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Nume Myocardial Infarction
Pagina Web
Clasificare globală Malacards Boli genetice
Clasificari ICD10 Acute myocardial infarction; Subsequent myocardial infarction
Clasificare anatomică Malacards Boli cardiovasculare
Boli din aceeaşi familie Acute Myocardial Infarction; Myocardial Infarction 2; Posterior Myocardial Infarction

Vezi şi

Boli A-Z Aarskog-Scott Syndrome Abdominal Obesity-Metabolic Syndrome 1 Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Acquired Amegakaryocytic Thrombocytopenia Acquired Hemophilia Acquired Hemophilia a Acquired Immunodeficiency Syndrome Acquired Metabolic Disease Acquired Thrombocytopenia Acquired Von Willebrand Syndrome Acrocallosal Syndrome Acromegaly Active Peptic Ulcer Disease Acute Adrenal Insufficiency Acute Anterolateral Myocardial Infarction Acute Cor Pulmonale Acute Inferolateral Myocardial Infarction Acute Insulin Response Acute Liver Failure Acute Lymphocytic Leukemia Acute Mountain Sickness Acute Myocardial Infarction Acute Myocarditis Acute Pancreatitis Acute Porphyria Acute Poststreptococcal Glomerulonephritis Acute Proliferative Glomerulonephritis Acute Promyelocytic Leukemia Acute Pulmonary Heart Disease Acute Pyelonephritis Acute Respiratory Distress Syndrome Acute Stress Disorder Acute Transverse Myelitis Adenocarcinoma Adenoma Adenomyosis Adjustment Disorder Adrenocortical Carcinoma, Hereditary Adult-Onset Still's Disease Adult Respiratory Distress Syndrome Afibrinogenemia Afibrinogenemia, Congenital Aganglionosis, Total Intestinal Aggressive Periodontitis Aging Aids Dementia Complex Aland Island Eye Disease Alcoholic Hepatitis Alcohol-Related Birth Defect 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 Alpha-Thalassemia Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amaurosis Fugax Amphetamine Abuse Amyloidosis Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Androgen Insensitivity Syndrome, Mild Anemia, Sideroblastic, and Spinocerebellar Ataxia Aneurysm Aneurysm of Interventricular Septum Angina Pectoris Angioedema Angiokeratoma Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Anterolateral Myocardial Infarction Anteroseptal Myocardial Infarction Antiphospholipid Syndrome Antipyrine Metabolism Antithrombin Iii Deficiency Anuria Aortic Aneurysm Aortic Aneurysm, Familial Abdominal, 1 Aortic Atherosclerosis Aortic Coarctation Aortic Disease Aortic Valve Disease 2 Aortitis Apert Syndrome Apical Myocardial Infarction Apnea, Obstructive Sleep Apolipoprotein C-Iii Deficiency Appendicitis Arcus Corneae Argentine Hemorrhagic Fever Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Arteries, Anomalies of Arteriosclerosis Arteriosclerosis Obliterans Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Aspirin Resistance Asthma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Ataxia-Telangiectasia Athabaskan Brainstem Dysgenesis Syndrome Atherosclerosis Susceptibility Atrial Fibrillation Atrial Fibrillation and Stroke Atrial Septal Aneurysm Atrioventricular Block Aural Atresia, Congenital Autoimmune Disease of Blood Autoimmune Myocarditis Autoinflammation, Lipodystrophy, and Dermatosis Syndrome Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Polycystic Kidney Disease Avoidant Personality Disorder Axenfeld-Rieger Syndrome Bacterial Meningitis Bacterial Vaginosis Basilar Artery Occlusion Behr Syndrome Benign Adult Familial Myoclonic Epilepsy Beriberi Bernard-Soulier Syndrome