Informaţii despre

Nume Acute Myocardial Infarction
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice
Clasificari ICD10 Acute transmural myocardial infarction of unspecified site
Clasificare anatomică Malacards Boli cardiovasculare
Boli din aceeaşi familie Myocardial Infarction 2; Posterior Myocardial Infarction

Vezi şi

Boli A-Z Acquired Thrombocytopenia Acrocallosal Syndrome Acute Adrenal Insufficiency Acute Anterolateral Myocardial Infarction Acute Cor Pulmonale Acute Kidney Failure Acute Mountain Sickness Acute Myocarditis Acute Pancreatitis Acute Porphyria Acute Poststreptococcal Glomerulonephritis Acute Pulmonary Heart Disease Acute Stress Disorder Adenocarcinoma Adenoma Adjustment Disorder Afibrinogenemia, Congenital Aging Aland Island Eye Disease Alexithymia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amaurosis Fugax Amphetamine Abuse Anauxetic Dysplasia 1 Aneurysm Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterolateral Myocardial Infarction Antiphospholipid Syndrome Anuria Aortic Coarctation Aortic Valve Disease 2 Aortitis Apolipoprotein C-Iii Deficiency Argentine Hemorrhagic Fever Arteries, Anomalies of Arteriosclerosis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atherosclerosis Susceptibility Atrial Fibrillation Atrial Fibrillation and Stroke Atrioventricular Block Aural Atresia, Congenital Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Polycystic Kidney Disease Bacterial Meningitis Basilar Artery Occlusion Behr Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Blue Toe Syndrome Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Broken Heart Syndrome Bronchopneumonia Cardiac Arrest Cardiac Arrhythmia Cardiac Rupture Cardiac Tamponade Cardiogenic Shock Cardiovascular Syphilis Carotid Artery Disease Carotid Artery Thrombosis Carotid Stenosis Central Serous Chorioretinopathy Cerebral Artery Occlusion Cerebral Falx Meningioma Cerebritis Cerebrotendinous Xanthomatosis Cerebrovascular Disease Chikungunya Chlamydia Cholecystitis Cholesterol Embolism Chops Syndrome Chronic Enteropathy Associated with Slco2a1 Gene Chronic Inflammatory Demyelinating Polyneuropathy Chronic Thromboembolic Pulmonary Hypertension Chronic Venous Insufficiency Churg-Strauss Syndrome Cluster Headache Cocaine Abuse Colitis Collecting Duct Carcinoma Colorado Tick Fever Colorectal Cancer Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Gerbode Defect Congenitally Corrected Transposition of the Great Arteries Congestive Heart Failure Conjugate Gaze Palsy Conjunctivitis Coronary Aneurysm Coronary Artery Aneurysm Coronary Artery Anomaly Coronary Artery Dissection, Spontaneous Coronary Artery Vasospasm Coronary Heart Disease 1 Coronary Restenosis Coronary Stenosis Coronary Thrombosis Cortical Blindness Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Creatine Phosphokinase, Elevated Serum Cutaneous Lupus Erythematosus Cytochrome P450 2d6 Variant Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Dementia Demyelinating Polyneuropathy Denys-Drash Syndrome Dextrocardia Dextrocardia with Situs Inversus Diabetes Mellitus Diabetic Autonomic Neuropathy Diastrophic Dysplasia Diffuse Alveolar Hemorrhage Diffuse Lymphatic Malformation Dirofilariasis Disseminated Intravascular Coagulation Double Discordia Dressler's Syndrome Dysbaric Osteonecrosis Dystonia 9 Eisenmenger Syndrome Encephalopathy Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Endocarditis Endotheliitis Essential Thrombocythemia Esterase C Euthyroid Sick Syndrome Exercise-Induced Anaphylaxis Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Familial Isolated Restrictive Cardiomyopathy Fanconi Anemia, Complementation Group E Fibrinolytic Defect Fibromuscular Dysplasia Gas Gangrene Generalized Anxiety Disorder Generalized Atherosclerosis Giant Hemangioma Glanzmann Thrombasthenia Glucose Intolerance Gout Granulomatous Hepatitis Graves' Disease Gray Platelet Syndrome Guillain-Barre Syndrome Headache Heart Cancer Heart Disease Helix Syndrome Hellp Syndrome Hemarthrosis Hemoglobinuria Hemopericardium Hemophilia Hemophilia a Hemorrhagic Disease Hemorrhagic Fever Hemorrhagic Fever with Renal Syndrome Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatorenal Syndrome Homocysteinemia Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hypereosinophilic Syndrome Hyperglycemia Hypersensitivity Vasculitis Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hypertensive