Informaţii despre

Nume Aortic Valve Disease 2
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Aortic (valve) stenosis; Aortic (valve) stenosis with insufficiency; Congenital stenosis of aortic valve; Rheumatic aortic stenosis; Rheumatic aortic stenosis with insufficiency
Clasificare anatomică Malacards Boli cardiovasculare
Boli din aceeaşi familie Aortic Valve Disease 1; Congenital Aortic Valve Insufficiency

Vezi şi

Boli A-Z Ablepharon-Macrostomia Syndrome Acquired Metabolic Disease Acquired Von Willebrand Syndrome Acute Myocardial Infarction Adamantinoma of Long Bones Adie Pupil Aging Aland Island Eye Disease Alkaptonuria Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aneurysm Angelman Syndrome Angina Pectoris Angiodysplasia Aniridia 1 Ankylosis Anorexia Nervosa 1 Anterolateral Myocardial Infarction Anuria Aortic Aneurysm Aortic Atherosclerosis Aortic Coarctation Aortic Disease Aortic Valve Atresia Aortic Valve Disease 1 Aortic Valve Insufficiency Apparent Mineralocorticoid Excess Arteries, Anomalies of Arteriosclerosis Arteriovenous Fistula Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Atrial Fibrillation Atrial Septal Defect 4 Atrial Standstill 1 Autosomal Dominant Polycystic Kidney Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System 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 Remodeling Disease Bone Resorption Disease Cardiac Conduction Defect Cardiac Rupture Cardiac Tamponade Cardiac Valvular Defect, Developmental Cardiogenic Shock Cardiomyopathy, Familial Hypertrophic, 1 Carotid Stenosis Central Sleep Apnea Cerebritis Cerebrovascular Disease Chlamydia Chromosomal Deletion Syndrome Chronic Actinic Dermatitis Chronic Angina Chronic Apical Periodontitis Chronic Thromboembolic Pulmonary Hypertension Congenital Aortic Valve Insufficiency Congenitally Corrected Transposition of the Great Arteries Congestive Heart Failure Coronary Arterial Fistulas Coronary Artery Anomaly Coronary Stenosis Craniosynostosis 7 Dental Pulp Calcification Dentin Dysplasia Dentin Dysplasia, Type Ii Diastolic Heart Failure Dilated Cardiomyopathy Discrete Subaortic Stenosis Double Discordia Ebstein Anomaly Endocardial Fibroelastosis Endocarditis Endosteal Hyperostosis, Autosomal Dominant Endotheliitis End Stage Renal Failure Fainting Familial Abdominal Aortic Aneurysm Familial Bicuspid Aortic Valve Familial Expansile Osteolysis Familial Hypertension Fibromuscular Dysplasia Generalized Atherosclerosis Glucocorticoid-Induced Osteoporosis Glucose Metabolism Disease Hajdu-Cheney Syndrome Heart Conduction Disease Heart Disease Heart Valve Disease Hemarthrosis Hemophilic Arthropathy Hepatic Adenomas, Familial Hepatoportal Sclerosis Hepatorenal Syndrome Holt-Oram Syndrome Hutchinson-Gilford Progeria Syndrome Hyperchlorhidrosis, Isolated Hypercholesterolemia, Autosomal Dominant, 3 Hyperparathyroidism Hypertension, Diastolic Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hypertensive Retinopathy Hypertrophic Cardiomyopathy Hypoaldosteronism Hypoplastic Left Heart Syndrome Hyporeninemic Hypoaldosteronism Hypoxia Idiopathic Edema Idiopathic Hypercalciuria Infective Endocarditis Inflammatory Myofibroblastic Tumor Intermediate Coronary Syndrome Intermittent Claudication Interstitial Nephritis Ischemic Bone Disease Ischemic Heart Disease Johnson Neuroectodermal Syndrome Kummell's Disease Late-Onset Focal Dermal Elastosis Limb Ischemia Lipomatosis Loeys-Dietz Syndrome 3 Lymphangiectasia, Pulmonary, Congenital Lymphangiectasis Malignant Hypertension Mediastinal Lipomatosis Mediastinitis Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 Mid-Dermal Elastolysis Migraine with or Without Aura 1 Mitral Valve Disease Mitral Valve Insufficiency Mitral Valve Stenosis Multicentric Carpotarsal Osteolysis Syndrome Multicentric Reticulohistiocytosis Muscle Hypertrophy Myocardial Infarction Myocarditis Ochronosis Osseous Heteroplasia, Progressive Osteofibrous Dysplasia Osteogenesis Imperfecta, Type Vi Osteogenic Sarcoma Osteonecrosis Otosclerosis Paget Disease of Bone 5, Juvenile-Onset Papillary Cystadenocarcinoma Patella, Chondromalacia of Pediatric Hypertension Pericardial Effusion Periodontal Disease Periodontitis Peripheral Artery Disease Plica Syndrome Pneumonia Polyarticular Onset Juvenile Idiopathic Arthritis Polycythemia Polycythemia Vera Postural Hypotension Pseudoxanthoma Elasticum Pseudoxanthoma Elasticum-Like Papillary Dermal Elastolysis Psoriatic Arthritis Pulmonary Atresia with Intact Ventricular Septum Pulmonary Edema Pulmonary Embolism Pulmonary Hypertension Pulmonary Valve Insufficiency Pulmonary Valve Stenosis Pure Autonomic Failure Pyomyositis Renal Artery Disease Renal Artery Obstruction Renal Dysplasia Renal Hypertension Renal Tubular Dysgenesis Renovascular Hypertension Retinitis Rheumatic Fever Rheumatic Fever-Related Antigen Rheumatic Heart Disease Root Resorption Salt and Pepper Developmental Regression Syndrome Situs Inversus Sleep Apnea Spondyloarthropathy 1 Spondyloocular Syndrome Stroke, Ischemic Supravalvular Aortic Stenosis Syncope Syndrome of Inappropriate Antidiuretic Hormone Synovitis Systemic Scleroderma Systolic Heart Failure Takayasu Arteritis Tetralogy of Fallot Tooth Ankylosis Tooth Resorption Transposition of the Great Arteries Tricuspid Valve Disease Tricuspid Valve Stenosis Tympanic Membrane Disease Undifferentiated Pleomorphic Sarcoma Uremia Urinary System Disease Vacterl Association Vascular Disease Ventricular Septal Defect Vitamin E, Familial Isolated Deficiency of Werner Syndrome Wolff-Parkinson-White Syndrome