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Nume Pulmonary Hypertension
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Other secondary pulmonary hypertension; Primary pulmonary hypertension
Clasificare anatomică Malacards Boli cardiovasculare; Boli respiratorii
Boli din aceeaşi familie Pulmonary Hypertension, Primary, 1; Pulmonary Hypertension, Primary, 2; Pulmonary Hypertension, Primary, 3; Pulmonary Hypertension, Primary, 4; Pulmonary Hypertension, Primary, Autosomal Recessive

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Boli A-Z 49,xxxxy Syndrome Aarskog-Scott Syndrome Acanthamoeba Keratitis Acheiria Achondroplasia Acquired Immunodeficiency Syndrome Acrocallosal Syndrome Acute Anterolateral Myocardial Infarction Acute Chest Syndrome Acute Cor Pulmonale Acute Mountain Sickness Acute Myocardial Infarction Acute Poststreptococcal Glomerulonephritis Acute Pulmonary Heart Disease Acute Respiratory Distress Syndrome Adams-Oliver Syndrome Adenocarcinoma Adenosquamous Pancreas Carcinoma Adie Pupil Adiponectin, Serum Level of, Quantitative Trait Locus 1 Adult Pulmonary Langerhans Cell Histiocytosis Adult Respiratory Distress Syndrome Afibrinogenemia, Congenital Aging Al Amyloidosis Aland Island Eye Disease Allergic Bronchopulmonary Aspergillosis Allergic Bronchopulmonary Aspergillosis, Familial Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 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 Alveolar Capillary Dysplasia Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins Amyloidosis Androgen Insensitivity Syndrome, Mild Aneurysm Angina Pectoris Angiodysplasia Angiomyolipoma Angiosarcoma Aniridia 1 Ankyloglossia Anorexia Nervosa 1 Anoxia Anterolateral Myocardial Infarction Anthracosis Antiphospholipid Syndrome Antisynthetase Syndrome Aortic Coarctation Aortic Disease Aortic Valve Disease 2 Aortopulmonary Window Argentine Hemorrhagic Fever Arterial Thoracic Outlet Syndrome Arteries, Anomalies of Arteriovenous Fistula Arteriovenous Malformation Arteriovenous Malformations of the Brain Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Aspergillosis Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrial Fibrillation Atrial Septal Aneurysm Atrioventricular Block Atrioventricular Septal Defect Autoimmune Disease Autonomic Dysfunction Axonal Neuropathy Basilar Artery Insufficiency B-Cell Lymphomas Beriberi Berylliosis Beta-Thalassemia Biliary Atresia Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Blue Rubber Bleb Nevus 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 Bornholm Eye Disease Brachydactyly, Type A2 Breast Cancer Bronchiectasis Bronchiolitis Bronchiolitis Obliterans Bronchopneumonia Bronchopulmonary Dysplasia Brunner Syndrome Bullous Impetigo Calcinosis Cantu Syndrome Capillary Hemangioma Capillary Leak Syndrome Cardiac Tamponade Cardiac Valvular Defect, Developmental Cardiogenic Shock Carotid Artery Thrombosis Cataract 5, Multiple Types Cataract 6, Multiple Types Central Retinal Artery Occlusion Central Retinal Vein Occlusion Central Sleep Apnea Cerebritis Cerebrovascular Disease Cervicitis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chorioamnionitis Choriocarcinoma Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Chromosome 8p Duplication Chronic Angina Chronic Granulomatous Disease Chronic Mountain Sickness Chronic Pulmonary Heart Disease Chronic Thromboembolic Pulmonary Hypertension Cohen-Gibson Syndrome Collagen Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Cytomegalovirus Congenital Dyserythropoietic Anemia Congenital Hepatic Fibrosis Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi Congenital Mitral Stenosis Congenital Mumps Congenital Plasminogen Deficiency Congenital Rubella Congenital Syphilis Congestive Heart Failure Conjugate Gaze Palsy Connective Tissue Disease Conotruncal Heart Malformations Conversion Disorder Corneal Neovascularization Coronary Arterial Fistulas Coronary Artery Anomaly Coronary Stenosis Coronary Thrombosis Corpus Callosum, Agenesis of, with Abnormal Genitalia Cor Triatriatum Cor Triatriatum Sinister Costello Syndrome Craniofacial-Deafness-Hand Syndrome