Bestrophinopathy, Autosomal Recessive Bipolar I Disorder Bladder Disease Bleeding Disorder, Platelet-Type, 11 Bleeding Disorder, Platelet-Type, 16 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, Gerbich 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 Bone Fracture Bone Inflammation Disease Brain Edema Brain Injury Branch Retinal Artery Occlusion Breast Myofibroblastoma Breath-Holding Spells Broken Heart Syndrome Bronchiectasis Bronchiolitis Obliterans Bronchogenic Cyst Bronchopneumonia Brucellosis Budd-Chiari Syndrome Buerger Disease Burns Calcinosis Cardiac Arrest Cardiac Arrhythmia Cardiac Rupture Cardiac Sarcoidosis Cardiac Tamponade Cardiogenic Shock Cardiomyopathy, Familial Hypertrophic, 1 Cardiovascular Syphilis Carotid Artery Disease Carotid Artery Occlusion Carotid Artery Thrombosis Carotid Stenosis Catamenial Pneumothorax Catastrophic Antiphospholipid Syndrome Central Nervous System Disease Central Nervous System Vasculitis Central Pontine Myelinolysis Central Retinal Artery Occlusion Central Retinal Vein Occlusion Central Serous Chorioretinopathy Central Sleep Apnea Cerebellofaciodental Syndrome Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 Cerebral Arteritis Cerebral Artery Occlusion Cerebral Atherosclerosis Cerebral Falx Meningioma Cerebral Palsy Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Cerebrotendinous Xanthomatosis Cerebrovascular Disease Cervical Cancer Cervicitis Chagas Disease Charles Bonnet Syndrome Chikungunya Chlamydia Cholangitis Cholecystitis Choledocholithiasis Cholesteatoma of Middle Ear Cholesterol Embolism Chops Syndrome Chorioamnionitis Chronic Angina Chronic Enteropathy Associated with Slco2a1 Gene Chronic Hiccups Chronic Inflammatory Demyelinating Polyneuropathy Chronic Monocytic Leukemia Chronic Mountain Sickness Chronic Thromboembolic Pulmonary Hypertension Chronic Venous Insufficiency Chronic Venous Leg Ulcers Churg-Strauss Syndrome Clopidogrel Resistance Cluster Headache Cocaine Abuse Colitis Collecting Duct Carcinoma Colorado Tick Fever Colorectal Cancer Common Cold Common Variable Immunodeficiency Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Regional Pain Syndrome Congenital Generalized Lipodystrophy Congenital Gerbode Defect Congenitally Corrected Transposition of the Great Arteries Congestive Heart Failure Conjunctivitis Conjunctivochalasis Conn's Syndrome Constrictive Pericarditis Contact Dermatitis Corneal Dystrophy, Fleck Corneal Ulcer Coronary Aneurysm Coronary Arterial Fistulas 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 Cor Triatriatum Cor Triatriatum Dexter Cor Triatriatum Sinister Coumarin Resistance Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Creatine Phosphokinase, Elevated Serum Crescentic Glomerulonephritis Crimean-Congo Hemorrhagic Fever Crouzon Syndrome with Acanthosis Nigricans Cryptogenic Cirrhosis Cutaneous Lupus Erythematosus Cutaneous Polyarteritis Nodosa Cysticercosis Cystitis Cytochrome P450 2d6 Variant Darier-White Disease Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Deep Angioma Defective Apolipoprotein B-100 Dementia Demyelinating Disease Demyelinating Polyneuropathy Dengue Hemorrhagic Fever Dengue Shock Syndrome Denys-Drash Syndrome Dermatomyositis Dextrocardia Dextrocardia with Situs Inversus Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diabetic Angiopathy Diabetic Autonomic Neuropathy Diabetic Macular Edema Diabetic Neuropathy Diaphragmatic Eventration Diastolic Heart