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

Hoyeraal-Hreidarsson Syndrome | Neurodermatitis | Diffuse Intrinsic Pontine Glioma | Cleidocranial Dysplasia | Azoospermia | Colitis, Collagenous | Glycogen Storage Disease Type 1b | Keratitis | Kaposiform Hemangioendothelioma | Panuveitis | Chondromyxoid Fibroma | Filariasis | Infantile Refsum Disease | Anemia | Microvillus Inclusion Disease | Hereditary Sensory Neuropathy Type 1 | Nephrotic Syndrome Type 1 | Tibial Muscular Dystrophy | Asthma, Nocturnal | Porokeratosis | Periodic Limb Movement Disorder | Infantile Nephropathic Cystinosis | Methylmalonic Aciduria And Homocystinuria, CblC Type | Fibronectin Glomerulopathy | Skin Carcinoma | Tinea | Primary Progressive Aphasia | Diarrhea | Mucolipidosis Type IV | Autosomal Recessive Congenital Ichthyosis | Achondrogenesis | Hereditary Coproporphyria | Benign Familial Pemphigus | Glycogen Storage Disease | Temtamy Preaxial Brachydactyly Syndrome | Bursitis | Epidermolytic Ichthyosis, Annular | T-cell Chronic Lymphocytic Leukemia | Exfoliative Dermatitis | Herpes Simplex Dermatitis | Pelizaeus-Merzbacher Disease | Schaaf-Yang Syndrome | Subacute Sclerosing Panencephalitis | Blue Nevus | Papulopustular Rosacea | Meier-Gorlin Syndrome | Spinocerebellar Ataxia Type 20 | Muscle Wasting | Hemophagocytic Lymphohistiocytosis | Charcot-Marie-Tooth Disease Type 4 | Spinocerebellar Ataxia Type 6 | Papilloma | Spinocerebellar Ataxia Type 23 | Ehlers-Danlos Syndrome | Leukocyte Adhesion Deficiency | Hypertension, Renal | Charcot-Marie-Tooth Disease Type 2D | Epidermolysis Bullosa Dystrophica | Esophagitis, Eosinophilic | Pseudohermaphroditism | Glycogen Storage Disease Type 1 | Adrenal Insufficiency | Costello Syndrome | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Heart Failure | Benign Hereditary Chorea | Chronic Idiopathic Myelofibrosis | Antenatal Bartter Syndrome Type 1 | Spinal Muscular Atrophy | Proximal Symphalangism | Vici Syndrome | Thyroiditis | Focal Dermal Hypoplasia | Hypobetalipoproteinemias | Klinefelter Syndrome | Glycogen Storage Disease Type 4 | Retinal Detachment | Metabolic Diseases | Galactosialidosis | Urea Cycle Disorder | Presbyopia | Astrocytoma, Anaplastic | Blau Syndrome | Dent Disease | Graft-versus-host Disease | Graves Disease | Glioblastoma | Lymphopenia | Fibrillation, Atrial | Twin-to-twin Transfusion Syndrome | Mabry Syndrome | Bipolar Disorder | Glycogen Storage Disease Type 5 | Adrenoleukodystrophy, X-linked | Usher Syndrome Type I | Thrombasthenia | Mosaic Variegated Aneuploidy Syndrome 2 | Silver-Russell Syndrome | Allergic Contact Dermatitis | Basan Syndrome | Choroiditis | Megaloblastic Anemia | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Wiedemann-Steiner Syndrome | Dystonia | Glomerulonephritis | Dysmorphophobia | Carpal Tunnel Syndrome | Otosclerosis | Migraine | Brachydactyly | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Asthma, Exercise-induced | Crigler-Najjar Syndrome | Lafora Disease | Chronic Granulomatous Disease, X-linked | Fanconi Syndrome | Lateral Meningocele Syndrome | Bethlem Myopathy | Alexander Disease | Smoldering Myeloma | Niemann-Pick Disease, Type B | Apparent Mineralocorticoid Excess Syndrome | Familial Dysautonomia | Gastritis | Japanese Encephalitis | Cancer, Skin | Mitochondrial DNA Depletion Syndrome 13 | Duane Retraction Syndrome | Long QT Syndrome Type 3 | Van Der Knaap Disease | Esthesioneuroblastoma | Pyruvate Carboxylase Deficiency Disease | Kashin-Beck Disease | Progressive Myoclonic Epilepsy | Hypertrophy | Autoimmune Hemolytic Anemia | Best Macular Dystrophy | Mucolipidosis Type III | Retinal Telangiectasia | Viral Meningitis | Spastic Paraplegia Type 7 | Retinitis | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Myelitis, Transverse | Craniofacial Dysostosis | Acrodermatitis Enteropathica | Congenital Myopathy | Ophthalmoplegia | Myeloid Leukemia | Varices | Hypohidrotic Ectodermal Dysplasia | Hemochromatosis Type 1 | Multiple Sclerosis, Secondary Progressive | Microcephalic Primordial Dwarfism | Polyarteritis Nodosa | Nicotine Dependence | Hypoproteinemia, Hypercatabolic | Astrocytoma | Apert Syndrome | Tardive Dyskinesia | Combined Pituitary Hormone Deficiency | Peutz-Jeghers Syndrome | Choroideremia | Distal Myopathy | Warsaw Breakage Syndrome | Conjunctivitis, Allergic | IgA Deficiency | Nicolaides-Baraitser Syndrome | Cancer, Prostate | Hemochromatosis | Arthritis, Reactive | Hyperphenylalaninemia | Left Ventricular Noncompaction | Congenital Aniridia | Glaucomatocyclitic Crisis | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Nasodigitoacoustic Syndrome | Robinow Syndrome | Diverticulitis | Cutaneous Lupus Erythematosus | Tendinopathy | Saethre-Chotzen Syndrome | Canavan Disease | H Syndrome | Hyperferritinemia-cataract Syndrome | Botulism | Goiter | Albinism | Plasma Cell Leukemia | Acral Lentiginous Melanoma | Beare-Stevenson Syndrome | Congenital Hereditary Endothelial Dystrophy Type I | Hereditary Elliptocytosis | Stargardt Disease | DOCK8 Immunodeficiency Syndrome | Waardenburg Syndrome Type 2E | Reye Syndrome | Mitochondrial Myopathy | Multiple Sulfatase Deficiency | 3-methylglutaconic Aciduria Type I | Leukoencephalopathy, Progressive Multifocal | Isobutyryl-CoA Dehydrogenase Deficiency | Sarcoidosis, Pulmonary | Specific Granule Deficiency | Crohn's Disease | Chondroma | Tetanus | Blastoma, Pleuropulmonary | Tinea Versicolor | Meningeal Melanocytoma | Osteogenesis Imperfecta Type II | Non-epidermolytic Palmoplantar Keratoderma | Okihiro Syndrome | Zellweger Syndrome | Senior-Loken Syndrome | Androgen Insensitivity | Epidermal Nevus Syndrome | Cryopyrin-associated Periodic Syndromes | Central Pain Syndrome | Macrophage Activation Syndrome | Infertility, Male | Adult Polyglucosan Body Disease | Multiple Sclerosis, Primary Progressive | Hyperparathyroidism-jaw Tumor Syndrome | Ocular Albinism Type 1 | Spinocerebellar Ataxia Type 14 | Ollier Disease | Peters-plus Syndrome | Optic Neuropathy | Acromesomelic Dysplasia | Monilethrix | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Trichothiodystrophy | Cyclic Vomiting Syndrome | Malonyl-CoA Decarboxylase Deficiency | Norrie Disease | Conjunctivitis | Prediabetes | Carcinoma, Small Cell | Polyneuropathy | Autosomal Recessive Bestrophinopathy | Lipid Metabolism Disorders | Early Infantile Epileptic Encephalopathy | 3-methylglutaconic Aciduria | Malaria, Cerebral | Retinal Coloboma | Phenylketonuria | Anal Fissure | Spinocerebellar Ataxia Type 5 | Congenital Torticollis | Renal Hypomagnesemia 3 | Apraxia | Waardenburg Syndrome Type 4 | X-linked Creatine Transporter Deficiency | Lymphoma | Paronychia | Wagner Disease | Iron Deficiency Anemia | Platelet Disorders | Corneal Ulcer | Guillain-Barre Syndrome | Gangliosidosis, GM1 | Atopic Dermatitis | Rash | Cystinuria | Joubert Syndrome 2 | Marfan