Disease

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

疾病靶点研报
B-cell Chronic Lymphocytic Leukemia

Note: If you'd like to get a target analysis report for B-cell Chronic Lymphocytic Leukemia, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of B-cell Chronic Lymphocytic Leukemia at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Adrenomyeloneuropathy | Lamellar Ichthyosis | B-cell Prolymphocytic Leukemia | Macrodactyly | Epilepsy Of Infancy With Migrating Focal Seizures | Meningioma, Benign | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Anti-NMDA Receptor Encephalitis | Pure Autonomic Failure | Scapuloperoneal Spinal Muscular Atrophy | Idiopathic Pulmonary Fibrosis | Renal Oncocytoma | Neuroleptic Malignant Syndrome | Farber Disease | Dentinogenesis Imperfecta | Meconium Ileus | LEOPARD Syndrome | Acute Myeloid Leukemia | Hermansky-Pudlak Syndrome | Porokeratosis | Chromosome 9q34.3 Deletion Syndrome | Ornithine Transcarbamylase Deficiency | Krabbe Disease | Thalassemia | Hemochromatosis Type 1 | Warsaw Breakage Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Hyperlipidemia Type V | Preaxial Polydactyly | Swine Influenza | Synpolydactyly | Genitopatellar Syndrome | Gastritis | Hepatitis E | Pseudomyxoma Peritonei | Iron Overload | Hypogonadism | Cutaneous T-cell Lymphoma | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Autism Spectrum Disorders | Chordoma | Sarcoma, Endometrial Stromal | Mevalonate Kinase Deficiency | Aplasia Cutis Congenita | Hepatic Veno-occlusive Disease | Ependymoma | Diabetes Insipidus, Nephrogenic | Lymphedema-distichiasis Syndrome | Connective Tissue Disorders | Rhabdomyosarcoma, Embryonal | Lichen Planus | Smoldering Myeloma | Familial Exudative Vitreoretinopathy | Gitelman Syndrome | Ataxia-ocular Apraxia 2 | Non-Langerhans Cell Histiocytosis | Galactosemia | Sarcoma, Ewing | Danon Disease | Marfan Syndrome | Sick Sinus Syndrome 1 | Monilethrix | Familial Cerebral Amyloid Angiopathy | Neurocutaneous Melanocytosis | Oligoastrocytoma | Shwachman-Bodian-Diamond Syndrome | Primary Sclerosing Cholangitis | Osteomyelitis | Lateral Meningocele Syndrome | Anxiety Disorders | Klinefelter Syndrome | Primary Progressive Nonfluent Aphasia | Hyperandrogenemia | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Bernard-Soulier Syndrome | Pitt-Hopkins Syndrome | Kearns-Sayre Syndrome | Beta-Propeller Protein-associated Neurodegeneration | Cardiomyopathy, Restrictive | Palsy, Cerebral | Chronic Neutrophilic Leukemia | Osmotic Demyelination Syndrome | Acromesomelic Dysplasia | Cataract | Filariasis | Urolithiasis | Diffuse Palmoplantar Keratoderma | Orthostatic Intolerance | Charcot-Marie-Tooth Disease Type 2T | Familial Episodic Pain Syndrome | Isovaleric Acidemia | Hemophilia | Genee-Wiedemann Syndrome | Marinesco-Sjogren Syndrome | Bone Giant Cell Tumor | Sarcosinemia | Renal Failure | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Insulin Resistance | Carcinoma In Situ | Brooke-Spiegler Syndrome | Corticobasal Syndrome | Niemann-Pick Disease, Type C | Lyme Disease | Astrocytoma, Anaplastic | Frontotemporal Dementia | Keratocystic Odontogenic Tumor | Hepatic Adenomatosis | Hypertelorism | Glycogen Storage Disease Type 0, Muscle | Diabetic Macular Edema | Whipple's Disease | Familial Isolated Hyperparathyroidism | Sleep Apnea, Obstructive | Familial Advanced Sleep Phase Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Autosomal Recessive Bestrophinopathy | Babesiosis | Myelodysplasia | Adenomyosis | Hemangioma | Astigmatism | Delirium | Muckle-Wells Syndrome | Uveitis, Anterior | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Craniofacial Dysostosis | Myocarditis | Cutaneous Mastocytosis | Multisystemic Smooth Muscle Dysfunction Syndrome | Early Infantile Epileptic Encephalopathy 28 | High Molecular Weight Kininogen Deficiency | Primary Progressive Aphasia | Oral Lichen Planus | Nestor-Guillermo Progeria Syndrome | Headache | Lassa Fever | Fibronectin Glomerulopathy | Primary Torsion Dystonia | Limb Girdle Muscular Dystrophy | Protein S Deficiency | Lymphomatoid Granulomatosis | Dysmorphophobia | Central Retinal Artery Occlusion | Charcot-Marie-Tooth Disease Type 4B1 | Lafora Disease | Yellow Fever | Blue Rubber Bleb Nevus Syndrome | Epidermolysis Bullosa Simplex, Localized | Pigment Dispersion Syndrome | VEXAS Syndrome | Leukemia | Addison Disease | Cohen Syndrome | Sulfite Oxidase Deficiency | Adenocarcinoma | Arthritis, Psoriatic | Bronchitis | Multiple System Atrophy | Scleroderma, Diffuse | Pulverulent Zonular Cataract | Stromal Corneal Dystrophy | Spondylosis | Inflammatory Bowel Disease | PHARC Syndrome | Mastitis | Malignant Fibrous Histiocytoma | Partington Syndrome | Mucolipidosis Type IV | Angiomyolipoma | Netherton Syndrome | Galloway-Mowat Syndrome | Hydrolethalus Syndrome | Hyperlipidemia | Zollinger-Ellison Syndrome | Astrocytoma | Skin Papilloma | Rheumatic Heart Disease | Lactose Intolerance | Viral Meningitis | ADNP Syndrome | Choriocarcinoma | Dystonia | Acrodermatitis Enteropathica | Cherubism | Kabuki Syndrome 2 | Neurofibroma, Plexiform | Behcet's Disease | Optic Neuritis | Cervicitis | Familial Retinal Arterial Macroaneurysm | Osteopetrosis | Angiodysplasia | Riboflavin Transporter Deficiency Neuronopathy | Lathosterolosis | Mesothelioma, Malignant | Cysticercosis | Dermatitis | Congenital Ichthyosiform Erythroderma | Focal Cortical Dysplasia Type 2 | Spondyloperipheral Dysplasia | Atelosteogenesis Type 1 | Cold-induced Sweating Syndrome | Hereditary Neuropathy With Liability To Pressure Palsies | Blepharoconjunctivitis | Antithrombin III Deficiency | Hypertension, Essential | Cardiofaciocutaneous Syndrome | Alcoholism | Exostoses | Erythrokeratodermia Variabilis | Myotonia | Portal Vein Thrombosis | Schizencephaly | Spasticity | Diamond-Blackfan Anemia | Mitochondrial DNA Depletion Syndrome | Stomatitis | Generalized Epilepsy With Febrile Seizures Plus | Congenital Heart Defects | Cone Dystrophy | Non-small Cell Lung Cancer | Papilloma | Cholesteryl Ester Storage Disease | Hypervalinemia | Mixed Connective Tissue Disease | Cat Eye Syndrome | Geleophysic Dysplasia | Left Ventricular Noncompaction | Hodgkin Lymphoma | Autoimmune Hemolytic Anemia | Myositis, Focal | Huntington's Disease | Avellino Corneal Dystrophy | Episodic Ataxia | Specific Granule Deficiency | Pyoderma Gangrenosum | SAPHO Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Epilepsy, Generalized | Localized Scleroderma | Pouchitis | Hypertension, Portal | Muir-Torre Syndrome | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Coma | Keratosis | Blau Syndrome | Focal Segmental Glomerulosclerosis | Waardenburg Syndrome Type 4 | Erectile Dysfunction | Senior-Loken Syndrome | Pleurisy | Hypermethioninemia | Knobloch Syndrome | Hydrocephalus, Normal Pressure | Polycystic Ovary Syndrome | Bardet-Biedl Syndrome | Postpoliomyelitis Syndrome | Multiple Sclerosis | Pierre Robin Syndrome | Bainbridge-Ropers Syndrome | Lung Diseases | Stickler Syndrome | Hypokalemic Periodic