Disease

Cutaneous Angiosarcoma

About the Disease
Skin Angiosarcoma, also known as angiosarcoma of skin, is related to angiosarcoma of the scalp and fanconi anemia, complementation group e. An important gene associated with Skin Angiosarcoma is SNRK (SNF Related Kinase). The drugs Nivolumab and Propranolol have been mentioned in the context of this disorder. Affiliated tissues include skin, breast and lymph node.

Common Targets
RBM10 | G4609 | Tubulin | G5243 | G3845

疾病靶点研报
Cutaneous Angiosarcoma

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

Other Diseases

Tardive Dyskinesia | Fascioliasis | Huntington's Disease | Congenital Hereditary Endothelial Dystrophy Type I | Multiple System Atrophy | Hepatic Veno-occlusive Disease | Postpartum Depression | Charcot-Marie-Tooth Disease Type 2D | Kabuki Syndrome | Botulism | Disseminated Intravascular Coagulation | Myoclonus-dystonia Syndrome | CEDNIK Syndrome | Meningitis | Mevalonate Kinase Deficiency | Antisynthetase Syndrome | Pontocerebellar Hypoplasia Type 7 | Astrocytoma | Hypohidrotic Ectodermal Dysplasia | Cholesteryl Ester Storage Disease | Kleine-Levin Syndrome | Neurocutaneous Syndromes | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Hyperglycemia | Familial Male-limited Precocious Puberty | Congenital Primary Aphakia | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Fanconi Anemia | Analgesia | Leukoplakia | Diabetes Insipidus | Intermittent Explosive Disorder | Spinocerebellar Ataxia | Bicuspid Aortic Valve | Giant Cell Glioblastoma | Craniosynostosis | Cocaine-Related Disorders | Riboflavin Transporter Deficiency Neuronopathy | Leri-Weill Dyschondrosteosis | Esthesioneuroblastoma | Migraine | Glycogen Storage Disease Type 0, Muscle | Sponastrime Dysplasia | Long QT Syndrome Type 1 | Progressive Familial Intrahepatic Cholestasis Type 1 | Renal Medullary Carcinoma | Postaxial Polydactyly | Aldosterone Deficiency | Monilethrix | Shwachman-Bodian-Diamond Syndrome | Leigh Syndrome | Carney-Stratakis Syndrome | Raynaud Phenomenon | Benign Familial Infantile Seizures | Eclampsia | Papillorenal Syndrome | Coronary Artery Disease | Vasculitis | Autosomal Recessive Spastic Paraplegia Type 75 | Hyperphenylalaninemia | Spondylo-ocular Syndrome | Supravalvular Aortic Stenosis | Inflammatory Myopathy | Greenberg Dysplasia | Erythema Nodosum | Kaposiform Hemangioendothelioma | Osmotic Demyelination Syndrome | Calcium Pyrophosphate Deposition Disease | AIDS Dementia Complex | Cramp Fasciculation Syndrome | Congenital Dysfibrinogenemia | Sitosterolemia | Waardenburg Syndrome Type 1 | Progressive Familial Intrahepatic Cholestasis Type 2 | Bethlem Myopathy | Otosclerosis | Arthritis | Opisthorchiasis | Vertigo | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Chronic Granulomatous Disease, X-linked | Adenoma, Villous | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Postpoliomyelitis Syndrome | Thymoma, Malignant | Anorectal Malformations | Kashin-Beck Disease | Agnathia-Otocephaly Complex | Early Infantile Epileptic Encephalopathy 13 | Premenstrual Syndrome | Familial Cerebral Amyloid Angiopathy | Fukuyama Congenital Muscular Dystrophy | Angioedema | Blastoma, Pleuropulmonary | Thyrotoxic Periodic Paralysis | Chromosome 16p11.2 Deletion Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Dysequilibrium Syndrome | Dermatitis | Usher Syndrome Type IIC | Ichthyosis Bullosa Of Siemens | Lipid Metabolism Disorders | Osteomyelitis | Hereditary Folate Malabsorption | Cutaneous Mastocytosis | Retinopathy, Diabetic | Hemolytic Anemia | Impulse Control Disorder | Harlequin Ichthyosis | Hypertensive Retinopathy | Sick Sinus Syndrome | Aarskog-Scott Syndrome | Parapsoriasis | Hemangioendothelioma | Diffuse Mesangial