Disease

Seminoma

About the Disease
Seminoma, also known as seminoma, pure, is related to testicular seminoma and extragonadal seminoma. An important gene associated with Seminoma is KIT (KIT Proto-Oncogene, Receptor Tyrosine Kinase), and among its related pathways/superpathways are Embryonic and Induced Pluripotent Stem Cells and Lineage-specific Markers and Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors. The drugs Granisetron and Cisplatin have been mentioned in the context of this disorder. Affiliated tissues include testis, lymph node and testes, and related phenotypes are endocrine/exocrine gland and reproductive system

Common Targets
DPPA3 | SCGB3A1 | SOX2 | POU5F1 | FLT3LG | TDRD1 | ERN2 | PIWIL2 | PIWIL4 | HIC1 | LEPR | DNAAF1 | MGMT | XIST | G3845 | PIWIL1 | MEST | RASSF1 | KIT | PRSS21

疾病靶点研报
Seminoma

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

Other Diseases

Hyperparathyroidism-jaw Tumor Syndrome | Diabetes Insipidus | Carcinoma, Merkel Cell | Asplenia | Renal Hypouricemia | Angioedema, Hereditary | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Angina Pectoris | Motor Neuron Diseases | Hyperammonemia | Thrombocythemia, Essential | Dysmorphophobia | Peters-plus Syndrome | Intestinal Hypomagnesemia 1 | Non-Langerhans Cell Histiocytosis | Cholera | Acral Lentiginous Melanoma | Relapsing Polychondritis | Tangier Disease | Polycythemia | ICF Syndrome | Pure Autonomic Failure | Clouston Hidrotic Ectodermal Dysplasia | Amebiasis | Progressive Familial Intrahepatic Cholestasis Type 2 | Creatine Deficiency Syndrome | Congenital Dyserythropoietic Anemia | Hypocalcemia | Paroxysmal Kinesigenic Dyskinesia | Hypokalemia | Thrombotic Microangiopathy | Stroke | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Alcoholism | Gastroenteritis, Eosinophilic | Spinocerebellar Ataxia Type 31 | Osteochondroma | Vitamin A Deficiency | Pycnodysostosis | Polyneuropathy | Antley-Bixler Syndrome | Sclerocornea | Persistent Fetal Circulation | Sensory Neuropathy | DEND Syndrome | Esophageal Motility Disorders | Multisystemic Smooth Muscle Dysfunction Syndrome | Pancreatitis | Coenzyme Q10 Deficiency | Retinitis Pigmentosa 3 | Farber Disease | Astrocytoma, Anaplastic | Zimmermann-Laband Syndrome | Globozoospermia | Xeroderma Pigmentosum | Anorectal Fistula | Gangliosidosis, GM1 | Pseudohypoparathyroidism Type 2 | Granular Corneal Dystrophy | Congenital Adrenal Hyperplasia | Gilbert Syndrome | Basal Ganglia Disease | LRBA Deficiency | Hemorrhagic Disorders | Myositis, Focal | Lymphoproliferative Disease, X-linked | Ganglioglioma | Familial Isolated Hyperparathyroidism | Peripheral Neuropathy | Open-angle Glaucoma | Pyruvate Decarboxylase Deficiency | Enlarged Vestibular Aqueduct | Eosinophilia | Gallstones | Birt-Hogg-Dube Syndrome | Neuroectodermal Tumors, Primitive | Immunoproliferative Disorders | Diverticulitis | Platelet Disorders | Aspergillosis | Leri-Weill Dyschondrosteosis | Hypercalcemia | Schindler Disease | Takayasu's Arteritis | Palsy, Cerebral | Torticollis | Uveitis, Anterior | Thin Basement Membrane Disease | Stuttering | Hemangioma | Thyroiditis, Autoimmune | Palmoplantar Keratoderma | Cryopyrin-associated Periodic Syndromes | Colorectal Adenoma | Hypobetalipoproteinemias | Hepatic Veno-occlusive Disease | Rhizomelic Chondrodysplasia Punctata | Glucagonoma | Bipolar Disorder | Crimean-Congo Hemorrhagic Fever | Primary Familial Brain Calcification | Diabetic Nephropathy | Genitopatellar Syndrome | Hyperparathyroidism, Primary | Colitis, Microscopic | Veno-occlusive Disease | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Rolandic Epilepsy | Acute Anterior Uveitis | Calcium Pyrophosphate Deposition Disease | Stevens-Johnson Syndrome | Vitamin B12 Deficiency | Hemophagocytic Lymphohistiocytosis | Adams-Oliver Syndrome | Takenouchi-Kosaki