Peripartum Cardiomyopathy

About the Disease
Peripartum Cardiomyopathy, also known as postpartum cardiomyopathy, is related to cardiac conduction defect and atrial standstill 1. An important gene associated with Peripartum Cardiomyopathy is MIR146A (MicroRNA 146a), and among its related pathways/superpathways are Striated muscle contraction pathway and MicroRNAs in cardiomyocyte hypertrophy. The drugs Selenium and Selenious acid have been mentioned in the context of this disorder. Affiliated tissues include heart, thyroid and brain, and related phenotypes are hypertension and fatigue

Common Targets
TNNC1 | TTN | SLC30A5 | MYH7 | BAG3

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

Other Diseases

Farber Disease | Milk Allergy | Ligneous Conjunctivitis | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Cardiomyopathy, Peripartum | Diabetic Nephropathy | Galloway-Mowat Syndrome | Chronic Neutrophilic Leukemia | Craniofacial Dysostosis | Swine Influenza | Warsaw Breakage Syndrome | Lissencephaly 2 | Cryoglobulinemia | Phosphoglycerate Dehydrogenase Deficiency | Portal Vein Thrombosis | Osteomalacia | Greig Cephalopolysyndactyly Syndrome | Lymphedema | Proteasome-associated Autoinflammatory Syndrome 2 | Ehlers-Danlos Syndrome | Scapuloperoneal Myopathy, X-linked Dominant | Intellectual Disability, Autosomal Dominant 5 | Ganglioglioma | Familial Mediterranean Fever | Tetanus | Congenital Sodium Diarrhea | Campomelic Dysplasia | Infantile Refsum Disease | Renal Tubular Dysgenesis | Strabismus | Renpenning Syndrome | Sialidosis | Ganglioneuroma | Dystonia Musculorum Deformans | Neuromyotonia | 3-hydroxy-3-methylglutaric Aciduria | Neurodermatitis | Chronic Myelomonocytic Leukemia | Cold Agglutinin Disease | Congenital Lipoid Adrenal Hyperplasia | Gangliosidosis | Holt-Oram Syndrome | Juvenile Polyposis | Hoyeraal-Hreidarsson Syndrome | Papillon-Lefevre Syndrome | Alzheimer Disease, Late Onset | Myositis, Focal | Babesiosis | Charcot-Marie-Tooth Disease, Type 2A | Fraser Syndrome | Cherubism | Glioma | Neurocutaneous Syndromes | Marfan Syndrome | Rhabdomyosarcoma, Embryonal | Spondylometaphyseal Dysplasia | Early Infantile Epileptic Encephalopathy 4 | VACTERL Association | Macular Corneal Dystrophy | Stroke, Hemorrhagic | Hepatitis C, Chronic | Congenital Stromal Corneal Dystrophy | Glycogen Storage Disease Type 5 | Osteosarcoma | Dengue Hemorrhagic Fever | AIDS Dementia Complex | Kleine-Levin Syndrome | Palmoplantar Keratoderma | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | ICF Syndrome | Meningioma | Hypogammaglobulinemia | X-linked Myotubular Myopathy | Osteoporosis | Bulimia Nervosa | Colitis, Lymphocytic | Neuromuscular Disorders | Sclerosing Cholangitis | Hydrocephalus | Borderline Personality Disorder | Polyneuropathy | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Myotonia | Rhinitis | Migraine | Coffin-Lowry Syndrome | McLeod Syndrome | Apert Syndrome | Gynecomastia | Encephalopathy, Glycine | Depression | Colitis, Collagenous | Down Syndrome | Postaxial Polydactyly | Peritonitis | Ocular Surface Squamous Neoplasia | Multiple Sclerosis | Pure Autonomic Failure | Oguchi Disease-2 | Glaucoma | Juvenile Myoclonic Epilepsy | C3 Glomerulopathy | Malnutrition | Schizencephaly | Muir-Torre Syndrome | Gitelman Syndrome | Posterior Polar Cataract | Roberts Syndrome | Retinitis | Skin Papilloma | Gallstones | Cyclic Vomiting Syndrome | Long QT Syndrome Type 2 | Ischemia | Spondylolisthesis | Basal Ganglia Disease, Biotin-responsive | Emery-Dreifuss Muscular Dystrophy | Aldosteronism | Myoclonic