Retinopathy Hyperthyroidism Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoaldosteronism Hypoglycemia Hypoparathyroidism Hypophosphatemia Hypoplastic Left Heart Syndrome Hypopyon Hypoxia Idiopathic Edema Idiopathic Inflammatory Myopathy Infective Endocarditis Inferior Myocardial Infarction Influenza Inherited Blood Coagulation Disease Insulin-Like Growth Factor I Intermediate Coronary Syndrome Intermittent Claudication Interstitial Myocarditis Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies Iritis Ischemia Ischemic Colitis Ischemic Heart Disease Ischemic Optic Neuropathy Kawasaki Disease Korean Hemorrhagic Fever Lactic Acidosis Laryngeal Cleft Lateral Myocardial Infarction Leech Infestation Legg-Calve-Perthes Disease Legionnaire Disease Legionnaires' Disease Lemierre's Syndrome Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Ligneous Conjunctivitis Limb Ischemia Lung Cancer Lung Disease Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphopenia Malignant Hypertension Malignant Renovascular Hypertension Marantic Endocarditis Meningococcemia Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration Metanephric Adenoma Middle Cerebral Artery Infarction Migraine with Aura Mitral Valve Insufficiency Mitral Valve Stenosis Miyoshi Muscular Dystrophy 1 Moebius Syndrome Mohr-Tranebjaerg Syndrome Morbid Obesity Mungan Syndrome Muscular Dystrophy, Duchenne Type Mycosis Fungoides Myelodysplastic Syndrome Myeloid Leukemia Myocardial Infarction Myocardial Infarction 2 Myocardial Stunning Myocarditis Myopathy Myositis Nephrotic Syndrome Neurodegeneration with Brain Iron Accumulation 2a Neuroleptic Malignant Syndrome Neuropathy Niemann-Pick Disease, Type a Nonarteritic Anterior Ischemic Optic Neuropathy Pancreatitis Papillon-Lefevre Syndrome Paraganglioma Parapsoriasis Patent Foramen Ovale Pediatric Systemic Lupus Erythematosus Peptic Ulcer Disease Pericardial Effusion Pericarditis Periodontal Disease Periodontitis Peripartum Cardiomyopathy Peripheral Artery Disease Peripheral Vascular Disease Peripheral Vertigo Pernicious Anemia Phaeochromocytoma Pharyngitis Pheochromocytoma Pituitary Adenoma 1, Multiple Types Plasminogen Activator Inhibitor-1 Deficiency Platelet Aggregation, Spontaneous Pleomorphic Liposarcoma Pneumonia Pneumothorax Polyarteritis Nodosa Polycystic Kidney Disease Polycythemia Polycythemia Vera Polymyositis Polyneuropathy Porphyria Portal Vein Thrombosis Posterior Myocardial Infarction Potocki-Lupski Syndrome Primary Lateral Sclerosis, Adult, 1 Primary Thrombocytopenia Prinzmetal's Variant Angina Progressive Familial Heart Block, Type Ib Prostate Sarcoma Prostatitis Protein C Deficiency Protein S Deficiency Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak Pseudoxanthoma Elasticum Pulmonary Edema Pulmonary Embolism Pulmonary Hypertension Pulmonary Tuberculosis Purpura Purpura Fulminans Qualitative Platelet Defect Renal Artery Obstruction Renal Hypertension Renovascular Hypertension Restrictive Cardiomyopathy Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Rett Syndrome Rheumatic Disease Rheumatoid Arthritis Richards-Rundle Syndrome Right Bundle Branch Block Robinow Syndrome, Autosomal Recessive Salt and Pepper Developmental Regression Syndrome Scrub Typhus Second-Degree Atrioventricular Block Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance Sensorineural Hearing Loss Serotonin Syndrome Short Bowel Syndrome Sickle Cell Anemia Sick Sinus Syndrome Silent Myocardial Infarction Sitosterolemia Situs Inversus Sleep Apnea Sleep Disorder Smith-Kingsmore Syndrome Spinal Cord Injury Status Asthmaticus Stroke, Ischemic Subclavian Steal Syndrome Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Sveinsson Chorioretinal Atrophy Syndrome of Inappropriate Antidiuretic Hormone Syphilis Systemic Lupus Erythematosus Systolic Heart Failure Thrombasthenia Thrombocytopenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thunderclap Headache Thyroiditis Tick Paralysis Toxic Myocarditis Transient Global Amnesia Transposition of the Great Arteries Treacher Collins Syndrome 1 Trichinosis Tularemia Valproate Embryopathy Van Der Woude Syndrome 1 Vascular Disease Vasculitis Vein Disease Venous Insufficiency Ventricular Septal Defect Vitamin B12 Deficiency Von Willebrand's Disease Von Willebrand Disease, Type 1 Wolff-Parkinson-White Syndrome Xanthomatosis Yemenite Deaf-Blind Hypopigmentation Syndrome Zygomycosis