Disease

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

疾病靶点研报
Peripartum Cardiomyopathy

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

Graft-versus-host Disease | Low Tension Glaucoma | VEXAS Syndrome | Chronic Myelomonocytic Leukemia | Leukoencephalopathy, Progressive Multifocal | Empyema | Adenosine Deaminase 2 Deficiency | Tetraplegia | Hydrolethalus Syndrome | Varices | Focal Segmental Glomerulosclerosis | Porokeratosis | Proteus Syndrome | Familial Hypobetalipoproteinemia | Hypophosphatemic Rickets, Autosomal Recessive, 1 | X-linked Myotubular Myopathy | Spinocerebellar Ataxia Type 40 | Hermansky-Pudlak Syndrome | Dysmorphophobia | Multiple Sclerosis, Chronic Progressive | Pontocerebellar Hypoplasia Type 7 | Von Willebrand Disease | Schizophrenia | Thalassemia, Beta | Sitosterolemia | Congenital Hemolytic Anemia | Anti-glomerular Basement Membrane Disease | Photosensitivity | Atrioventricular Septal Defect | Polycystic Kidney, Autosomal Dominant | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Urofacial Syndrome | Charcot-Marie-Tooth Disease | GLUT1 Deficiency Syndrome | Citrullinemia | Heroin Dependence | Leukocyte Adhesion Deficiency | Antenatal Bartter Syndrome Type 1 | Asplenia | Acne | MIRAGE Syndrome | Thyroid Dysgenesis | Adenomyosis | Spinal Muscular Atrophy | Osteogenesis Imperfecta Type V | Wiedemann-Steiner Syndrome | Long QT Syndrome Type 2 | ACTH-independent Macronodular Adrenal Hyperplasia | Pseudohypoparathyroidism Type 2 | Hyper IgE Syndrome | Glutaric Aciduria Type 3 | Prostatitis | Birk-Barel Syndrome | Haim-Munk Syndrome | Multiple Sclerosis, Relapsing-remitting | Danon Disease | Tyrosinemia Type 2 | Nanophthalmos | Retinal Detachment | Hypervalinemia | Epidermolysis Bullosa Acquisita | Amyloidosis | Ehlers-Danlos Syndrome | Mitochondrial DNA Depletion Syndrome 13 | Progressive Familial Intrahepatic Cholestasis Type 3 | Spinocerebellar Ataxia Type 13 | Congenital Diaphragmatic Hernia | Alpha-1 Antitrypsin Deficiency | Neurocutaneous Syndromes | Epidermal Nevus Syndrome | Subcortical Band Heterotopia | Tinea Versicolor | Hypertension, Portal | Bare Lymphocyte Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Endocarditis | Nemaline Myopathy 8 | Panniculitis | Congenital Hereditary Endothelial Dystrophy Type I | Jawad Syndrome | Anterior Segment Dysgenesis | Coenzyme Q10 Deficiency | Narcolepsy | Angioimmunoblastic T-cell Lymphoma | Chronic Inflammatory Demyelinating Polyneuropathy | Atopy | Congenital Central Hypoventilation Syndrome | Autonomic Nervous System Disorders | Arts Syndrome | Sulfite Oxidase Deficiency | Alopecia | Cancer, Prostate | Botulism | Thrombotic Microangiopathy | Veno-occlusive Disease | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Dermatitis | Hereditary Hemorrhagic Telangiectasia | Hypertension, Pulmonary | Bronchitis | Ellis-Van Creveld Syndrome | Kindler Syndrome | Cluster Headache | Neovascular Glaucoma | Keratocystic Odontogenic Tumor | Toxic Epidermal Necrolysis | MELAS Syndrome | Cryptococcal Meningitis | Spinal And Bulbar Muscular Atrophy | Lichen Sclerosus | Rhabdomyosarcoma | Anorchia | Colitis | Sepiapterin Reductase Deficiency | Lateral Meningocele Syndrome | Liver Failure | Eczema | HIBCH Deficiency | Renal Oncocytoma | DEND Syndrome | Glioblastoma Multiforme | Cholangiocarcinoma | Anodontia | IgA Deficiency | Astrocytoma | Malaria | Hereditary Folate Malabsorption | Jalili Syndrome | Spinocerebellar Ataxia Type 16 | Gastrointestinal Disorders | Rolandic Epilepsy | Blepharo-cheilo-odontic Syndrome | Protein C Deficiency | Retinitis | Geleophysic Dysplasia | 3-methylglutaconic Aciduria Type IV | Muscle Wasting | Amblyopia | Spinocerebellar Ataxia Type 8 | Encephalocele | Speech Disorders | Pneumonia, Mycoplasma | Retinal Telangiectasia | Metabolic Syndrome | Alopecia Totalis | Spinocerebellar Ataxia Type 2 | Ameloblastic Carcinoma | Syncope | Sleep Disorder | Intermittent Explosive Disorder | Glycogen Storage Disease Type 3 | Chromosome 8q21.11 Deletion Syndrome | Avian Influenza | Blepharitis | Open-angle Glaucoma | Epidermolysis Bullosa | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Spondylo-ocular Syndrome | Congenital Hypofibrinogenemia | Aceruloplasminemia | Fuchs Dystrophy | Glycogen Storage Disease Type 1a | Infantile Nephropathic Cystinosis | Alagille Syndrome | LMNA-related Congenital Muscular Dystrophy | Epithelioid Hemangioma | Arteriosclerosis | Inborn Errors Of Metabolism | Scapuloperoneal Myopathy, X-linked Dominant | Beta-Propeller Protein-associated Neurodegeneration | Macular Corneal Dystrophy Type 1 | Angioedema, Hereditary | Fahr Disease | Stroke, Ischemic | Hepatitis D | Mohr-Tranebjaerg Syndrome | Mixed Connective Tissue Disease | Schaaf-Yang Syndrome | Pelvic Inflammatory Disease | Spinal Cord Diseases | Hypercalciuria | Joubert Syndrome | Strabismus | Sorsby Fundus Dystrophy | Angina Pectoris | Fucosidosis | Alzheimer Disease, Late Onset | GATA2 Deficiency | Vici Syndrome | Histoplasmosis | Carcinoma, Small Cell | Schwartz-Jampel-Aberfeld Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Porphyria Cutanea Tarda | Marinesco-Sjogren Syndrome | Autosomal Recessive Spastic Paraplegia Type 54 | Hyperparathyroidism, Secondary | Lymphoproliferative Disorders | Schistosomiasis Mansoni | Osteoporosis-pseudoglioma Syndrome | Pemphigus Vulgaris | Diabetes Insipidus | Prolymphocytic Leukemia | Congenital Dyserythropoietic Anemia Type 1 | Bronchitis, Chronic | Alexander Disease | Polyneuropathy | Polycystic Kidney, Autosomal Recessive | Blau Syndrome | Usher Syndrome | Aspartylglycosaminuria | Spinal Muscular Atrophy Type 2 | Encephalitis, Tick-borne | Ataxia-ocular Apraxia 2 | Goiter | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Benign Recurrent Intrahepatic Cholestasis 1 | Tatton-Brown-Rahman Syndrome | Alpha-mannosidosis | Retinal Diseases | Atopic Dermatitis | Onchocerciasis | Metachromatic Leukodystrophy | Schizencephaly | VACTERL/VATER Association | Synpolydactyly | Dental Caries | Polymyositis | HUPRA Syndrome | Atherosclerosis | Hypohidrotic Ectodermal Dysplasia, X-linked | Primary Cutaneous Amyloidosis | Borderline Personality Disorder | Sleep Apnea, Central | Erythema Multiforme | Chronic Enteropathy Associated With SLCO2A1 Gene | Paraganglioma | D-2-Hydroxyglutaric Aciduria | Carcinoma, Merkel Cell | Familial Glucocorticoid Deficiency | Tyrosinemia Type 1 | Thin Basement Membrane Disease | Best Macular Dystrophy | Hyperekplexia | Neurofibroma | Aldosteronism | Diarrhea | Hypersomnia | Neurofibromatosis Type 2 | PHARC Syndrome | Stiff-man Syndrome | Coffin-Lowry Syndrome | Oligoasthenoteratozoospermia | Ischemia | Rheumatoid Arthritis | Diamond-Blackfan Anemia | Patent Foramen Ovale | Alazami