B-cell Chronic Lymphocytic Leukemia
B-cell Chronic Lymphocytic Leukemia
About the Disease
Leukemia, Chronic Lymphocytic, also known as chronic lymphocytic leukemia, is related to richter's syndrome and chronic lymphocytic leukemia/small lymphocytic lymphoma, and has symptoms including angina pectoris, chest pain and edema. An important gene associated with Leukemia, Chronic Lymphocytic is TP53 (Tumor Protein P53), and among its related pathways/superpathways are miRNA regulation of DNA damage response and DNA damage response (only ATM dependent). The drugs Valganciclovir and Ofatumumab have been mentioned in the context of this disorder. Affiliated tissues include Blood, and related phenotypes are cellular immunodeficiency and chronic lymphatic leukemia
Common Targets
CCL26 | CCR6 | PIK3CD | IKZF1 | TNFSF13 | G6352 | BCR | CCR4 | G4609 | CCR7 | TNFSF13B | FCGR3A | CCL7 | CCL8 | MS4A1 | CD22 | CCL11 | DCX (DDB1-CUL4-X-box) E3 protein ligase complex | G7422 | CCR8 | TLR9 | CCL13 | CCL1 | CCR9 | IKZF3 | HEATR9 | CCR1 | ROR1 | LYN | FCGR2A | Ikzf1 | CCL18 | CRBN | G7124 | CCL20 | FYN | CD28 | CD160 | PIK3CG | DKK4 | CD19 | G7157 | ABL1 | G673 | FGF2 | CD37 | CCL24 | AMP-activated protein kinase (AMPK) | BTK | TNFRSF13B | G29126 | CAT | PLCG2 | CCR3 | CD3 Complex (T Cell Receptor Complex) | MYD88 | MALT1 | GHSR
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Other Diseases
Alopecia Totalis | Lymphoproliferative Disease, X-linked | Endometriosis | Blastomycosis | Pseudo-pseudohypoparathyroidism | Encephalopathy, Hepatic | Charcot-Marie-Tooth Disease Type 2D | Eiken Syndrome | Asthma, Nocturnal | Craniofacial Dysostosis | Hypolipoproteinemia | Loeys-Dietz Syndrome Type 4 | Acrodermatitis Enteropathica | Leukocyte Adhesion Deficiency Type 1 | Glanzmann Thrombasthenia | Pantothenate Kinase-associated Neurodegeneration | Progressive Familial Intrahepatic Cholestasis Type 3 | Meckel-Gruber Syndrome | Hypoplastic Left Heart Syndrome | Nemaline Myopathy 8 | Spinocerebellar Ataxia Type 6 | Renpenning Syndrome | Takenouchi-Kosaki Syndrome | Polymicrogyria | Norrie Disease | Schnyder Crystalline Corneal Dystrophy | Focal Dermal Hypoplasia | Uterine Leiomyoma | Usher Syndrome Type I | Intestinal Hypomagnesemia 1 | Cockayne Syndrome | Goiter, Nodular | Mitochondrial DNA Depletion Syndrome | MIRAGE Syndrome | Pathological Gambling | Hidradenitis | Delayed Sleep Phase Syndrome | Majeed Syndrome | Epidermolysis Bullosa Dystrophica | Waardenburg Syndrome | Hepatitis | Autosomal Recessive Bestrophinopathy | Fibromuscular Dysplasia | Chondroma | Sclerosteosis 2 | Dengue Shock Syndrome | Primary Sclerosing Cholangitis | Eosinophilic Asthma | Urolithiasis | Multiple Sclerosis, Chronic Progressive | Exostoses | Filariasis | Acute Coronary Syndrome | Cerebellar Ataxia, Cayman Type | Oguchi Disease-2 | Hyperbilirubinemia | Primary Progressive Aphasia | Greig Cephalopolysyndactyly Syndrome | Sporadic Inclusion Body Myositis | Craniopharyngioma | Ovarian Sex Cord-stromal Tumor | Erythromelalgia | Schamberg Disease | Early Infantile Epileptic Encephalopathy 4 | Meleda Disease | Non-Hodgkin Lymphoma | Gastritis, Atrophic | Spinocerebellar Ataxia Type 38 | Hepatitis E | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Spina Bifida | Cryopyrin-associated Periodic Syndromes | Lateral Meningocele Syndrome | Okihiro Syndrome | Axenfeld-Rieger Syndrome | Follicular Dendritic Cell Sarcoma | Spermatocele | Tic Disorder | Moyamoya Disease | Teratozoospermia | Lung Diseases | Hyperinsulinism-hyperammonemia Syndrome | Juvenile Myoclonic Epilepsy | Fabry's Disease | Acute Myeloid Leukemia | Chiari Malformation Type I | Hyperthyroidism | Hypercalcemia | Familial Advanced Sleep Phase Syndrome | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Microvillus Inclusion Disease | Premature Ejaculation | Epilepsy | Vascular Calcification | Spinocerebellar Ataxia | VACTERL Association | Cherubism | IgA Nephropathy | Cirrhosis | Multiple Sulfatase Deficiency | Vertebrobasilar Insufficiency | Congenital Myasthenic Syndrome | Peyronie's Disease | High Molecular Weight Kininogen Deficiency | Cavitary Optic Disc Anomalies | Nicotine Addiction | Kernicterus | Mycosis Fungoides | Personality Disorders | Sarcoidosis | Chudley-McCullough Syndrome | Hypocalcemia | Aceruloplasminemia | Epidermolysis Bullosa Acquisita | Mesothelioma, Malignant | Ligneous 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Sclerosis, Primary Progressive | Prostatitis | Tinea | Communication Disorders | Impetigo | Crisponi Syndrome | Dysplastic Nevus | Non-small Cell Lung Cancer | Multicystic Renal Dysplasia | Osteoporosis | Von Willebrand Disease | Optic Neuropathy, Anterior Ischemic | Myelitis | Ameloblastic Carcinoma | Congenital Bile Acid Synthesis Defect | Heart Failure | Optic Neuritis | Metaphyseal Chondrodysplasia, Schmid Type | Lassa Fever | Spondylometaphyseal Dysplasia | Hairy Cell Leukemia | Sturge-Weber Syndrome | Lymphangiomatosis | Myocardial Infarction | Diabetic Nephropathy | Familial Dysautonomia | Aplastic Anemia | Gastroenteritis, Eosinophilic | Raynaud Phenomenon | Pulmonary Capillary Hemangiomatosis | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Cerebellofaciodental Syndrome | Tay-Sachs Disease | Glutaric Aciduria Type 3 | Congenital Ichthyosiform Erythroderma | Glycogen Storage Disease Type 5 | GATA2 Deficiency | Congenital Diaphragmatic Hernia | Anxiety Disorders | Primrose Syndrome | Proteasome-associated Autoinflammatory Syndrome 2 | Neurofibromatosis | Methemoglobinemia Type IV | Adrenal Insufficiency | Esophagitis, Eosinophilic | Epithelioid Hemangioma | Cystitis, Interstitial | Gastrointestinal Disorders | IgA Deficiency | Hepatoblastoma | Acromicric Dysplasia | Hypertension, Pulmonary | Myasthenia | Peritonitis | Spinocerebellar Ataxia Type 8 | Brenner Tumor | Netherton Syndrome | Keratitis | Multifocal Motor Neuropathy | Erysipelas | Lipid Storage Diseases | Wolman Disease | Fanconi Syndrome | Retinal Diseases | Spinocerebellar Ataxia Type 12 | Obsessive-compulsive Disorder | Thrombosis | Niemann-Pick Disease, Type C | Peutz-Jeghers Syndrome | Joubert Syndrome 2 | Sporadic Hemiplegic Migraine | Erythema Multiforme | CHARGE Syndrome | Ependymoma | Congenital Nephrotic Syndrome | Graves Disease | Papilloma | Nephritis, Interstitial | Venous Insufficiency | Still Disease | Borderline Personality Disorder | Histiocytic Sarcoma | Spinocerebellar Ataxia Type 28 | HELLP Syndrome | Beta-Propeller Protein-associated Neurodegeneration | Congenital Central Hypoventilation Syndrome | Hashimoto Thyroiditis | Mixed Connective Tissue Disease | Thrombophlebitis | Arthritis, Reactive | Arthropathy | Peripheral Neuropathy | Rosacea | Milk Allergy | Hydrolethalus Syndrome | Cabezas Syndrome | Disseminated Intravascular Coagulation | Ichthyosis Bullosa Of Siemens | Bare Lymphocyte Syndrome | Ornithine Transcarbamylase Deficiency | Hepatitis, Autoimmune | COACH Syndrome | Aicardi-Goutieres