Non-Hodgkin Lymphoma
About the Disease
Lymphoma, also known as non-hodgkin malignant lymphoma nos, is related to lymphoma, hodgkin, classic and lymphoma, non-hodgkin, familial. An important gene associated with Lymphoma is PTPN11 (Protein Tyrosine Phosphatase Non-Receptor Type 11), and among its related pathways/superpathways are IL-9 Signaling Pathways and NF-kappaB Signaling. The drugs Ferrous succinate and Posaconazole have been mentioned in the context of this disorder. Affiliated tissues include t cells, bone marrow and myeloid, and related phenotypes are immune system and hematopoietic system
Common Targets / Biomarkers
MSH6 | APEH | BAG6 | ALK | MSH2 | PLK1 | GSTP1 | CCR3 | TNFRSF9 | JAK3 | ADAM10 | CCL26 | TNFRSF10B | IL2RB | JAK1 | PIK3CG | FAM110B | SIRT2 | HLA-DQB1 | BCL2 | CXCR5 | KDR | MPO | FCGR2B | BIVM-ERCC5 | CEBPE | NTRK2 | NT5C2 | CSNK1E | KCNH2 | DNA Methyltransferase (DNMT) (nonspecified subtype) | PARP3 | Vascular endothelial growth factors (VEGF) (nonspecified subtype) | ERCC5 | ATM | NBN | CD74 | Cyclin B (nonspecified subtype) | MDM4 | Protein farnesyltransferase | AURKA | EGFR | SNCA | ABL1 | DNA-Directed DNA Polymerase Complex | GTF2H1 | HDAC10 | GSR | OGDH | MALT1 | IL-15 receptor | JAK2 | IL12B | FAP | FBN1 | STAT3 | Pyruvate Dehydrogenase Complex | THBS1 | HLA-DMB | CCR6 | ASXL1 | MYD88 | CDK2 | IL1RN | IL6 | TERT | TFRC | ORAI1 | CCNH | NFATC1 | HDAC2 | TNFRSF10A | BTK | CTPS1 | HOXA9 | NAE1 | FAM221A | Heat shock protein 90 (nonspecified subtype) | PRMT5 | HOXB13 | PRDM1 | CNRIP1 | IFNGR1 | ELANE | PRKAA2 | Calcium release-activated channel (CRAC) | PRKCA | CDK6 | IL2RA | CHEK1 | MNX1 | Protein Kinase B (PKB/Akt) (nonspecified subtype) | CCR4 | CCR7 | AURKB | CCL5 | C11orf65 | AXL | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | TLR4 | LAG3 | BMX | Ribonucleoside-diphosphate reductase | Protein kinase C (nonspecified subtype) | MSH5 | VWA5B1 | GATA6 | EED | TYK2 | EML4 | HLA class II histocompatibility antigen DR (HLA-DR) | EGF | PDCD1 | EBF3 | BCL2L1 | PIM3 | TNFSF13B | CD3 Complex (T Cell Receptor Complex) | mTOR complex 1 | TXN | IL7R | CDK4 | CD2 | CCL7 | KIT | ADAM17 | TOP1 | IKZF1 | CD274 | HLA-B | CDK9/Cyclin T1 | FLRT2 | LY75 | HDAC11 | NOD2 | NOTCH4 | BRCA2 | CCL8 | CXCR4 | CACNG8 | NCF4 | DPP7 | BCR | MAP2K1 | DRD2 | XIAP | RHOH | BRD4 | ZNF503 | HLA-DRB1 | PIK3CD | AVEN | TGFB1I1 | NRN1 | DPP8 | MAL | PLXNC1 | IFNGR2 | Adenosine deaminase (nonspecified subtype) | DNA Topoisomerase II (nonspecified subtype) | ARID5B | ROS1 | CCN2 | FOXP4 | GABRG3 | CDK9 | ADA | HDAC3 | IRF4 | POLQ | SH3BP4 | FZD8 | MSI1 | CCL11 | XPO1 | ZAP70 | CD40 | SIRPA | SOD2 | CD52 | CD38 | INA | PARP1 | Interleukin-12 (IL-12) | NTRK3 | SEPTIN9 | DPP4 | PDGFRB | CD22 | HLA-DRA | SYK | BAX | PIKFYVE | CCL13 | Tyrosine Kinase (nonspecified subtype) | HDAC1 | JUP | MCL1 | MUC1 | CCNT1 | CDK20 | ITGA5 | LSP1 | EZH1 | PTGS1 | SUMO activating enzyme complex | FABP5 | FCGR3A | CCR8 | PRF1 | PAX5 | DSP | MRE11 | MYC | FCRL2 | NEDD8-activating enzyme E1 | TMEM260 | AIF1 | NTRK1 | SYT6 | IL5 | CCL1 | HEATR9 | HLA-A | Interferon alpha/beta Receptor (nonspecified subtype) | CSNK1A1 | CD7 | ABCG2 | BCL2A1 | DCX (DDB1-CUL4-X-box) E3 protein ligase complex | BCL2L11 | CD70 | Polycomb Repressive Complex 2 | TNFAIP3 | MTOR | MS4A1 | CDK1/Cyclin B | MERTK | CCR9 | IGF1R | FLT4 | mTOR complex 2 | CCND3 | CCR1 | MSMB | IKZF3 | KIF11 | EP300 | ADRA1D | KDM1A | CCL18 | Mitogen-Activated Protein Kinase (nonspecified subtype) | CD80 | PRKAG1 | FLT1 | H1-3 | TYRO3 | RAD51 | CDK2/Cyclin A | CD3E | HLA-DRB3 | TNFRSF13C | BCL2L2 | RYR3 | ROR1 | NR3C1 | BLK | TP53 | Ikzf1 | CLPTM1L | TNFRSF17 | B2M | CCL20 | CLPP | Janus Kinase (nonspecified subtype) | PRKCB | Glutaminase (nonspecified subtype) | MBP | PIM1 | VCP | FCGR2A | NPAT | PON1 | POLA1 | CXCR2 | METAP2 | LYN | SPART | TIMP2 | TIGIT | Tubulin | MMP2 | MAP2K2 | PTGS2 | CD79B | TLR9 | PPP1R14A | Cyclin A (nonspecified subtype) | EPHX1 | VDR | NAMPT | CCL24 | PARP2 | TNFRSF8 | TYMS | CTLA4 | HLA-DRB5 | PIK3CA | CD47 | CD28 | CCR5 | PAK4 | CD37 | MYCN | ERBB2 | GSPT1 | TNF | KMT2D | NQO1 | LGALS1 | CREBBP | PRRC2A | DPP9 | BIRC5 | GPER1 | 11beta-Hydroxysteroid Dehydrogenase (nonspecified subtype) | DNAH14 | PDGFRA | FLT3 | DHFR | TNFRSF13B | TDP1 | PTPRC | IL10 | ATR | IL6R | MTHFR | DRD3 | FCRL5 | TAP2 | MTR | Proteasome Complex | TOP2A | ALDH1L1 | Histone deacetylase (nonspecified subtype) | EZH2 | TOGARAM1 | ABCB1 | CDK1 | PTPRO | ASRGL1 | CDK7 | C2 | VEGFA | POU2AF1 | CD19 | GOLGA7
Other Diseases
Non-Langerhans Cell Histiocytosis | Non-proliferative Diabetic Retinopathy | Non-small Cell Lung Cancer | Noonan Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Norrie Disease | Nutrition Disorders | Obesity | Obesity, Morbid | Obsessive-compulsive Disorder | Ocular Albinism Type 1 | Ocular Hypertension | Ocular Surface Squamous Neoplasia | Oculocutaneous Albinism | Oculocutaneous Albinism Type 1 | Oculocutaneous Albinism Type 2 | Oculocutaneous Albinism Type 4 | Oculodentodigital Dysplasia | Oculopharyngeal Muscular Dystrophy | Odonto-onycho-dermal Dysplasia | Oguchi Disease-2 | Okihiro Syndrome | Oligoasthenoteratozoospermia | Oligoastrocytoma | Oligodendroglioma | Oligospermia | Ollier Disease | Olmsted Syndrome | Omenn Syndrome | Onchocerciasis | Open-angle Glaucoma | Ophthalmia, Sympathetic | Ophthalmoplegia | Opisthorchiasis | Optic Nerve Diseases | Optic Nerve Hypoplasia, Bilateral | Optic Neuropathy | Optic Neuropathy, Anterior Ischemic | Oral Lichen Planus | Ornithine Transcarbamylase Deficiency | Orotic Aciduria | Orthostatic Intolerance | Osmotic Demyelination Syndrome | Osteitis | Osteoarthritis | Osteochondroma | Osteochondrosis | Osteogenesis Imperfecta | Osteogenesis Imperfecta Type II | Osteogenesis Imperfecta Type III | Osteogenesis Imperfecta Type IV | Osteogenesis Imperfecta Type V | Osteogenesis Imperfecta Type VI | Osteoglophonic Dysplasia | Osteomalacia | Osteomyelitis | Osteonecrosis | Osteonecrosis Of The Jaw | Osteopathia Striata With Cranial Sclerosis | Osteopetrosis | Osteoporosis | Osteoporosis, Postmenopausal | Osteoporosis-pseudoglioma Syndrome | Osteosarcoma | Osteosclerosis | Otitis Externa | Otitis Media | Otopalatodigital Syndrome Type 2 | Otosclerosis | Ovarian Hyperstimulation Syndrome | Ovarian Sex Cord-stromal Tumor | Overactive Bladder | Pachyonychia Congenita | Paget's Disease Of The Breast | Pain | Palmoplantar Keratoderma | Palsy, Cerebral | Pancreatitis | Pancreatitis, Chronic | Pancytopenia | Panic Disorder | Panniculitis | Pantothenate Kinase-associated Neurodegeneration | Panuveitis | Papilledema | Papilloma | Papillon-Lefevre Syndrome | Papillorenal Syndrome | Papulopustular Rosacea | Paraganglioma | Paraplegia | Parapsoriasis | Parkinson Disease 6, Autosomal Recessive Early-onset | Parkinson's Disease | Parkinsonism | Paronychia | Paroxysmal Kinesigenic Dyskinesia | Paroxysmal Nocturnal Hemoglobinuria | Partington Syndrome | Parvovirus B19 Infection | PASLI Disease | Patent Ductus Arteriosus | Patent Foramen Ovale | Paternal Uniparental Disomy Of Chromosome 14 | Pathological Gambling | Pearson Syndrome | Peeling Skin Syndrome Type B | Peeling Skin Syndrome, Acral Type | Pelizaeus-Merzbacher Disease | Pelvic Inflammatory Disease | Pemphigoid | Pemphigus | Pemphigus Foliaceus | Pemphigus Vulgaris | Pendred Syndrome | Pericarditis | Periodic Limb Movement Disorder | Periodontitis | Peripheral Neuropathy | Peripheral T-cell Lymphoma | 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