Paralysis | Molybdenum Cofactor Deficiency | Fanconi Anemia | Takenouchi-Kosaki Syndrome | Anuria | X-linked Myotubular Myopathy | Fibromuscular Dysplasia | Greenberg Dysplasia | Acute Kidney Injury | Congenital Hereditary Endothelial Dystrophy Type I | Pseudohypoparathyroidism Type 1A | Glomerulonephritis, Membranoproliferative | Onchocerciasis | Syphilis | Hypercalcemia | Cri-du-chat Syndrome | Pseudoachondroplasia | Necrobiosis Lipoidica | Kidney Stones | Trichotillomania | Congenital Myopathy | Diabetes Gestational | Vogt-Koyanagi-Harada Syndrome | Fraser Syndrome | Adrenal Insufficiency | Aicardi-Goutieres Syndrome | Kashin-Beck Disease | Hypopituitarism | Omenn Syndrome | Tremor | Myoclonic Atonic Epilepsy | Fibrodysplasia Ossificans Progressiva | Learning Disability | Pulmonary Vein Stenosis | Pneumonia, Viral | Primary Cutaneous Amyloidosis | Skin Carcinoma | VACTERL/VATER Association | Spondyloarthritis | Pontocerebellar Hypoplasia Type 2 | Leber Hereditary Optic Neuropathy | Conjunctivitis, Allergic | Schistosomiasis | Sleep Disorder | Meningococcal Infections | Restrictive Dermopathy | Hypolipoproteinemia | Hypercholesterolemia | Anorchia | Acute Generalized Exanthematous Pustulosis | Epidermolysis Bullosa Acquisita | HUPRA Syndrome | Gout | Thyroiditis | Cancer, Skin | Congenital Primary Aphakia | Unverricht-Lundborg Syndrome | Colitis, Lymphocytic | Metabolic Syndrome | Atopic Dermatitis | Wolcott-Rallison Syndrome | Anodontia | Pneumococcal Meningitis | Myoclonus-dystonia Syndrome | Christianson Syndrome | Inflammatory Myopathy | Corneal Ulcer | Lichen Sclerosus | Lipid Storage Diseases | HANAC Syndrome | Thyroiditis, Autoimmune | Osteogenesis Imperfecta Type I | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Tenosynovial Giant Cell Tumor | Fahr Disease | Prurigo Nodularis | Generalized Epilepsy And Paroxysmal Dyskinesia | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Hereditary Sensory Neuropathy Type 1 | Syncope | NDH Syndrome | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Venous Insufficiency | Chudley-McCullough Syndrome | Carbohydrate Metabolism Disorders | Crohn's Disease | Hypohidrotic Ectodermal Dysplasia | Klippel-Feil Syndrome | Peutz-Jeghers Syndrome | Thyroid Hormone Resistance | Early Infantile Epileptic Encephalopathy 1 | Ebstein Anomaly | Histiocytic Sarcoma | Acute Motor Axonal Neuropathy | Bruck Syndrome | Cerebellar Ataxia, Cayman Type | Duodenal Atresia | Leukoencephalopathy, Progressive Multifocal | Charcot-Marie-Tooth Disease, Type 2C | Prolymphocytic Leukemia | Exotropia | Creatine Deficiency Syndrome Due To AGAT Deficiency | Osteogenesis Imperfecta Type V | Non-proliferative Diabetic Retinopathy | Angioimmunoblastic T-cell Lymphoma | Oguchi Disease-2 | Hyperacusis | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Cheilitis | Corneal Edema | Aneurysm, Abdominal Aortic | Cyclic Vomiting Syndrome | Hidradenitis Suppurativa | Gerodermia Osteodysplastica | Benign Hereditary Chorea | Megalencephaly | Eccrine Porocarcinoma | Hennekam Lymphangiectasia-lymphedema Syndrome | Microcephalic Primordial Dwarfism | Sotos Syndrome | Hemolytic Uremic Syndrome, Atypical | Perry Syndrome | Tuberculosis | Cardiac Sarcoidosis | ACTH-independent Macronodular Adrenal Hyperplasia | Sporadic Hemiplegic Migraine | Ophthalmoplegia | Hypodontia | Vestibular Disease | Peritonitis | Hemorrhagic Disorders | Guttate Psoriasis | Smith-Lemli-Opitz Syndrome | Combined Pituitary Hormone Deficiency | Craniosynostosis | Leishmaniasis, Visceral