Informaţii despre

Nume Factor Xiii Deficiency
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Hereditary deficiency of other clotting factors
Clasificare anatomică Malacards Boli de sânge

Vezi şi

Boli A-Z Acquired Hemophilia Acquired Hemophilia a Acute Cor Pulmonale Acute Myocardial Infarction Acute Pulmonary Heart Disease Afibrinogenemia Afibrinogenemia, Congenital Alcohol-Related Birth Defect Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Amaurosis Fugax Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Autoimmune Encephalitis Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Blue Toe Syndrome Budd-Chiari Syndrome Cardiac Rupture Carotid Artery Occlusion Carotid Artery Thrombosis Catastrophic Antiphospholipid Syndrome Cerebral Sinovenous Thrombosis Cerebritis Chronic Myelomonocytic Leukemia Colitis Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Coronary Thrombosis Cryofibrinogenemia Cryptogenic Cirrhosis Disseminated Intravascular Coagulation Dysbaric Osteonecrosis Dysfibrinogenemia Encephalitis Epilepsy 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 Fournier Gangrene Giant Hemangioma Glanzmann Thrombasthenia Glomerulonephritis Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Hepatic Adenomas, Familial Hepatic Veno-Occlusive Disease Hepatitis Hepatitis C Inferior Vena Cava Interruption Inflammatory Bowel Disease Inherited Blood Coagulation Disease Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Ischemic Colitis Korean Hemorrhagic Fever Legg-Calve-Perthes Disease Lemierre's Syndrome Leukemia Livedoid Vasculopathy Liver Cirrhosis Marantic Endocarditis Meningococcemia Myeloid Leukemia Myocardial Infarction Pdgfrb-Associated Chronic Eosinophilic Leukemia Peripheral Vertigo Plasmacytoma Plasminogen Activator Inhibitor-1 Deficiency Polycystic Kidney Disease Portal Vein Thrombosis Post-Thrombotic Syndrome Priapism Protein S Deficiency Prothrombin Deficiency Pulmonary Embolism Purpura Purpura Fulminans Quebec Platelet Disorder Retinal Artery Occlusion Rheumatoid Arthritis Sagittal Sinus Thrombosis Severe Hemophilia a Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sticky Platelet Syndrome Stroke, Ischemic Tetraamelia Syndrome, Autosomal Recessive Thrombocytopenia Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Vaginitis Vein Disease Von Willebrand's Disease Von Willebrand Disease, Type 1