Informaţii despre

Nume Blood Platelet Disease
Pagina Web www.malacards.org
Clasificare anatomică Malacards Blood diseases

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Boli A-Z Acquired Hemophilia Acquired Hemophilia a Acquired Von Willebrand Syndrome Acute Leukemia Acute Myocardial Infarction Adie Pupil Afibrinogenemia Afibrinogenemia, Congenital Alcohol-Related Birth Defect Alpha-2-Plasmin Inhibitor Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amegakaryocytic Thrombocytopenia, Congenital Angina Pectoris Aniridia 1 Anomalous Left Coronary Artery from the Pulmonary Artery Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Autoimmune Disease of Blood Autosomal Dominant Macrothrombocytopenia Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 16 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Protein Disease Blue Toe Syndrome Bombay Phenotype Bone Marrow Cancer Branch Retinal Artery Occlusion Budd-Chiari Syndrome Carotid Artery Thrombosis Catastrophic Antiphospholipid Syndrome Cerebral Arteritis Cerebral Falx Meningioma Cerebral Sinovenous Thrombosis Chediak-Higashi Syndrome Chronic Myelomonocytic Leukemia Cleft Lip Cold Urticaria Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Syphilis Core Binding Factor Acute Myeloid Leukemia Coronary Thrombosis Dengue Hemorrhagic Fever Disseminated Intravascular Coagulation Dyskeratosis Congenita, Autosomal Dominant 6 Early Congenital Syphilis Endocardium Disease Essential Thrombocythemia Evans' Syndrome Exanthema Subitum Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Fetal and Neonatal Alloimmune Thrombocytopenia Fournier Gangrene Genitopatellar Syndrome Giant Hemangioma Glanzmann Thrombasthenia Gray Platelet Syndrome Hairy Cell Leukemia Hantavirus Pulmonary Syndrome Hellp Syndrome Hemarthrosis Hematologic Cancer Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis a Hepatitis D Hypersplenism Immune System Disease Infective Endocarditis Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intestinal Pseudo-Obstruction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemic Colitis Ischemic Optic Neuropathy Korean Hemorrhagic Fever Latent Syphilis Leech Infestation Legg-Calve-Perthes Disease Leukemia Leukemia, Chronic Myeloid Leukocyte Adhesion Deficiency, Type Iii Livedoid Vasculopathy Liver Cirrhosis Lupus Erythematosus Marantic Endocarditis Megakaryocytic Leukemia Mild Hemophilia a Mitral Valve Stenosis Myelofibrosis Myeloid Leukemia Myh-9 Related Disease Nonarteritic Anterior Ischemic Optic Neuropathy Orbital Granuloma Pancytopenia Pdgfrb-Associated Chronic Eosinophilic Leukemia Peripheral Vertigo Platelet Aggregation, Spontaneous Platelet Disorder, Familial, with Associated Myeloid Malignancy Polycythemia Polycythemia Vera Portal Hypertension Portal Vein Thrombosis Post-Thrombotic Syndrome Primary Syphilis Primary Thrombocytopenia Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pseudo-Von Willebrand Disease Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Quebec Platelet Disorder Refractory Anemia Retinal Artery Occlusion Retinal Vascular Occlusion Sagittal Sinus Thrombosis Severe Congenital Neutropenia Severe Hemophilia a Sneddon Syndrome Spinal Cord Infarction Splenic Disease Splenomegaly Sticky Platelet Syndrome Stormorken Syndrome Stroke, Ischemic Sudden Sensorineural Hearing Loss Syphilitic Meningitis Systemic Lupus Erythematosus Tertiary Syphilis Thrombasthenia Thrombocythemia 1 Thrombocytopenia Thrombocytopenia 1 Thrombocytopenia 3 Thrombocytopenia-Absent Radius Syndrome Thrombocytopenia Due to Platelet Alloimmunization Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Varicose Veins Vein Disease Velocardiofacial Syndrome Venous Insufficiency Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Von Willebrand Disease, Type 3 White Platelet Syndrome