Informaţii despre

Nume Hypertension, Essential
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Hypertensive heart and renal disease, unspecified
Clasificare anatomică Malacards Boli cardiovasculare; Boli de sânge
Boli din aceeaşi familie Benign Essential Hypertension; Benign Secondary Hypertension; Hypertension, Essential 1; Hypertension, Essential 2; Hypertension, Essential 3; Hypertension, Essential 4; Hypertension, Essential 5; Hypertension, Essential 6; Hypertension, Essential 7; Hypertension, Essential 8; Malignant Essential Hypertension; Malignant Hypertension; Malignant Secondary Hypertension

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Boli A-Z Abdominal Obesity-Metabolic Syndrome 1 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 Abetalipoproteinemia Acanthosis Nigricans Acquired Generalized Lipodystrophy Acquired Metabolic Disease Acrocallosal Syndrome Acromegaly Acute Mountain Sickness Acute Myocardial Infarction Acute Poststreptococcal Glomerulonephritis Adenoma Adie Pupil Adrenal Adenoma Adrenal Carcinoma Adrenal Cortex Disease Adrenal Gland Disease Adrenal Gland Hyperfunction Adult Syndrome Aging Aland Island Eye Disease Alcohol Abuse Aldosterone-Producing Adenoma Allergic Urticaria Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amyloidosis Aa Anauxetic Dysplasia 1 Aneurysm Angina Pectoris Angioedema Aniridia 1 Anorexia Nervosa 1 Anterolateral Myocardial Infarction Antiphospholipid Syndrome Anuria Aortic Atherosclerosis Aortic Coarctation Aortic Valve Disease 2 Apert Syndrome Apnea, Obstructive Sleep Apolipoprotein C-Iii Deficiency Apparent Mineralocorticoid Excess Arcus Corneae Arteries, Anomalies of Arteriolosclerosis Arteriosclerosis Arteriosclerosis Obliterans Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 3 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Atherosclerosis Susceptibility Atrial Fibrillation Autonomic Dysfunction Autonomic Nervous System Disease Autonomic Neuropathy Autosomal Dominant Polycystic Kidney Disease Bartter Disease Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness Bartter Syndrome, Type 4b, Neonatal, with Sensorineural Deafness Benign Essential Hypertension Benign Secondary Hypertension Bestrophinopathy, Autosomal Recessive 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 Brachydactyly Buerger Disease Bulimia Nervosa 1 Bulimia Nervosa 2 C1 Inhibitor Deficiency Cardiogenic Shock Carotid Artery Disease Carotid Artery Thrombosis Carotid Intimal Medial Thickness 2 Cell Type Benign Neoplasm Central Serous Chorioretinopathy Central Sleep Apnea Cerebritis Cerebrovascular Disease Chronic Angina Chronic Thromboembolic Pulmonary Hypertension Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Collagen Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Hepatic Fibrosis Congestive Heart Failure Conjunctivitis Conn's Syndrome Coronary Artery Anomaly Coronary Artery Vasospasm Coronary Heart Disease 1 Coronary Stenosis Coronary Thrombosis Corticosteroid-Binding Globulin Deficiency Cytochrome P450 2d6 Variant Cytomegalovirus Infection Dementia Dermatomyositis Diabetes Insipidus Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diabetic Angiopathy Diastolic Heart Failure Diffuse Glomerulonephritis Dirofilariasis Dysautonomia Dysbaric Osteonecrosis Eating Disorder Eclampsia Eisenmenger Syndrome Endocrine Organ Benign Neoplasm Endocrine Pancreas Disease Endotheliitis End Stage Renal Failure Essential Thrombocythemia Familial Hyperaldosteronism Familial Hyperlipidemia Familial Hypertension Fatty Liver Disease Fetal Macrosomia Fibrinolytic Defect Fibromuscular Dysplasia Generalized Atherosclerosis Gestational Diabetes Gitelman Syndrome Glomerulonephritis Glucose Intolerance Glucose Metabolism Disease Heart Disease Hemifacial Spasm Hemorrhage, Intracerebral Hemorrhagic Disease Hepatic Adenomas, Familial Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatopulmonary Syndrome Hepatorenal Syndrome Hereditary Angioedema Homocysteinemia Hyperaldosteronism, Familial, Type I Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Familial