Syndrome | Phosphoglycerate Dehydrogenase Deficiency | Prune Belly Syndrome | Opisthorchiasis | Tracheal Disorders | Diabetic Neuropathy | Myhre Syndrome | Antisocial Personality Disorder | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Hypersensitivity | Priapism | Atelosteogenesis Type 1 | Early Infantile Epileptic Encephalopathy 13 | Chondrodysplasia Punctata 2, X-linked Dominant | Nephropathy | Hemangioblastoma | Pancreatitis, Chronic | Macrophagic Myofasciitis | Neurotoxicity | Jalili Syndrome | Spinal Muscular Atrophy Type 3 | Coloboma | Congenital Hereditary Endothelial Dystrophy Type II | Oligoastrocytoma | Oguchi Disease-2 | Synpolydactyly | Myofibrillar Myopathy | Hemolytic Uremic Syndrome | Diabetic Encephalopathy | Chondrosarcoma | Cholesteryl Ester Storage Disease | Epidermolytic Palmoplantar Keratoderma | Astrocytoma | Hyperuricemic Nephropathy, Familial Juvenile | Blastoma, Pleuropulmonary | Cherubism | Pneumococcal Meningitis | Crouzon Syndrome With Acanthosis Nigricans | Myelodysplasia | Centronuclear Myopathy | N-acetylglutamate Synthase Deficiency | Charcot-Marie-Tooth Disease, Type 2A | Achromatopsia | High Molecular Weight Kininogen Deficiency | Tonsillitis | Hyperoxaluria | PHARC Syndrome | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Usher Syndrome Type I | Amelanotic Melanoma | Ectrodactyly | Hypertension, Pulmonary | Cancer, Prostate | Best Macular Dystrophy | Cellulitis | Frank-ter Haar Syndrome | Renal Tubular Acidosis | Autosomal Recessive Spastic Paraplegia Type 54 | Glycogen Storage Disease Type 4 | Fowler's Syndrome | Coronary Artery Disease | LEOPARD Syndrome | Glycogen Storage Disease Type 0, Muscle | Portal Vein Thrombosis | Keratitis | Cholecystitis | Ventricular Septal Defect | Retinoblastoma | Personality Disorders | Benign Familial Infantile Seizures | Congenital Aniridia | Macrophage Activation Syndrome | Colon Adenoma | Epidermodysplasia Verruciformis | Ureteropelvic Junction Obstruction | Hyperkalemic Periodic Paralysis | Cornelia De Lange Syndrome | Myeloid Leukemia | Multiple Sulfatase Deficiency | Leukocyte Adhesion Deficiency | Incontinentia Pigmenti | Epidermolysis Bullosa | Desbuquois Syndrome | Stomatitis | Fanconi Anemia | Teratozoospermia | Alopecia | Dowling-Degos Disease | Glycogen Storage Disease Type 3 | Chiari Malformation Type I | Infertility | Episodic Ataxia Type 2 | Hypotrichosis Simplex | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Mucolipidosis Type II | Urolithiasis | Inflammatory Joint Disease | Multiple Sclerosis, Relapsing-remitting | Necrotizing Autoimmune Myopathy | MELAS Syndrome | Pheochromocytoma | Tylosis With Esophageal Cancer | Adenosine Deaminase Deficiency | Postpartum Depression | Lyme Disease | Kashin-Beck Disease | Brachial Plexus Neuropathy | Geleophysic Dysplasia | Thrombophlebitis | Cholestasis | Autosomal Recessive Congenital Ichthyosis | Hyperinsulinism-hyperammonemia Syndrome | Congenital Nephrotic Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Erectile Dysfunction | Neuronal Ceroid Lipofuscinosis | Scapuloperoneal Spinal Muscular Atrophy | Distal Myopathy 2 | Disseminated Intravascular Coagulation | Contact Dermatitis | Microcephaly | Asperger Syndrome | Nestor-Guillermo Progeria Syndrome | Charcot-Marie-Tooth Disease Type 2D | Primary Progressive Aphasia | Congenital Hypofibrinogenemia | Infantile Neuroaxonal Dystrophy | Photosensitivity | Periventricular Nodular Heterotopia | Carotid Artery Disease | Cancer, Brain | Heimler Syndrome | Lipid Storage Myopathy | Nephronophthisis | Graft-versus-host Disease | Coma | Gastritis, Atrophic | Lafora Disease | Progressive Familial Intrahepatic Cholestasis Type 3 | Poirier-Bienvenu Neurodevelopmental Syndrome | Granuloma Annulare | Gastric Atrophy | Transthyretin-related Amyloidosis | Plasma Cell Dyscrasia | Mucolipidosis Type IV | COACH Syndrome | Usher Syndrome Type IIC | Esophagitis | Pseudohypoparathyroidism Type 1A | Hypopigmentation | Tyrosine Hydroxylase Deficiency | Mandibuloacral Dysplasia With Type A Lipodystrophy | Pneumonia, Bacterial | Polymyositis | Tenosynovial Giant Cell Tumor | Glioblastoma Multiforme | Chondrodysplasia Punctata | Angiodysplasia | Hemochromatosis Type 2 | Periventricular Leukomalacia | Mixed Connective Tissue Disease | Proctitis | Acne | VEXAS Syndrome | Diastrophic Dysplasia | Cri-du-chat Syndrome | Chronic Inflammatory Demyelinating Polyneuropathy | Charcot-Marie-Tooth Disease, Type 2C | Rhinitis | Lissencephaly 2 | Microcephalic Primordial Dwarfism | Loeys-Dietz Syndrome Type 4 | Withdrawal Syndrome | Optic Nerve Hypoplasia, Bilateral | Pachyonychia Congenita | Hashimoto Thyroiditis | Congenital Dysfibrinogenemia | Endometrial Hyperplasia | Niemann-Pick Disease | Amish Infantile Epilepsy Syndrome | Juvenile Polyposis | Ectopia Lentis, Isolated, Autosomal Recessive | Frontotemporal Dementia | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Hypertension | Arthrogryposis | Multiple Sclerosis, Chronic Progressive | Familial Glucocorticoid Deficiency | Borderline Personality Disorder | Microcephaly, Seizures, And Developmental Delay | Sitosterolemia | Inflammatory Linear Verrucous Epidermal Nevus | Hennekam Lymphangiectasia-lymphedema Syndrome | Salla Disease | Combined Pituitary Hormone Deficiency | Aceruloplasminemia | Cerebrotendinous Xanthomatosis | Muir-Torre Syndrome | Oligodendroglioma | Basal Ganglia Cerebrovascular Disease | Anemia | Achondrogenesis | Hypophosphatasia | D-2-Hydroxyglutaric Aciduria | Proteasome-associated Autoinflammatory Syndrome 2 | Chronic Granulomatous Disease | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Mitochondrial DNA Depletion Syndrome 13 | Hyperbilirubinemia | Milk Allergy | Hypohidrotic Ectodermal Dysplasia | Acrodysostosis | Hereditary Xerocytosis | Malaria, Cerebral | Optic Nerve Diseases | Smith-Kingsmore Syndrome | Oligoasthenoteratozoospermia | Erdheim-Chester Disease | Pyelonephritis | Retinal Coloboma | Splenomegaly | Cholangitis | Pernicious Anemia | Subcortical Band Heterotopia | Dyggve-Melchior-Clausen Disease | Central Core Disease | Amyotrophic Lateral Sclerosis, Juvenile | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Cardiomyopathy, Peripartum | Pontocerebellar Hypoplasia Type 7 | Bronchitis | Pain | Deafness, Dystonia, And Cerebral Hypomyelination | Pemphigus | Amenorrhea | Trismus-pseudocamptodactyly Syndrome | Oculocutaneous Albinism | Bronchiolitis | Transient Bullous Dermolysis Of The Newborn | Syncope | Joubert Syndrome | Pyruvate Kinase Deficiency | Leishmaniasis, Cutaneous | Fukuyama Congenital Muscular Dystrophy | Kallmann Syndrome | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Epidermolysis Bullosa Dystrophica | Saethre-Chotzen Syndrome | Hepatitis A | Seborrheic Dermatitis | Benign Familial Pemphigus | Chronic Kidney Disease | Conjunctivitis, Allergic | Oculodentodigital Dysplasia | Congenital Muscular Dystrophy | Tetraplegia | Choroiditis | Sick Sinus Syndrome | Myocarditis | Thyrotoxic Periodic Paralysis | C3 Glomerulonephritis | Histoplasmosis | Prader-Willi Syndrome | Pontocerebellar Hypoplasia | Addison Disease | Herpes Genitalis | Pure Red Cell Aplasia | Fundus Albipunctatus | Optic Atrophy 2 | Anorchia | Polydactyly | Proopiomelanocortin Deficiency | Cystinuria | Generalized Epilepsy With Febrile Seizures Plus | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Localized Scleroderma | Beta-Propeller Protein-associated Neurodegeneration | Polycystic Kidney, Autosomal Recessive | Rash | Dent Disease | Schaaf-Yang Syndrome | Epilepsy, Generalized | Cerebral Cavernous Malformations | Polyarteritis Nodosa | Non-proliferative Diabetic Retinopathy