Thalassemia, Beta
Thalassemia, Beta
About the Disease
Beta-Thalassemia, also known as beta thalassemia, is related to thrombocytopenia with beta-thalassemia, x-linked and hemoglobin lepore-beta-thalassemia syndrome. An important gene associated with Beta-Thalassemia is HBB (Hemoglobin Subunit Beta), and among its related pathways/superpathways are Response to elevated platelet cytosolic Ca2+ and Golgi-to-ER retrograde transport. The drugs Busulfan and Metformin have been mentioned in the context of this disorder. Affiliated tissues include liver, spleen and bone, and related phenotypes are splenomegaly and pallor
Common Targets
PPARG | CYP2D6 | HAMP | GDF11 | ATRX | CFP | HDAC1 | PRMT5 | KEAP1 | BCL11A | G5243 | G9429 | CYP1A1 | HDAC3 | TNFSF11 | ZNF644 | EHMT1 | PKLR | PDE9A | EED | VDR | ABCC2 | TMPRSS6 | XDH | NOS3 | FTSJ1 | SLC6A9 | XPO1 | CYP24A1 | WIZ | IL1B | LOC105378010 | DCX (DDB1-CUL4-X-box) E3 protein ligase complex | ERFE | INHBA | CYP1A2 | GATAD2A | Transforming growth factor beta (nonspecified subtype) | NF-kappaB (NFkB) | HBB | Polycomb Repressive Complex 2 | SLC40A1 | CCR5 | GC | G1786 | G7124 | KLF1 | Proteasome Complex | UGT1A1 | NFIX | EHMT2 | HBBP1 | CRBN | HBD | HBG1 | HBG2 | CD19 | EPAS1 | CYP27B1 | MBD2 | HDAC2 | G4780 | UGT1A3 | TNFRSF11B | DDC | HFE | G2475

Note: If you'd like to get a target analysis report for Thalassemia, Beta, 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 Thalassemia, Beta at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Delirium | Asplenia | Kleine-Levin Syndrome | Cancer, Kidney | Schindler Disease | Keratitis | Poikiloderma With Neutropenia | Familial Glucocorticoid Deficiency | Adenomyosis | Carcinoma, Transitional Cell | Gerodermia Osteodysplastica | Plasmacytoma | Sialidosis Type I | Wiskott-Aldrich Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Carcinoma, Squamous Cell | Neurodegeneration With Brain Iron Accumulation | Trachoma | Epidermolysis Bullosa Acquisita | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Maple Syrup Urine Disease | Osteogenesis Imperfecta Type VI | Hyperacusis | Pregnancy, Ectopic | Leukodystrophies | Bietti Crystalline Dystrophy | Optic Neuropathy | Menetrier Disease | Nemaline Myopathy 8 | Veno-occlusive Disease | Hypoproteinemia, Hypercatabolic | Conjunctivitis | Rothmund-Thomson Syndrome | Waardenburg Syndrome Type 1 | Cramp Fasciculation Syndrome | Stroke | Hemoglobinopathies | Rosacea | Sorsby Fundus Dystrophy | Primary Ovarian Insufficiency | Spinocerebellar Ataxia Type 16 | Hereditary Mixed Polyposis Syndrome | Angioedema, Hereditary | Paroxysmal Kinesigenic Dyskinesia | Camptocormia | Cirrhosis | Amelogenesis Imperfecta | Tularemia | Dysferlinopathy | Anovulation | Inflammatory Bowel Disease | Wolcott-Rallison Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Anterior Segment Dysgenesis | Mosaic Variegated Aneuploidy Syndrome 2 | Familial Hypertrophic Cardiomyopathy | Tangier Disease | Hyperandrogenemia | Larsen Syndrome | Presbycusis | Inflammatory Joint Disease | Avellino Corneal Dystrophy | Renal Hypomagnesemia 3 | Lissencephaly 2 | Gitelman Syndrome | Familial Retinal Arterial Macroaneurysm | Melnick-Needles Syndrome | Specific Granule Deficiency | Esophagitis, Eosinophilic | Rickets | Parvovirus B19 Infection | Agammaglobulinemia | Thyroid Dyshormonogenesis | Pendred Syndrome | Ependymoma | Epiphyseal Chondrodysplasia, Miura Type | Sarcoma, Alveolar Soft Part | Hyperuricemic Nephropathy, Familial Juvenile | Hypersensitivity | Bladder Exstrophy | Chronic Thromboembolic Pulmonary Hypertension | Bacterial Meningitis | Chronic Neutrophilic Leukemia | Macular Corneal Dystrophy Type 1 | Gliosarcoma | DOCK8 Immunodeficiency Syndrome | Guanidinoacetate Methyltransferase Deficiency | Polycythemia | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Hyperammonemia | Charcot-Marie-Tooth Disease Axonal Type 2N | Hypercholesterolemia | Sarcoma, Endometrial