Disease

Peripheral T-cell Lymphoma

About the Disease
Peripheral T-Cell Lymphoma, also known as lymphoma t-cell peripheral, is related to angioimmunoblastic t-cell lymphoma and burkitt lymphoma, and has symptoms including pruritus An important gene associated with Peripheral T-Cell Lymphoma is TNFRSF8 (TNF Receptor Superfamily Member 8), and among its related pathways/superpathways are ERK Signaling and Signal Transduction. The drugs Coenzyme M and Denileukin diftitox have been mentioned in the context of this disorder. Affiliated tissues include bone marrow, thymus and t cells, and related phenotypes are no effect and no effect

Common Targets
DLEC1 | FAM110B | ICOS | KIR3DL2 | G6774 | Protein farnesyltransferase | CXCR5 | AFF4 | SRGAP3 | TLR8 | PIK3R5 | HDAC10 | TNFRSF21 | DDX25 | HDAC2 | ADAMTS14 | PASK | HDAC6 | G5133 | THBS1 | MTERF2 | KIT | FOXO1 | ALDH1A2 | NINL | DENND4B | CIITA | MYD88 | G29126 | NF-kappaB (NFkB) | LATS1 | IL2RG | G207 | VAV1 | CHD1 | CSF1R | PASD1 | CD3 Complex (T Cell Receptor Complex) | Ribonucleoside-diphosphate reductase | DNMT3A | FAT1 | G5728 | KMT2C | HOXA9 | Geranylgeranyl transferase type-1 | CD58 | G673 | VAV2 | STAT6 | AURKB | PDCD11 | KDM4C | FAM221A | G598 | BRCA2 | LCK | IKZF1 | MAP3K2 | DUSP22 | CCR4 | LRRK1 | IDH1 | FGFR3 | BRD2 | GFI1 | DNA Topoisomerase II (nonspecified subtype) | CARD11 | MNX1 | ASXL3 | ADAMTS5 | G4851 | PRDM2 | PDGFRB | EML4 | PIK3CB | PIK3R1 | GATA6 | CHD2 | EBF3 | PEG3 | ADCK1 | VWA5B1 | BRD4 | PIK3CD | XIAP | ING1 | RIOK2 | PIK3R4 | TRAF6 | HDAC3 | HDAC11 | CDK9 | GORAB | FLRT2 | HDAC1 | CACNG8 | FAT2 | TENM1 | G4609 | G2475 | TP63 | NAV2 | DCAF10 | NUP133 | CLIP1 | XPO1 | NRN1 | RNF213 | G7157 | FLT4 | ZNF503 | COQ8A | G5595 | Tyrosine Kinase (nonspecified subtype) | SIRPA | TGFB1I1 | CD38 | FCGR3A | GABRG3 | CD52 | PDPK1 | FOXP4 | SYK | PDCD6 | TET2 | DDX20 | SH3BP4 | PTPN23 | ITK | FLT1 | MIB1 | EBF2 | CMYA5 | BIRC6 | AURKAIP1 | DAPK1 | EZH1 | CHD3 | BCORL1 | AATK | ITGA5 | JUP | CXCL12 | CDK20 | G920 | EBF1 | PCLO | Tubulin | FYB1 | CCND3 | EPHB6 | G836 | SYT6 | ALMS1 | CD7 | LTBP1 | PNP | SETD2 | BCL9 | KMT2A | HMCN1 | STK3 | RARB | CACNA1D | LRRN3 | IDH2 | RAD51 | PLCG1 | STAB1 | GPI | G4193 | NFRKB | IKZF3 | GTF2IRD1 | ADRA1D | CHD8 | GAK | PIK3CA | CTLA4 | LAMA2 | PIM1 | CLTC | COL19A1 | MDN1 | TLL1 | Janus Kinase (nonspecified subtype) | LYN | Ikzf1 | FAF1 | B2M | NFAT5 | MCM4 | IRF8 | ST18 | TIGIT | PAX8 | PDGFRA | CD47 | ACTA1 | BRIP1 | KDR | KMT2D | FYN | CD28 | STX11 | NOTCH2 | CREBBP | TNFRSF8 | ALPK2 | VHL | BCL6 | Histone deacetylase (nonspecified subtype) | Proteasome Complex | DHFR | PDGFA | MBD4 | TTC3 | DDX3X | G2146 | CD37 | CUL9 | G238 | COL6A3 | KLF9 | RARG | G3845 | PHLPP1 | APC | CDK12 | PKD2L1 | DDX55 | DNAH14 | G596 | CDH23 | MAP3K1 | CRBN | JAK3 | CTNNB1 | STAT5B | G472 | CD5 | JAK1 | RHOA | PIK3CG | DPH5 | RELN | EPHA6 | AURKA | DNA Methyltransferase (DNMT) (nonspecified subtype) | ABL2 | JAK2 | GRIK4 | BIRC2 | PLCG2 | MDM4 | MST1R

疾病靶点研报
Peripheral T-cell Lymphoma