Failure Diastrophic Dysplasia Diffuse Alveolar Hemorrhage Diffuse Lymphatic Malformation Dilated Cardiomyopathy Dirofilariasis Disseminated Intravascular Coagulation Double Discordia Dowling-Degos Disease 1 Dressler's Syndrome Drug Metabolism, Poor, Cyp2c19-Related Duane Retraction Syndrome 1 Duodenal Ulcer Duodenitis Dysbaric Osteonecrosis Dysfibrinogenemia Dyspepsia Dystonia 9 Eales Disease Eclampsia Ehlers-Danlos Syndrome Eisenmenger Syndrome Encephalomalacia Encephalopathy Endocardial Fibroelastosis Endocarditis Endometrial Disease Endometriosis Endometritis Endotheliitis End Stage Renal Failure Enhanced S-Cone Syndrome Enteropathy-Associated T-Cell Lymphoma Epilepsy Epileptic Encephalopathy, Childhood-Onset Epithelial Recurrent Erosion Dystrophy Esophageal Cancer Essential Thrombocythemia Esterase C Euthyroid Sick Syndrome Evans' Syndrome Exercise-Induced Anaphylaxis Extrinsic Allergic Alveolitis Extrinsic Cardiomyopathy Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Familial Hyperlipidemia Familial Hypertension Familial Lcat Deficiency Familial Mediterranean Fever Fanconi Anemia, Complementation Group E Fascioliasis Fatty Liver Disease Fetal and Neonatal Alloimmune Thrombocytopenia Fibrinolytic Defect Fibromatosis, Gingival, 2 Fibromuscular Dysplasia Fibrosarcoma Fibrosing Mediastinitis Filariasis Fournier Gangrene Funisitis Gallbladder Disease Gastritis Gastroenteritis Gastroesophageal Reflux Gastroschisis Generalized Anxiety Disorder Generalized Eruptive Histiocytosis Genitopatellar Syndrome Giant Hemangioma Gigantism Gingival Disease Gingival Fibromatosis Gingival Overgrowth Gingivitis Glanzmann Thrombasthenia Glucose Intolerance Glucose Metabolism Disease Goiter Gout Granulocytopenia Graves' Disease Gray Platelet Syndrome Guillain-Barre Syndrome Hantavirus Pulmonary Syndrome Headache Heart Aneurysm Heart Cancer Heart Disease Hellp Syndrome Hemarthrosis Hemifacial Spasm Hemoglobinuria Hemolytic Anemia Hemopericardium Hemophilia Hemophilia a Hemophilia B Hemorrhage, Intracerebral Hemorrhagic Disease Hemorrhagic Fever Hemorrhagic Fever with Renal Syndrome Hemorrhagic Shock and Encephalopathy Syndrome Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatic Lipase Deficiency Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Hepatitis E Hepatopulmonary Syndrome Hepatorenal Syndrome Hereditary Hemorrhagic Telangiectasia Hernia, Hiatus Heterophyiasis Hidradenitis Hidradenitis Suppurativa Hinman Syndrome Homocysteinemia Homocystinuria Homocystinuria Due to Cystathionine Beta-Synthase Deficiency Homozygous Familial Hypercholesterolemia Human Immunodeficiency Virus Infectious Disease Huntington Disease-Like 3 Hydronephrosis Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Familial Hypereosinophilic Syndrome Hyperglycemia Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hyperlipoproteinemia, Type V Hypersensitivity Reaction Type Iii Disease Hypersensitivity Vasculitis Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertension, Essential Hypertensive Heart Disease Hypertensive Nephropathy Hypertensive Retinopathy Hyperthyroidism Hypertriglyceridemia, Familial Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoaldosteronism Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypocalcemia, Autosomal Dominant 1 Hypoglycemia Hypoglycemic Coma Hypogonadism Hypokalemia Hypolipoproteinemia Hypoparathyroidism Hypophosphatemia Hypoplastic Left Heart Syndrome Hypopyon Hyporeninemic