Disease

Choriocarcinoma

About the Disease
Choriocarcinoma, also known as chorioepithelioma, is related to gestational choriocarcinoma and placental choriocarcinoma. An important gene associated with Choriocarcinoma is H19 (H19 Imprinted Maternally Expressed Transcript), and among its related pathways/superpathways are Peptide hormone metabolism and Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors. The drugs Bleomycin and Carboplatin have been mentioned in the context of this disorder. Affiliated tissues include placenta, testis and ovary, and related phenotypes are Increased shRNA abundance (Z-score > 2) and Increased shRNA abundance (Z-score > 2)

Common Targets
ENG | FLT1 | G7157 | CSF1R

疾病靶点研报
Choriocarcinoma

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

Other Diseases

Nance-Horan Syndrome | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Ichthyosis, X-linked | Spastic Paraplegia Type 7 | Genee-Wiedemann Syndrome | Nephritis, Interstitial | Aldosterone Synthase Deficiency | GATA2 Deficiency | Spondylosis | Familial Partial Lipodystrophy | Chronic Kidney Disease | Distal Myopathy 2 | Chronic Mucocutaneous Candidiasis | Smith-Kingsmore Syndrome | Renal Dysplasia | Mycosis Fungoides | Whipple's Disease | Reticular Dysgenesis | NDH Syndrome | Granuloma Annulare | Brenner Tumor | Coronary Artery Disease | Prune Belly Syndrome | Paraplegia | Primary Carnitine Deficiency | Stuttering | Kaposiform Hemangioendothelioma | Thyrotoxic Periodic Paralysis | LEOPARD Syndrome | Familial Hemiplegic Migraine | Nicotine Addiction | High Molecular Weight Kininogen Deficiency | Hennekam Lymphangiectasia-lymphedema Syndrome | Hereditary Multiple Exostoses | Retinoschisis | Cold-induced Sweating Syndrome | Megaloblastic Anemia | Cholecystitis | LMNA-related Congenital Muscular Dystrophy | Sotos Syndrome | Eclampsia | ACTH-independent Macronodular Adrenal Hyperplasia | Treacher Collins Syndrome | Tendinitis | Hemochromatosis Type 1 | Feingold Syndrome | Osteochondrosis | Myocardial Infarction | Carbonic Anhydrase VA Deficiency | Waardenburg Syndrome Type 4 | Congenital Fiber-type Disproportion Myopathy | Withdrawal Syndrome | Chondrodysplasia Punctata | Hypoparathyroidism | Focal Facial Dermal Dysplasia | Pierre Robin Syndrome | MELAS Syndrome | Lesch-Nyhan Syndrome | Antithrombin III Deficiency | Renal Tubular Dysgenesis | Optic Neuropathy, Anterior Ischemic | Inflammatory Bowel Disease | Proteus Syndrome | Meningococcal Meningitis | Cold Agglutinin Disease | Osteomalacia | Prurigo Nodularis | Lafora Disease | Basan Syndrome | Asthma, Nocturnal | Lactose Intolerance | Salla Disease | Micropenis | Muir-Torre Syndrome | Pneumonia, Bacterial | Primary Hyperoxaluria Type 1 | Leukocyte Adhesion Deficiency Type 1 | Spitz Nevus | Pulmonary Vein Stenosis | Hemangioblastoma | Hernia, Inguinal | Noonan Syndrome-like Disorder With Loose Anagen Hair | Lymphoproliferative Disorders | Hypertension, Renal | Mitochondrial DNA Depletion Syndrome | Ameloblastoma | Paraganglioma, Carotid Body | Pulmonary Stenosis | Benign Recurrent Intrahepatic Cholestasis 1 | Cryptorchidism | Lymphangiomatosis | 5-oxoprolinase Deficiency | Nemaline Myopathy 8 | Mountain Sickness | Evans Syndrome | Persistent Hyperplastic Primary Vitreous | Spinocerebellar Ataxia Type 17 | Gingivitis | Thrombosis | Omenn Syndrome | Histoplasmosis | Spinocerebellar Ataxia Type 31 | Myasthenia | DNA Ligase IV Deficiency | Ocular Hypertension | Adrenomyeloneuropathy | Addison Disease | Apraxia | Protein S Deficiency | Osteogenesis Imperfecta Type V | KBG Syndrome | Hypermethioninemia | Wieacker-Wolff Syndrome | Liver Diseases | Sturge-Weber Syndrome | Ganglioglioma | Peeling