Disease

Follicular Dendritic Cell Sarcoma

About the Disease
Follicular Dendritic Cell Sarcoma, also known as dendritic cell sarcoma, follicular, is related to castleman disease and angioimmunoblastic t-cell lymphoma, and has symptoms including fatigue, fever and night sweats. An important gene associated with Follicular Dendritic Cell Sarcoma is CR1 (Complement C3b/C4b Receptor 1 (Knops Blood Group)), and among its related pathways/superpathways are Innate Immune System and Class I MHC mediated antigen processing and presentation. The drugs Pembrolizumab and Antineoplastic Agents, Immunological have been mentioned in the context of this disorder. Affiliated tissues include lymph nodes, lung and lymph node, and related phenotype is immune system.

Common Targets
NF2 | G7157 | VHL | CTNNB1

疾病靶点研报
Follicular Dendritic Cell Sarcoma

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

Other Diseases

Acne Vulgaris | Pigment Dispersion Syndrome | Cervicitis | Polycystic Kidney, Autosomal Recessive | Zellweger Syndrome | Alpha-mannosidosis | Jacobsen Syndrome | Necrobiosis Lipoidica | Biotinidase Deficiency | Homocystinuria | Hereditary Neuropathy With Liability To Pressure Palsies | Palmoplantar Keratoderma | Myelofibrosis | Epidermal Nevus Syndrome | Heroin Dependence | Anti-glomerular Basement Membrane Disease | Osteoporosis | Porphyria Cutanea Tarda | Erythrokeratodermia Variabilis | Kaposi Sarcoma | Sleep Apnea, Obstructive | Chylothorax, Congenital | Spinocerebellar Ataxia | Tularemia | Pseudoachondroplasia | Hemochromatosis Type 1 | Dysthymia | Holoprosencephaly | Fascioliasis | Mucolipidosis Type III | Megaloblastic Anemia | Temporal Lobe Epilepsy | Neovascular Glaucoma | Anemia | Neural Tube Defect | Cocaine-Related Disorders | Cutis Laxa | Polyradiculopathy | Spinocerebellar Ataxia Type 8 | Microcephalic Primordial Dwarfism | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Malnutrition | Frontotemporal Dementia | Congenital Mirror Movements | Spondylocostal Dysostosis | Coma | Eating Disorder | Primary Hyperoxaluria | Charcot-Marie-Tooth Disease Type 3 | Down Syndrome | Melanoma, Malignant | Maple Syrup Urine Disease | Wiedemann-Steiner Syndrome | Schuurs-Hoeijmakers Syndrome | Tendinitis | Optic Neuritis | Trachoma | Cancer, Skin | Hydrops Fetalis | Patent Ductus Arteriosus | Cancer, Kidney | Split Hand-foot Malformation | Kernicterus | Melanocytic Nevus | Aplasia Cutis Congenita | Leishmaniasis, Cutaneous | Saul-Wilson Syndrome | Heart Septal Defects | Epidermolytic Ichthyosis, Annular | Pituitary Dwarfism | Eiken Syndrome | Currarino Syndrome | Chronic Leukemia | Beta-Propeller Protein-associated Neurodegeneration | Acute Lymphocytic Leukemia | Trichuriasis | Still Disease | Hepatic Adenomatosis | Pneumonia, Mycoplasma | Cystitis, Interstitial | Pyruvate Kinase Deficiency | Glycogen Storage Disease Type 9 | Cystitis | Dengue Hemorrhagic Fever | Liebenberg Syndrome | Hemangioma | Focal Segmental Glomerulosclerosis | Dowling-Degos Disease | Liver Failure | Transient Bullous Dermolysis Of The Newborn | Diabetes Gestational | Cohen Syndrome | Cerebellar Ataxia, Cayman Type | Cryptorchidism | Myelodysplasia | Cenani-Lenz Syndactyly Syndrome | Amish Infantile Epilepsy Syndrome | Adenoma, Pituitary | Arterial Tortuosity Syndrome | Meier-Gorlin Syndrome | Schizophrenia, Paranoid | Centronuclear Myopathy | Birt-Hogg-Dube Syndrome | Sjogren Syndrome | Acute Chest Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Gerstmann-Straussler-Scheinker Syndrome | Trichothiodystrophy | Pulmonary