Hypoaldosteronism Hypoxia Idiopathic Edema Idiopathic Inflammatory Myopathy Idiopathic Interstitial Pneumonia Idiopathic Neutropenia Iga Glomerulonephritis Ige Responsiveness, Atopic Immune-Complex Glomerulonephritis Immune System Disease Immunoglobulin E Concentration, Serum Infectious Myocarditis Infective Endocarditis Inferior Myocardial Infarction Inferior Vena Cava Interruption Inferolateral Myocardial Infarct Inflammatory Myofibroblastic Tumor Influenza Inguinal Hernia Inherited Blood Coagulation Disease Insulin-Like Growth Factor I Intermediate Coronary Syndrome Intermittent Claudication Internal Hemorrhoid Interstitial Nephritis Intestinal Disease Intestinal Impaction Intracranial Aneurysm Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Intracranial Vasospasm Intramuscular Hemangioma Intussusception Iritis Ischemia Ischemic Colitis Ischemic Heart Disease Ischemic Optic Neuropathy Johnson Neuroectodermal Syndrome Joint Disorders Juvenile Rheumatoid Arthritis Kartagener Syndrome Kawasaki Disease Keratoconjunctivitis Sicca Kidney Papillary Necrosis Korean Hemorrhagic Fever Lactic Acidosis Laryngeal Cleft Lateral Myocardial Infarction Lecithin:cholesterol Acyltransferase Deficiency Leech Infestation Left Ventricular Noncompaction Legg-Calve-Perthes Disease Legionellosis Legionnaire Disease Legionnaires' Disease Lemierre's Syndrome Lentigo Maligna Melanoma Leptospirosis Leukemia Leukodystrophy, Hypomyelinating, 3 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukostasis Limb Ischemia Lipid Metabolism Disorder Lipodermatosclerosis Lipodystrophy Lipomatosis, Multiple Lipoprotein Glomerulopathy Lissencephaly 1 Livedoid Vasculopathy Liver Cirrhosis Liver Disease Loeys-Dietz Syndrome Logopenic Progressive Aphasia Lung Cancer Lung Disease Lupus Erythematosus Lutheran Suppressor, X-Linked Lyme Disease Lymphadenitis Lymphangiosarcoma Lymph Node Disease Lymphoma Lymphopenia Macs Syndrome Macular Holes Macular Retinal Edema Malignant Essential Hypertension Malignant Hypertension Malignant Otitis Externa Malignant Renovascular Hypertension Malignant Secondary Hypertension Malignant Spiradenoma Mallory-Weiss Syndrome Mannose-Binding Lectin Deficiency Marantic Endocarditis Marfan Syndrome Meckel Syndrome, Type 1 Mediastinitis Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 Melanoma Meningitis Meningococcal Infection Meningococcemia Meningoencephalitis Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 Mercury Poisoning Mesangial Proliferative Glomerulonephritis Mesenteric Vascular Occlusion Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration Metanephric Adenoma Microcystic Meningioma Microvascular Complications of Diabetes 1 Microvascular Complications of Diabetes 3 Microvascular Complications of Diabetes 5 Middle Cerebral Artery Infarction Migraine with Aura Migraine with or Without Aura 1 Mild Hemophilia a Miller-Dieker Lissencephaly Syndrome Mitral Valve Insufficiency Mitral Valve Stenosis Mixed Connective Tissue Disease Miyoshi Muscular Dystrophy 1 Moderate and Severe Traumatic Brain Injury Moebius Syndrome Mohr-Tranebjaerg Syndrome Monocytic Leukemia Mononeuritis Multiplex Morbid Obesity Mucocutaneous Leishmaniasis Mucolipidosis Ii Alpha/beta Mucositis Multicentric Castleman Disease Multiple Chemical Sensitivity Multiple Cranial Nerve Palsy Multiple Sclerosis Multiple Symmetrical Lipomatosis Mungan Syndrome Myasthenia Gravis Mycosis Fungoides Myelitis Myelodysplastic Syndrome Myeloid