Crest Syndrome Crimean-Congo Hemorrhagic Fever Critical Limb Ischemia Cryoglobulinemia, Familial Mixed Cutis Laxa Cystic Fibrosis Cytomegalovirus Infection Denys-Drash Syndrome Dermatomyositis Developmental Dysplasia of the Hip 1 Dextrocardia Dextrocardia with Situs Inversus Diabetic Macular Edema Diaphragmatic Hernia, Congenital Diastolic Heart Failure Diffuse Pulmonary Fibrosis Diffuse Scleroderma Dilated Cardiomyopathy Dirofilariasis Disseminated Intravascular Coagulation Double Discordia Double Outlet Left Ventricle Down Syndrome Duane Retraction Syndrome 1 Dysbaric Osteonecrosis Dysfibrinogenemia Dyskinesia of Esophagus Echinococcosis Eclampsia Ehrlichiosis Eisenmenger Syndrome Emphysema, Congenital Lobar Encephalopathy Endocardial Fibroelastosis Endomyocardial Fibrosis Endotheliitis End Stage Renal Failure Eosinophilia-Myalgia Syndrome Epileptic Encephalopathy, Childhood-Onset Epithelial Recurrent Erosion Dystrophy Esophageal Cancer Essential Thrombocythemia Esterase C Fanconi Anemia, Complementation Group E Fibrinolytic Defect Fibrochondrogenesis Fibrodysplasia Ossificans Progressiva Fibromuscular Dysplasia Fibrosing Mediastinitis Gallbladder Adenocarcinoma Gapo Syndrome Gastric Cancer Gestational Choriocarcinoma Giant Hemangioma Gigantism Gigantomastia Glomeruloid Hemangioma Glucose Intolerance Glycogen Storage Disease Graves' Disease Hantavirus Pulmonary Syndrome Heart Disease Heart Valve Disease Hellp Syndrome Hemangioendothelioma Hematopoietic Stem Cell Transplantation Hemochromatosis, Neonatal Hemoglobinopathy Hemolytic Anemia Hemolytic-Uremic Syndrome Hemophagocytic Lymphohistiocytosis Hemorrhagic Disease Hemorrhagic Fever Hemosiderosis Hepatic Adenomas, Familial Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatopulmonary Syndrome Hepatorenal Syndrome Hereditary Hemorrhagic Telangiectasia Hereditary Spherocytosis Heritable Pulmonary Arterial Hypertension Heterotaxy Heterotaxy, Visceral, 1, X-Linked Histiocytosis Holt-Oram Syndrome Homocystinuria Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type Human Herpesvirus 8 Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertension, Essential Hypertensive Heart Disease Hypertensive Retinopathy Hyperthyroidism Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Pyloric Stenosis Hyperuricemia Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome Hypoaldosteronism Hypoascorbemia Hyporeninemic Hypoaldosteronism Hypoxia Idiopathic Edema Idiopathic Hypercalciuria Idiopathic Interstitial Pneumonia Immunodeficiency 21 Impetigo Impotence Incontinentia Pigmenti Inferior Myocardial Infarction Interatrial Communication Intermittent Claudication Interstitial Lung Disease Intestinal Atresia Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Intravascular Large B-Cell Lymphoma Ischemia Ischemic Colitis Ischemic Optic Neuropathy Juvenile Myelomonocytic Leukemia Juvenile Polyposis Syndrome Juvenile Rheumatoid Arthritis Kawasaki Disease Klippel-Feil Syndrome Korean Hemorrhagic Fever Lactic Acidosis Langerhans Cell Histiocytosis Laryngotracheitis Leech Infestation Left Ventricular Noncompaction Legg-Calve-Perthes Disease Leiomyosarcoma Leopard Syndrome Leprosy 2 Leukemia Leukostasis Ligneous Conjunctivitis Limb Ischemia Limited Scleroderma Lipodermatosclerosis Lipomatosis, Multiple Liver Cirrhosis Liver Disease Lung Disease Lupus Erythematosus Lymphangioleiomyomatosis Lymphangitis Lymphedema Lymphoma Macroglobulinemia Macrophage Activation Syndrome Malignant Hypertension Malignant Renovascular Hypertension Malignant Secondary Hypertension Malonyl-Coa Decarboxylase Deficiency Marantic Endocarditis Marfan Syndrome Meconium Aspiration Syndrome Mediastinitis Megakaryocytic Leukemia Methemoglobinemia Microcephaly Microvascular Complications of Diabetes 5 Migraine with Aura Migraine with or Without Aura 1 Mitochondrial Disorders Mitral Atresia Mitral Valve Disease Mitral Valve Stenosis Mixed Connective Tissue Disease Mohr-Tranebjaerg Syndrome Moyamoya Disease 1 Mucopolysaccharidosis, Type Vii Multiple Synostoses Syndrome Mumps Muscle Hypertrophy Myelofibrosis Myocardial Infarction Myocardial Stunning