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 / Biomarkers
G9940 | G90362 | G29851 | G3812 | G6774 | P5575 | G643 | G27125 | G9901 | G51311 | G23533 | G83933 | G27242 | G29118 | G3066 | G140766 | G23178 | G10013 | G5133 | G7057 | G80298 | G3815 | G2308 | G8854 | G22981 | G9909 | G4261 | G4615 | G29126 | P6058 | G9113 | G3561 | G207 | G7409 | G1105 | G1436 | G139135 | P8262 | Ribonucleoside-diphosphate reductase | G1788 | G2195 | G5728 | G58508 | G3205 | P5577 | G965 | G673 | G7410 | G6778 | G9212 | G22984 | G23081 | G340277 | G598 | G675 | G3932 | G10320 | G10746 | G56940 | G1233 | G79705 | G3417 | G2261 | G6046 | G2672 | DNA Topoisomerase II (nonspecified subtype) | G84433 | G3110 | G80816 | G11096 | G4851 | G7799 | G5159 | G27436 | G5291 | G5295 | G2627 | G1106 | G253738 | G5178 | G57143 | G127731 | G23476 | G5293 | G331 | G3621 | G55781 | G30849 | G7189 | G8841 | G79885 | G1025 | G92344 | G23768 | G3065 | G59283 | G2196 | G10178 | G4609 | G2475 | G8626 | G89797 | G79269 | G55746 | G6249 | G7514 | G51299 | G57674 | G7157 | G2324 | G84858 | G56997 | G5595 | Tyrosine Kinase (nonspecified subtype) | G140885 | G7041 | G952 | G2214 | G2567 | G1043 | G5170 | G116113 | G6850 | G10016 | G54790 | G11218 | G23677 | G25930 | G3702 | G2321 | G57534 | G64641 | G202333 | G57448 | G54998 | G1612 | G2145 | G1107 | G63035 | G9625 | G3678 | G3728 | G6387 | G23552 | G920 | G1879 | G27445 | P6884 | G2533 | G896 | G2051 | G836 | G148281 | G7840 | G924 | G4052 | G4860 | G29072 | G607 | G4297 | G83872 | G6788 | G5915 | G776 | G54674 | G3418 | G5888 | G5335 | G23166 | G2821 | G4193 | G4798 | G22806 | G9569 | G146 | G57680 | G2580 | G5290 | G1493 | G3908 | G5292 | G1213 | G1310 | G23195 | G7092 | Janus Kinase (nonspecified subtype) | G4067 | G10320 | G11124 | G567 | G10725 | G4173 | G3394 | G9705 | G201633 | G7849 | G5156 | G961 | G58 | G83990 | G3791 | G8085 | G2534 | G940 | G8676 | G4853 | G1387 | G943 | G115701 | G7428 | G604 | Histone deacetylase (nonspecified subtype) | P13024 | G1719 | G5154 | G8930 | G7267 | G1654 | G2146 | G951 | G23113 | G238 | G1293 | G687 | G5916 | G3845 | G23239 | G324 | G51755 | G9033 | G57696 | G127602 | G596 | G64072 | G4214 | G51185 | G3718 | G1499 | G6777 | G472 | G921 | G3716 | G387 | G5294 | G51611 | G5649 | G285220 | G6790 | DNA Methyltransferase (DNMT) (nonspecified subtype) | G27 | G3717 | G2900 | G329 | G5336 | G4194 | G4486
Other Diseases
Peritonitis | Perivascular Epithelioid Cell Tumor | Periventricular Leukomalacia | Periventricular Nodular Heterotopia | Pernicious Anemia | Peroxisomal Disorder | Persistent Fetal Circulation | Persistent Hyperplastic Primary Vitreous | Persistent Mullerian Duct Syndrome | Persistent Truncus Arteriosus | Personality Disorders | Peters-plus Syndrome | Peutz-Jeghers Syndrome | Peyronie's Disease | Pfeiffer Syndrome | PHARC Syndrome | Phenylketonuria | Phenylketonuria II | Pheochromocytoma | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Phosphoglycerate Dehydrogenase Deficiency | Photosensitivity | Pierpont Syndrome | Pierre Robin Syndrome | Pierson Syndrome | Pigment Dispersion Syndrome | Pilomatrix Carcinoma | Pineoblastoma | Pitt-Hopkins Syndrome | Pituitary Disorders | Pituitary Dwarfism | Pituitary Stalk Interruption Syndrome | Placenta Previa | Plasma Cell Dyscrasia | Plasma Cell Leukemia | Plasmacytoma | Platelet Disorders | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Pleomorphic Xanthoastrocytoma | Pleural Tuberculosis | Pleurisy | Pneumococcal Meningitis | Pneumoconiosis | Pneumonia, Bacterial | Pneumonia, Mycoplasma | Pneumonia, Viral | Pneumothorax | POEMS Syndrome | Poikiloderma With Neutropenia | Poirier-Bienvenu Neurodevelopmental Syndrome | Polyarteritis Nodosa | Polycystic Kidney, Autosomal Dominant | Polycystic Kidney, Autosomal Recessive | Polycystic Liver | Polycystic Ovary Syndrome | Polycythemia | Polycythemia Vera | Polydactyly | Polymicrogyria | Polymyalgia Rheumatica | Polymyositis | Polyneuropathy | Polyomavirus Nephropathy | Polyradiculopathy | Pompe Disease | Pontocerebellar Hypoplasia | Pontocerebellar Hypoplasia Type 2 | Porencephaly | Poretti-Boltshauser Syndrome | Porokeratosis | Porphyria | Porphyria Cutanea Tarda | Porphyria, Acute Intermittent | Porphyria, Variegate | Portal Vein Thrombosis | Postaxial Polydactyly | Posterior Polar Cataract | Postpartum Depression | Postpoliomyelitis Syndrome | Potocki-Shaffer Syndrome | Pouchitis | Prader-Willi Syndrome | Pre-eclampsia | Preaxial Polydactyly | Precocious Puberty | Prediabetes | Pregnancy, Ectopic | Premature Ejaculation | Premenstrual Syndrome | Presbycusis | Presbyopia | Priapism | Primary Aldosteronism | Primary Biliary Cholangitis | Primary Carnitine Deficiency | Primary Cutaneous Amyloidosis | Primary Erythromelalgia | Primary Familial Brain Calcification | Primary Hyperoxaluria | Primary Hyperoxaluria Type 1 | Primary Hyperoxaluria Type 3 | Primary Lateral Sclerosis | Primary Ovarian Insufficiency | Primary Pigmented Nodular Adrenocortical Disease | Primary Progressive Aphasia | Primary Progressive Nonfluent Aphasia | Primary Sclerosing Cholangitis | Primary Torsion Dystonia | Primrose Syndrome | Proctitis | Progressive Encephalopathy-optic Atrophy Syndrome | Progressive External Ophthalmoplegia | Progressive Familial Intrahepatic Cholestasis | Progressive Familial Intrahepatic Cholestasis Type 1 | Progressive Familial Intrahepatic Cholestasis Type 2 | Progressive Familial Intrahepatic Cholestasis Type 3 | Progressive Myoclonic Epilepsy | Progressive Osseous Heteroplasia | Prolactinoma | Prolidase Deficiency | Prolymphocytic Leukemia | Proopiomelanocortin Deficiency | Prostatitis | Proteasome-associated Autoinflammatory Syndrome 2 | Protein C Deficiency | Protein S Deficiency | Proximal Symphalangism | Prune Belly Syndrome | Prurigo Nodularis | Pseudo-pseudohypoparathyroidism | Pseudoachondroplasia | Pseudoexfoliation Syndrome | Pseudohermaphroditism | Pseudohypoaldosteronism | Pseudohypoparathyroidism Type 1A | Pseudohypoparathyroidism Type 1B | Pseudohypoparathyroidism Type 1C | Pseudohypoparathyroidism Type 2 | Pseudomyxoma Peritonei | Psoriasis | Pterygium | Pulmonary Alveolar Microlithiasis | Pulmonary Alveolar Proteinosis | Pulmonary Capillary Hemangiomatosis | Pulmonary Sclerosing Hemangioma | Pulmonary Stenosis | Pulmonary Tuberculosis | Pulmonary Vein Stenosis | Pulmonary Veno-occlusive Disease | Pulverulent Zonular Cataract | Pupil Disorders | Pure Autonomic Failure | Pure Red Cell Aplasia | Purpura | Purpura, Thrombotic Thrombocytopenic | Pycnodysostosis | Pyelonephritis | Pyloric Stenosis, Infantile Hypertrophic | Pyoderma Gangrenosum | Pyruvate Carboxylase Deficiency Disease | Pyruvate Decarboxylase Deficiency | Pyruvate Dehydrogenase Deficiency | Pyruvate Kinase Deficiency | Raine Syndrome | Rash | Raynaud Phenomenon | Recurrent Respiratory Papillomatosis | Reflex Epilepsy | Relapsing Polychondritis | REM Sleep Behavior Disorder | Renal Dysplasia | Renal Failure | Renal Hypomagnesemia 3 | Renal Hypouricemia | Renal Medullary Carcinoma | Renal Oncocytoma | Renal Tubular Acidosis | Renal Tubular Dysgenesis | Renal-hepatic-pancreatic Dysplasia | Renpenning Syndrome | Restless Legs Syndrome | Restrictive Dermopathy | Reticular Dysgenesis | Retinal Coloboma | Retinal Degeneration | Retinal Detachment | Retinal Diseases | Retinal Dystrophy | Retinal Telangiectasia | Retinal Vasculitis | Retinitis | Retinitis Pigmentosa | Retinitis Pigmentosa 3 | Retinoblastoma | Retinopathy Of Prematurity | Retinopathy, Diabetic | Retinoschisis | Rett Syndrome | Reye Syndrome | Rhabdoid Tumor | Rhabdomyosarcoma | Rhabdomyosarcoma, Alveolar | Rhabdomyosarcoma, Embryonal | Rheumatic Heart Disease | Rheumatoid Arthritis | Rhinitis | Rhizomelic Chondrodysplasia Punctata | Riboflavin Transporter Deficiency Neuronopathy | Richter's Syndrome | Rickets | Rift Valley Fever | Roberts Syndrome | Robinow Syndrome | Rolandic Epilepsy | Rosacea | Rothmund-Thomson Syndrome | Rotor Syndrome | Rubeosis Iridis | Rubinstein-Taybi Syndrome | Saethre-Chotzen Syndrome | Salla Disease | Sandhoff Disease | SAPHO Syndrome | Sarcoidosis | Sarcoidosis, Pulmonary | Sarcoma | Sarcoma, Alveolar Soft Part | Sarcoma, Endometrial Stromal | Sarcoma, Ewing | Sarcomatoid Carcinoma Of The Lung | Sarcosinemia | Saul-Wilson Syndrome | Scabies | Scapuloperoneal Myopathy, X-linked Dominant | Scapuloperoneal Spinal Muscular Atrophy | Schaaf-Yang Syndrome | Schamberg Disease | Schindler Disease | Schistosomiasis | Schistosomiasis Mansoni | Schizencephaly | Schizophrenia | Schizotypal Personality Disorder | Schnitzler Syndrome | Schnyder Crystalline Corneal Dystrophy | Schuurs-Hoeijmakers Syndrome | Schwannoma | Schwannomatosis | Schwartz-Jampel-Aberfeld Syndrome | Scleritis | Sclerocornea | Scleroderma | Scleroderma, Diffuse | Sclerosing Cholangitis | Sclerosteosis | Sclerosteosis 2 | Scoliosis | Seasonal Mood Disorder | Seborrheic Dermatitis | Seizures | Seizures-scoliosis-macrocephaly Syndrome | Seminoma | Sengers Syndrome | Senior-Loken Syndrome | Sensorineural Hearing Loss | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Sensory Neuropathy | Sepiapterin Reductase Deficiency | Sertoli Cell-only Syndrome | Sezary Syndrome | Shock, Cardiogenic | Short-chain Acyl-CoA Dehydrogenase Deficiency | Shprintzen-Goldberg Syndrome | Shwachman-Bodian-Diamond Syndrome | Sialoadenitis | Sick Sinus Syndrome | Sick Sinus Syndrome 1 | Sickle Cell Anemia | Sickle