Stenosis | Agnathia-Otocephaly Complex | Vitamin B12 Deficiency | Epilepsy | L-2-Hydroxyglutaric Aciduria | Cyclic Vomiting Syndrome | DICER1 Syndrome | 3C Syndrome | Vertebrobasilar Insufficiency | Empyema | Waldenstrom Macroglobulinemia | Papilledema | Spinocerebellar Ataxia Type 17 | Takayasu's Arteritis | Syncope | Familial Retinal Arterial Macroaneurysm | Fibronectin Glomerulopathy | Dementia, Vascular | Relapsing Polychondritis | Benign Hereditary Chorea | Macular Corneal Dystrophy Type 1 | Overactive Bladder | IgA Deficiency | Acquired Partial Lipodystrophy | Poikiloderma With Neutropenia | Osteochondroma | Cannabis Abuse | Arthritis, Gouty | 5-oxoprolinase Deficiency | Scapuloperoneal Myopathy, X-linked Dominant | Abetalipoproteinemia | Carcinoma, Squamous Cell | Vitiligo | Hypohidrotic Ectodermal Dysplasia | Polycystic Liver | Riboflavin Transporter Deficiency Neuronopathy | Anuria | Adenomyosis | Hyperthyroidism | Poretti-Boltshauser Syndrome | Chronic Granulomatous Disease, X-linked | Leiomyoma | Absence Epilepsy | Tylosis With Esophageal Cancer | Nager Acrofacial Dysostosis | Borjeson-Forssman-Lehmann Syndrome | Facioscapulohumeral Muscular Dystrophy Type 2 | Hidradenitis Suppurativa | Congenital Central Hypoventilation Syndrome | Withdrawal Syndrome | Multiple Sulfatase Deficiency | Pancreatitis, Chronic | Colon Adenoma | Thyroid Hormone Resistance | Microcephaly | Zygomycosis | Delayed Sleep Phase Syndrome | Meconium Ileus | Inflammatory Bowel Disease | Pancytopenia | Keratocystic Odontogenic Tumor | Hyperinsulinemia | Charcot-Marie-Tooth Disease, Type 6 | Uveitis | Osteomalacia | Seizures | Pyruvate Decarboxylase Deficiency | Stroke, Ischemic | Bulimia Nervosa | Ichthyosis Bullosa Of Siemens | Oguchi Disease-2 | Neurofibromatosis | Porphyria | Cherubism | Arthritis, Reactive | Hemolytic Uremic Syndrome | Congenital Generalized Lipodystrophy | Intestinal Obstruction | Chloridorrhea, Congenital | Neuropathy | Carey-Fineman-Ziter Syndrome | Martsolf Syndrome | Familial Cerebral Amyloid Angiopathy | Localized Scleroderma | Hemangioblastoma | Otosclerosis | Posterior Polar Cataract | Pain | Paraganglioma, Carotid Body | Polymicrogyria | McLeod Syndrome | Sleep Apnea | Progressive Myoclonic Epilepsy | Nance-Horan Syndrome | Mycosis Fungoides | Androgenic Alopecia | Proteus Syndrome | Essential Fructosuria | Steel Syndrome | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Poirier-Bienvenu Neurodevelopmental Syndrome | Thrombophlebitis | Sick Sinus Syndrome 1 | Stevens-Johnson Syndrome | Spondyloarthritis | Early Infantile Epileptic Encephalopathy | Cancer, Brain | Diamond-Blackfan Anemia | Huntington's Disease | Thrombocythemia, Essential | Cholangiocarcinoma | Intracerebral Hemorrhage | Pleurisy | Jalili Syndrome | Hypercholesterolemia, Familial | Exotropia | Intestinal Hypomagnesemia 1 | Acute Leukemia | Diffuse Palmoplantar Keratoderma | Mohr-Tranebjaerg Syndrome | Pregnancy, Ectopic | Lymphoproliferative Disease, X-linked | Measles | Autoimmune Autonomic Ganglionopathy | Aldosteronism | Fahr Disease | Autoimmune Disease | Compartment Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Congenital Hypofibrinogenemia | Lymphoma, Mantle Cell | Silver-Russell Syndrome | Cardiac Arrest | Periodontitis | AIDS | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Viral Meningitis | Eczema | Colitis | REM Sleep Behavior Disorder | Pre-eclampsia | Rothmund-Thomson Syndrome | Adrenoleukodystrophy, X-linked | Lentigo | Retinal Diseases | Early Infantile Epileptic Encephalopathy 28 | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Malonyl-CoA Decarboxylase Deficiency | Tuberculosis | Common Variable Immunodeficiency | Mannosidase Deficiency Diseases | Chronic Idiopathic Myelofibrosis | Lung Diseases | Congenital Torticollis | Hypertension, Renal | Acute Coronary Syndrome | Cholestasis | Lissencephaly 2 | Usher Syndrome | Herpes Simplex Dermatitis | Glaucomatocyclitic Crisis | Nephronophthisis | Anorchia | Beare-Stevenson Syndrome | Carney-Stratakis Syndrome | Osteogenesis Imperfecta Type VI | Hyperparathyroidism, Primary | Antiphospholipid Syndrome | Hemolytic Uremic Syndrome, Atypical | Angiodysplasia | Mosaic Variegated Aneuploidy Syndrome 2 | KBG Syndrome | Growth Hormone Excess | Communication Disorders | Hereditary Elliptocytosis | Keratoconjunctivitis | Renal Tubular Dysgenesis | Lymphangioleiomyomatosis | Fuchs Heterochromic Iridocyclitis | Netherton Syndrome | Multifocal Motor Neuropathy | Neuroendocrine Cancer | Silicosis | Hypersensitivity Pneumonitis | Wieacker-Wolff Syndrome | Pierpont Syndrome | Celiac Disease | Agoraphobia | Mucolipidosis Type IV | Subcortical Band Heterotopia | Milk Allergy | Ameloblastoma | Myositis, Focal | Gnathodiaphyseal Dysplasia | Pernicious Anemia | Chondrosarcoma | Kidney Stones | VACTERL/VATER Association | Thanatophoric Dysplasia | Hypoplastic Left Heart Syndrome | Liddle Syndrome | Chromosome 9q34.3 Deletion Syndrome | Skin Fragility-woolly Hair Syndrome | Brenner Tumor | Osteopetrosis | B-cell Prolymphocytic Leukemia | Hepatitis D | Hemochromatosis | Congenital Stromal Corneal Dystrophy | Rhabdoid Tumor | Glycogen Storage Disease | Varices | Sarcosinemia | Knobloch Syndrome | Oculocutaneous Albinism Type 2 | Hyperparathyroidism, Secondary | WAGR Syndrome | Hyperferritinemia-cataract Syndrome | Neuromyotonia | Carcinoid Tumor | Keratitis | Duane Retraction Syndrome | Sialidosis | Carotid Artery Disease | Arteriosclerosis | Common Cold | Multiple Sclerosis, Secondary Progressive | Ganglioneuroma | Non-bullous Congenital Ichthyosiform Erythroderma | Oligoasthenoteratozoospermia | Bruck Syndrome | Spinocerebellar Ataxia Type 7 | Peters-plus Syndrome | Conjunctivitis, Allergic | Keratosis, Seborrheic | Bare Lymphocyte Syndrome | Congenital Nystagmus | Nephrotic Syndrome Type 1 | Pachyonychia Congenita | Glutaric Aciduria Type 3 | Osteogenesis Imperfecta | Ectodermal Dysplasia | Hydronephrosis | Chordoma | Amblyopia | Osteogenesis Imperfecta Type II | Weill-Marchesani Syndrome | Oligodendroglioma | Corticobasal Syndrome | Olmsted Syndrome | Coffin-Lowry Syndrome | Fraser Syndrome | Blood Protein Disorders | Limb Girdle Muscular Dystrophy | Primary Pigmented Nodular Adrenocortical Disease | Micro Syndrome | Fundus Albipunctatus | Renal Dysplasia | Wolfram Syndrome | Smoldering Myeloma | Corneal Edema | Spinocerebellar Ataxia Type 6 | Galactosialidosis | Familial Hypertrophic Cardiomyopathy | Cryoglobulinemia | Hyperlipidemia Type V | Hyperbilirubinemia | GATA2 Deficiency | Joubert Syndrome | Carcinoma, Merkel Cell | Protein C Deficiency | Crohn's Disease | Exfoliative Dermatitis | Rotor Syndrome | Lymphopenia | Diarrhea | Marinesco-Sjogren Syndrome | Fetal Akinesia Deformation Sequence | Progressive Familial Intrahepatic Cholestasis | Angioedema | Von Willebrand Disease | Budd-Chiari Syndrome | Toxoplasmosis | Mucolipidosis | Autism Spectrum Disorders | Epiphyseal Chondrodysplasia, Miura Type | Blue Rubber Bleb Nevus Syndrome | Perivascular Epithelioid Cell Tumor | Postpartum Depression | Alkaptonuria | Ectrodactyly | Rickets