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
G3604 | G3718 | G3716 | G5777 | G3560 | G5294 | G596 | G6401 | G643 | G2213 | G51185 | G29851 | G5820 | G1454 | G3055 | G1198 | DNA Methyltransferase (DNMT) (nonspecified subtype) | G972 | G6790 | G1956 | G919 | G5693 | G83933 | G4967 | G3553 | G3717 | G51311 | G10892 | P5683 | G8651 | G2191 | G975 | G7133 | G939 | G79695 | G6774 | P26505 | G3569 | G4615 | G2335 | G55384 | G1017 | G3557 | G7015 | G10013 | G3561 | G8741 | G3066 | G695 | G8797 | G6595 | G1503 | Heat shock protein 90 (nonspecified subtype) | G3660 | G10419 | G340348 | G1/S-specific cyclin-E (nonspecified subtype) | G406947 | G3587 | G3559 | G207 | G4049 | P6058 | G55823 | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | G660 | P11442 | G7297 | G5133 | G27436 | G598 | P8262 | G3594 | G415116 | G10673 | G7295 | G1030 | G973 | G3566 | G80829 | G57396 | G10320 | G29126 | G914 | G3577 | G55743 | G79885 | G5291 | G7852 | G3588 | G399 | G5966 | G3123 | G23476 | G5293 | G29121 | G3965 | G3036 | DNA Topoisomerase II (nonspecified subtype) | Adenosine deaminase (nonspecified subtype) | G8841 | G1025 | G100 | G3662 | G1859 | G958 | G960 | P42808 | G8788 | G140885 | G1043 | G8444 | G1029 | G933 | G1244 | G51135 | G3122 | G3702 | G6850 | Pim Kinase (nonspecified subtype) | G10232 | G3065 | P16126 | G2214 | G2145 | G4609 | G3145 | G208 | G3567 | G2932 | G1452 | G9429 | P16964 | G4153 | G931 | G970 | G3251 | G2475 | G386607 | G2952 | G896 | Glycylpeptide N-tetradecanoyltransferase (nonspecified subtype) | G55289 | G10563 | P5753 | G3802 | G22806 | G654 | G941 | G5888 | G5915 | G916 | G3125 | G1116 | G115650 | G898 | G640 | Chromobox protein homolog (nonspecified subtype) | G4919 | G10320 | G9854 | G608 | G1195 | G3803 | G6619 | G101928376 | G5925 | G1798 | G5292 | G2212 | G9149 | G3558 | G5422 | G7293 | CDK2/Cyclin E | G201633 | P6884 | G3804 | G974 | G971 | G54106 | G3707 | G8764 | G10333 | G1493 | G10525 | G355 | G3127 | G5290 | G961 | G3014 | G940 | G3654 | G1234 | G8445 | G925 | G951 | G2064 | G4613 | G7124 | G213 | G10000 | G3956 | G340061 | G332 | G5916 | G1524 | G2322 | G2944 | G3586 | Ribosomal Protein S6 Kinase, 70kDa (p70S6K) (nonspecified subtype) | G1196 | G4524 | P13024 | G6891 | G3565 | G7428 | G2146 | G5243 | G930 | G1022 | G5450 | G11040 | G3107 | G238
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