Neonatal Scleroderma Neonatal Thyrotoxicosis Nephrotic Syndrome Netherton Syndrome Neurofibromatosis, Type Iv, of Riccardi Neuropathy Nodular Regenerative Hyperplasia Nonarteritic Anterior Ischemic Optic Neuropathy Nonspecific Interstitial Pneumonia Norrie Disease Obesity-Hypoventilation Syndrome Oliver Syndrome Omphalocele Open-Angle Glaucoma Opitz Gbbb Syndrome, Type I Orthostatic Intolerance Osteonecrosis Osteopetrosis Pallister-Hall Syndrome Panniculitis Parkes Weber Syndrome Patent Ductus Arteriosus 1 Patent Ductus Venosus Patent Foramen Ovale Pericardial Effusion Perinephritis Peripartum Cardiomyopathy Peripheral Artery Disease Peritonitis Persistent Fetal Circulation Syndrome Pheochromocytoma Pitt-Hopkins Syndrome Placenta Accreta Placental Abruption Placental Insufficiency Plasma Cell Leukemia Plasminogen Activator Inhibitor-1 Deficiency Platelet Aggregation, Spontaneous Platelet Membrane Fluidity Pneumoconiosis Pneumonia Poems Syndrome Poland Syndrome Polycythemia Polycythemia Vera Polydactyly Polymicrogyria, Bilateral Perisylvian, X-Linked Polymyositis Portal Hypertension Postaxial Acrofacial Dysostosis Post-Thrombotic Syndrome Pre-Eclampsia Premature Ejaculation Priapism Primary Biliary Cirrhosis Primary Effusion Lymphoma Prinzmetal's Variant Angina Protein C Deficiency Protein-Losing Enteropathy Protein S Deficiency Pulmonary Alveolar Microlithiasis Pulmonary Alveolar Proteinosis Pulmonary Arteriovenous Malformation Pulmonary Artery Agenesis Pulmonary Artery Leiomyosarcoma Pulmonary Aspergilloma Pulmonary Disease, Chronic Obstructive Pulmonary Edema Pulmonary Edema of Mountaineers Pulmonary Embolism Pulmonary Emphysema Pulmonary Fibrosis Pulmonary Hemosiderosis Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis Pulmonary Hypertension, Neonatal Pulmonary Hypertension, Primary, 1 Pulmonary Hypertension, Primary, 2 Pulmonary Interstitial Glycogenosis Pulmonary Sarcoidosis Pulmonary Vein Stenosis Pulmonary Venoocclusive Disease Pulmonary Venoocclusive Disease 1, Autosomal Dominant Pulmonary Venoocclusive Disease 2, Autosomal Recessive Pulmonic Stenosis Pure Autonomic Failure Purpura Pyloric Stenosis Pyogenic Granuloma Raynaud Disease Renal Artery Disease Renal Artery Obstruction Renal Hypertension Renovascular Hypertension Resting Heart Rate, Variation in Restless Legs Syndrome Restrictive Cardiomyopathy Retinal Artery Occlusion Retinal Detachment Retinal Vein Occlusion Retinitis Rheumatic Disease Rheumatic Fever Rheumatic Fever-Related Antigen Rheumatoid Arthritis Rheumatoid Vasculitis Right Bundle Branch Block Rubella Salt and Pepper Developmental Regression Syndrome Sarcoidosis 2 Sarcoma Scalp-Ear-Nipple Syndrome Schistosomiasis Sensorineural Hearing Loss Severe Combined Immunodeficiency Sexual Disorder Shone Complex Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly Sickle Cell Anemia Sickle Cell Disease Silicosis Single Ventricular Heart Sinusitis Situs Inversus Sleep Apnea Smith-Lemli-Opitz Syndrome Spinal Stenosis Splenomegaly Spondyloepiphyseal Dysplasia Congenita Spondyloocular Syndrome Storage Pool Platelet Disease Stroke, Ischemic Sudden Arrhythmia Death Syndrome Sveinsson Chorioretinal Atrophy Swyer-James Syndrome Syncope Syndrome of Inappropriate Antidiuretic Hormone Syphilis Systemic Lupus Erythematosus Systemic Scleroderma Systolic Heart Failure Takayasu Arteritis Telangiectasis Tetralogy of Fallot Thalassemia Thoracic Outlet Syndrome Thoracoabdominal Syndrome Thrombocytopenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Toxic Oil Syndrome Transposition of the Great Arteries Tricuspid Atresia Tricuspid Valve Insufficiency Tricuspid Valve Prolapse Tropical Endomyocardial Fibrosis Twin-to-Twin Transfusion Syndrome Tympanosclerosis Undifferentiated Pleomorphic Sarcoma Unilateral Absence of a Pulmonary Artery Univentricular Heart Urea Cycle Disorder Van Der Woude Syndrome 1 Varicose Veins Vascular Cancer Vascular Disease Vasculitis Vasculogenic Impotence Vein Disease Vein of Galen Aneurysm Ventricular Septal Defect Waldenstrom Macroglobulinemia Wdha Syndrome Weber Syndrome Whipple Disease Wilson-Mikity Syndrome Xanthomatosis