Skin Syndrome, Acral Type | Hyperglycemia | Peeling Skin Syndrome Type B | Blood Protein Disorders | Angioedema, Acquired | Phenylketonuria II | Hypertension, Essential | Necrobiosis Lipoidica | Chronic Periodontitis | Familial Exudative Vitreoretinopathy | Transient Bullous Dermolysis Of The Newborn | Hodgkin Lymphoma | Thanatophoric Dysplasia Type 1 | Hypothalamic Obesity | Atherosclerosis | Anovulation | C3 Glomerulonephritis | Primary Hyperoxaluria | Argininosuccinic Aciduria | Dysthymia | Pontocerebellar Hypoplasia Type 7 | Anterior Segment Dysgenesis | Aneurysm, Thoracic Aortic | Bicuspid Aortic Valve | Bursitis | Schaaf-Yang Syndrome | Cystinuria | Usher Syndrome Type II | Guttate Psoriasis | Tremor | Iron Overload | Diffuse Palmoplantar Keratoderma | Distal Spinal Muscular Atrophy | Learning Disability | Spinocerebellar Ataxia Type 1 | Neuroma | Pyruvate Carboxylase Deficiency Disease | Van Der Knaap Disease | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Myoclonic Atonic Epilepsy | Chronic Lymphocytic Leukemia | Charcot-Marie-Tooth Disease Axonal Type 2N | Lymphoproliferative Disease, X-linked | Sarcoidosis | Kearns-Sayre Syndrome | Mast Cell Leukemia | Hypertensive Nephropathy | Pleomorphic Xanthoastrocytoma | Creatine Deficiency Syndrome | Early Infantile Epileptic Encephalopathy 4 | Lathosterolosis | Epidermolysis Bullosa Acquisita | Joubert Syndrome | Tyrosinemia Type 2 | Muscle Wasting | Hyperlipidemia Type V | Globozoospermia | Cholelithiasis | Pfeiffer Syndrome | Nephropathy | Hereditary Neuropathy With Liability To Pressure Palsies | Ichthyosis Hystrix, Curth-Macklin Type | Sialidosis | Multicentric Carpotarsal Osteolysis Syndrome | Esophageal Motility Disorders | Achromatopsia | Donnai-Barrow Syndrome | Epidermolytic Palmoplantar Keratoderma | Congenital Adrenal Hyperplasia 1 | Hypoproteinemia, Hypercatabolic | Heroin Dependence | Synpolydactyly | Primary Aldosteronism | Blepharoconjunctivitis | Yellow Fever | Pemphigus | Eiken Syndrome | Intestinal Tuberculosis | Iron Deficiency Anemia | Familial Episodic Pain Syndrome | Myotonia | Pheochromocytoma | Compartment Syndrome | Riboflavin Transporter Deficiency Neuronopathy | Multisystemic Smooth Muscle Dysfunction Syndrome | Leukodystrophies | Pulmonary Alveolar Microlithiasis | Recurrent Respiratory Papillomatosis | Carcinoid Tumor | Hyperthermia, Malignant | Charcot-Marie-Tooth Disease Type 2D | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Paraganglioma | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Juvenile Polyposis | Protein C Deficiency | Seborrheic Dermatitis | Calcium Pyrophosphate Deposition Disease | McKusick Type Metaphyseal Chondrodysplasia | Paronychia | Dentinogenesis Imperfecta | Lymphopenia | Spondyloepiphyseal Dysplasia Tarda, X-linked | Malaria | Asthma | Ichthyosis | T-cell Prolymphocytic Leukemia | Left Ventricular Noncompaction | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Lewy Body Dementia | Hypercalciuria | Retinal Detachment | Hypobetalipoproteinemias | Meningeal Melanocytoma | Diabetic Neuropathy | Periventricular Leukomalacia | Spinal Muscular Atrophy | Interstitial Lung Diseases | Spinocerebellar Ataxia Type 16 | Granular Corneal Dystrophy | Hypokalemic Periodic Paralysis | Anorectal Fistula | Glycogen Storage Disease Type 4 | Fahr Disease | Enterocolitis, Necrotizing | Budd-Chiari Syndrome | Papilledema | Coloboma | Scleritis | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Pituitary Disorders | Stevens-Johnson Syndrome | Choroiditis | Acanthosis Nigricans | Diabetes Type 1 | Osteoglophonic Dysplasia | Pupil Disorders | Leprosy | Renal Failure | Gestational Trophoblastic Disease | Perry Syndrome | Presbyopia | Hypertension | Rosacea | Hyperprolactinemia | Primary Progressive Nonfluent Aphasia | Gallstones | Hydrocephalus | Hyperparathyroidism, Primary | Episodic Ataxia | Bone Marrow Necrosis | Sleep Apnea, Central | Situs Inversus | Skin Carcinoma | Facioscapulohumeral Muscular Dystrophy Type 1 | Congenital Stromal Corneal Dystrophy | Hereditary Elliptocytosis | Dyslipidemia | Atelosteogenesis Type 2 | Aphasia | Krabbe Disease | Alstrom Syndrome | Lipid Storage Diseases | Wolcott-Rallison Syndrome | Acute Lung Injury | Acromesomelic Dysplasia | Craniolenticulosutural Dysplasia | Neovascular Glaucoma | Hypervalinemia | Charcot-Marie-Tooth Disease Type 4E | Asplenia | Sickle Cell Disease | Autoimmune Autonomic Ganglionopathy | Methylmalonic Aciduria And Homocystinuria, CblC Type | Galloway-Mowat Syndrome | Cutaneous Angiosarcoma | Keratopathy | Von Hippel-Lindau Disease | Blepharospasm | Menetrier Disease | Hereditary Coproporphyria | Blepharophimosis Syndrome | Acute Anterior Uveitis | Apert Syndrome | Muscular Dystrophy | Menkes Disease | Paracoccidioidomycosis | Lymphomatoid Granulomatosis | Dengue Hemorrhagic Fever | Leri-Weill Dyschondrosteosis | Corneal Ulcer | Empyema | Niemann-Pick Disease, Type A | Meckel-Gruber Syndrome | Cone Dystrophy | Crouzon Syndrome With Acanthosis Nigricans | Autosomal Recessive Spastic Paraplegia Type 35 | Mevalonate Kinase Deficiency | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Saul-Wilson Syndrome | Charcot-Marie-Tooth Disease, Type 2C | Conjunctivitis, Allergic | Ameloblastic Carcinoma | Macrodactyly | Neuromyelitis Optica | Vitamin D Deficiency | Stroke, Ischemic | Dengue Shock Syndrome | Nijmegen Breakage Syndrome | Borderline Personality Disorder | Gray Platelet Syndrome | Atrial Septal Defect | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Renal Hypouricemia | Currarino Syndrome | Epidermolysis Bullosa Simplex, Localized | Maple Syrup Urine Disease | Dysgerminoma | Spinocerebellar Ataxia Type 15 | Myhre Syndrome | Infertility | Hydrolethalus Syndrome | Lassa Fever | Common Cold | Keratosis, Actinic | Neutropenia | Crimean-Congo Hemorrhagic Fever | Restrictive Dermopathy | Osteosclerosis | Cenani-Lenz Syndactyly Syndrome | Lateral Meningocele Syndrome | Delayed Sleep Phase Syndrome | Niemann-Pick Disease, Type B | Oculocutaneous Albinism Type 4 | Thyroid Dysgenesis | Cervical Dystonia | Frontometaphyseal Dysplasia | Thrombophlebitis | Epidermolysis Bullosa | Osmotic Demyelination Syndrome | Acne | Nicotine Dependence | Heart Failure | Erythematotelangiectatic Rosacea | Influenza | Congenital Bile Acid Synthesis Defect | Juvenile Hyaline Fibromatosis | Nemaline Myopathy 10 | Congenital Hypofibrinogenemia | Chitayat Syndrome | Dyggve-Melchior-Clausen Disease | Chondrodysplasia Punctata 1, X-linked Recessive | Hyperparathyroidism, Secondary | Anosmia, Congenital | Congenital Dysfibrinogenemia | Pearson Syndrome | Melanoma | Peripheral T-cell Lymphoma | C3 Glomerulopathy | Bainbridge-Ropers Syndrome | Cabezas Syndrome | Colitis | Leukoplakia, Oral | Toxic Epidermal Necrolysis | Hyperuricemic Nephropathy, Familial Juvenile | Acute Chest Syndrome | Mastitis | Granular Corneal Dystrophy Type 1 | Carcinoma, Transitional Cell | Congestive Heart Failure | Epidermolytic Ichthyosis, Annular | Varicocele | Synovitis | Arrhythmogenic Right Ventricular Cardiomyopathy | Aceruloplasminemia | Carcinoma, Small Cell | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Alpha-thalassemia Myelodysplasia Syndrome | Meesmann Corneal Dystrophy | Cerebral Cavernous Malformations | Leber Hereditary Optic Neuropathy | Pseudohypoparathyroidism Type 1B | Immunoproliferative Disorders | Angina Pectoris