Disease

T-cell Leukemia

About the Disease
Leukemia, T-Cell, Chronic, also known as chronic t-cell leukemia, is related to adult t-cell leukemia/lymphoma and t-cell acute lymphoblastic leukemia. The drugs Valproic acid and Zidovudine have been mentioned in the context of this disorder. Affiliated tissues include bone marrow, t cells and bone.

Common Targets
Tumor-Associated Glycoprotein 72 (TAG-72) | CD3 Complex (T Cell Receptor Complex) | TNFRSF18 | CDKN2B-AS1 | IL-2 receptor | HLA-A | G920 | CD7 | CTLA4 | Major Histocompatibility Complex Class I | Sarcoplasmic/Endoplasmic Reticulum Calcium ATPase (SERCA) (nonspecified subtype) | TRBV12-3 | IGF2BP2 | CD5 | JAK2 | TRBC1

疾病靶点研报
T-cell Leukemia

Note: If you'd like to get a target analysis report for T-cell 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 T-cell Leukemia at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Thyrotoxic Periodic Paralysis | Conjunctivitis, Allergic | Prolymphocytic Leukemia | Cohen Syndrome | Thalassemia | Encephalitis | Bardet-Biedl Syndrome | Aldosterone Deficiency | Traboulsi Syndrome | Hyperinsulinemia | Idiopathic Pulmonary Fibrosis | Myoclonus-dystonia Syndrome | Anti-glomerular Basement Membrane Disease | Gastric Atrophy | Epithelial-myoepithelial Carcinoma | Dystonia | Chorea-acanthocytosis | Hepatorenal Syndrome | Congenital Absence Of Vas Deferens | Benign Hereditary Chorea | Encephalopathy, Glycine | Subacute Sclerosing Panencephalitis | Encephalocele | 3-M Syndrome | Hypoplastic Left Heart Syndrome | Conn Syndrome | Alopecia Totalis | Glutaric Aciduria Type 2 | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Photosensitivity | Congenital Heart Defects | Pierre Robin Syndrome | Agammaglobulinemia | Wagner Disease | Blomstrand Osteochondrodysplasia | Hyperkeratosis | Alopecia | Beckwith-Wiedemann Syndrome | Wiedemann-Steiner Syndrome | Histoplasmosis | Medulloblastoma | Spinal Muscular Atrophy | Paracoccidioidomycosis | Delirium | Leukemia | Angioedema, Acquired | Trismus-pseudocamptodactyly Syndrome | Pontocerebellar Hypoplasia | Von Hippel-Lindau Disease | Spinocerebellar Ataxia Type 13 | Usher Syndrome Type IIC | Palsy, Cerebral | Gigantism | Waardenburg Syndrome Type 2A | Rubeosis Iridis | Schistosomiasis | Amenorrhea | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Transcobalamin Deficiency | Hyperekplexia | Diarrhea | Heterotaxy | Malaria, Cerebral | Short-chain Acyl-CoA Dehydrogenase Deficiency | Seborrheic Dermatitis | Blepharophimosis Syndrome | Craniometaphyseal Dysplasia | Chondrodysplasia Punctata 2, X-linked Dominant | Congenital Ichthyosiform Erythroderma | Carbonic Anhydrase VA Deficiency | Intracerebral Hemorrhage | Pilomatrix Carcinoma | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Charcot-Marie-Tooth Disease Type 4D | Renal-hepatic-pancreatic Dysplasia | Sickle Cell Anemia | Diabetes Insipidus, Neurogenic | Wiskott-Aldrich Syndrome | Fetal Alcohol Syndrome | Dupuytren Disease | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Otosclerosis | Shwachman-Bodian-Diamond Syndrome | Osteomyelitis | Coffin-Lowry Syndrome | Larsen Syndrome | McLeod Syndrome | Guillain-Barre Syndrome | Pseudohypoparathyroidism Type 1A | Tangier Disease | Spondylolisthesis | Roberts Syndrome | Japanese Encephalitis | Cardiac Sarcoidosis | Facioscapulohumeral Muscular Dystrophy Type 2 | Esophageal Motility Disorders | Bernard-Soulier Syndrome | Potocki-Shaffer Syndrome | Neurofibroma, Plexiform | Cancer, Bladder | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Low Tension Glaucoma | Borderline Personality Disorder | Central Retinal Artery Occlusion | Thyroid Hormone Resistance | Autosomal Recessive Spastic Paraplegia Type 54 | Histiocytic Sarcoma | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Endophthalmitis | Iron Deficiency Anemia | Porphyria, Acute Intermittent | Stargardt Disease | Leukoplakia, Oral | Cherubism | Heterotopic Ossification | Episodic Ataxia Type 1 | Herpes Simplex Dermatitis | Evans Syndrome | Glutathione Synthetase Deficiency | Familial Partial Lipodystrophy | Meesmann Corneal Dystrophy | Hyperlipidemia, Familial Combined | Bacterial Meningitis | Axenfeld-Rieger Syndrome | Anemia | Pituitary Dwarfism | Hyperprolactinemia | SAPHO Syndrome | Metanephric Adenoma | Trichomegaly | Restrictive Dermopathy | Rothmund-Thomson Syndrome | Familial Hemiplegic Migraine | Acute Tubular Necrosis | IMAGe Syndrome | Splenomegaly | Malaria | Branchiootorenal Syndrome | Blue Nevus | Periventricular Leukomalacia | Maternally Inherited Diabetes And Deafness | Moyamoya Disease | Glycogen Storage Disease Type 1a | Fibromuscular Dysplasia | Agranulocytosis | Granular Corneal Dystrophy | Congenital Hemolytic Anemia | Prediabetes | Usher Syndrome | Adenylosuccinate Lyase Deficiency | Dystonia-parkinsonism, X-linked | Osteosarcoma | Pyoderma Gangrenosum | Motor Neuron Diseases | Shprintzen-Goldberg Syndrome | Pseudohypoparathyroidism Type 1C | Pyelonephritis | Acute Chest Syndrome | Hyperbilirubinemia | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Withdrawal Syndrome | Episodic Ataxia Type 2 | Supravalvular Aortic Stenosis | Osteopetrosis | Panuveitis | Osteonecrosis | Lysosomal Acid Lipase Deficiency | Cancer, Breast | Papilledema | Anxiety Disorders | POEMS Syndrome | Ganglioneuroma | Paraganglioma, Carotid Body | Jacobsen Syndrome | Malnutrition | Retinal Vasculitis | Filariasis | Myocarditis | Subcortical Band Heterotopia | Primary Progressive Nonfluent Aphasia | Ectopia Lentis, Isolated, Autosomal Recessive | Menetrier Disease | Plasma Cell Dyscrasia | Cholangitis | Vitamin D Deficiency | Trichorhinophalangeal Syndrome | Neuropathy | Hypopituitarism | Crohn's Disease | Scleritis | Pityriasis Rubra Pilaris | Thrombotic Microangiopathy | Cholestasis | Recurrent Respiratory Papillomatosis | ICF Syndrome | Leigh Syndrome | Macular Degeneration | Glaucoma | Hepatitis A | Hypertensive Nephropathy | Waardenburg Syndrome Type 2E | Pierson Syndrome | Retinal Dystrophy, Early-onset Severe | Odonto-onycho-dermal Dysplasia | Bartter Syndrome | Peutz-Jeghers Syndrome | Leber Hereditary Optic Neuropathy | Congenital Heart Block | NGLY1 Deficiency | Antithrombin III Deficiency | Fukuyama Congenital Muscular Dystrophy | Multiple Sclerosis, Primary Progressive | Keloid | Glycogen Storage Disease Type 1 | Crisponi Syndrome | Goldenhar Syndrome | Neurogenic Bladder | Anosmia, Congenital | Acromicric Dysplasia | Epidermolysis Bullosa Acquisita | Noonan Syndrome-like Disorder With Loose Anagen Hair | X-linked Creatine Transporter Deficiency | Diabetic Macular Edema | Parkinson Disease 6, Autosomal Recessive Early-onset | Hydrocephalus, Normal Pressure | Sarcoma, Alveolar Soft Part | Adenosine Deaminase 2 Deficiency | Albinism | Progressive Encephalopathy-optic Atrophy Syndrome | Facioscapulohumeral Muscular Dystrophy Type 1 | Craniolenticulosutural Dysplasia | Fanconi Anemia | Light Chain Amyloidosis | Pregnancy, Ectopic | Congenital Bile Acid Synthesis Defect | Erythropoietic Protoporphyria | Fuchs Heterochromic Iridocyclitis | Urea Cycle Disorder | Periodontitis | Cone Dystrophy | Charcot-Marie-Tooth Disease Type 2D | Obesity, Morbid | Hereditary Neuropathy With Liability To Pressure Palsies | Alpers Syndrome | Colitis | Pituitary Disorders | Meconium Ileus | Primary Carnitine Deficiency | Premature Ejaculation | Neuronal Ceroid Lipofuscinosis | Spinocerebellar Ataxia Type 