Informaţii despre

Nume Coronary Thrombosis
Pagina Web www.malacards.org
Clasificari ICD10 Acute myocardial infarction; Subsequent myocardial infarction
Clasificare anatomică Malacards Blood diseases; Cardiovascular diseases

Vezi şi

Boli A-Z Acquired Von Willebrand Syndrome Acute Cor Pulmonale Acute Myocardial Infarction Acute Pancreatitis Acute Pulmonary Heart Disease Afibrinogenemia, Congenital Aging Al-Raqad Syndrome Alzheimer Disease 3 Anauxetic Dysplasia 1 Aneurysm Angel-Shaped Phalangoepiphyseal Dysplasia Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Argentine Hemorrhagic Fever Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Autosomal Dominant Macrothrombocytopenia Behr Syndrome Bernard-Soulier 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 Branchiootic Syndrome 1 Brooke-Spiegler Syndrome Budd-Chiari Syndrome Burns Cardiac Arrest Cardiac Tamponade Cardiogenic Shock Carotid Artery Thrombosis Catastrophic Antiphospholipid Syndrome Central Serous Chorioretinopathy Cerebritis Chronic Venous Insufficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Conjunctivitis Coronary Aneurysm Coronary Arterial Fistulas Diabetes Mellitus Disseminated Intravascular Coagulation Dysbaric Osteonecrosis Dysfibrinogenemia Eisenmenger Syndrome Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Endocarditis Endotheliitis Essential Thrombocythemia Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fetal and Neonatal Alloimmune Thrombocytopenia Fibrinolytic Defect Fournier Gangrene Genitopatellar Syndrome Giant Hemangioma Glanzmann Thrombasthenia Gray Platelet Syndrome Hansen's Disease Hellp Syndrome Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hypereosinophilic Syndrome Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Immune System Disease Infective Endocarditis Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemia Ischemic Colitis Ischemic Optic Neuropathy Kawasaki Disease Korean Hemorrhagic Fever Leech Infestation Legg-Calve-Perthes Disease Lemierre's Syndrome Marantic Endocarditis May-Hegglin Anomaly Mediastinitis Meningococcemia Myocardial Infarction Neurodegeneration with Brain Iron Accumulation 2a Nonarteritic Anterior Ischemic Optic Neuropathy Pancreatitis Plasminogen Activator Inhibitor-1 Deficiency Platelet Aggregation, Spontaneous Portal Vein Thrombosis Posterior Myocardial Infarction Post-Thrombotic Syndrome Primary Thrombocytopenia Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Pseudo-Von Willebrand Disease Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Renal Glucosuria Retinal Artery Occlusion Rheumatic Heart Disease Sagittal Sinus Thrombosis Sebastian Syndrome Single Ventricular Heart Sticky Platelet Syndrome Stroke, Ischemic Subacute Bacterial Endocarditis Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Thrombasthenia Thrombocytopenia Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Vascular Disease Vein Disease Venous Insufficiency Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 3