Epilepsy With Ragged Red Fibers | Hyperkeratosis | Brooke-Spiegler Syndrome | Pneumothorax | Pantothenate Kinase-associated Neurodegeneration | Gangliosidosis, GM1 | Mesothelioma, Malignant | Intermittent Explosive Disorder | Long QT Syndrome Type 1 | Bartsocas-Papas Syndrome | Hyperparathyroidism | Botulism | Cancer, Brain | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Trichotillomania | Atelosteogenesis Type 2 | Subacute Sclerosing Panencephalitis | Glucagonoma | Multicystic Renal Dysplasia | Prader-Willi Syndrome | Brachydactyly | Diffuse Intrinsic Pontine Glioma | Mixed Connective Tissue Disease | Lymphoma Lymphoblastic | Leprosy | Anorectal Fistula | CDKL5 Deficiency Disorder | Schizophrenia | Spinocerebellar Ataxia Type 7 | Erythromelalgia | Infantile Nephropathic Cystinosis | Communication Disorders | Neuroma | Craniopharyngioma | Myelomeningocele | Dyslipidemia | Vitamin D Deficiency | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Ovarian Sex Cord-stromal Tumor | Nestor-Guillermo Progeria Syndrome | Pleurisy | T-cell Chronic Lymphocytic Leukemia | Polymyalgia Rheumatica | Seizures-scoliosis-macrocephaly Syndrome | Sarcoma, Ewing | Zimmermann-Laband Syndrome | Pyruvate Kinase Deficiency | Bainbridge-Ropers Syndrome | Anorchia | Cerebellar Ataxia, Cayman Type | Cholestasis, Intrahepatic | Sweet Syndrome | Hemoglobinopathies | Hypolipoproteinemia | REM Sleep Behavior Disorder | Ovarian Hyperstimulation Syndrome | Mastitis | Hyperandrogenemia | Diabetic Neuropathy | Spinocerebellar Ataxia Type 17 | Crisponi Syndrome | Hydrops Fetalis | Congenital Hypofibrinogenemia | Spasticity | Spinal Muscular Atrophy Type 3 | Heimler Syndrome | Craniofrontonasal Syndrome | Senior-Loken Syndrome | Cushing Syndrome | Familial Isolated Hyperparathyroidism | Peutz-Jeghers Syndrome | Nager Acrofacial Dysostosis | Pycnodysostosis | Aphasia | Patent Foramen Ovale | Retinitis Pigmentosa | Alveolar Capillary Dysplasia | Myocarditis | Hyperammonemia | Spinocerebellar Ataxia Type 12 | Benign Hereditary Chorea | Vitamin K Deficiency | Tyrosine Hydroxylase Deficiency | Waldenstrom Macroglobulinemia | Blepharitis | Fibrillation, Atrial | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Endocarditis | Autonomic Neuropathy | Silver-Russell Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Hyperinsulinemia | Meningococcal Infections | Diffuse Mesangial Sclerosis | Conjunctivitis | Vascular Cognitive Impairment | Venous Insufficiency | Angioedema, Acquired | Arrhythmogenic Right Ventricular Cardiomyopathy | Small Lymphocytic Lymphoma | Granular Corneal Dystrophy Type 1 | Ocular Albinism Type 1 | Paroxysmal Kinesigenic Dyskinesia | Autoimmune Hemolytic Anemia | Pontocerebellar Hypoplasia Type 2 | Trachoma | Stomatitis | Leukocyte Adhesion Deficiency Type 1 | Sotos Syndrome | Oligospermia | Budd-Chiari Syndrome | Niemann-Pick Disease, Type C | Guttate Psoriasis | Spinocerebellar Ataxia Type 23 | GLUT1 Deficiency Syndrome | Arthritis, Gouty | Blood Protein Disorders | Neuropathy | Wolfram Syndrome | Tietze Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Bethlem Myopathy | Lymphangioma | Torticollis | Rotor Syndrome | Progressive Osseous Heteroplasia | Macrophage Activation Syndrome | Otitis Media | Galactosialidosis | Pearson Syndrome | Hyperkalemic Periodic Paralysis | Infertility | Hypospadias | Rubinstein-Taybi Syndrome | Acromicric Dysplasia | Vestibular Disease | Neurotoxicity | Saul-Wilson Syndrome | Enlarged Vestibular Aqueduct | Smith-Lemli-Opitz Syndrome | Hereditary Xerocytosis | Autoimmune Disease | Graft-versus-host