27 | Nutrition Disorders | Hereditary Sensory Neuropathy Type 1 | Hyperostosis | Adenoma, Pleomorphic | Presbyopia | LMNA-related Congenital Muscular Dystrophy | Primary Torsion Dystonia | Niemann-Pick Disease, Type A | Hemophagocytic Lymphohistiocytosis | Glycogen Storage Disease | HELLP Syndrome | Nephropathy | Cervical Dystonia | VEXAS Syndrome | Lafora Disease | Porphyria, Variegate | Transient Bullous Dermolysis Of The Newborn | Niemann-Pick Disease, Type B | Lymphedema | Neuroma | Spitz Nevus | Reye Syndrome | Peeling Skin Syndrome, Acral Type | Trichothiodystrophy | Pancreatitis, Chronic | Hypertension, Renal | Porencephaly | Tinea | Muir-Torre Syndrome | Epilepsy Of Infancy With Migrating Focal Seizures | Cyst | Galactosemia | Vitelliform Macular Dystrophy | Autosomal Recessive Spastic Paraplegia Type 35 | Primary Hyperoxaluria Type 1 | Galloway-Mowat Syndrome | Dermatitis Herpetiformis | Arthropathy | Familial Episodic Pain Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Asphyxia Neonatorum | Schamberg Disease | Arteriosclerosis | Analgesia | Amyotrophic Lateral Sclerosis | Blepharoconjunctivitis | Essential Fructosuria | Proximal Symphalangism | Thyroiditis | Hereditary Coproporphyria | Neurotoxicity | Hypogonadism | Wolman Disease | Endocarditis | Aldosterone Synthase Deficiency | Measles | Parapsoriasis | Hereditary Mixed Polyposis Syndrome | Lymphoma | Cutaneous Mastocytosis | Aphasia | Kabuki Syndrome 2 | Cutis Laxa | Diffuse Mesangial Sclerosis | Proopiomelanocortin Deficiency | Lymphoproliferative Disorders | Diabetes Mellitus, Transient Neonatal | Nephrotic Syndrome Type 1 | Exocrine Pancreatic Insufficiency | Basan Syndrome | Pulverulent Zonular Cataract | Hyperglycemia | Hemangioma | Adrenoleukodystrophy, X-linked | Cystitis | Ebstein Anomaly | Johanson-Blizzard Syndrome | Patent Ductus Arteriosus | Sclerosing Cholangitis | Nemaline Myopathy 10 | Primary Progressive Aphasia | Aspergillosis | Asthma | Chronic Thromboembolic Pulmonary Hypertension | Williams Syndrome | Gliosarcoma | MELAS Syndrome | Vitiligo | Chronic Lymphocytic Leukemia | Necrobiosis Lipoidica | Sick Sinus Syndrome | Chronic Kidney Disease | Neonatal Progeroid Syndrome | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Behcet's Disease | Kaposi Sarcoma | Ghosal Syndrome | Waardenburg Syndrome Type 1 | 3-methylglutaconic Aciduria Type I | Vitreoretinopathy, Proliferative | Mitochondrial Disease | Hypereosinophilic Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Adrenal Insufficiency | Distal Myopathy | GATA2 Deficiency | Antenatal Bartter Syndrome Type 1 | Carbohydrate Metabolism Disorders | Otitis Media | Sleep Apnea, Central | Superficial Spreading Melanoma | Spinocerebellar Ataxia Type 5 | Mitochondrial DNA Depletion Syndrome 13 | Trigonocephaly | Epidermal Nevus Syndrome | Meleda Disease | Zellweger Syndrome | Heart Failure | Iron Overload | Netherton Syndrome | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Autonomic Neuropathy | Chromosome 5q Deletion Syndrome | Walker-Warburg Syndrome | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Hyperbilirubinemia, Neonatal | Charcot-Marie-Tooth Disease Type 3 | Eating Disorder | Pleural Tuberculosis | Strabismus | Allan-Herndon-Dudley Syndrome | Chitayat Syndrome | Hypothyroidism | Inborn Errors Of Metabolism | Compartment Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Paroxysmal Kinesigenic Dyskinesia | Colitis, Microscopic | Arteriovenous Malformations | Familial Isolated Hyperparathyroidism | Coronary Artery Disease | Endometriosis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Polycythemia | Lennox-Gastaut Syndrome | Polymyositis | Acromesomelic Dysplasia | Diabetic Nephropathy