Disease

Takotsubo Cardiomyopathy

About the Disease
Broken Heart Syndrome, also known as takotsubo cardiomyopathy, is related to cervical intraepithelial neoplasia and myocardial stunning. The drugs Acetylcarnitine and Folic acid have been mentioned in the context of this disorder. Affiliated tissues include heart, brain and endothelial, and related phenotypes are mildly reduced left ventricular ejection fraction and chest pain

Common Targets
ADRB1 | ADRB2

疾病靶点研报
Takotsubo Cardiomyopathy

Note: If you'd like to get a target analysis report for Takotsubo Cardiomyopathy, 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 Takotsubo Cardiomyopathy at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Abetalipoproteinemia | Hyperprolactinemia | Diabetic Encephalopathy | Cystinuria | Oculopharyngeal Muscular Dystrophy | Lipodystrophy | Maternally Inherited Diabetes And Deafness | Ameloblastic Carcinoma | Ameloblastoma | Meesmann Corneal Dystrophy | Antisynthetase Syndrome | Osteogenesis Imperfecta | Polycystic Liver | Aldosteronism | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Epidermolysis Bullosa Simplex, Localized | Pituitary Stalk Interruption Syndrome | TARP Syndrome | Vulvovaginitis | Nephrotic Syndrome Type 1 | Allan-Herndon-Dudley Syndrome | Tendinitis | Restless Legs Syndrome | Coronary Restenosis | Niemann-Pick Disease, Type B | Distal Myopathy | Macrodactyly | Fetal Alcohol Syndrome | Withdrawal Syndrome | Hepatitis, Chronic | Hyperhomocysteinemia | Nemaline Myopathy 10 | Ovarian Sex Cord-stromal Tumor | Erythropoietic Protoporphyria | Carbonic Anhydrase VA Deficiency | Shprintzen-Goldberg Syndrome | Kawasaki Disease | Angioimmunoblastic T-cell Lymphoma | Myositis | Plasma Cell Dyscrasia | Chromosome 16p11.2 Deletion Syndrome | Perry Syndrome | Smoldering Myeloma | Arthritis, Reactive | Mitochondrial Encephalomyopathy | Herpes Genitalis | Stuve-Wiedemann Syndrome | Rhabdomyosarcoma | Lissencephaly 2 | Kleine-Levin Syndrome | Hyperkalemic Periodic Paralysis | Corneal Neovascularization | Meningioma | Empyema | DEND Syndrome | Aplastic Anemia | Pericarditis | Familial Male-limited Precocious Puberty | Hypercholesterolemia | Tumoral Calcinosis | Hypotonia-cystinuria Syndrome | Primary Progressive Aphasia | Congenital Generalized Lipodystrophy | Addison Disease | Encephalopathy, Hepatic | Dyskeratosis Congenita | Acute Tubular Necrosis | Thyroid Dysgenesis | Myeloid Leukemia | Dermatofibrosarcoma | Congenital Mirror Movements | Lipid Storage Diseases | Spondylometaphyseal Dysplasia | Histoplasmosis | Basal Ganglia Cerebrovascular Disease | Hypertensive Retinopathy | Tangier Disease | Hepatitis C, Chronic | Cardiac Sarcoidosis | Rickets | Mosaic Variegated Aneuploidy Syndrome 2 | AIDS Dementia Complex | Cutaneous Angiosarcoma | Lattice Corneal Dystrophy Type 1 | Infantile Spasm | WAGR Syndrome | Shock, Cardiogenic | Glomerulonephritis | Coloboma | Osteoglophonic Dysplasia | Behavioral Variant Of Frontotemporal Dementia | Angiomyolipoma | Trachoma | Pemphigoid | Giant Cell Arteritis | Beare-Stevenson Syndrome | Glutathione Synthetase Deficiency | Carcinoma, Signet Ring Cell | Malaria, Cerebral | Fibrosarcoma | Spinocerebellar Ataxia Type 13 | Glycogen Storage Disease Type 1a | Zollinger-Ellison Syndrome | Pontocerebellar Hypoplasia Type 2 | Vitreoretinopathy, Proliferative | ACTH-independent Macronodular Adrenal Hyperplasia | Ophthalmoplegia | IgA Deficiency | Omenn Syndrome | Amelogenesis Imperfecta | Glioma | Myoclonic Epilepsy With Ragged Red Fibers | Bronchitis | Neurodevelopmental Disorders | Loeys-Dietz Syndrome