Lymphoma, B-cell
About the Disease
B-Cell Lymphoma, also known as lymphoma, b-cell, is related to marginal zone b-cell lymphoma and lymphoma, mucosa-associated lymphoid type. An important gene associated with B-Cell Lymphoma is MIR17 (MicroRNA 17), and among its related pathways/superpathways are Cytokine Signaling in Immune system and NF-kappaB Signaling. The drugs Lomustine and Rivoceranib have been mentioned in the context of this disorder. Affiliated tissues include t cells, b cells and bone marrow, and related phenotypes are endocrine/exocrine gland and cellular
Common Targets / Biomarkers
TNFRSF9 | JAK3 | JAK1 | PTPN6 | IL2RB | PIK3CG | BCL2 | SELE | CXCR5 | FCGR2B | CRBN | ICOS | PVT1 | CSNK1E | HCK | CLK3 | DNA Methyltransferase (DNMT) (nonspecified subtype) | CD74 | AURKA | EGFR | CD247 | PSMB5 | HDAC10 | OGDH | IL1B | JAK2 | TLR8 | MALT1 | IL-15 receptor | SOCS1 | FAP | CD81 | TNFRSF1B | CD27 | GALNT12 | STAT3 | Pyruvate Dehydrogenase Complex | IL6 | MYD88 | FN1 | MEG3 | CDK2 | IL1RN | TERT | HDAC6 | IL2RG | TNFSF13 | HDAC2 | BTK | TNFRSF10A | SMARCA2 | CTPS1 | Heat shock protein 90 (nonspecified subtype) | IRF2 | PRMT5 | TSPAN33 | G1/S-specific cyclin-E (nonspecified subtype) | MIR155 | IL10RA | IL2RA | AKT1 | LTA | NF-kappaB (NFkB) | VPS11 | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | BMX | HLA class II histocompatibility antigen DR (HLA-DR) | TYK2 | PDCD1 | EML4 | BCL2L1 | CD3 Complex (T Cell Receptor Complex) | IL12RB1 | PIM3 | TNFSF13B | TXN | CDKN2B | CD79A | IL4R | ZFP91 | CLK4 | IKZF1 | CD274 | CD2 | CXCR1 | CHFR | HDAC11 | PIK3CB | CXCR4 | IL10RB | RHOH | REL | HLA-DRB1 | BRD4 | PIK3CD | CLEC2D | LGALS9 | HAS1 | DNA Topoisomerase II (nonspecified subtype) | Adenosine deaminase (nonspecified subtype) | HDAC3 | CDK9 | ADA | IRF4 | DYRK1A | CD40 | CD44 | CD8 | DLK1 | SIRPA | CD52 | DYRK3 | CDKN2A | CD22 | ABCC2 | IRAK4 | HLA-DRA | ITK | SYK | Pim Kinase (nonspecified subtype) | MSLN | HDAC1 | Reverse transcriptase (Telomerase) | FCGR3A | EZH1 | MYC | HMBS | AKT2 | IL5 | GSK3B | CSNK1A1 | ABCG2 | DCX (DDB1-CUL4-X-box) E3 protein ligase complex | MBL2 | MS4A1 | CD70 | HPRT1 | MTOR | ZFP91-CNTF | GSTT1 | CCND3 | Glycylpeptide N-tetradecanoyltransferase (nonspecified subtype) | ACOXL | CXCL13 | Integrin alphaLbeta2 (LFA-1) receptor | KIR2DL1 | IKZF3 | BMP6 | CD80 | RAD51 | RARB | CD3E | HLA-DRB3 | CHI3L1 | TNFRSF13C | CCNE1 | BLK | Chromobox protein homolog (nonspecified subtype) | ROR1 | Ikzf1 | C2CD2L | TNFRSF17 | CLK1 | KIR2DL2 | SNAPC3 | IL12A-AS1 | RB1 | DPAGT1 | PIM1 | FCGR2A | DYRK1B | IL2 | POLA1 | TNFRSF4 | CDK2/Cyclin E | TIGIT | Tubulin | KIR2DL3 | CD79B | CD72 | TLR9 | ITPKB | TNFRSF14 | TLR6 | CTLA4 | HYOU1 | FAS | HLA-DRB5 | PIK3CA | CD47 | H2AX | CD28 | IRAK1 | CCR5 | DYRK2 | CD8A | CD37 | ERBB2 | MYCN | TNF | ALB | AKT3 | LGALS1 | STING1 | BIRC5 | RARG | CX3CR1 | FLT3 | GSTM1 | IL10 | Ribosomal Protein S6 Kinase, 70kDa (p70S6K) (nonspecified subtype) | CLK2 | MTHFR | Proteasome Complex | TAP2 | IL4 | VHL | EZH2 | ABCB1 | CD19 | CDK7 | POU2AF1 | PIM2 | HLA-C | ALK
Other Diseases
Lymphoma, Follicular | Lymphoma, Mantle Cell | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Lymphomatoid Granulomatosis | Lymphoproliferative Disease, X-linked | Lymphoproliferative Disorders | Lysosomal Acid Lipase Deficiency | Mabry Syndrome | Macrodactyly | Macrophage Activation Syndrome | Macrophagic Myofasciitis | Macular Corneal Dystrophy | Macular Corneal Dystrophy Type 1 | Macular Degeneration | Majeed Syndrome | Major Depression | Malaria | Malaria, Cerebral | Malignant Fibrous Histiocytoma | Malignant Peripheral Nerve Sheath Tumor | Malnutrition | Malonyl-CoA Decarboxylase Deficiency | Mandibuloacral Dysplasia With Type A Lipodystrophy | Mannosidase Deficiency Diseases | Maple Syrup Urine Disease | Marfan Syndrome | Marinesco-Sjogren Syndrome | Marshall-Smith Syndrome | Martsolf Syndrome | Mast Cell Leukemia | Mastitis | Maternally Inherited Diabetes And Deafness | McCune-Albright Syndrome | McKusick Type Metaphyseal Chondrodysplasia | McLeod Syndrome | Measles | Meckel-Gruber Syndrome | Meconium Ileus | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Medulloblastoma | Meesmann Corneal Dystrophy | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Megalencephaly | Megaloblastic Anemia | Meier-Gorlin Syndrome | Melanocytic Nevus | Melanoma | Melanoma, Malignant | Melanoma, Uveal | MELAS Syndrome | Meleda Disease | Melnick-Needles Syndrome | Membranous Nephropathy | Meniere's Disease | Meningeal Melanocytoma | Meningioma | Meningioma, Benign | Meningitis | Meningococcal Infections | Meningococcal Meningitis | Menkes Disease | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Mesothelioma, Malignant | Metabolic Diseases | Metabolic Syndrome | Metachondromatosis | Metachromatic Leukodystrophy | Metaphyseal Chondrodysplasia, Schmid Type | Metatropic Dysplasia | Methemoglobinemia | Methemoglobinemia Type IV | Methylmalonic Acidemia | Methylmalonic Aciduria And Homocystinuria, CblC Type | Mevalonate Kinase Deficiency | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Microcephalic Primordial Dwarfism | Microcephaly | Microcephaly, Seizures, And Developmental Delay | Micropenis | Microphthalmia | Microphthalmia, Syndromic 7 | Microtia | Microvillus Inclusion Disease | Migraine | Milk Allergy | MIRAGE Syndrome | Mitochondrial Cytopathy | Mitochondrial Disease | Mitochondrial DNA Depletion Syndrome | Mitochondrial DNA Depletion Syndrome 13 | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Mitochondrial Encephalomyopathy | Mitochondrial Myopathy | Mixed Connective Tissue Disease | Miyoshi Myopathy | Mohr-Tranebjaerg Syndrome | Molybdenum Cofactor Deficiency | Monilethrix | Mood Disorder | Mosaic Variegated Aneuploidy Syndrome 2 | Motion Sickness | Motor Neuron Diseases | Mountain Sickness | Moyamoya Disease | Muckle-Wells Syndrome | Mucolipidosis | Mucolipidosis Type II | Mucolipidosis Type III | Mucolipidosis Type IV | Mucormycosis | Muir-Torre Syndrome | Multicentric Carpotarsal Osteolysis Syndrome | Multicystic Renal Dysplasia | Multifocal Motor Neuropathy | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Multiple Epiphyseal Dysplasia | Multiple Hamartoma Syndrome | Multiple Myeloma | Multiple Sclerosis | Multiple Sclerosis, Chronic Progressive | Multiple Sclerosis, Primary Progressive | Multiple Sclerosis, Relapsing-remitting | Multiple Sclerosis, Secondary Progressive | Multiple Sulfatase Deficiency | Multiple System Atrophy | Mumps | Muscle Wasting | Muscular Dystrophy | Myasthenia | Myasthenia Gravis | Mycosis Fungoides | Myelitis | Myelitis, Transverse | Myelodysplasia | Myelofibrosis | Myeloid Leukemia | Myelomeningocele | Myhre Syndrome | Myocardial Infarction | Myocarditis | Myoclonic Atonic Epilepsy | Myoclonic Epilepsy With Ragged Red Fibers | Myoclonus | Myoclonus-dystonia Syndrome | Myofibrillar Myopathy | Myofibromatosis | Myopathy | Myopia | Myosin Storage Myopathy | Myositis | Myositis, Focal | Myotonia | Myotonic Disorders | N-acetylglutamate Synthase Deficiency | Nail-Patella Syndrome | Nance-Horan Syndrome | Nanophthalmos | Narcolepsy | Nasodigitoacoustic Syndrome | NDH Syndrome | Necrobiosis Lipoidica | Necrotizing Autoimmune Myopathy | Nemaline Myopathy | Nemaline Myopathy 10 | Nemaline Myopathy 8 | Neonatal Progeroid Syndrome | Neovascular Glaucoma | Nephritis, Interstitial | Nephroblastoma | Nephrocalcinosis | Nephronophthisis | Nephropathy | Nephrosclerosis | Nephrotic Syndrome | Nephrotic Syndrome Type 1 | Nestor-Guillermo Progeria Syndrome | Netherton Syndrome | Neural Tube Defect | Neuroblastoma | Neurocutaneous Melanocytosis | Neurocutaneous Syndromes | Neurocysticercosis | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Neurodegeneration With Brain Iron Accumulation | Neurodermatitis | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Neurodevelopmental Disorders | Neuroectodermal Tumors, Primitive | Neuroendocrine Cancer | Neurofibroma | Neurofibroma, Plexiform | Neurofibromatosis | Neurofibromatosis Type 1 | Neurofibromatosis Type 2 | Neurofibromatosis-Noonan Syndrome | Neurofibrosarcoma | Neurogenic Bladder | Neuroleptic Malignant Syndrome | Neuroma | Neuromuscular Disorders | Neuromyelitis Optica | Neuromyotonia | Neuronal Ceroid Lipofuscinosis | Neuropathy | Neutropenia | Nevus | NGLY1 Deficiency | Nicolaides-Baraitser Syndrome | Nicotine Addiction | Nicotine Dependence | Niemann-Pick Disease | Niemann-Pick Disease, Type A | Niemann-Pick Disease, Type B | Niemann-Pick Disease, Type C | Nijmegen Breakage Syndrome | Non-bullous Congenital Ichthyosiform Erythroderma | Non-epidermolytic Palmoplantar Keratoderma | Non-Hodgkin Lymphoma | 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