Hyperglycemia Hyperinsulinemic Hypoglycemia Hyperinsulinism Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertension, Essential 1 Hypertension, Essential 2 Hypertension, Essential 3 Hypertension, Essential 4 Hypertension, Essential 5 Hypertension, Essential 6 Hypertension, Essential 7 Hypertension, Essential 8 Hypertensive Heart Disease Hypertensive Nephropathy Hypertensive Retinopathy Hypertriglyceridemia, Familial Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoaldosteronism Hypokalemia Hypolipoproteinemia Hyporeninemic Hypoaldosteronism Ichthyosis Prematurity Syndrome Idiopathic Edema Idiopathic Recurrent Pericarditis Iga Glomerulonephritis Impotence Insulin Autoimmune Syndrome Insulin-Like Growth Factor I Intermittent Claudication Interstitial Nephritis Interstitial Pneumonitis, Desquamative, Familial Intracranial Vasospasm Ischemia Ischemic Heart Disease Ischemic Optic Neuropathy Kawasaki Disease Kidney Disease Kwashiorkor Lecithin:cholesterol Acyltransferase Deficiency Legg-Calve-Perthes Disease Leukodystrophy, Hypomyelinating, 3 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Liddle Syndrome Limb Ischemia Lipid Metabolism Disorder Lipoid Congenital Adrenal Hyperplasia Liver Cirrhosis Liver Disease Loeffler Syndrome Logopenic Progressive Aphasia Lutheran Suppressor, X-Linked Malignant Essential Hypertension Malignant Hypertension Malignant Otitis Externa Malignant Renovascular Hypertension Malignant Secondary Hypertension Mandibulofacial Dysostosis with Alopecia Meningococcal Infection Mental Depression Microvascular Complications of Diabetes 3 Microvascular Complications of Diabetes 5 Migraine with Aura Migraine with or Without Aura 1 Mineral Metabolism Disease Mitral Valve Disease Mitral Valve Stenosis Mohr-Tranebjaerg Syndrome Mood Disorder Morbid Obesity Multicystic Dysplastic Kidney Multiple Symmetrical Lipomatosis Mungan Syndrome Muscle Hypertrophy Myocardial Infarction Myocardial Stunning Nephrosclerosis Netherton Syndrome Neurogenic Hypertension Neuronitis Nonalcoholic Steatohepatitis Nonarteritic Anterior Ischemic Optic Neuropathy Nutritional Deficiency Disease Obesity-Hypoventilation Syndrome Oppositional Defiant Disorder Optic Perineuritis Organ System Benign Neoplasm Orthostatic Intolerance Orthostatic Proteinuria Overnutrition Pancreatic Islet Cell Tumors Pancreatitis Panic Disorder Pediatric Hypertension Pericardial Effusion Perinephritis Peripheral Artery Disease Persistent Fetal Circulation Syndrome Pitt-Hopkins Syndrome Placental Insufficiency Plasminogen Activator Inhibitor-1 Deficiency Platelet Aggregation, Spontaneous Platelet Membrane Fluidity Pleural Disease Polycystic Liver Disease Portal Hypertension Postaxial Acrofacial Dysostosis Posterior Urethral Valves Postural Hypotension Prediabetes Syndrome Pre-Eclampsia Premenstrual Tension Prinzmetal's Variant Angina Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak Pseudohypoaldosteronism Pulmonary Edema Pulmonary Embolism Pulmonary Hypertension Pure Autonomic Failure Raynaud Disease Renal Artery Disease Renal Dysplasia Renal Fibrosis Renal Glucosuria Renal Hypertension Renal Infectious Disease Renal Tuberculosis Renal Tubular Dysgenesis Renal Tubular Transport Disease Renovascular Hypertension Resting Heart Rate, Variation in Retinal Vein Occlusion Retinitis Right Bundle Branch Block Salt and Pepper Developmental Regression Syndrome Satb2-Associated Syndrome Severe Pre-Eclampsia Short-Rib Thoracic Dysplasia 5 with or Without Polydactyly Shwartzman Phenomenon Sleep Apnea Spindle Cell Hemangioma Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Steroid Inherited Metabolic Disorder Stroke, Ischemic Syncope Syndrome of Inappropriate Antidiuretic Hormone Systemic Scleroderma Systolic Heart Failure Takayasu Arteritis Tangier Disease Taqi Polymorphism Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Unilateral Absence of a Pulmonary Artery Uremia Ureteral Obstruction Urinary System Disease Van Der Woude Syndrome 1 Vascular Disease Vasculitis Vasculogenic Impotence Venous Insufficiency Xanthomatosis