Note: If you'd like to get a target analysis report for Peripheral T-cell Lymphoma, 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 Peripheral T-cell Lymphoma at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Precocious Puberty | Hepatopulmonary Syndrome | Dominant Optic Atrophy | Glycogen Storage Disease Type 9 | Fraser Syndrome | Charcot-Marie-Tooth Disease Type 4D | Cardiomyopathy, Peripartum | Congenital Muscular Dystrophy | Acne Vulgaris | Opisthorchiasis | Infertility, Male | Cancer, Prostate | Esotropia | Primary Hyperoxaluria Type 1 | Skin Fragility-woolly Hair Syndrome | Hypotonia-cystinuria Syndrome | Polyarteritis Nodosa | Primary Ovarian Insufficiency | Obsessive-compulsive Disorder | Glaucoma | Vitamin K Deficiency | Vitreoretinal Degeneration, Snowflake Type | Astigmatism | Pain | Charcot-Marie-Tooth Disease Type 4B1 | Gilbert Syndrome | Nijmegen Breakage Syndrome | Vogt-Koyanagi-Harada Syndrome | Osteitis | Chorea-acanthocytosis | Cerebrovascular Disorders | Leiomyoma | Chondrodysplasia Punctata 2, X-linked Dominant | Sezary Syndrome | Prediabetes | Primary Erythromelalgia | Viral Meningitis | Tyrosine Hydroxylase Deficiency | Congenital Hemolytic Anemia | Charcot-Marie-Tooth Disease Type 4 | Encephalopathy, Hepatic | Vascular Calcification | Kabuki Syndrome 2 | Sclerosing Cholangitis | Tatton-Brown-Rahman Syndrome | Restrictive Dermopathy | Long QT Syndrome Type 2 | Parvovirus B19 Infection | Herpes Simplex Dermatitis | Jaundice, Obstructive | Aceruloplasminemia | Infertility | Bernard-Soulier Syndrome | Blomstrand Osteochondrodysplasia | Gynecomastia | Beare-Stevenson Syndrome | Myoclonus-dystonia Syndrome | Currarino Syndrome | Kearns-Sayre Syndrome | Spastic Paraplegia Type 7 | Dwarfism | Lamellar Ichthyosis | Endocarditis | Hidradenitis Suppurativa | Common Cold | Spondylometaphyseal Dysplasia | Vestibular Disease | Polymyalgia Rheumatica | Polyradiculopathy | Alpha-thalassemia Myelodysplasia Syndrome | Bartter Syndrome | Atopy | Silver-Russell Syndrome | Non-bullous Congenital Ichthyosiform Erythroderma | Imerslund-Grasbeck Syndrome | Sengers Syndrome | Duane Retraction Syndrome | Congenital Stationary Night Blindness | Stevens-Johnson Syndrome | Pompe Disease | Multiple Sulfatase Deficiency | Neuroleptic Malignant Syndrome | Hereditary Sensory Neuropathy Type 1 | Craniopharyngioma | Familial Dysautonomia | Dengue Hemorrhagic Fever | Spinocerebellar Ataxia Type 23 | Deafness, Dystonia, And Cerebral Hypomyelination | Ligneous Conjunctivitis | Infantile Nephropathic Cystinosis | Sialidosis Type I | Aspartylglycosaminuria | Shwachman-Bodian-Diamond Syndrome | Cutis Laxa | Pitt-Hopkins Syndrome | Aldosterone Synthase Deficiency | Corneal Ulcer | Hereditary Spastic Paraplegia | Liebenberg Syndrome | Wieacker-Wolff Syndrome | Periventricular Nodular Heterotopia | Optic Neuritis | Schaaf-Yang Syndrome | Molybdenum Cofactor Deficiency | Encephalitis, Tick-borne | Autosomal Recessive Bestrophinopathy | Brachydactyly | Hypoparathyroidism | Schwannoma | Costello Syndrome | Von Willebrand Disease | Infantile Spasm | Mitochondrial Encephalomyopathy | Hepatitis A | Osteoglophonic Dysplasia | Zollinger-Ellison Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Retinal Dystrophy | C3 Glomerulonephritis | Otopalatodigital Syndrome Type 2 | Becker Muscular Dystrophy | Myelodysplasia | Lymphangioleiomyomatosis | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Hereditary Hemorrhagic Telangiectasia Type 2 | Rett Syndrome | Glomerulonephritis, Membranous | Prolymphocytic Leukemia | Bloom Syndrome | Aicardi-Goutieres Syndrome | Intestinal Obstruction | Inflammatory Myofibroblastic Tumor | Hyperhomocysteinemia | Cohen Syndrome | Vitiligo | Intestinal Hypomagnesemia 1 | Glaucoma, Congenital | Lathosterolosis | Spinocerebellar Ataxia Type 10 | Crimean-Congo