Syndrome | Scapuloperoneal Spinal Muscular Atrophy | T-cell Chronic Lymphocytic Leukemia | Jawad Syndrome | Gingivitis | Hermansky-Pudlak Syndrome | Obesity, Morbid | Guillain-Barre Syndrome | Allan-Herndon-Dudley Syndrome | Porphyria Cutanea Tarda | Infantile Nephropathic Cystinosis | Urticaria | Hyperuricemic Nephropathy, Familial Juvenile | Primary Biliary Cholangitis | Benign Recurrent Intrahepatic Cholestasis 1 | CREST Syndrome | Cardiomyopathy, Restrictive | Uremic Pruritus | Congenital Dyserythropoietic Anemia Type 4 | Sarcoma, Ewing | Hyperglycemia | X-linked Charcot-Marie-Tooth Disease | Alcoholism | Crouzon Syndrome With Acanthosis Nigricans | Apparent Mineralocorticoid Excess Syndrome | Irritable Bowel Syndrome | Cone Dystrophy | Silicosis | Renal Tubular Dysgenesis | Retinitis Pigmentosa | Dentinogenesis Imperfecta | Sleep Apnea, Central | Distal Myopathy 2 | Epidermolytic Palmoplantar Keratoderma | Hypoproteinemia, Hypercatabolic | Thromboembolism | Ollier Disease | Congenital Disorders Of Glycosylation Type II | Cannabis Abuse | Dowling-Degos Disease | Schnitzler Syndrome | Pearson Syndrome | Paraganglioma, Carotid Body | Torticollis | 3-methylglutaconic Aciduria | Smith-Kingsmore Syndrome | Xeroderma Pigmentosum | Lupus Erythematosus | Leber Congenital Amaurosis | Frontotemporal Dementia | Schwannoma | Hernia, Inguinal | Hodgkin Lymphoma | Pneumoconiosis | Spondylocarpotarsal Synostosis Syndrome | Benign Hereditary Chorea | Strabismus | Cryptorchidism | Hypotension, Orthostatic | Wieacker-Wolff Syndrome | Osteoporosis, Postmenopausal | Walker-Warburg Syndrome | Maple Syrup Urine Disease | Hemolytic Uremic Syndrome, Atypical | Superficial Spreading Melanoma | Cancer, Colon | HANAC Syndrome | Spinocerebellar Ataxia Type 13 | Parkinson Disease 6, Autosomal Recessive Early-onset | Globozoospermia | Hereditary Spherocytosis | Adams-Oliver Syndrome | Epidermolytic Hyperkeratosis | Chediak-Higashi Syndrome | Motion Sickness | Common Variable Immunodeficiency | Polycystic Kidney, Autosomal Dominant | Chorea | Colorectal Adenoma | Zygomycosis | Anal Fissure | Epithelial-myoepithelial Carcinoma | Patent Ductus Arteriosus | Premenstrual Syndrome | Achromatopsia | Conjunctivitis | Headache | X-linked Sideroblastic Anemia | Myopathy | Cataract | Auriculocondylar Syndrome | Anorexia Nervosa | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Oligodendroglioma | Bone Marrow Necrosis | Carotid Artery Disease | Anovulation | Mumps | Low Tension Glaucoma | Polycythemia | Tatton-Brown-Rahman Syndrome | Unverricht-Lundborg Syndrome | Autosomal Recessive Congenital Ichthyosis | Pseudoachondroplasia | Contact Dermatitis | Waardenburg Syndrome Type 2A | Myhre Syndrome | Prolactinoma | Palsy, Cerebral | Neurodevelopmental Disorders | Obesity | Glioblastoma | Epilepsy Of Infancy With Migrating Focal Seizures | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Cardiac Arrest | Sialidosis Type I | Stiff-man Syndrome | Atopic Dermatitis | Nail-Patella Syndrome | Periventricular Nodular Heterotopia | Scoliosis | Hyperkalemic Periodic Paralysis | VACTERL/VATER Association | Spinocerebellar Ataxia Type 21 | Medulloblastoma | Dermatitis | Hereditary Folate Malabsorption | Sickle Cell Disease | Osteochondrosis | Hyperparathyroidism | Cryptosporidiosis | Macrophage Activation Syndrome | Syphilis | Benign Familial Neonatal Convulsions | Dyslipidemia | Retinopathy, Diabetic | 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