Disease

Gestational Trophoblastic Disease

About the Disease
Gestational Trophoblastic Neoplasm, also known as hydatidiform mole, is related to partial hydatidiform mole and placental site trophoblastic tumor. An important gene associated with Gestational Trophoblastic Neoplasm is NLRP7 (NLR Family Pyrin Domain Containing 7), and among its related pathways/superpathways are Peptide hormone metabolism and Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors. The drugs Amifostine and Nitroglycerin have been mentioned in the context of this disorder. Affiliated tissues include placenta, lung and t cells, and related phenotypes are endocrine/exocrine gland and reproductive system

Common Targets
DNA-Directed RNA Polymerase (nonspecified subtype)

疾病靶点研报
Gestational Trophoblastic Disease

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

Other Diseases

Episodic Ataxia Type 1 | Gastroschisis | Focal Dermal Hypoplasia | Sorsby Fundus Dystrophy | Mitochondrial DNA Depletion Syndrome 13 | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Waardenburg Syndrome Type 2A | Nephrotic Syndrome | Malignant Peripheral Nerve Sheath Tumor | Retinoblastoma | Gastritis | Periventricular Nodular Heterotopia | Avian Influenza | Nail Disorder, Nonsyndromic Congenital | Pontocerebellar Hypoplasia Type 2 | Esotropia | Spina Bifida | Sclerosteosis 2 | Spitz Nevus | Acute Lymphocytic Leukemia | Congenital Stromal Corneal Dystrophy | Primary Torsion Dystonia | Congenital Lipoid Adrenal Hyperplasia | Leukemia | Vitreoretinopathy, Proliferative | Epidermolytic Hyperkeratosis | Sialoadenitis | Cataract | Glycogen Storage Disease | Lactose Intolerance | Influenza | Rickets | Pseudohypoparathyroidism Type 1C | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Sialidosis Type I | Desbuquois Syndrome | Congenital Fiber-type Disproportion Myopathy | Benign Familial Neonatal Convulsions | Blepharophimosis Syndrome | McLeod Syndrome | Saethre-Chotzen Syndrome | Cutaneous Lupus Erythematosus | Pyruvate Decarboxylase Deficiency | Vitamin B12 Deficiency | Multiple Epiphyseal Dysplasia | Heterotaxy | Sengers Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Familial Advanced Sleep Phase Syndrome | Congenital Adrenal Hyperplasia | Thanatophoric Dysplasia | Ichthyosis | Lipid Storage Diseases | Ichthyosis Hystrix, Curth-Macklin Type | PASLI Disease | Azoospermia | Alexander Disease | Osteogenesis Imperfecta Type VI | Renal-hepatic-pancreatic Dysplasia | Biotinidase Deficiency | Allergic Contact Dermatitis | Ataxia-ocular Apraxia 2 | Hypersensitivity | Stargardt Disease | Eclampsia | Proteasome-associated Autoinflammatory Syndrome 2 | Hypercalciuria | Otosclerosis | Melanoma, Malignant | Hypertension, Renal | Infertility | Cannabis Abuse | Mucolipidosis | Opisthorchiasis | Alpers Syndrome | Leukoplakia | Fascioliasis | Atherosclerosis | Filariasis | Tuberculosis | Myoclonic Atonic Epilepsy | Hyperparathyroidism, Primary | Chondrodysplasia Punctata | Klinefelter Syndrome | Pyruvate Carboxylase Deficiency Disease | Chronic Neutrophilic Leukemia | Insulin Resistance | Trichuriasis | Gilbert Syndrome | Thrombocythemia, Essential | Astrocytoma, Anaplastic | Neuroendocrine Cancer | Restrictive Dermopathy | Plasma Cell Dyscrasia | Medulloblastoma | Hyperoxaluria | Tumoral Calcinosis | Chronic Lymphocytic Leukemia | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Rosacea | Cerebellar Ataxia, Cayman Type | Sick Sinus Syndrome | Dystonia | Spinocerebellar Ataxia Type 23 | Acromicric Dysplasia | Aromatic L-amino Acid Decarboxylase Deficiency | Wolfram Syndrome | Frontotemporal Dementia | AIDS