Disease

Tenosynovial Giant Cell Tumor

About the Disease
Pigmented Villonodular Synovitis, also known as localized pigmented villonodular synovitis, is related to villonodular synovitis and synovitis, and has symptoms including pain An important gene associated with Pigmented Villonodular Synovitis is PTPN11 (Protein Tyrosine Phosphatase Non-Receptor Type 11), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Granisetron and Etoposide have been mentioned in the context of this disorder. Affiliated tissues include lymph node, testis and bone marrow, and related phenotypes are Increased shRNA abundance (Z-score > 2) and Increased shRNA abundance (Z-score > 2)

Common Targets
CCN1 | IFIT1B | H3-3B | SOGA3 | ASB7 | FANCE | CC2D1A | TNFSF11 | G4318 | OSGIN1 | ANKRD61 | TENM1 | FLT3 | MIDEAS | PFKFB4 | SESTD1 | IDH2 | FDPS | CBL | SLC45A1 | RUFY1 | CXCR2 | IKZF3 | CSF2 | DNAH7 | IGFBP4 | KMT2D | ZNF665 | KIT | ATN1 | SLC15A5 | MMP1 | LRRC3C | MAN2B1 | MYO3A | PCDHB6 | IKBKE | KIF26A | CSF1R | PDGFRB | ZNF687 | PPARG | ASXL1 | ZXDB | ZNF366 | H3-3A | MED13L

