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Nume Patent Foramen Ovale
Pagina Web www.malacards.org
Clasificare globală Malacards Fetal diseases; Rare diseases
Clasificari ICD10 Atrial septal defect
Clasificare anatomică Malacards Cardiovascular diseases

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Boli A-Z Acanthamoeba Keratitis Acute Cor Pulmonale Acute Myocardial Infarction Acute Respiratory Distress Syndrome Adrenal Carcinoma Afibrinogenemia Afibrinogenemia, Congenital Aganglionosis, Total Intestinal Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Al-Raqad Syndrome Alzheimer Disease 3 Amaurosis Fugax Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aneurysm Angina Pectoris Angiolipoma Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Aortic Aneurysm Aortic Atherosclerosis Aortic Valve Prolapse Argentine Hemorrhagic Fever Argininosuccinic Aciduria Arteriovenous Fistula Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Ataxia Neuropathy Spectrum Athyreosis Atrial Fibrillation Atrial Heart Septal Defect Atrial Septal Aneurysm Atrial Septal Defect 1 Atrial Septal Defect 3 Atrioventricular Block Atrioventricular Septal Defect Autism Spectrum Disorder Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Blood Protein Disease 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 Branchiootic Syndrome 1 Branch Retinal Artery Occlusion Broken Heart Syndrome Brucellosis Budd-Chiari Syndrome Buerger Disease Cardiac Tamponade Carotid Stenosis Catastrophic Antiphospholipid Syndrome Central Retinal Artery Occlusion Central Retinal Vein Occlusion Cerebral Palsy Cerebral Palsy, Ataxic, Autosomal Recessive Cerebral Sinovenous Thrombosis Cerebritis Cerebrovascular Disease Cervicitis Char Syndrome Chromosomal Triplication Cluster Headache Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complete Atrioventricular Canal-Ventricle Hypoplasia Syndrome Congenitally Corrected Transposition of the Great Arteries Conotruncal Heart Malformations Cor Triatriatum Cor Triatriatum Dexter Cryptogenic Cirrhosis Cyanosis, Transient Neonatal Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Diaphragmatic Hernia, Congenital Disseminated Intravascular Coagulation Double Discordia Down Syndrome Dysfibrinogenemia Ebstein Anomaly Eclampsia Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Endocarditis Endotheliitis Eosinophilic Granulomatosis with Polyangiitis Factor V Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Familial Atrial Fibrillation Fanconi Anemia, Complementation Group E Fibrinolytic Defect Fibroblastic Rheumatism Fournier Gangrene Galactose Epimerase Deficiency Headache Heart Cancer Heart Septal Defect Hellp Syndrome Hemicrania Continua Hemiplegic Migraine Hemoglobin E Disease Hemoglobinuria Hemorrhagic Disease Hepatic Adenomas, Familial Hepatic Infarction Hepatic Vascular Disease Hereditary Spherocytosis Holt-Oram Syndrome Homocysteinemia Homocystinuria Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoparathyroidism, Familial Isolated Hypoplastic Left Heart Syndrome Hypoxia Immune System Disease Infective Endocarditis Inferior Myocardial Infarction Inferior Vena Cava Interruption Influenza Interatrial Communication Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Ischemia Ischemic Colitis Ischemic Optic Neuropathy Levocardia Lipomatosis Livedoid Vasculopathy Lymphoma Marantic Endocarditis May-Thurner Syndrome Medial Medullary Syndrome Mesenteric Vascular Occlusion Migraine with Aura Migraine Without Aura Muscular Dystrophy Myocardial Infarction Myoma Neuronitis Nonarteritic Anterior Ischemic Optic Neuropathy Obesity-Hypoventilation Syndrome Opitz Gbbb Syndrome, Type Ii Osteonecrosis Paracetamol Poisoning Paroxysmal Nocturnal Hemoglobinuria Partial Atrioventricular Canal Pectus Carinatum Peripheral Vertigo Persistent Eustachian Valve Placenta Disease Placental Abruption Platelet Aggregation, Spontaneous Polydactyly Porencephaly Portal Vein Thrombosis Post-Thrombotic Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Premature Chromatid Separation Trait Priapism Progressive Nodular Histiocytosis Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Arterio-Veinous Fistula Pulmonary Arteriovenous Fistulas Pulmonary Arteriovenous Malformation Pulmonary Edema Pulmonary Embolism Pulmonary Hypertension Pulmonary Valve Disease Pulmonary Valve Stenosis Pulmonic Stenosis Purpura Purpura Fulminans Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Sagittal Sinus Thrombosis Scleromyxedema Severe Pre-Eclampsia Sickle Cell Disease Sleep Apnea Sleep Disorder Sneddon Syndrome Spinal Cord Infarction Splenic Infarction Sporadic Hemiplegic Migraine Sticky Platelet Syndrome Stroke, Ischemic Sudden Sensorineural Hearing Loss Sveinsson Chorioretinal Atrophy Tetralogy of Fallot Thrombasthenia Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Toxoplasmoză Transient Cerebral Ischemia Transient Global Amnesia Transposition of the Great Arteries Varicose Veins Vein Disease Ventricular Septal Defect