Disease | Hemochromatosis | Periventricular Nodular Heterotopia | Multicentric Carpotarsal Osteolysis Syndrome | Cardiospondylocarpofacial Syndrome | Transcobalamin Deficiency | Sarcoma | Dental Caries | Thalassemia | Ophthalmia, Sympathetic | Presbyopia | Familial Retinal Arterial Macroaneurysm | Spinocerebellar Ataxia Type 14 | Waardenburg Syndrome Type 2E | Temporal Lobe Epilepsy | Spitz Nevus | Fuchs Dystrophy | Chronic Enteropathy Associated With SLCO2A1 Gene | Antenatal Bartter Syndrome Type 1 | Hereditary Hemorrhagic Telangiectasia | Purpura, Thrombotic Thrombocytopenic | Eating Disorder | Tetraplegia | Rosacea | Hypopigmentation | Dystrophy, Cone-rod | Metachromatic Leukodystrophy | Neuroblastoma | Toxic Epidermal Necrolysis | Haim-Munk Syndrome | Benign Familial Infantile Seizures | Acute Tubular Necrosis | Transthyretin-related Amyloidosis | PHARC Syndrome | Encephalitis | Hypoalbuminemia | Myasthenia | ADNP Syndrome | Chronic Inflammatory Demyelinating Polyneuropathy | Patent Ductus Arteriosus | Cleidocranial Dysplasia | Cancer, Bladder | Acquired Partial Lipodystrophy | Hepatic Adenomatosis | Genitopatellar Syndrome | Blomstrand Osteochondrodysplasia | Renal Failure | Neuroendocrine Cancer | Wiedemann-Steiner Syndrome | Melanoma, Malignant | Erysipelas | Pfeiffer Syndrome | Tibial Muscular Dystrophy | Melanoma | Chondroma | Oculocutaneous Albinism Type 2 | Erythema Nodosum | Oculocutaneous Albinism | Fibromuscular Dysplasia | Whipple's Disease | Focal Cortical Dysplasia Type 2 | Cockayne Syndrome | HUPRA Syndrome | Greenberg Dysplasia | Chondrodysplasia Punctata 1, X-linked Recessive | CHOPS Syndrome | Connective Tissue Disorders | Methylmalonic Acidemia | Chanarin-Dorfman Syndrome | Rhabdoid Tumor | Best Macular Dystrophy | Gerodermia Osteodysplastica | Lattice Corneal Dystrophy | Bronchitis | Pityriasis Rubra Pilaris | Cholesteryl Ester Storage Disease | Cutis Laxa | SAPHO Syndrome | Spondylosis | Werner's Syndrome | Nance-Horan Syndrome | Juvenile Myelomonocytic Leukemia | Osteogenesis Imperfecta Type I | Nicotine Dependence | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Angiodysplasia | Dermatitis Herpetiformis | Acanthosis Nigricans | Hemimegalencephaly | Prostatitis | Aldosterone Deficiency | Leukodystrophies | Focal Segmental Glomerulosclerosis | Methemoglobinemia Type IV | Alpha-1 Antitrypsin Deficiency | Vogt-Koyanagi-Harada Syndrome | Rhabdomyosarcoma | Palsy, Cerebral | Hereditary Inclusion Body Myopathy | Facioscapulohumeral Muscular Dystrophy Type 2 | Polydactyly | Pemphigus | Central Retinal Artery Occlusion | Myotonic Disorders | Sorsby Fundus Dystrophy | Hypotrichosis Simplex | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Congenital Ichthyosiform Erythroderma | Glaucomatocyclitic Crisis | 3-methylglutaconic Aciduria | Diabetes Gestational | Celiac Disease | Adenocarcinoma | Congenital Generalized Lipodystrophy | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Oculopharyngeal Muscular Dystrophy | Fragile X Syndrome | Hyperbilirubinemia | Hemosiderosis | Chediak-Higashi Syndrome | Lamellar Ichthyosis | Mood Disorder | Adenomatoid Tumor | Leishmaniasis, Visceral | Monilethrix | Preaxial Polydactyly | Optic Neuritis | Porphyria Cutanea Tarda | Traboulsi Syndrome | Perry Syndrome | Neurodegeneration With Brain Iron Accumulation | Congenital Dyserythropoietic Anemia | Congenital Afibrinogenemia | Cervical Dystonia | Hypertension, Renal | Pseudohypoparathyroidism Type 1B | Chorea | Amish Infantile Epilepsy Syndrome | Kabuki Syndrome | Renal-hepatic-pancreatic Dysplasia