Dementia Complex | Snyder-Robinson Syndrome | Holoprosencephaly | Fanconi Anemia | Osteopathia Striata With Cranial Sclerosis | Cardiomyopathy, Hypertrophic | Congenital Dysfibrinogenemia | Silicosis | Chronic Mucocutaneous Candidiasis | Acute Lung Injury | Familial Exudative Vitreoretinopathy | Pouchitis | Pitt-Hopkins Syndrome | Trichothiodystrophy | Gingivitis | Pulmonary Capillary Hemangiomatosis | Creatine Deficiency Syndrome | Nephropathy | Hereditary Pyropoikilocytosis | Lissencephaly 2 | Ganglioglioma | Malaria, Cerebral | Costello Syndrome | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Coronary Restenosis | Epidermolysis Bullosa Dystrophica | Glanzmann Thrombasthenia | Epidermodysplasia Verruciformis | Cerebral Cavernous Malformations | Still Disease | Optic Neuropathy | Neuropathy | Glycogen Storage Disease Type 3 | Pulmonary Sclerosing Hemangioma | Lymphoma, Follicular | Vitamin A Deficiency | Keratopathy | Pulmonary Vein Stenosis | Dyslipidemia | Familial Hemiplegic Migraine | Hepatitis, Autoimmune | Microvillus Inclusion Disease | Muckle-Wells Syndrome | Hypotension, Orthostatic | Osteogenesis Imperfecta Type IV | Erdheim-Chester Disease | Heart Block | Neuroleptic Malignant Syndrome | Bronchiectasis | Geleophysic Dysplasia | Acromesomelic Dysplasia | Evans Syndrome | Antiphospholipid Syndrome | Bare Lymphocyte Syndrome | Diffuse Intrinsic Pontine Glioma | Eccrine Porocarcinoma | Generalized Epilepsy With Febrile Seizures Plus | Amyloidosis | Cardiomyopathy, Peripartum | Progressive Familial Intrahepatic Cholestasis | Gray Platelet Syndrome | Malonyl-CoA Decarboxylase Deficiency | Cancer, Bladder | Cancer, Breast | Hyperinsulinism-hyperammonemia Syndrome | Onchocerciasis | Epidermolysis Bullosa Simplex, Localized | Sezary Syndrome | Polymyositis | Bartter Syndrome | Lennox-Gastaut Syndrome | Hypertension, Pulmonary | Spinocerebellar Ataxia | Bernard-Soulier Syndrome | Mitochondrial Cytopathy | Premature Ejaculation | Partington Syndrome | Familial Thoracic Aortic Aneurysm | Intracranial Hypertension | Myofibrillar Myopathy | Seborrheic Dermatitis | Charcot-Marie-Tooth Disease, Type 1A | Myoclonus | T-cell Leukemia | Aneurysm, Abdominal Aortic | Haim-Munk Syndrome | Supravalvular Aortic Stenosis | Batten Disease | Leber Congenital Amaurosis | Osteosarcoma | Kaposiform Hemangioendothelioma | Olmsted Syndrome | Autonomic Nervous System Disorders | Cystitis | Hydrocephalus | Maple Syrup Urine Disease | Cholestasis | Metatropic Dysplasia | Spondyloarthritis | Pompe Disease | Hepatic Steatosis | Basal Ganglia Cerebrovascular Disease | Exotropia | Thyroiditis | IgA Nephropathy | Hyperprolactinemia | Peutz-Jeghers Syndrome | Micropenis | Congenital Hypofibrinogenemia | Congenital Primary Aphakia | Antisynthetase Syndrome | D-2-Hydroxyglutaric Aciduria | Nemaline Myopathy 8 | Glutathione Synthetase Deficiency | Spinal Cord Diseases | Oculocutaneous Albinism Type 4 | Scleroderma, Diffuse | Cryptorchidism | Diverticulitis | Congenital Adrenal Hyperplasia 1 | Blastoma, Pleuropulmonary | Fabry's Disease | Asperger Syndrome | Sarcosinemia | Pleomorphic Xanthoastrocytoma | Schindler Disease | Alpha-mannosidosis | Dermatitis | Bronchitis | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Varicocele | Amenorrhea | Rolandic Epilepsy | Lafora Disease | Acrodermatitis Enteropathica | Ameloblastoma | Schnyder Crystalline Corneal Dystrophy | Episodic Ataxia | Aplastic Anemia | Conjunctivitis, Allergic | Tinea | Neurocutaneous Syndromes | Retinal Dystrophy | Coronary Artery Disease | Hemimegalencephaly | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Extramammary