Syndrome | Hypotension, Orthostatic | 3-hydroxy-3-methylglutaric Aciduria | Tardive Dyskinesia | Paroxysmal Nocturnal Hemoglobinuria | Erythropoietic Protoporphyria | Crohn's Disease | Papulopustular Rosacea | Orthostatic Intolerance | Peroxisomal Disorder | Multisystemic Smooth Muscle Dysfunction Syndrome | Mucolipidosis Type II | Uveitis, Anterior | Cryoglobulinemia | Iron Deficiency Anemia | Alpers Syndrome | Fibrosarcoma | Primary Progressive Nonfluent Aphasia | Congenital Ichthyosiform Erythroderma | Kallmann Syndrome | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Fanconi Syndrome | Anuria | Arthropathy | Wolfram Syndrome | Rhabdoid Tumor | Tinea | C3 Glomerulopathy | Papilledema | Autoimmune Polyendocrine Syndrome | Hepatitis, Chronic | Hyperoxaluria | Angioedema, Acquired | Rubeosis Iridis | Amish Infantile Epilepsy Syndrome | Stargardt Disease | Antithrombin III Deficiency | Argininosuccinic Aciduria | Exfoliative Dermatitis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Bullous Pemphigoid | Shock, Cardiogenic | Phenylketonuria II | Autoimmune Disease | Chloridorrhea, Congenital | Zellweger Syndrome | Duane Retraction Syndrome | Dowling-Degos Disease | ADNP Syndrome | Glioblastoma | Sarcoma, Ewing | Esophagitis | Wagner Disease | Pernicious Anemia | Pancreatitis, Chronic | Congenital Primary Aphakia | Hypokalemic Periodic Paralysis | Rhizomelic Chondrodysplasia Punctata | Potocki-Shaffer Syndrome | Polycystic Ovary Syndrome | Migraine | Lipid Metabolism Disorders | Hamartoma | Progressive Osseous Heteroplasia | Enterocolitis, Necrotizing | Alveolar Capillary Dysplasia | Malaria, Cerebral | Psoriasis | Panuveitis | Giant Cell Arteritis | Myelitis, Transverse | Idiopathic Pulmonary Fibrosis | Erythrokeratodermia Variabilis | Necrotizing Autoimmune Myopathy | Lipoma | Coloboma | Gestational Trophoblastic Disease | Polycythemia | Persistent Hyperplastic Primary Vitreous | Familial Retinal Arterial Macroaneurysm | Senior-Loken Syndrome | Keratosis | Nicotine Dependence | Neurodegeneration With Brain Iron Accumulation | Familial Partial Lipodystrophy | Lafora Disease | Mitochondrial DNA Depletion Syndrome | Holoprosencephaly | Centronuclear Myopathy | Renal Hypouricemia | Seminoma | Jacobsen Syndrome | Synovitis | Mevalonate Kinase Deficiency | Hypospadias | Melanoma, Uveal | Dwarfism | Eiken Syndrome | Warsaw Breakage Syndrome | Mycosis Fungoides | Leprosy | Pituitary Dwarfism | Esophageal Carcinoma | Li-Fraumeni Syndrome | Chromosome 9q34.3 Deletion Syndrome | Hidradenitis | Viral Meningitis | N-acetylglutamate Synthase Deficiency | Long QT Syndrome Type 3 | Epidermolysis Bullosa Simplex, Localized | Triple A Syndrome | Niemann-Pick Disease, Type B | Pain | Congenital Nephrotic Syndrome | Juvenile Hyaline Fibromatosis | Actinomycetoma | Obesity | Analgesia | Osteosclerosis | Nephrotic Syndrome Type 1 | Marfan Syndrome | Dubin-Johnson Syndrome | Atelosteogenesis Type 2 | Maple Syrup Urine Disease | Hashimoto Thyroiditis | 5-oxoprolinase Deficiency | Crimean-Congo Hemorrhagic Fever | Chordoma | Restrictive Dermopathy | AIDS Dementia Complex | Multiple System Atrophy | Seizures | Low Phospholipid Associated Cholelithiasis | Still Disease | Cataplexy | Knobloch Syndrome | Spermatocele | Trigonocephaly | Hemosiderosis | Astigmatism | Colitis, Microscopic | Benign Hereditary Chorea | Sponastrime Dysplasia