Lymphoma
About the Disease
Lymphosarcoma, also known as lymphoma, diffuse, is related to lymphoma, non-hodgkin, familial and lymphoma, hodgkin, classic. An important gene associated with Lymphosarcoma is BCL6 (BCL6 Transcription Repressor), and among its related pathways/superpathways are Direct p53 effectors and Interleukin-4 and Interleukin-13 signaling. The drugs Crofelemer and Aprepitant have been mentioned in the context of this disorder. Affiliated tissues include t cells, bone marrow and myeloid.
Common Targets / Biomarkers
G3604 | G3718 | G22900 | G5347 | G114548 | G3716 | G8795 | Fibroblast Growth Factor Receptor (FGFR) (nonspecified subtype) | G3560 | G25816 | G11200 | G5294 | G329 | G596 | G90362 | G3791 | G51185 | G5820 | G7515 | G6714 | G4915 | G7006 | G4790 | G2706 | Na+/H+ Exchanger (NHE) (nonspecified subtype) | Vascular endothelial growth factors (VEGF) (nonspecified subtype) | G6790 | G2209 | G1956 | G57124 | P16165 | G25 | G3824 | G83933 | G100133941 | G2936 | G3553 | G3717 | G10892 | G440 | G2350 | G10769 | G6774 | G5789 | G3569 | G4615 | G2335 | G1017 | Serine/Threonine Kinase (nonspecified subtype) | G7015 | G7037 | Tyrosine-Protein Kinases Src (nonspecified subtype) | G1445 | G4149 | G9970 | Tachykinin Receptor (nonspecified subtype) | P16704 | G10013 | G3561 | G3066 | G2263 | G909 | G6624 | G695 | G646 | P5755 | P5859 | G10964 | G3205 | CDK5/p25 | Heat shock protein 90 (nonspecified subtype) | G1601 | G7376 | G10419 | Inhibitor of Apoptosis Proteins (IAPs) (nonspecified subtype) | G6240 | G3091 | G595 | G340348 | G3752 | G3163 | G1/S-specific cyclin-E (nonspecified subtype) | G406947 | G8140 | G5578 | G3559 | G1021 | G80213 | G1111 | G11213 | G207 | Protein Kinase B (PKB/Akt) (nonspecified subtype) | G1233 | G1432 | P6058 | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | G3902 | G558 | G660 | G4026 | G7099 | G10062 | Ribonucleoside-diphosphate reductase | Calcium channel (nonspecified subtype) | Protein kinase C (nonspecified subtype) | G201294 | P11442 | G127731 | G7297 | G5133 | G8726 | G27436 | Lipoxygenase (nonspecified subtype) | G598 | G6046 | G1263 | G6241 | G1436 | P8262 | G415116 | G8784 | G10673 | P12327 | G7295 | G57396 | G1020 | G1723 | G1019 | G10320 | G29126 | G3815 | G1633 | G7150 | G4780 | G9020 | G3563 | Glutamate Transporter (nonspecified subtype) | CDK9/Cyclin T1 | G6474 | G5291 | G115350 | G7852 | G675 | G2618 | G383 | G59283 | G1543 | G3383 | G5604 | G399 | P12578 | G5966 | P5614 | G3123 | G331 | G2261 | G23476 | G65110 | G5293 | G84858 | G51299 | DNA Topoisomerase II (nonspecified subtype) | G8856 | Adenosine deaminase (nonspecified subtype) | G6098 | G8841 | G1025 | G673 | G4137 | G2567 | G100 | G115352 | G3662 | G3600 | G1859 | G5170 | G958 | G960 | Inhibitory kappaB Kinase (IKK) (nonspecified subtype) | Chaperone (nonspecified subtype) | G7162 | G3400 | G140885 | G7514 | G1043 | G7535 | G952 | Histone acetyltransferase (HAT) (nonspecified subtype) | P5756 | G4690 | P39377 | G933 | G1244 | P5833 | G4916 | G51135 | G3122 | G3702 | G6850 | G22914 | G105374265 | G10801 | G1088 | G5159 | Pim Kinase (nonspecified subtype) | CDK4/Cyclin D | Na+/K+-ATPase (nonspecified subtype) | G581 | G3065 | P16126 | G4170 | G4582 | G2214 | G904 | G2145 | G23552 | G5580 | G3678 | G5742 | G5468 | G1604 | G4609 | P40594 | G6582 | G79368 | G208 | G43 | G841 | G920 | G330 | G4914 | G2819 | G10434 | Heme Oxygenase (HO) (nonspecified subtype) | G1452 | Interferon (nonspecified subtype) | G9429 | P16964 | Cyclin D (nonspecified subtype) | G924 | G931 | G970 | G597 | G2475 | Pyruvate dehydrogenase kinase (nonspecified subtype) | G127833 | G4311 | P19878 | G3921 | G7128 | G3663 | G23414 | G4860 | G2952 | G1147 | G1612 | G3480 | P12328 | G2324 | G2538 | G896 | G966 | G10563 | G22806 | G3832 | G4322 | G1544 | Transforming growth factor beta (nonspecified subtype) | G3556 | Sodium channel (nonspecified subtype) | Caspase (nonspecified subtype) | G2913 | G5888 | P23180 | G2321 | G836 | G11313 | G2260 | G916 | G3125 | G100528032 | G115650 | CDK2/Cyclin A | G7042 | G4318 | G23274 | G599 | G898 | G640 | Heat shock protein 70 (nonspecified subtype) | G4919 | G2908 | G7157 | G10320 | G608 | G151888 | G1195 | P11025 | G2264 | G374383 | Adenosine receptor (nonspecified subtype) | G5292 | G4193 | G1024 | G8019 | G3558 | G5422 | G953 | G7293 | G3579 | Chemokine receptor (nonspecified subtype) | G6427 | G10988 | CDK2/Cyclin E | G201633 | G84868 | P6884 | G5588 | G10928 | Focal Adhesion Kinases (FAK) (nonspecified subtype) | G4313 | G79728 | G1786 | G5605 | G2615 | G974 | G5743 | G54106 | G3082 | G10733 | G3707 | G10135 | Cyclin A (nonspecified subtype) | G604 | G1493 | G943 | G3075 | G4233 | G7298 | G4586 | G3127 | P5678 | G5290 | G961 | G2625 | G7490 | G940 | G3654 | G1234 | G951 | G2064 | G7124 | G213 | G10000 | G2935 | G3956 | G340061 | G332 | G56616 | G2322 | G127602 | G5156 | G3586 | G1719 | G4144 | G83903 | G5788 | P16740 | Ribosomal Protein S6 Kinase, 70kDa (p70S6K) (nonspecified subtype) | G1196 | G7294 | P13024 | G5979 | G6506 | G4255 | G83416 | G3820 | G7428 | P11049 | G6374 | G7153 | G921 | Histone deacetylase (nonspecified subtype) | G2146 | G5243 | G983 | G930 | G1022 | G80150 | G5450 | G11040 | G23097 | G54806 | G3606 | G7292 | G238 | G28639 | G3162
Other Diseases
Lymphoma Lymphoblastic | Lymphoma, AIDS-related | Lymphoma, B-cell | 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