Hemorrhagic Fever | Cutaneous Angiosarcoma | Leri-Weill Dyschondrosteosis | Glycogen Storage Disease Type 6 | Sleep Apnea, Central | Sickle Cell Anemia | Cryptosporidiosis | Coffin-Lowry Syndrome | Osteogenesis Imperfecta Type VI | Basal Cell Nevus Syndrome | Autoimmune Polyendocrine Syndrome | Dysferlinopathy | Heroin Dependence | Sarcoma | IgA Nephropathy | Skin Carcinoma | Rolandic Epilepsy | Benign Familial Infantile Seizures | Martsolf Syndrome | Hemochromatosis Type 2 | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Persistent Fetal Circulation | Tuberculosis | Myelitis, Transverse | Hemolytic Anemia | Hypereosinophilic Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Mesothelioma, Malignant | Multicystic Renal Dysplasia | Protein S Deficiency | Papillon-Lefevre Syndrome | Dermatofibrosarcoma | VEXAS Syndrome | Tendinopathy | 3-methylglutaconic Aciduria | Vitreoretinopathy, Proliferative | Azoospermia | Unverricht-Lundborg Syndrome | Language Disorders | Acute Chest Syndrome | MIRAGE Syndrome | Paroxysmal Nocturnal Hemoglobinuria | Synpolydactyly | Diabetes Insipidus, Nephrogenic | Epidermolytic Ichthyosis, Annular | Asthma, Exercise-induced | Sickle Cell Disease | Pemphigus Foliaceus | Bronchiectasis | Esophageal Carcinoma | Wagner Disease | Light Chain Amyloidosis | Congenital Disorders Of Glycosylation Type II | Thyroid Hormone Resistance | Bronchitis | Tetraplegia | McLeod Syndrome | Congenital Mirror Movements | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Pleomorphic Xanthoastrocytoma | Leber Congenital Amaurosis | Hoyeraal-Hreidarsson Syndrome | Kindler Syndrome | Hypertrophy | Nephrotic Syndrome Type 1 | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Metanephric Adenoma | Nephrotic Syndrome | Congenital Adrenal Hyperplasia | Neurodegeneration With Brain Iron Accumulation | Orotic Aciduria | Milk Allergy | Kaposi Sarcoma | Vici Syndrome | Oral Lichen Planus | Poikiloderma With Neutropenia | Charcot-Marie-Tooth Disease, Type 2 | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Tuberculous Meningitis | Encephalopathy, Glycine | Urea Cycle Disorder | Amyloidosis | B-cell Chronic Lymphocytic Leukemia | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Antisocial Personality Disorder | Batten Disease | LMNA-related Congenital Muscular Dystrophy | Diabetic Macular Edema | Van Der Knaap Disease | Ocular Hypertension | Donnai-Barrow Syndrome | Ataxia-ocular Apraxia 2 | 3-methylglutaconic Aciduria Type IV | Hepatitis, Autoimmune | Achondrogenesis | Hepatitis C, Chronic | Inflammatory Linear Verrucous Epidermal Nevus | Erectile Dysfunction | Duodenal Atresia | Alopecia Areata | Guanidinoacetate Methyltransferase Deficiency | Malignant Fibrous Histiocytoma | Bullous Pemphigoid | Lymphoma | Juvenile Xanthogranuloma | Malignant Peripheral Nerve Sheath Tumor | Early Infantile Epileptic Encephalopathy 13 | Trichomegaly | Temporal Lobe Epilepsy | Perivascular Epithelioid Cell Tumor | Hyperphenylalaninemia | Hemophagocytic Lymphohistiocytosis | Carbamoyl Phosphate Synthetase I Deficiency | Epidermolysis Bullosa Simplex, Generalized | Lassa Fever | Goldenhar Syndrome | Hereditary Hemorrhagic Telangiectasia | Stickler Syndrome | Alpha-1 Antitrypsin Deficiency | Connective Tissue Disorders | Pityriasis Rubra Pilaris | Primary Lateral Sclerosis | Acanthosis Nigricans | Waldenstrom Macroglobulinemia | Familial Retinal Arterial Macroaneurysm | Osteopathia Striata With Cranial Sclerosis | Growth Hormone Excess | Ileitis | Retinopathy Of Prematurity | Dysfibrinogenemia | Spinocerebellar Ataxia Type 31 | Charcot-Marie-Tooth Disease, Type 6 | Sorsby Fundus Dystrophy | Early Infantile Epileptic Encephalopathy 1 | Nephrocalcinosis | Nicolaides-Baraitser Syndrome | Spinocerebellar Ataxia Type 8 | Hypokalemia | Diabetes Insipidus | Charcot-Marie-Tooth Disease Type 2D | Veno-occlusive Disease | Chylothorax, Congenital | Congenital Generalized Lipodystrophy | Basan Syndrome | Oligospermia | Episodic Ataxia Type 2 | Thanatophoric Dysplasia | Walker-Warburg Syndrome | Menkes Disease | Absence Epilepsy | NGLY1 Deficiency | Adult Polyglucosan Body Disease | Dementia, Vascular | Creutzfeldt-Jakob Disease | Leprosy | Stargardt Disease | Cri-du-chat Syndrome | Knobloch Syndrome | Osteoporosis | Camptocormia | Leiomyosarcoma | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Pantothenate Kinase-associated Neurodegeneration | Aromatic L-amino Acid Decarboxylase Deficiency | Aphasia | Hemochromatosis | Guttate Psoriasis | Immunoproliferative Disorders | Juvenile Myoclonic Epilepsy | Corneal Edema | AIDS Dementia Complex | Non-Hodgkin Lymphoma | Joubert Syndrome | Parapsoriasis | Uterine Leiomyoma | Oculocutaneous Albinism Type 4 | Spondylolisthesis | Hypophosphatasia | Antenatal Bartter Syndrome Type 1 | PHARC Syndrome | Epicondylitis | Hereditary Neuropathy With Liability To Pressure Palsies | Hemophilia | Superficial Spreading Melanoma | Castleman Disease | Desbuquois Syndrome | Leukoencephalopathy, Progressive Multifocal | Exfoliative Dermatitis | Sensory Neuropathy | 3C Syndrome | Sarcoidosis | Learning Disability | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Myelitis | Progressive Familial Intrahepatic Cholestasis Type 2 | Cerebellofaciodental Syndrome | Anovulation | Panic Disorder | Intermittent Claudication | Hernia, Inguinal | Conduct Disorder | Blepharophimosis Syndrome | Holt-Oram Syndrome | Galactosemia | Preaxial Polydactyly | Tinea | Psoriasis | Agoraphobia | Polyomavirus Nephropathy | Hyperuricemia | Papilloma | Fetal Akinesia Deformation Sequence | Facioscapulohumeral Muscular Dystrophy | Encephalopathy | Optic Neuropathy, Anterior Ischemic | Spina Bifida | WAGR Syndrome | Trichothiodystrophy | Ebstein Anomaly | Gray Platelet Syndrome | Communication Disorders | Progressive Encephalopathy-optic Atrophy Syndrome | Early Infantile Epileptic Encephalopathy 4 | GLUT1 Deficiency Syndrome | Lateral Meningocele Syndrome | Acrocallosal Syndrome | Acute Leukemia | Myotonic Disorders | Low Phospholipid Associated Cholelithiasis | Kernicterus | Perry Syndrome | Reye Syndrome | Homocystinuria | Genitopatellar Syndrome | Meckel-Gruber Syndrome | Celiac Disease | Lipid Storage Myopathy | Chromosome 5q Deletion Syndrome | Auriculocondylar Syndrome | Sialidosis | Hyperlipidemia | Large Granular Lymphocytic Leukemia | Wolfram Syndrome 2 | Arthritis, Psoriatic | Jacobsen Syndrome | Endometriosis | Histiocytic Sarcoma | Bare Lymphocyte Syndrome | Hemosiderosis | NDH Syndrome | Dowling-Degos Disease | Fibrosis | Familial Advanced Sleep Phase Syndrome | Hypotrichosis Simplex | Fibrosarcoma | Subacute Sclerosing Panencephalitis | Congenital Dyserythropoietic Anemia Type 1 | Hermansky-Pudlak Syndrome | Saul-Wilson Syndrome | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Behavioral Variant Of Frontotemporal Dementia