Paget's Disease | Spondylocarpotarsal Synostosis Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | Pseudohypoaldosteronism | Jalili Syndrome | Cellulitis | Camptocormia | Carney-Stratakis Syndrome | Gastric Atrophy | Congenital Bile Acid Synthesis Defect | Pseudohypoparathyroidism Type 1A | Anti-glomerular Basement Membrane Disease | Pneumonia, Viral | Hypertension | Charcot-Marie-Tooth Disease, Type 2A | Hyperthermia, Malignant | C3 Glomerulopathy | Primary Progressive Nonfluent Aphasia | Benign Familial Pemphigus | Nicolaides-Baraitser Syndrome | Hypodontia | Mucolipidosis Type II | Hypokalemic Periodic Paralysis | Acrocallosal Syndrome | CDKL5 Deficiency Disorder | Hyperekplexia | Myotonia | Keratosis | Scabies | Glutaric Aciduria Type 2 | Achromatopsia | Celiac Disease | Cancer, Colon | Spinocerebellar Ataxia Type 15 | Hyperkalemic Periodic Paralysis | Takotsubo Cardiomyopathy | Usher Syndrome | ADNP Syndrome | Long QT Syndrome Type 3 | Herpes Simplex Dermatitis | Histiocytic Sarcoma | Wieacker-Wolff Syndrome | Vitelliform Macular Dystrophy | Erythema Multiforme | Silver-Russell Syndrome | Glomerulonephritis, Membranoproliferative | Perivascular Epithelioid Cell Tumor | Down Syndrome | Isovaleric Acidemia | Postpoliomyelitis Syndrome | Retinal Dystrophy, Early-onset Severe | Orotic Aciduria | Syphilis | Leber Hereditary Optic Neuropathy | Hyperthyroidism | Currarino Syndrome | Corneal Dystrophies, Hereditary | Hydrolethalus Syndrome | Rhabdoid Tumor | Senior-Loken Syndrome | Arthritis, Psoriatic | Pilomatrix Carcinoma | Primary Aldosteronism | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Glomerulonephritis | Osmotic Demyelination Syndrome | Pemphigus | Meleda Disease | Spinal And Bulbar Muscular Atrophy | Spinocerebellar Ataxia Type 21 | Pyelonephritis | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Macular Corneal Dystrophy Type 1 | Congenital Diaphragmatic Hernia | Yellow Fever | Colitis, Lymphocytic | Alveolar Capillary Dysplasia | Becker Muscular Dystrophy | Primary Erythromelalgia | Cornelia De Lange Syndrome | Craniosynostosis | Hemangioma | Charcot-Marie-Tooth Disease Type 4B1 | CHOPS Syndrome | Gitelman Syndrome | Bone Marrow Necrosis | Iron Deficiency Anemia | Diabetes | Paracoccidioidomycosis | Gaucher Disease | Sickle Cell Disease | Central Pain Syndrome | Hemochromatosis Type 1 | Osteosclerosis | Retinal Telangiectasia | Tyrosinemia | Hereditary Sensory Neuropathy Type 1 | Sturge-Weber Syndrome | Encephalitis | Glycogen Storage Disease Type 1 | Tinea Versicolor | Acute Motor Axonal Neuropathy | Purpura, Thrombotic Thrombocytopenic | Perry Syndrome | Lathosterolosis | Leigh Syndrome | Wolcott-Rallison Syndrome | Greenberg Dysplasia | Tracheal Disorders | Lymphoma, B-cell | Syndactyly | Leri Pleonosteosis | Cholecystitis | Pancytopenia | Kaposi Sarcoma | Bethlem Myopathy | Progressive Osseous Heteroplasia | Diabetic Nephropathy | Angioedema | Macular Degeneration | Myofibromatosis | Cherubism | Diabetic Encephalopathy | Glutaric Aciduria Type 3 | Hepatic Veno-occlusive Disease | Allan-Herndon-Dudley Syndrome | Reye Syndrome | Polyneuropathy | CEDNIK Syndrome | Pyloric Stenosis, Infantile Hypertrophic | Duchenne Muscular Dystrophy | Hereditary Sensory And Autonomic Neuropathy | Okihiro Syndrome | Cryopyrin-associated Periodic Syndromes | Nanophthalmos | Delirium | Esthesioneuroblastoma | Pheochromocytoma | Anodontia | Common Variable Immunodeficiency | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Cystinuria | Japanese Encephalitis | Epidermolysis Bullosa | Vogt-Koyanagi-Harada Syndrome | Odonto-onycho-dermal Dysplasia