Leukemia Myeloma, Multiple Myeloproliferative Syndrome, Transient Myocardial Infarction 2 Myocardial Stunning Myocarditis Myopathy Myxedema Neonatal Stroke Nephrosclerosis Nephrotic Syndrome Nervous System Disease Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuroleptic Malignant Syndrome Neuronitis Neuropathy Neutrophil Actin Dysfunction Niemann-Pick Disease, Type a Nodular Goiter Non-a-E Hepatitis Nonalcoholic Steatohepatitis Nonarteritic Anterior Ischemic Optic Neuropathy Nutritional Deficiency Disease Obesity-Hypoventilation Syndrome Obstructive Jaundice Ocular Motor Apraxia Odontogenic Myxoma Oral Lichen Planus Orofacial Granulomatosis Orthostatic Intolerance Osteomyelitis Osteomyelitis, Sterile Multifocal, with Periostitis and Pustulosis Osteonecrosis Osteoporotic Fracture Osteosclerotic Myeloma Otitis Media Ovarian Hyperstimulation Syndrome Overnutrition Palindromic Rheumatism Pancreatitis Papillon-Lefevre Syndrome Paraganglioma Paralytic Ileus Parapsoriasis Paroxysmal Nocturnal Hemoglobinuria Patent Foramen Ovale Pediatric Angiosarcoma Pediatric Hypertension Pediatric Systemic Lupus Erythematosus Pelvic Inflammatory Disease Pelvic Organ Prolapse Peptic Ulcer Disease Pericardial Effusion Pericardial Mesothelioma Pericarditis Pericardium Cancer Perinatal Necrotizing Enterocolitis Periodontal Disease Periodontitis Periodontosis Peripartum Cardiomyopathy Peripheral Artery Disease Peripheral Vascular Disease Peripheral Vertigo Peritonitis Pernicious Anemia Pertussis Phaeochromocytoma Pharyngitis Pheochromocytoma Pituitary Adenoma 1, Multiple Types Pituitary Apoplexy Pituitary Hormone Deficiency, Combined, 2 Placenta Disease Placental Abruption Plasminogen Activator Inhibitor-1 Deficiency Plasmodium Vivax Malaria Platelet Aggregation, Spontaneous Platelet Groups--Ko System Pleomorphic Liposarcoma Pleural Disease Pleurisy Pneumonia Pneumothorax Poems Syndrome Polyarteritis Nodosa Polycystic Kidney Disease Polycythemia Polycythemia Vera Polymorphic Reticulosis Polymyositis Polyneuropathy Porphyria Portal Hypertension Portal Vein Thrombosis Posterior Myocardial Infarction Posterior Urethral Valves Posteroinferior Myocardial Infarction Posterolateral Myocardial Infarction Post-Thrombotic Syndrome Postural Hypotension Potocki-Lupski Syndrome Prediabetes Syndrome Pre-Eclampsia Prekallikrein Deficiency Priapism Prieto X-Linked Mental Retardation Syndrome Primary Lateral Sclerosis, Adult, 1 Primary Progressive Multiple Sclerosis Primary Thrombocytopenia Prinzmetal's Variant Angina Progressive Familial Heart Block, Type Ib Prolymphocytic Leukemia Prostate Cancer Prostate Disease Prostatitis Protein C Deficiency Protein S Deficiency Protein Z Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Psammomatous Meningioma Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak Pseudo-Von Willebrand Disease Pseudoxanthoma Elasticum Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Arteriovenous Malformation Pulmonary Atresia with Intact Ventricular Septum Pulmonary Disease, Chronic Obstructive Pulmonary Edema Pulmonary Embolism Pulmonary Embolism and Infarction Pulmonary Hypertension Pulmonary Sarcoidosis Pulmonary Tuberculosis Pulmonic Stenosis Pulpitis Pure Autonomic Failure Purpura Purpura Fulminans Purulent Labyrinthitis Pyelonephritis Q Fever Qualitative Platelet Defect Quebec Platelet Disorder Raynaud Disease Relapsing-Remitting Multiple Sclerosis Renal Artery Disease Renal Artery Obstruction Renal