Type 4 | Non-Hodgkin Lymphoma | Atrioventricular Septal Defect | Hypermethioninemia | Erdheim-Chester Disease | Chylothorax, Congenital | Paraplegia | Analgesia | Reflex Epilepsy | Encephalopathy, Glycine | Eiken Syndrome | Aneurysm, Thoracic Aortic | Gerstmann-Straussler-Scheinker Syndrome | AIDS | Hypothyroidism | Coma | Acromicric Dysplasia | Low Phospholipid Associated Cholelithiasis | Leukoencephalopathy, Progressive Multifocal | Vascular Calcification | Keratitis-ichthyosis-deafness Syndrome | Pigment Dispersion Syndrome | MELAS Syndrome | Wiedemann-Steiner Syndrome | Hemolytic Uremic Syndrome | Greenberg Dysplasia | Mitochondrial Disease | Cancer, Prostate | Chondrosarcoma | Familial Cerebral Amyloid Angiopathy | Osteogenesis Imperfecta Type VI | McCune-Albright Syndrome | Early Infantile Epileptic Encephalopathy 28 | Bainbridge-Ropers Syndrome | Thalassemia | Porphyria, Acute Intermittent | Turner's Syndrome | Stiff-man Syndrome | Avellino Corneal Dystrophy | Mountain Sickness | Microtia | Episodic Ataxia Type 1 | Succinic Semialdehyde Dehydrogenase Deficiency | Currarino Syndrome | Nephritis, Interstitial | Muscle Wasting | Light Chain Amyloidosis | Pyruvate Decarboxylase Deficiency | Esophagitis, Eosinophilic | Dysplastic Nevus | Pierre Robin Syndrome | Congenital Heart Block | Gallstones | Cardiac Arrest | Schistosomiasis | Beckwith-Wiedemann Syndrome | Peyronie's Disease | Chronic Enteropathy Associated With SLCO2A1 Gene | Erectile Dysfunction | Superficial Spreading Melanoma | Hemophilia | Polycystic Kidney, Autosomal Recessive | Lafora Disease | Leukodystrophies | Pilomatrix Carcinoma | Trichothiodystrophy | Glanzmann Thrombasthenia | Craniopharyngioma | Tenosynovial Giant Cell Tumor | Hypospadias | Dermatitis | Epidermolysis Bullosa Simplex | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Antisocial Personality Disorder | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Osteomyelitis | Epithelioid Hemangioma | Oculocutaneous Albinism Type 4 | Inflammatory Myofibroblastic Tumor | VACTERL/VATER Association | Colitis, Collagenous | Melanocytic Nevus | Juvenile Hyaline Fibromatosis | Arthrogryposis | Hemophagocytic Lymphohistiocytosis | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Sclerosteosis | Large Granular Lymphocytic Leukemia | Emery-Dreifuss Muscular Dystrophy | Microphthalmia | Charcot-Marie-Tooth Disease, Type 2C | Avian Influenza | Acute Motor Axonal Neuropathy | Progressive Encephalopathy-optic Atrophy Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Waardenburg Syndrome Type 4A | Tonsillitis | X-linked Acrogigantism | Macrophage Activation Syndrome | Sarcoidosis, Pulmonary | Renal Oncocytoma | Polydactyly | Hyperostosis | Photosensitivity | Acne Vulgaris | Donnai-Barrow Syndrome | Acrodermatitis Enteropathica | Tinea Versicolor | Chitayat Syndrome | Incontinentia Pigmenti | Krabbe Disease | Corneal Dystrophy And Perceptive Deafness | Primary Hyperoxaluria Type 1 | Meckel-Gruber Syndrome | Histiocytosis | Angiosarcoma | Blepharo-cheilo-odontic Syndrome | Familial Pheochromocytoma-paraganglioma | LRBA Deficiency | Oculocutaneous Albinism Type 2 | Hepatitis B, Chronic | Ganglioneuroma | Porphyria, Variegate | Papillon-Lefevre Syndrome | Potocki-Shaffer Syndrome | Encephalocele | Liver Failure, Acute Infantile | Fibrodysplasia Ossificans Progressiva | Polyneuropathy | Heart Block | Intracerebral Hemorrhage | Cystinosis | Myofibromatosis | Bernard-Soulier Syndrome | Peters-plus Syndrome | Woodhouse-Sakati Syndrome | Actinomycetoma | Paronychia | Lymphangioleiomyomatosis | Pseudohypoparathyroidism