Cell Disease | Silicosis | Silver-Russell Syndrome | Sitosterolemia | Situs Inversus | Sjogren Syndrome | Skin Carcinoma | Skin Fragility-woolly Hair Syndrome | Skin Papilloma | Sleep Apnea | Sleep Apnea, Central | Sleep Apnea, Obstructive | Sleep Disorder | Small Lymphocytic Lymphoma | Smith-Kingsmore Syndrome | Smith-Lemli-Opitz Syndrome | Smith-Magenis Syndrome | Smoldering Myeloma | Snyder-Robinson Syndrome | Sorsby Fundus Dystrophy | Sotos Syndrome | Spastic Paraplegia Type 7 | Spasticity | Specific Granule Deficiency | Speech Disorders | Spina Bifida | Spinal And Bulbar Muscular Atrophy | Spinal Cord Diseases | Spinal Muscular Atrophy | Spinal Muscular Atrophy Type 2 | Spinal Muscular Atrophy Type 3 | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Spinocerebellar Ataxia Type 1 | Spinocerebellar Ataxia Type 10 | Spinocerebellar Ataxia Type 12 | Spinocerebellar Ataxia Type 13 | Spinocerebellar Ataxia Type 14 | Spinocerebellar Ataxia Type 15 | Spinocerebellar Ataxia Type 16 | Spinocerebellar Ataxia Type 17 | Spinocerebellar Ataxia Type 2 | Spinocerebellar Ataxia Type 20 | Spinocerebellar Ataxia Type 21 | Spinocerebellar Ataxia Type 23 | Spinocerebellar Ataxia Type 27 | Spinocerebellar Ataxia Type 28 | Spinocerebellar Ataxia Type 3 | Spinocerebellar Ataxia Type 31 | Spinocerebellar Ataxia Type 38 | Spinocerebellar Ataxia Type 40 | Spinocerebellar Ataxia Type 42 | Spinocerebellar Ataxia Type 5 | Spinocerebellar Ataxia Type 6 | Spinocerebellar Ataxia Type 7 | Spinocerebellar Ataxia Type 8 | Spitz Nevus | Spitzoid Melanoma | Splenomegaly | Split Hand-foot Malformation | Sponastrime Dysplasia | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Spondylo-ocular Syndrome | Spondyloarthritis | Spondylocarpotarsal Synostosis Syndrome | Spondylocostal Dysostosis | Spondyloepiphyseal Dysplasia Tarda, X-linked | Spondylolisthesis | Spondylometaphyseal Dysplasia | Spondyloperipheral Dysplasia | Spondylosis | Sporadic Hemiplegic Migraine | Sporadic Inclusion Body Myositis | Stargardt Disease | Steel Syndrome | Stevens-Johnson Syndrome | Stickler Syndrome | Stiff-man Syndrome | Still Disease | Stomatitis | Strabismus | Stroke | Stroke, Hemorrhagic | Stroke, Ischemic | Stromal Corneal Dystrophy | Sturge-Weber Syndrome | Stuttering | Stuve-Wiedemann Syndrome | Subacute Sclerosing Panencephalitis | Subcortical Band Heterotopia | Succinic Semialdehyde Dehydrogenase Deficiency | Sulfite Oxidase Deficiency | Superficial Spreading Melanoma | Supravalvular Aortic Stenosis | Sweet Syndrome | Swine Influenza | Syncope | Syndactyly | Synovitis | Synpolydactyly | Syphilis | Systemic Lupus Erythematosus | Systemic Mastocytosis | T-cell Chronic Lymphocytic Leukemia | T-cell Leukemia | T-cell Lymphoma, Subcutaneous Panniculitis-like | T-cell Prolymphocytic Leukemia | Takayasu's Arteritis | Takenouchi-Kosaki Syndrome | Takotsubo Cardiomyopathy | Tangier Disease | Tardive Dyskinesia | TARP Syndrome | Tatton-Brown-Rahman Syndrome | Tay-Sachs Disease | Temporal Lobe Epilepsy | Temtamy Preaxial Brachydactyly Syndrome | Tendinitis | Tendinopathy | Tenosynovial Giant Cell Tumor | Teratozoospermia | Tetanus | Thalassemia