Fibrosis Renal Hypertension Renal Tubular Dysgenesis Renovascular Hypertension Respiratory System Disease Resting Heart Rate, Variation in Restrictive Cardiomyopathy Retinal Artery Occlusion Retinal Ischemia Retinal Vascular Disease Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Rett Syndrome Rheumatic Disease Rheumatic Heart Disease Rheumatoid Arthritis Rheumatoid Nodulosis Rheumatoid Vasculitis Richards-Rundle Syndrome Right Bundle Branch Block Ring Chromosome 2 Robinow Syndrome, Autosomal Recessive Rosacea Sagittal Sinus Thrombosis Salmonellosis Salt and Pepper Developmental Regression Syndrome Sarcoidosis 1 Sarcoidosis 2 Schistosomiasis Scorpion Envenomation Scott Syndrome Scrub Typhus Secondary Progressive Multiple Sclerosis Second-Degree Atrioventricular Block Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance Seminoma Sensorineural Hearing Loss Septal Myocardial Infarction Septic Arthritis Serotonin Syndrome Severe Acute Respiratory Syndrome Severe Hemophilia a Severe Pre-Eclampsia Short Bowel Syndrome Shwartzman Phenomenon Sickle Cell Anemia Sickle Cell Disease Sick Sinus Syndrome Silent Myocardial Infarction Sinusitis Sitosterolemia Situs Inversus Sleep Apnea Sleep Disorder Smith-Kingsmore Syndrome Smith-Lemli-Opitz Syndrome Sneddon Syndrome Sorsby Fundus Dystrophy Spastic Entropion Spinal Cord Infarction Spinal Cord Injury Splenic Disease Splenic Infarction Spondylarthropathy Spondylitis Spondyloarthropathy Spondyloocular Syndrome Spondylosis Spotted Fever Squamous Cell Carcinoma Squamous Cell Carcinoma of the Hypopharynx Stachybotrys Chartarum Status Asthmaticus Sticky Platelet Syndrome Stroke, Ischemic Stromal Keratitis Subacute Bacterial Endocarditis Subclavian Steal Syndrome Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Superior Limbic Keratoconjunctivitis Supravalvular Aortic Stenosis Sveinsson Chorioretinal Atrophy Swine Influenza Syncope Syndrome of Inappropriate Antidiuretic Hormone Synovitis Syphilis Syringocystadenoma Papilliferum Systemic Lupus Erythematosus Systolic Heart Failure Takayasu Arteritis Tangier Disease T-Cell Adult Acute Lymphocytic Leukemia T-Cell Prolymphocytic Leukemia Temporal Arteritis Testicular Cancer Testicular Seminoma Thalassemia Third-Degree Atrioventricular Block Thoracoabdominal Syndrome Thrombasthenia Thrombocytopenia Thrombocytopenia Due to Platelet Alloimmunization Thrombocytopenic Purpura, Autoimmune 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 Toxic Shock Syndrome Toxoplasmoză Transient Global Amnesia Transposition of the Great Arteries Transverse Myelitis Traumatic Brain Injury Treacher Collins Syndrome 1 Trichinosis Tricuspid Atresia Tricuspid Valve Insufficiency Trypanosomiasis Tuberculous Meningitis Tularemia Twin-to-Twin Transfusion Syndrome Typhoid Fever Undifferentiated Pleomorphic Sarcoma Unilateral Absence of a Pulmonary Artery Uremia Urinary System Disease Uterine Anomalies Valproate Embryopathy Van Der Woude Syndrome 1 Varicose Veins Vascular Dementia Vascular Disease Vascular Hemostatic Disease Vasculitis Vasculogenic Impotence Vein Disease Venous Insufficiency Ventricular Septal Defect Viral Encephalitis Viral Meningitis Vitamin B12 Deficiency Vitamin E, Familial Isolated Deficiency of Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Von Willebrand Disease, Type 3 Witkop Syndrome Wolff-Parkinson-White Syndrome Xanthoma Disseminatum Xanthomatosis Yemenite Deaf-Blind Hypopigmentation Syndrome Zygomycosis