Sclerosis | Anorchia | Cantu Syndrome | Cartilage Disorders | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Takotsubo Cardiomyopathy | Polyarteritis Nodosa | Encephalitis, Tick-borne | Anovulation | Yellow Fever | Coffin-Lowry Syndrome | Hypogammaglobulinemia | Porphyria, Variegate | Sleep Apnea | Allan-Herndon-Dudley Syndrome | Non-Hodgkin Lymphoma | Fucosidosis | Hyperlipidemia | Spinocerebellar Ataxia Type 21 | Cervical Dystonia | Fibronectin Glomerulopathy | Acromegaly | Salla Disease | Rothmund-Thomson Syndrome | Hypertension | Polyomavirus Nephropathy | Walker-Warburg Syndrome | Teratozoospermia | Benign Recurrent Intrahepatic Cholestasis 1 | Wieacker-Wolff Syndrome | Pontocerebellar Hypoplasia Type 2 | Granular Corneal Dystrophy Type 1 | Pathological Gambling | Traboulsi Syndrome | Spinocerebellar Ataxia Type 16 | Idiopathic Multicentric Castleman Disease | Blepharoconjunctivitis | Diabetes Mellitus, Transient Neonatal | Malignant Fibrous Histiocytoma | Antenatal Bartter Syndrome Type 1 | Prader-Willi Syndrome | Parkinsonism | Obsessive-compulsive Disorder | Melnick-Needles Syndrome | Enhanced S-cone Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Genitopatellar Syndrome | Paroxysmal Kinesigenic Dyskinesia | Ameloblastoma | Oculocutaneous Albinism | Colitis, Lymphocytic | Ataxia-ocular Apraxia 2 | Impetigo | Esophageal Carcinoma | Congenital Ichthyosiform Erythroderma | Lymphoproliferative Disease, X-linked | Panniculitis | Intracranial Hypertension | Hyperthermia, Malignant | Angioedema, Hereditary | Martsolf Syndrome | Neurogenic Bladder | Schindler Disease | Cardiomyopathy, Restrictive | Perivascular Epithelioid Cell Tumor | Branchiootorenal Syndrome | Urea Cycle Disorder | Cutaneous Angiosarcoma | Niemann-Pick Disease, Type C | Myoclonic Epilepsy With Ragged Red Fibers | Leishmaniasis, Cutaneous | Wolfram Syndrome 2 | Sweet Syndrome | Congenital Diaphragmatic Hernia | Chordoid Glioma | Liver Failure | Spermatocele | Epilepsy, Generalized | Exotropia | Mosaic Variegated Aneuploidy Syndrome 2 | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Hypoalbuminemia | Nephropathy | Corticobasal Syndrome | Rhabdomyosarcoma, Embryonal | Azoospermia | Giant Cell Arteritis | Familial Partial Lipodystrophy | Progressive Familial Intrahepatic Cholestasis Type 3 | Cavitary Optic Disc Anomalies | Pierre Robin Syndrome | Dementia | Cutaneous Lupus Erythematosus | Myosin Storage Myopathy | Partington Syndrome | Acanthosis Nigricans | Hypogonadism | Gardner Syndrome | Colitis | Vascular Cognitive Impairment | Melanocytic Nevus | Cancer, Kidney | Polymyositis | Episodic Ataxia | Juvenile Polyposis | Progressive Encephalopathy-optic Atrophy Syndrome | Bipolar Disorder | Congenital Disorders Of Glycosylation Type II | Glycogen Storage Disease Type 1 | Sleep Disorder | Granuloma Annulare | Long QT Syndrome Type 3 | Mohr-Tranebjaerg Syndrome | Alexander Disease | Arrhythmogenic Right Ventricular Cardiomyopathy | Joubert Syndrome | Extramammary Paget's Disease | Chordoma | Lichen Sclerosus | Epidermolysis Bullosa Dystrophica | Porphyria, Acute Intermittent | Gingivitis | Fetal Alcohol Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Polycystic Kidney, Autosomal Dominant | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Schwartz-Jampel-Aberfeld Syndrome | REM Sleep Behavior Disorder | Sarcoidosis, Pulmonary | Polycystic Liver | Chondromyxoid Fibroma | Orthostatic Intolerance | Hemimegalencephaly | Pituitary Disorders | Glycogen Storage Disease Type 9 | Mitochondrial Disease | Peripheral Neuropathy | Multiple Sclerosis, Secondary Progressive | Adrenoleukodystrophy, X-linked | Molybdenum Cofactor Deficiency | Pityriasis Rubra Pilaris | Pontocerebellar Hypoplasia | Poretti-Boltshauser Syndrome | Open-angle Glaucoma | Fuchs Heterochromic Iridocyclitis | Familial Hypertrophic Cardiomyopathy | IgA Nephropathy | Hereditary Spastic Paraplegia | Diabetes Type 1 | Pyloric Stenosis, Infantile Hypertrophic | Antisocial Personality Disorder | Bietti Crystalline Dystrophy | Bloom Syndrome | Nemaline Myopathy | Choriocarcinoma | Retinoblastoma | Tibial Muscular Dystrophy | Warsaw Breakage Syndrome | Carcinoma, Squamous Cell | Microcephaly, Seizures, And Developmental Delay | Encephalopathy, Ethylmalonic | Ichthyosis Hystrix, Curth-Macklin Type | Williams Syndrome | Oculocutaneous Albinism Type 1 | Ellis-Van Creveld Syndrome | Fuchs Dystrophy | LRBA Deficiency | X-linked Sideroblastic Anemia | Neurofibromatosis Type 1 | Pulmonary Capillary Hemangiomatosis | Cataplexy | Multisystemic Smooth Muscle Dysfunction Syndrome | Low Phospholipid Associated Cholelithiasis | X-linked Charcot-Marie-Tooth Disease | Chitayat Syndrome | Small Lymphocytic Lymphoma | Asthma | Pneumoconiosis | Frank-ter Haar Syndrome | CDKL5 Deficiency Disorder | Hydrolethalus Syndrome | Autoimmune Disease | Nephrotic Syndrome | VACTERL/VATER Association | Heart Septal Defects | Chronic Granulomatous Disease | Farber Disease | Atherosclerosis | Renal Failure | Dystonia-parkinsonism, X-linked | Episodic Ataxia Type 1 | Localized Scleroderma | Vitiligo | Goiter, Nodular | Spastic Paraplegia Type 7 | Hyperkeratosis | Alcoholism | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Epilepsy | Sertoli Cell-only Syndrome | Marshall-Smith Syndrome | Patent Foramen Ovale | Meniere's Disease | Schistosomiasis Mansoni | Giant Axonal Neuropathy | Hartsfield Syndrome | Geleophysic Dysplasia | Familial Hyperaldosteronism | Malaria, Cerebral | POEMS Syndrome | Triple A Syndrome | Multicystic Renal Dysplasia | Inflammatory Joint Disease | Crouzon Syndrome With Acanthosis Nigricans | Sclerosing Cholangitis | Stuttering | Anencephaly | Gastrointestinal Disorders | Keratoconjunctivitis | Keloid | Cerebral Amyloid Angiopathy | Colon Adenoma | Neurocysticercosis | Schizophrenia, Paranoid | Schwannomatosis | Corneal Edema | ICF Syndrome | Duane Retraction Syndrome | Hyperparathyroidism-jaw Tumor Syndrome | Neuroblastoma | DNA Ligase IV Deficiency | Trismus-pseudocamptodactyly Syndrome | Gastritis, Atrophic | Pouchitis | Antiphospholipid Syndrome | Myasthenia | Glucagonoma | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Peeling Skin Syndrome Type B | Congenital Bilateral Absence Of Vas Deferens | Cardiomyopathy, Peripartum | Palmoplantar Keratoderma | Bernard-Soulier Syndrome | Nephrosclerosis | Optic Nerve Diseases | Parkinson Disease 6, Autosomal Recessive Early-onset | Glutaric Aciduria Type 3 | Lipoma | Hyperekplexia | Hyperostosis | Scleritis | Endophthalmitis | Corneal Dystrophies, Hereditary | Neuroendocrine Cancer | Hemoglobinopathies | T-cell Lymphoma, Subcutaneous Panniculitis-like | Diverticulitis | Coronary Restenosis | Chorea-acanthocytosis | Distal Spinal Muscular Atrophy | Chanarin-Dorfman Syndrome | Pantothenate Kinase-associated Neurodegeneration | Gynecomastia | GM2-gangliosidosis AB Variant | Arthritis, Reactive | Metabolic Syndrome | Bullous Pemphigoid | Raine Syndrome | Large Granular Lymphocytic Leukemia | Wiedemann-Steiner Syndrome | Optic Neuropathy | Hemorrhagic Disorders | Beare-Stevenson Syndrome | Fragile X Syndrome | Emery-Dreifuss Muscular Dystrophy | 3-methylglutaconic Aciduria | Urticaria | Hyperuricemic Nephropathy, Familial Juvenile | Transthyretin-related Amyloidosis | Cerebellofaciodental Syndrome | Keratosis, Seborrheic | Majeed Syndrome | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Encephalocele | Iron Metabolism Disorders | Epidermolytic Ichthyosis, Annular