Informaţii despre

Nume Hemophilia a
Pagina Web www.malacards.org
Clasificare globală Malacards Genetic diseases; Rare diseases
Clasificari ICD10 Hereditary factor VIII deficiency
Clasificare anatomică Malacards Blood diseases
Boli din aceeaşi familie Acquired Hemophilia; Acquired Hemophilia a; Hemophilia B; Severe Hemophilia a; Severe Hemophilia B

Vezi şi

Boli A-Z Acquired Hemophilia Acquired Hemophilia a Acquired Von Willebrand Syndrome Acute Myocardial Infarction Acute Pancreatitis Adrenoleukodystrophy Afibrinogenemia Afibrinogenemia, Congenital Aging Aicardi Syndrome Alcohol-Related Birth Defect Allergic Rhinitis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Aneurysm Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Antiphospholipid Syndrome Antithrombin Iii Deficiency Aortic Aneurysm Arteriovenous Malformation Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Ataxia Neuropathy Spectrum Autoimmune Disease Autoimmune Pancreatitis Beta-Adrenergic Stimulation, Response to Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, I System Blood Platelet 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 Budd-Chiari Syndrome Bullous Pemphigoid Cardiac Tamponade Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism Carotid Artery Occlusion Carotid Artery Thrombosis Catastrophic Antiphospholipid Syndrome Cerebral Arteritis Cerebral Hemorrhage Cerebral Sinovenous Thrombosis Cerebritis Charcot-Marie-Tooth Disease Choledocholithiasis Chorioamnionitis Chronic Neutrophilic Leukemia Colitis Color Blindness Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Constrictive Pericarditis Coronary Thrombosis Cytophagic Histiocytic Panniculitis Diabetes Mellitus Disseminated Intravascular Coagulation Endocarditis Endotheliitis Epidermolysis Bullosa Epidermolysis Bullosa Acquisita Esophageal Cancer Essential Thrombocythemia Factor V and Factor Viii, Combined Deficiency of, 2 Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Fibromatosis Fournier Gangrene Glanzmann Thrombasthenia Gonadal Dysgenesis Gynecomastia Hemarthrosis Hematopoietic Stem Cell Transplantation Hemolytic-Uremic Syndrome Hemophilia Hemophilia B Hemophilic Arthropathy Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatitis Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Human Coronavirus Sensitivity Human Immunodeficiency Virus Type 1 Ichthyosis Prematurity Syndrome Infant Gynecomastia Inferior Myocardial Infarction Inherited Blood Coagulation Disease Intracranial Thrombosis Intussusception Ischemic Colitis Leech Infestation Leukemia Liver Disease Lung Cancer Lung Disease Lupus Erythematosus Mallory-Weiss Syndrome Mandibular Arteriovenous Malformation Marfan Syndrome Mild Hemophilia a Moderately Severe Hemophilia a Moyamoya Disease 1 Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Vii Mucositis Multiple Sclerosis Muscular Dystrophy Muscular Dystrophy, Duchenne Type Myasthenia Gravis Myelodysplastic Syndrome Myelofibrosis Myeloma, Multiple Myocardial Infarction Ovarian Cyst Pancreatitis Parietal Foramina 1 Pemphigus Pemphigus Foliaceus Pemphigus Vulgaris Pericardial Effusion Pericarditis Pneumonia Polyarteritis Nodosa Portal Vein Thrombosis Post-Thrombotic Syndrome Prostate Cancer Prostatitis Protein C Deficiency Protein S Deficiency Proteus Syndrome Prothrombin Deficiency Prothrombin Deficiency, Congenital Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Embolism Pulmonary Valve Stenosis Purpura Pustular Psoriasis Qualitative Platelet Defect Quebec Platelet Disorder Renal Glucosuria Retinal Artery Occlusion Rheumatoid Arthritis Rhinitis Sagittal Sinus Thrombosis Schizophrenia Scott Syndrome Septic Arthritis Severe Hemophilia a Severe Hemophilia B Stroke, Ischemic Systemic Lupus Erythematosus Thrombocytopenia Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Tooth Disease Turner Syndrome Vein Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Von Willebrand Disease, Type 3 West Syndrome