Disease

Malignant Thymoma

About the Disease
Thymic Carcinoma, also known as malignant thymoma, is related to lymphoepithelioma-like thymic carcinoma and thymus adenocarcinoma. An important gene associated with Thymic Carcinoma is KIT (KIT Proto-Oncogene, Receptor Tyrosine Kinase), and among its related pathways/superpathways are Cytoskeletal Signaling and Hippo-Merlin signaling dysregulation. The drugs Paclitaxel and Pembrolizumab have been mentioned in the context of this disorder. Affiliated tissues include thymus, thyroid and bone marrow, and related phenotypes are mediastinal lymphadenopathy and neoplasm of the thymus

Common Targets
PDGFRB | DNMT3A | Uncharacterized LOC101928822, transcript variant X1 | GH1 | POLE | GTF2I | Somatostatin receptor (nonspecified subtype) | PIK3CA | FLT4 | FGFR1 | FLT1 | SPTA1 | KDR | DNMT3B | SMARCA4 | RICTOR | RET | SST | SMAD2 | BCOR | PDGFRA | MGMT | WT1 | HIF1A-AS2 | VCP | TNFRSF4 | G472 | TOP2A | ARID1A | KIT | G7157 | PRKN | FGFR2 | TNFRSF9 | HIF1A | KDM5A | G1029 | KDM6A | NRAS | EPHB1 | ERCC1 | NF2 | TYK2