疾病靶点研报
Tenosynovial Giant Cell Tumor

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

Other Diseases

Urofacial Syndrome | Agranulocytosis | Epidermolysis Bullosa Dystrophica | Acute Anterior Uveitis | Neuronal Ceroid Lipofuscinosis | Fibrosarcoma | Gitelman Syndrome | Cervical Dystonia | Hypertension, Portal | Epicondylitis | Nicolaides-Baraitser Syndrome | Greig Cephalopolysyndactyly Syndrome | Hyperglycemia | Sclerosteosis | Trigonocephaly | Keloid | Myofibromatosis | Diabetic Encephalopathy | Superficial Spreading Melanoma | Melnick-Needles Syndrome | Vitamin B12 Deficiency | Persistent Truncus Arteriosus | Kohlschutter-Tonz Syndrome | Carney-Stratakis Syndrome | Craniofacial Dysostosis | Dental Caries | Christianson Syndrome | Craniosynostosis | Hemimegalencephaly | Achromatopsia | Aphasia | Neurocysticercosis | Alopecia | Dermatomyositis | Scapuloperoneal Myopathy, X-linked Dominant | Dowling-Degos Disease | Steel Syndrome | Double Outlet Right Ventricle | Endometrial Hyperplasia | Glutaric Aciduria Type 2 | Rolandic Epilepsy | Hemoglobinopathies | Craniofrontonasal Syndrome | Neurocutaneous Syndromes | Hemorrhoids | Congenital Dyserythropoietic Anemia Type 1 | Dermatofibrosarcoma | Alstrom Syndrome | Cushing Syndrome | Acute Generalized Exanthematous Pustulosis | Renal Medullary Carcinoma | Hemochromatosis Type 2 | PHARC Syndrome | Salla Disease | Connective Tissue Disorders | Sarcosinemia | Peritonitis | IMAGe Syndrome | Erythema Nodosum | Disseminated Intravascular Coagulation | Inflammatory Bowel Disease | Tonsillitis | Small Lymphocytic Lymphoma | Sturge-Weber Syndrome | Okihiro Syndrome | Wilson's Disease | Glutaric Aciduria Type 3 | Osteomalacia | Hyperammonemia | Transient Bullous Dermolysis Of The Newborn | Diffuse Palmoplantar Keratoderma | Pilomatrix Carcinoma | Ichthyosis, X-linked | Melanoma, Malignant | Rash | Rubeosis Iridis | Globozoospermia | Waardenburg Syndrome | Hyperparathyroidism-jaw Tumor Syndrome | Hypogammaglobulinemia | FG Syndrome | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Trachoma | Gingivitis | Hypogonadism | Atelosteogenesis Type 1 | Giant Axonal Neuropathy | HANAC Syndrome | Myelodysplasia | Common Cold | Neutrophilia | Blood Protein Disorders | Gestational Trophoblastic Disease | Polymyositis | Borderline Personality Disorder | Idiopathic Multicentric Castleman Disease | Avian Influenza | Pigment Dispersion Syndrome | Chiari Malformation Type I | Cryptosporidiosis | Uterine Leiomyoma | Palmoplantar Keratoderma | Charcot-Marie-Tooth Disease Type 2D | Intracranial Hypertension | Androgenic Alopecia | Neurotoxicity | Communication Disorders | Hereditary Elliptocytosis | Guillain-Barre Syndrome | Cold Agglutinin Disease | Histoplasmosis | Primary Cutaneous Amyloidosis | Pitt-Hopkins Syndrome | Cockayne Syndrome | Polycystic Ovary Syndrome | Waardenburg Syndrome Type 4 | Porencephaly | Intestinal Tuberculosis | Silver-Russell Syndrome | Hyperuricemia | Nephronophthisis | Goiter | Cardiomyopathy, Dilated, 1L | Eczema | Congenital Lipoid Adrenal Hyperplasia | Infantile Spasm | Congenital Bilateral Absence Of Vas Deferens | Thyroiditis, Autoimmune | Vitamin D Deficiency | Hereditary Pyropoikilocytosis | Holt-Oram Syndrome | Congenital Dyserythropoietic Anemia Type 4 | Myoclonus | Still Disease | Hepatitis, Chronic | Sweet Syndrome | Macrodactyly | B-cell Prolymphocytic Leukemia | Meconium Ileus | Protein S Deficiency | Hyperinsulinemic Hypoglycemia | Hypertensive Retinopathy | Duane Retraction Syndrome | Craniometaphyseal Dysplasia | Cocaine-Related Disorders | Bronchitis, Chronic | Cervicitis | Osteomyelitis | Hydrops Fetalis | Nail Disorder, Nonsyndromic Congenital | Pancytopenia | Infectious Diarrhea | Autism | Congenital Myopathy | Ichthyosis Bullosa Of Siemens | Familial Digital Arthropathy-brachydactyly | Mastitis | Thanatophoric Dysplasia Type 1 | Chromosome 9q34.3 Deletion Syndrome | Lymphoproliferative Disorders | Pemphigus | Myeloid Leukemia | Oculocutaneous Albinism | Thyroid Hormone Resistance | Glucagonoma | Antithrombin III Deficiency | Autosomal Recessive Spastic Paraplegia Type 54 | Usher Syndrome Type IIC | Asphyxia Neonatorum | Wagner Disease | Systemic Lupus Erythematosus | Contact Dermatitis | Granular Corneal Dystrophy Type 1 | Spinocerebellar Ataxia Type 16 | Hepatitis B, Chronic | Nephrocalcinosis | Vici Syndrome | Spitz Nevus | Keratoconjunctivitis | Blepharospasm | Mucolipidosis Type III | Camurati-Engelmann Disease | Primary Progressive Nonfluent Aphasia | Epidermolysis Bullosa Simplex, Generalized | Microphthalmia | Rhabdoid Tumor | Blepharitis | Meier-Gorlin Syndrome | Chronic Lymphocytic Leukemia | Costello Syndrome | Panniculitis | Tylosis With Esophageal Cancer | Aspartylglycosaminuria | Azoospermia | CREST Syndrome | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Torticollis | Corticobasal Syndrome | Reticular Dysgenesis | Retinoschisis | Acquired Partial Lipodystrophy | Alopecia Areata | Hemophagocytic Lymphohistiocytosis | Majeed Syndrome | Tetraplegia | Retinopathy Of Prematurity | Atherosclerosis | Lentigo | McKusick Type Metaphyseal Chondrodysplasia | Congenital Nystagmus | Goiter, Nodular | Trichorhinophalangeal Syndrome | Basan Syndrome | Shock, Cardiogenic | Spinocerebellar Ataxia Type 31 | Meckel-Gruber Syndrome | Congenital Hereditary Endothelial Dystrophy Type II | Pulmonary Alveolar Microlithiasis | Lipoma | Dementia | Gilbert Syndrome | Cranial Nerve Disease | Autonomic Neuropathy | Gynecomastia | Spinocerebellar Ataxia Type 42 | Periodic Limb Movement Disorder | Wolfram Syndrome | Pleomorphic Xanthoastrocytoma | Bainbridge-Ropers Syndrome | Hyperoxaluria | Coloboma | Congenital Hereditary Endothelial Dystrophy Type I | Delirium | Posterior Polar Cataract | Anorexia Nervosa | Alkaptonuria | Blue Nevus | Familial Male-limited Precocious Puberty | Lichen Planus | Chronic Enteropathy Associated With SLCO2A1 Gene | Sleep Apnea | Diabetes Mellitus, Transient Neonatal | Keratoacanthoma | Hypertelorism | Adenosine Deaminase 2 Deficiency | Goldenhar Syndrome | Gyrate Atrophy Of The Choroid And Retina | Distal Spinal Muscular Atrophy | Cerebral Cavernous Malformations | Colitis | Depression | Paraganglioma | Nicotine Addiction | Lymphoma Lymphoblastic | Citrullinemia | Anemia | Gliosarcoma | Autonomic Nervous System Disorders | Primary Lateral Sclerosis | Rheumatoid Arthritis | Basal Ganglia Disease | Cornelia De Lange Syndrome | Turner's Syndrome | Leukoplakia | Metanephric Adenoma | Iron Metabolism Disorders | Creutzfeldt-Jakob Disease | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Thrombocythemia, Essential | Arthritis, Psoriatic | Gallstones | Down Syndrome | Cardiomyopathy, Restrictive | Microcephaly, Seizures, And Developmental Delay | Kawasaki Disease | Leigh Syndrome | Congenital Heart Block | Renal-hepatic-pancreatic Dysplasia | Renal Failure | Aspergillosis | Congenital Disorders Of Glycosylation | Galactosemia | Amish Infantile Epilepsy Syndrome | Purpura, Thrombotic Thrombocytopenic | Retinitis Pigmentosa 3 | Pulmonary Sclerosing Hemangioma | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Celiac Disease | Diabetes Gestational | Heavy Chain Disease | Brachial Plexus Neuropathy | Pendred Syndrome | Maple Syrup Urine Disease | DEND Syndrome | Chromosome 16p11.2 Deletion Syndrome | Toxoplasmosis | Poikiloderma With Neutropenia | Carney Triad | Plasma Cell Dyscrasia | Liver Failure, Acute Infantile | Epidermolytic Ichthyosis, Annular | Galloway-Mowat Syndrome | Multifocal Motor Neuropathy | Chondroma | Epithelioid Hemangioma | Pachyonychia Congenita | Systemic Mastocytosis | Mannosidase Deficiency Diseases | Facioscapulohumeral Muscular Dystrophy Type 2 | Acrodysostosis | Autoimmune Polyendocrine Syndrome | Arthropathy | Myoclonic Epilepsy With Ragged Red Fibers | Persistent Fetal Circulation | Charcot-Marie-Tooth Disease Type 4 | Huntington's Disease | Botulism | Bronchiectasis | Lymphangioleiomyomatosis | Cryopyrin-associated Periodic Syndromes | Epidermolytic Palmoplantar Keratoderma | Basal Ganglia Disease, Biotin-responsive | Primary Hyperoxaluria Type 3 | Graves Disease | Von Hippel-Lindau Disease | Congenital Stationary Night Blindness | Veno-occlusive Disease | Cystinuria | Potocki-Shaffer Syndrome | Gout | Pemphigoid | Spondylocostal Dysostosis | Thalassemia | Chronic Mucocutaneous Candidiasis | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Pneumonia, Bacterial | Rhabdomyosarcoma, Alveolar | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Mountain Sickness | Hepatic Adenomatosis | Spondylolisthesis | Cardiomyopathy, Peripartum | Hypersomnia | Becker Muscular Dystrophy | Polymicrogyria | Frontotemporal Dementia | Netherton Syndrome | Obesity | Calcium Pyrophosphate Deposition Disease | Incontinentia Pigmenti | Anal Fissure | Spinocerebellar Ataxia Type 1 | Desbuquois Syndrome | Cancer, Breast | Autosomal Recessive Congenital Ichthyosis | Polycystic Kidney, Autosomal Recessive | Melanoma | Endocarditis | ICF Syndrome | Anthrax | Primary Hyperoxaluria Type 1 | Pierre Robin Syndrome | Erythromelalgia | Ependymoma | Familial Hypobetalipoproteinemia | Lipid Metabolism Disorders | Familial Episodic Pain Syndrome | Walker-Warburg Syndrome | Inflammatory Myofibroblastic Tumor | Chronic Idiopathic Myelofibrosis | Osteogenesis Imperfecta Type II | Polycythemia | Fuchs Heterochromic Iridocyclitis | Eosinophilia | Absence Epilepsy | Chorioretinitis | Myoclonus-dystonia Syndrome | Interstitial Lung Diseases | Mood Disorder | Familial Glucocorticoid Deficiency | Adenoma, Pleomorphic | Addison Disease | Progressive Familial Intrahepatic Cholestasis Type 2 | Smoldering Myeloma | Blomstrand Osteochondrodysplasia | Varicocele | Juvenile Hyaline Fibromatosis | Dengue Hemorrhagic Fever | Cheilitis | Congenital Sodium Diarrhea | Keratitis-ichthyosis-deafness Syndrome | Cardiofaciocutaneous Syndrome | Aldosteronism | Myasthenia | Osteoporosis, Postmenopausal | Arteriosclerosis | Restless Legs Syndrome | Lattice Corneal Dystrophy | Rosacea | Aneurysm, Thoracic Aortic