndrome | Reye Syndrome | Amish Infantile Epilepsy Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | T-cell Leukemia | Pityriasis Rubra Pilaris | Ameloblastoma | Succinic Semialdehyde Dehydrogenase Deficiency | Dermatomyositis | Primary Ovarian Insufficiency | Conjunctivitis | Left Ventricular Noncompaction | Scabies | Schindler Disease | Leprosy | Myasthenia Gravis | Hemophagocytic Lymphohistiocytosis | Anodontia | Congenital Heart Defects | Dentinogenesis Imperfecta | Pancytopenia | Insulinoma | Wagner Disease | Stomatitis | Hydrocephalus | Retinal Detachment | Takenouchi-Kosaki Syndrome | Spondylometaphyseal Dysplasia | Lupus Erythematosus | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Knobloch Syndrome | Adult Polyglucosan Body Disease | Bone Giant Cell Tumor | Neuromuscular Disorders | Cystitis, Interstitial | Alopecia Totalis | 5-oxoprolinase Deficiency | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Trichotillomania | Distal Myopathy 2 | Glutaric Aciduria Type 3 | Leukemia-lymphoma, Adult T-cell | Hypertension, Essential | Veno-occlusive Disease | Maternally Inherited Diabetes And Deafness | Whipple's Disease | Benign Familial Neonatal Convulsions | Speech Disorders | Zollinger-Ellison Syndrome | Waardenburg Syndrome Type 1 | Contact Dermatitis | Scapuloperoneal Spinal Muscular Atrophy | Aspartylglycosaminuria | High Molecular Weight Kininogen Deficiency | Neutropenia | Myotonia | Primary Hyperoxaluria Type 1 | Blepharospasm | Spinocerebellar Ataxia Type 13 | Epidermolytic Ichthyosis, Annular | Frontometaphyseal Dysplasia | Malaria, Cerebral | Snyder-Robinson Syndrome | Silicosis | Multifocal Motor Neuropathy | Crigler-Najjar Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Esophageal Carcinoma | Hyperekplexia | Acute Generalized Exanthematous Pustulosis | Renal Tubular Acidosis | Distal Spinal Muscular Atrophy | Pelizaeus-Merzbacher Disease | Holt-Oram Syndrome | Tatton-Brown-Rahman Syndrome | Hypopigmentation | Evans Syndrome | Mitochondrial Cytopathy | Thrombotic Microangiopathy | Ocular Albinism Type 1 | Nijmegen Breakage Syndrome | C3 Glomerulonephritis | Connective Tissue Disorders | Tinea Versicolor | Kernicterus | Hyperparathyroidism-jaw Tumor Syndrome | Feingold Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Cholangitis | Burn-McKeown Syndrome | Rubeosis Iridis | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Sitosterolemia | Exotropia | Platelet Disorders | Atelosteogenesis Type 1 | Nevus | Nail-Patella Syndrome | Ocular Hypertension | Insulin Resistance | Diffuse Intrinsic Pontine Glioma | Glycogen Storage Disease Type 0, Muscle | Lymphoma, B-cell | Focal Cortical Dysplasia Type 2 | Granular Corneal Dystrophy | Acute Myeloid Leukemia | Corticobasal Syndrome | Pancreatitis | Spinocerebellar Ataxia | Spinocerebellar Ataxia Type 10 | Essential Fructosuria | Vertigo | Sweet Syndrome | Otitis Media | Mountain Sickness | Sick Sinus Syndrome | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Oculocutaneous Albinism | Pneumococcal Meningitis | Retinal Dystrophy, Early-onset Severe | Spinocerebellar Ataxia Type 15 | Hereditary Spherocytosis | Hereditary Neuropathy With Liability To Pressure Palsies | Osteomyelitis | Cancer, Brain | Orotic Aciduria | Diabetic Nephropathy | Keratosis, Actinic | Generalized Epilepsy And Paroxysmal Dyskinesia | Myositis, Focal | Chondromyxoid Fibroma | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Epicondylitis | Dominant Optic Atrophy | Dysplastic Nevus | Frontotemporal Dementia | Hypokalemia | Hereditary Folate Malabsorption | Pfeiffer Syndrome | Primary Torsion Dystonia | Sotos Syndrome | Mucolipidosis Type II | Kabuki Syndrome | Ophthalmia, Sympathetic | Uremic Pruritus | Riboflavin Transporter Deficiency Neuronopathy | Retinoblastoma | L-2-Hydroxyglutaric Aciduria | Osteoporosis | Dental Caries | Hyperinsulinemic Hypoglycemia | Neonatal Progeroid Syndrome | Chronic Mucocutaneous Candidiasis | Carney-Stratakis Syndrome | Myocardial Infarction | Hyperprolactinemia | Sensorineural Hearing Loss | 3-methylglutaconic Aciduria Type I | Cryptorchidism | Chondroma | Congenital Bile Acid Synthesis Defect | Leiomyosarcoma | Diabetes Insipidus, Neurogenic | Overactive Bladder | Prune Belly Syndrome | Marfan Syndrome | Acromicric Dysplasia | Mesothelioma, Malignant | Lassa Fever | Hereditary Inclusion Body Myopathy | Neurofibroma | Joubert Syndrome | Neurocysticercosis | Wieacker-Wolff Syndrome | Yellow Fever | Niemann-Pick Disease | Mevalonate Kinase Deficiency | Stiff-man Syndrome | Trichuriasis | Smith-Kingsmore Syndrome | Periodontitis | Galactosialidosis | Van Der Knaap Disease