Type 1A | Basal Cell Nevus Syndrome | Carey-Fineman-Ziter Syndrome | Cavitary Optic Disc Anomalies | Cornelia De Lange Syndrome | Epilepsy, Generalized | Dengue Shock Syndrome | Hyperparathyroidism | Conduct Disorder | Spitz Nevus | Amebiasis | Oguchi Disease-2 | Chondromyxoid Fibroma | Down Syndrome | Gigantism | Hypersomnia | Prune Belly Syndrome | Pneumonia, Viral | PHARC Syndrome | Neuroleptic Malignant Syndrome | Esthesioneuroblastoma | Influenza | Reticular Dysgenesis | Wieacker-Wolff Syndrome | Lymphedema | Chondrodysplasia Punctata | Retinoblastoma | DICER1 Syndrome | Rheumatoid Arthritis | Rheumatic Heart Disease | Trimethylaminuria | Familial Hemiplegic Migraine | Cheilitis | Maple Syrup Urine Disease | Paroxysmal Kinesigenic Dyskinesia | Cleidocranial Dysplasia | Amyotrophic Lateral Sclerosis | Epidermolytic Ichthyosis, Annular | Central Retinal Artery Occlusion | Neurodegeneration With Brain Iron Accumulation | Hypersensitivity | Chromosome 9q34.3 Deletion Syndrome | Hydronephrosis | Glycogen Storage Disease Type 6 | Cluster Headache | Bloom Syndrome | Rhabdoid Tumor | Meleda Disease | Williams Syndrome | Ependymoma | Overactive Bladder | Pendred Syndrome | Schistosomiasis Mansoni | Paraganglioma | Keloid | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Waardenburg Syndrome Type 4 | Desbuquois Syndrome | Anti-glomerular Basement Membrane Disease | Werner's Syndrome | Synovitis | Thrombocytopenia | Spinocerebellar Ataxia Type 28 | Cholestasis, Intrahepatic | Arteriosclerosis | Ectodermal Dysplasia | Encephalopathy, Ethylmalonic | Van Der Knaap Disease | Chloridorrhea, Congenital | Spinocerebellar Ataxia Type 1 | Presbyopia | Stroke, Hemorrhagic | Kernicterus | Lentigo | Goiter | Spinal Muscular Atrophy Type 2 | Lymphoma | Alkaptonuria | Speech Disorders | Primary Pigmented Nodular Adrenocortical Disease | Hartsfield Syndrome | Thyroiditis | Pneumonia, Mycoplasma | REM Sleep Behavior Disorder | Canavan Disease | Metachondromatosis | Familial Mediterranean Fever | Pneumonia, Bacterial | Carcinoma, Small Cell | Pure Autonomic Failure | Familial Dysautonomia | Low Tension Glaucoma | Dystonia-parkinsonism, X-linked | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Adenomatoid Tumor | Adams-Oliver Syndrome | Craniolenticulosutural Dysplasia | Retinal Telangiectasia | Nephronophthisis | Spinal Cord Diseases | Basal Ganglia Disease | Meningococcal Infections | Hydrolethalus Syndrome | Otosclerosis | Acute Kidney Injury | Colitis, Microscopic | Usher Syndrome Type II | Pyelonephritis | Diabetes Insipidus | Cardiomyopathy, Dilated, 1L | Retinopathy Of Prematurity | Schizencephaly | HELLP Syndrome | Paraganglioma, Carotid Body | Choriocarcinoma | Retinal Dystrophy | Acral Lentiginous Melanoma | Sialidosis | Myopathy | Palmoplantar Keratoderma | Pterygium | Spondylolisthesis | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Apparent Mineralocorticoid Excess Syndrome | Anuria | Pyoderma Gangrenosum | Impetigo | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Specific Granule Deficiency | FG Syndrome | Best Macular Dystrophy | Esotropia | Diabetic Nephropathy | Sensory Neuropathy | Poirier-Bienvenu Neurodevelopmental Syndrome | Spinocerebellar Ataxia Type 5 | Hereditary Inclusion Body Myopathy | Pontocerebellar Hypoplasia | Amish Infantile Epilepsy Syndrome | Paracoccidioidomycosis | Imerslund-Grasbeck Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Crigler-Najjar Syndrome | DiGeorge Syndrome | Creatine Deficiency Syndrome Due To AGAT Deficiency | Leukemia-lymphoma, Adult T-cell | Spinocerebellar Ataxia Type 17