Syndrome | Rhabdomyosarcoma, Embryonal | Glycogen Storage Disease Type 6 | Uveitis | Nijmegen Breakage Syndrome | Small Lymphocytic Lymphoma | Lymphoma, Follicular | Scoliosis | Seizures-scoliosis-macrocephaly Syndrome | Sezary Syndrome | Eosinophilic Asthma | Xeroderma Pigmentosum Variant Type | Cardiomyopathy, Hypertrophic | Dysgerminoma | Vitelliform Macular Dystrophy | Neurofibroma, Plexiform | Angioedema | Pleomorphic Xanthoastrocytoma | Ichthyosis, X-linked | Pycnodysostosis | Tay-Sachs Disease | Trachoma | Odonto-onycho-dermal Dysplasia | Aplastic Anemia | Kallmann Syndrome | Ichthyosis Bullosa Of Siemens | Usher Syndrome Type II | Glanzmann Thrombasthenia | Sick Sinus Syndrome 1 | Pneumoconiosis | Prurigo Nodularis | Pneumonia, Viral | Carcinoid Tumor | Hyperuricemic Nephropathy, Familial Juvenile | Inborn Errors Of Metabolism | Imerslund-Grasbeck Syndrome | Retinal Diseases | Pemphigus | Muir-Torre Syndrome | Deafness, Dystonia, And Cerebral Hypomyelination | 3-methylglutaconic Aciduria Type IV | Diabetes Insipidus, Nephrogenic | Gastroenteritis | Methemoglobinemia | Chromosome 9q34.3 Deletion Syndrome | Arthritis, Psoriatic | Tonsillitis | NDH Syndrome | Primary Hyperoxaluria | Cardiomyopathy, Dilated, 1L | Neuroma | Osteoporosis | Primary Progressive Nonfluent Aphasia | Melnick-Needles Syndrome | Trichorhinophalangeal Syndrome | Moyamoya Disease | Polymyositis | Teratozoospermia | Stroke, Ischemic | Schnyder Crystalline Corneal Dystrophy | Paternal Uniparental Disomy Of Chromosome 14 | Cantu Syndrome | Sjogren Syndrome | Evans Syndrome | Renal Oncocytoma | Delayed Sleep Phase Syndrome | Disseminated Superficial Actinic Porokeratosis | Camurati-Engelmann Disease | Synpolydactyly | Pyelonephritis | Neurofibromatosis-Noonan Syndrome | Facioscapulohumeral Muscular Dystrophy Type 1 | Rheumatoid Arthritis | Paroxysmal Nocturnal Hemoglobinuria | Cerebral Cavernous Malformations | Birk-Barel Syndrome | Peroxisomal Disorder | Neurofibrosarcoma | Olmsted Syndrome | Cheilitis | Erythropoietic Protoporphyria | Progressive Osseous Heteroplasia | Hyperinsulinemic Hypoglycemia | Pancreatitis, Chronic | Muscular Dystrophy | Hypothalamic Obesity | Trimethylaminuria | Agranulocytosis | Carcinoma, Squamous Cell | Herpes Genitalis | Jaundice, Obstructive | Autoimmune Polyendocrinopathy Syndrome Type I | Uremic Pruritus | Adenosine Deaminase 2 Deficiency | Common Variable Immunodeficiency | Spinocerebellar Ataxia Type 10 | Leukoplakia, Oral | Chitayat Syndrome | Familial Hemiplegic Migraine | Fibrosis | Tic Disorder | Genitopatellar Syndrome | Autonomic Nervous System Disorders | X-linked Myotubular Myopathy | Metabolic Syndrome | Hemophilia | Angioimmunoblastic T-cell Lymphoma | Hereditary Multiple Exostoses | Lattice Corneal Dystrophy Type 1 | Hypersomnia | Oculocutaneous Albinism Type 1 | Thrombosis | Asphyxia Neonatorum | Early Infantile Epileptic Encephalopathy 13 | Osteogenesis Imperfecta Type IV | Tricho-hepato-enteric Syndrome | Congenital Generalized Lipodystrophy | Charcot-Marie-Tooth Disease Type 4D | Bartsocas-Papas Syndrome | Schistosomiasis Mansoni | Protein C Deficiency | Hypotrichosis Simplex | Thrombocythemia, Essential | Renal Failure | Venous Insufficiency | T-cell Leukemia | Retinal Dystrophy, Early-onset Severe | Emery-Dreifuss Muscular Dystrophy | Contact Dermatitis | Thrombotic Microangiopathy | Spondylometaphyseal Dysplasia | Asperger Syndrome | Meconium Ileus