Stromal | Adenomatoid Tumor | Tyrosine Hydroxylase Deficiency | Acrodermatitis Enteropathica | Juvenile Myoclonic Epilepsy | Myofibrillar Myopathy | Coronary Artery Disease | PASLI Disease | Nephropathy | Sweet Syndrome | Vertebrobasilar Insufficiency | Perivascular Epithelioid Cell Tumor | Steel Syndrome | Primary Progressive Nonfluent Aphasia | Polydactyly | Oculocutaneous Albinism | Allan-Herndon-Dudley Syndrome | Hemolytic Anemia | Pathological Gambling | Blepharoconjunctivitis | Microcephaly, Seizures, And Developmental Delay | Mitochondrial Myopathy | Dengue Hemorrhagic Fever | Polycystic Ovary Syndrome | Majeed Syndrome | Mitochondrial Encephalomyopathy | Acromicric Dysplasia | Hemolytic Uremic Syndrome, Atypical | Obesity, Morbid | Craniosynostosis | Behavioral Variant Of Frontotemporal Dementia | Encephalopathy, Glycine | Crouzon Syndrome With Acanthosis Nigricans | Diverticulitis | Analgesia | Gardner Syndrome | Duchenne Muscular Dystrophy | Cryoglobulinemia | Spinocerebellar Ataxia Type 31 | Congenital Myasthenic Syndrome | Saethre-Chotzen Syndrome | Epithelioid Hemangioma | Sotos Syndrome | Duodenal Atresia | Homocystinuria | Plasma Cell Leukemia | Transcobalamin Deficiency | Micro Syndrome | Neurofibroma | Cysticercosis | Thrombophilia | Loeys-Dietz Syndrome Type 4 | Leukocyte Adhesion Deficiency | Hyperinsulinemia | Lamellar Ichthyosis | Focal Segmental Glomerulosclerosis | Carey-Fineman-Ziter Syndrome | Ventricular Septal Defect | Stickler Syndrome | Geleophysic Dysplasia | Melanoma, Malignant | Bernard-Soulier Syndrome | Hypercalciuria | Alopecia | Hypoplastic Left Heart Syndrome | Usher Syndrome Type III | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Sarcoma, Ewing | Schaaf-Yang Syndrome | Craniofrontonasal Syndrome | Cutaneous T-cell Lymphoma | Macrophagic Myofasciitis | Retinal Diseases | Lattice Corneal Dystrophy Type 1 | Gastric Atrophy | Sarcoidosis | Hypoglycemia | Keratopathy | Glanzmann Thrombasthenia | Optic Nerve Hypoplasia, Bilateral | Chromosome 16p11.2 Deletion Syndrome | Iron Metabolism Disorders | Takayasu's Arteritis | Hepatitis C, Chronic | Headache | Carcinoma, Signet Ring Cell | Cervical Dystonia | Vasculitis | Sertoli Cell-only Syndrome | Lymphoproliferative Disorders | Dengue Shock Syndrome | Lymphopenia | Fetal Alcohol Syndrome | REM Sleep Behavior Disorder | Glycogen Storage Disease Type 0, Muscle | Neurofibromatosis Type 1 | Hyperthyroidism | Charcot-Marie-Tooth Disease Type 2D | Schnitzler Syndrome | Marinesco-Sjogren Syndrome | Central Retinal Artery Occlusion | Hemimegalencephaly | Trichorhinophalangeal Syndrome | Fetal Akinesia Deformation Sequence | Smith-Kingsmore Syndrome | Diabetes Insipidus | Cancer, Prostate | Lymphangiomatosis | Colitis, Microscopic | Lipid Storage Diseases | Glycogen Storage Disease Type 5 | Rhabdomyosarcoma | Hemochromatosis Type 1 | Intestinal Pseudo-obstruction | Chronic Granulomatous Disease | Long QT Syndrome Type 1 | Hypercholesterolemia, Familial | CDKL5 Deficiency Disorder | CEDNIK Syndrome | Dent Disease | Acral Lentiginous Melanoma | Absence Epilepsy | Borjeson-Forssman-Lehmann Syndrome | Agoraphobia | Uveitis, Anterior | Burn-McKeown Syndrome | Spondylolisthesis | Branchiootorenal Syndrome | Maternally Inherited Diabetes And Deafness | Prader-Willi Syndrome | Polycythemia Vera | Blastoma, Pleuropulmonary | Hereditary Neuropathy With Liability To Pressure Palsies | Primary Hyperoxaluria Type 1 | Hyperparathyroidism, Primary | Split Hand-foot Malformation | Familial Thoracic Aortic Aneurysm | Scapuloperoneal Spinal Muscular Atrophy | Hereditary Sensory Neuropathy Type 1 | Adult Polyglucosan Body Disease | Choroiditis | Hyperoxaluria | Stuttering | Charcot-Marie-Tooth Disease Type 2E | Arthritis, Reactive | Cri-du-chat Syndrome | Spinocerebellar Ataxia Type 3 | Ichthyosis Bullosa Of Siemens | Pelvic Inflammatory Disease | Erythromelalgia | Acute Myeloid Leukemia | Malnutrition | Niemann-Pick Disease, Type A | Diamond-Blackfan Anemia | Carney Triad | Charcot-Marie-Tooth Disease Type 3 | PHARC Syndrome | Histiocytosis | Parkinson Disease 6, Autosomal Recessive Early-onset | Meniere's Disease | Tendinitis | Ligneous Conjunctivitis | Haim-Munk Syndrome | Lymphangioma | Epidermal Nevus Syndrome | Renal Oncocytoma | Antiphospholipid Syndrome | Glycogen Storage Disease Type 9 | Osteogenesis Imperfecta Type I | Granular Corneal Dystrophy | Leishmaniasis, Cutaneous | Lymphoma, Follicular | Aldosterone Deficiency | Ophthalmia, Sympathetic | Chronic Myelomonocytic Leukemia | Raine Syndrome | Hypotonia-cystinuria Syndrome | Cornelia De Lange Syndrome | Chronic Inflammatory Demyelinating Polyneuropathy | Kabuki Syndrome 2 | Ulcerative Colitis | Carney-Stratakis Syndrome | Peters-plus Syndrome | Pleomorphic Xanthoastrocytoma | Anemia | Lymphomatoid Granulomatosis | Costello Syndrome | Aspartylglycosaminuria | Sarcoidosis, Pulmonary | GATA2 Deficiency | Hemosiderosis | Colitis, Lymphocytic | Spondylocostal Dysostosis | Cholecystitis | Still Disease | Focal Cortical Dysplasia Type 2 | Trimethylaminuria | Graft-versus-host Disease | Amenorrhea | Rhabdomyosarcoma, Embryonal | Communication Disorders | Charcot-Marie-Tooth Disease Type 4B1 | Hemorrhagic Disorders | Fuchs Dystrophy | Acute Tubular Necrosis | Autism | Multiple System Atrophy | Heart Failure | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Azoospermia | Fabry's Disease | Potocki-Shaffer Syndrome | Hemangioblastoma | Pseudohypoparathyroidism Type 1B | Jawad Syndrome | Erythropoietic Protoporphyria | Dubin-Johnson Syndrome | Diabetic Nephropathy | Pemphigoid | Persistent Fetal Circulation | Temporal Lobe Epilepsy | Phenylketonuria | Constipation | Neurodermatitis | Lymphoma, Mantle Cell | Trichomegaly | Glioblastoma | Neovascular Glaucoma | Sturge-Weber Syndrome | DRESS Syndrome | Cardiospondylocarpofacial Syndrome | Pigment Dispersion Syndrome | Sickle Cell Disease | Mood Disorder | Neurogenic Bladder | Cannabis Abuse | Hypokalemic Periodic Paralysis | Reflex Epilepsy | Syndactyly | Congenital Poikiloderma | Schizophrenia, Paranoid | Proximal Symphalangism | Precocious Puberty | 3-methylglutaconic Aciduria Type I | Long QT Syndrome Type 2 | Bronchitis | Deafness, Dystonia, And Cerebral Hypomyelination | Episodic Ataxia Type 2 | Hennekam Lymphangiectasia-lymphedema Syndrome | HELLP Syndrome | Growth Hormone Excess | Long QT Syndrome Type 3 | Castleman Disease | Hodgkin Lymphoma | Epilepsy Of Infancy With Migrating Focal Seizures | Donnai-Barrow Syndrome | Renal Hypouricemia | Poretti-Boltshauser Syndrome | Crohn's Disease | Retinitis Pigmentosa 3 | Tremor | Vitamin A Deficiency | Medulloblastoma | Mitochondrial DNA Depletion Syndrome | Synpolydactyly | Acrocallosal Syndrome | Influenza | Hemochromatosis Type 2 | Schnyder Crystalline Corneal Dystrophy | Paternal Uniparental Disomy Of Chromosome 14 | Pituitary Stalk Interruption Syndrome | Pierpont Syndrome | Optic Atrophy 2 | Kallmann Syndrome | Pitt-Hopkins Syndrome | Myelitis, Transverse | Hepatitis A | Carpenter Syndrome | Necrotizing Autoimmune Myopathy | Episodic Ataxia Type 1 | Marfan Syndrome | Esophageal Adenocarcinoma | Hypotrichosis | Cerebrovascular Disorders | Fowler's Syndrome | Fibronectin Glomerulopathy | Spinal Cord Diseases | Coenzyme Q10 Deficiency | Stevens-Johnson Syndrome | Pulmonary Vein Stenosis | Unverricht-Lundborg Syndrome | Tyrosinemia Type 2 | Ovarian Hyperstimulation Syndrome | Arterial Tortuosity Syndrome | Neurodevelopmental Disorders | Patent Foramen Ovale | Ichthyosis Hystrix, Curth-Macklin Type | Pericarditis | Schwannoma | Temtamy Preaxial Brachydactyly Syndrome | Cardiomyopathy, Restrictive | Lathosterolosis | Kaposiform Hemangioendothelioma | Nutrition Disorders | Combined Deficiency Of Factor V And Factor VIII | Congenital Heart Block | Posterior Polar Cataract | Glycogen Storage Disease Type 1b