疾病靶点研报
Malignant Thymoma

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

Other Diseases

Antley-Bixler Syndrome | Diamond-Blackfan Anemia | Paraplegia | Cousin Syndrome | Atrioventricular Septal Defect | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Myopathy | Hypersensitivity Pneumonitis | Pulmonary Alveolar Proteinosis | Cancer, Kidney | Agoraphobia | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Apraxia | Parvovirus B19 Infection | Atrial Septal Defect | Schwannomatosis | Pseudohypoparathyroidism Type 1C | GATA2 Deficiency | Medulloblastoma | Hereditary Mixed Polyposis Syndrome | Ornithine Transcarbamylase Deficiency | Spinocerebellar Ataxia Type 3 | Mixed Connective Tissue Disease | Retinoblastoma | Creutzfeldt-Jakob Disease | Bloom Syndrome | Cold-induced Sweating Syndrome | Spastic Paraplegia Type 7 | Pericarditis | VACTERL/VATER Association | Lung Diseases | Shock, Cardiogenic | Anti-glomerular Basement Membrane Disease | Ectodermal Dysplasia | Brachydactyly | Stroke | Hyperekplexia | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Neuromyelitis Optica | Lichen Planus | Oguchi Disease-2 | Adrenoleukodystrophy, X-linked | Urticaria | Waardenburg Syndrome Type 1 | Lymphangiomatosis | Diabetes Type 1 | Ganglioneuroma | Dentinogenesis Imperfecta | Spinocerebellar Ataxia Type 2 | Renal Tubular Acidosis | Vertebrobasilar Insufficiency | Cryopyrin-associated Periodic Syndromes | Posterior Polar Cataract | Chronic Enteropathy Associated With SLCO2A1 Gene | Inborn Errors Of Metabolism | Parkinson Disease 6, Autosomal Recessive Early-onset | Immunoproliferative Disorders | Lymphoma, Follicular | Gout | Sarcoidosis | Angina Pectoris | Ovarian Sex Cord-stromal Tumor | Scleritis | Mountain Sickness | Acute Leukemia | Microcephalic Primordial Dwarfism | Pulmonary Vein Stenosis | Acne | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Batten Disease | Seminoma | Acute Kidney Injury | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Orthostatic Intolerance | Pemphigus Vulgaris | Lymphoma | Avian Influenza | Primary Erythromelalgia | Hypogonadism | Thyroiditis | Micropenis | Liver Failure, Acute Infantile | Sclerosteosis | Ectopia Lentis, Isolated, Autosomal Recessive | Stuve-Wiedemann Syndrome | Lafora Disease | Pancytopenia | Chronic Beryllium Disease | Subcortical Band Heterotopia | Cryoglobulinemia | Polymyositis | Sulfite Oxidase Deficiency | Familial Retinal Arterial Macroaneurysm | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Basal Ganglia Disease, Biotin-responsive | Hypertension, Renal | Hypoparathyroidism | Hemophilia | Craniometaphyseal Dysplasia | Congenital Ichthyosiform Erythroderma | Congenital Torticollis | Obsessive-compulsive Disorder | Adenomyosis | Achondrogenesis | Hyperglycemia | Coronary Artery Disease | Fraser Syndrome | Primary Progressive Nonfluent Aphasia | Papillon-Lefevre Syndrome | Psoriasis | Osteosarcoma | Primary Hyperoxaluria Type 1 | Contact Dermatitis | Holoprosencephaly | Hyperinsulinism-hyperammonemia Syndrome | Frontotemporal Dementia | T-cell Lymphoma, Subcutaneous Panniculitis-like | Intracranial Hypertension | Sorsby Fundus Dystrophy | Osteochondrosis | Corneal Edema | Pseudoachondroplasia | Microcephaly | Spasticity | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Pyruvate Dehydrogenase Deficiency | Sengers Syndrome | Carey-Fineman-Ziter Syndrome | Portal Vein Thrombosis | Pemphigoid | Gigantism | Poikiloderma With Neutropenia | Scapuloperoneal Myopathy, X-linked Dominant | Lissencephaly 2 | Greenberg Dysplasia | Niemann-Pick Disease, Type A | Hypodontia | Congenital Tufting Enteropathy | Vascular Cognitive Impairment | Sleep Apnea, Obstructive | Multiple Sclerosis | Keratitis-ichthyosis-deafness Syndrome | Von Willebrand Disease | L-2-Hydroxyglutaric Aciduria | Juvenile Myelomonocytic Leukemia | Kaposi Sarcoma | Optic Neuritis | Cohen Syndrome | Lassa Fever | Hemangioma | Asthma | Cervicitis | Hypertensive Nephropathy | Thromboembolism | Primary Ovarian Insufficiency | Intracerebral Hemorrhage | Epithelial-myoepithelial Carcinoma | Absence Epilepsy | Hyperbilirubinemia | Carcinoma, Squamous Cell | Growth Hormone Excess | Nemaline Myopathy 10 | Carcinoid Tumor | Polymicrogyria | Lipid Metabolism Disorders | Argininosuccinic Aciduria | Esophagitis, Eosinophilic | Hepatitis B, Chronic | Occipital Neuralgia | Optic Nerve Hypoplasia, Bilateral | Blastomycosis | Poirier-Bienvenu Neurodevelopmental Syndrome | Rothmund-Thomson Syndrome | Tonsillitis | Oligoasthenoteratozoospermia | 3C Syndrome | Hepatopulmonary Syndrome | Osteopathia Striata With Cranial Sclerosis | Giant Axonal Neuropathy | Hepatitis A | Dystrophy, Cone-rod | Cardiospondylocarpofacial Syndrome | Coloboma | Leukocyte Adhesion Deficiency | Menetrier Disease | Asplenia | Thyrotoxic Periodic Paralysis | Basal Ganglia Cerebrovascular Disease | Asthma, Nocturnal | Autonomic Nervous System Disorders | Necrotizing Autoimmune Myopathy | Neuropathy | Follicular Dendritic Cell Sarcoma | Multifocal Motor Neuropathy | Neovascular Glaucoma | Xeroderma Pigmentosum Variant Type | Measles | Malignant Fibrous Histiocytoma | Pre-eclampsia | Angioedema, Hereditary | Hereditary Spastic Paraplegia | Celiac Disease | Meningioma | Tyrosine Hydroxylase Deficiency | Hyperammonemia | Dysthymia | Vertigo | Viral Meningitis | Retinal Dystrophy, Early-onset Severe | Fibronectin Glomerulopathy | Mabry Syndrome | Blepharophimosis Syndrome | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Common Variable Immunodeficiency | Hepatic Steatosis | Birt-Hogg-Dube Syndrome | Skin Carcinoma | Erythrokeratodermia Variabilis | Currarino Syndrome | Biotinidase Deficiency | Meningioma, Benign | Retinitis Pigmentosa 3 | Osteogenesis Imperfecta | Large Granular Lymphocytic Leukemia | Genee-Wiedemann Syndrome | Hepatorenal Syndrome | Lymphangioleiomyomatosis | Down Syndrome | Erythromelalgia | CHOPS Syndrome | N-acetylglutamate Synthase Deficiency | Branchiootorenal Syndrome | Nance-Horan Syndrome | Intestinal Pseudo-obstruction | Gynecomastia | Larsen Syndrome | Prader-Willi Syndrome | Hypohidrotic Ectodermal Dysplasia, X-linked | Amelanotic Melanoma | Transthyretin-related Amyloidosis | Osteoporosis-pseudoglioma Syndrome | Aceruloplasminemia | DICER1 Syndrome | Cartilage Disorders | IgA Nephropathy | Neurogenic Bladder | Mitochondrial Disease | Uremic Pruritus | Familial Hypobetalipoproteinemia | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Cardiac Arrest | Familial Glucocorticoid Deficiency | Gerodermia Osteodysplastica | Spinocerebellar Ataxia Type 21 | PHARC Syndrome | Neurocysticercosis | VEXAS Syndrome | Jaundice, Obstructive | Eiken Syndrome | Usher Syndrome Type IIC | Familial Exudative Vitreoretinopathy | WAGR Syndrome | Neuroma | Duodenal Atresia | Mumps | Basan Syndrome | Epiphyseal Chondrodysplasia, Miura Type | Crigler-Najjar Syndrome | Pulmonary Veno-occlusive Disease | Epidermolytic Ichthyosis, Annular | Pseudoexfoliation Syndrome | Peroxisomal Disorder | Meningococcal Infections | Spitz Nevus | Mastitis | Thrombophlebitis | Myelitis, Transverse | Hyperparathyroidism, Secondary | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Yellow Fever | Motion Sickness | Ureteropelvic Junction Obstruction | Pouchitis | Charcot-Marie-Tooth Disease, Type 2A | Thrombocytopenia | Craniofrontonasal Syndrome | Tricho-hepato-enteric Syndrome | Hemangioblastoma | Epithelioid Hemangioma | Acrodermatitis Enteropathica | Cockayne Syndrome | Dubin-Johnson Syndrome | Gestational Trophoblastic Disease | Uremia | Stromal Corneal Dystrophy | Leber Congenital Amaurosis | Ollier Disease | Dent Disease | Chronic Thromboembolic Pulmonary Hypertension | Pathological Gambling | Postpartum Depression | Tetanus | Glomerulonephritis, Membranous | Congenital Heart Block | Myosin Storage Myopathy | Walker-Warburg Syndrome | Retinopathy, Diabetic | Hereditary Elliptocytosis | Hypertension | Antisynthetase Syndrome | Vitreoretinal Degeneration, Snowflake Type | Carbamoyl Phosphate Synthetase I Deficiency | Pupil Disorders | Charcot-Marie-Tooth Disease Type 4 | Erdheim-Chester Disease | Common Cold | Giant Cell Glioblastoma | Periodontitis | Premenstrual Syndrome | Acne Vulgaris | Sleep Apnea | Urolithiasis | Lymphoma Lymphoblastic | Nephronophthisis | Benign Familial Neonatal Convulsions | Glycogen Storage Disease Type 1b | Triphalangeal Thumb-polysyndactyly Syndrome | Neurofibrosarcoma | Glycogen Storage Disease Type 6 | Acrodysostosis | Brugada Syndrome 1 | Persistent Mullerian Duct Syndrome | Cerebral Amyloid Angiopathy | Nevus | Costello Syndrome | Fucosidosis | Splenomegaly | Peters-plus Syndrome | Dupuytren Disease | Schistosomiasis Mansoni | Tay-Sachs Disease | Bronchitis | Metachromatic Leukodystrophy | Stargardt Disease | Acute Lung Injury | Epidermolysis Bullosa Dystrophica | Amebiasis | Acute Motor Axonal Neuropathy | Milk Allergy | Hermansky-Pudlak Syndrome | Bardet-Biedl Syndrome | Multiple Myeloma | Myotonic Disorders | Mucolipidosis Type II | Pneumococcal Meningitis | Chromosome 17q21.31 Deletion Syndrome | Benign Hereditary Chorea | Plasma Cell Leukemia | Small Lymphocytic Lymphoma | Placenta Previa | Rhabdomyosarcoma, Alveolar | Borjeson-Forssman-Lehmann Syndrome | Nicotine Dependence | Dyslexia | Myelodysplasia | Homocystinuria | LRBA Deficiency | Schaaf-Yang Syndrome | Stiff-man Syndrome | Pineoblastoma | Chronic Myelomonocytic Leukemia | Tuberculous Meningitis | Mannosidase Deficiency Diseases | Meningococcal Meningitis | Macular Corneal Dystrophy Type 1 | Bronchiolitis | Epidermolytic Hyperkeratosis | Long QT Syndrome Type 1 | Usher Syndrome Type I | Bone Giant Cell Tumor | Endophthalmitis | Chorioretinitis | Glaucomatocyclitic Crisis | Sturge-Weber Syndrome | Pyruvate Carboxylase Deficiency Disease | Hypersensitivity | Cone Dystrophy | Still Disease | Alpha-thalassemia Myelodysplasia Syndrome | Hepatic Veno-occlusive Disease | Hyperinsulinemic Hypoglycemia | Glycogen Storage Disease Type 0, Muscle | Dyslipidemia | Spinocerebellar Ataxia Type 31 | Schuurs-Hoeijmakers Syndrome | Palsy, Cerebral | Osteogenesis Imperfecta Type II | Paracoccidioidomycosis | Spinal And Bulbar Muscular Atrophy | Hypervalinemia