Informaţii despre

Nume Factor X Deficiency
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; 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 Acquired Von Willebrand Syndrome Acute Liver Failure Acute Myocardial Infarction Adie Pupil Adrenal Cortical Hypofunction Afibrinogenemia Afibrinogenemia, Congenital Aging Al Amyloidosis Alcohol-Related Birth Defect Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Amyloidosis, Familial Visceral Androgen Insensitivity Syndrome, Mild Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Antithrombin Iii Deficiency Arthrochalasia Ehlers-Danlos Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Branch Retinal Artery Occlusion Budd-Chiari Syndrome Burns Cardiac Tamponade Carotid Artery Thrombosis Catastrophic Antiphospholipid Syndrome Central Retinal Vein Occlusion Cerebral Falx Meningioma Cerebral Sinovenous Thrombosis Chromosome 13q Duplication Congenital Disorder of Glycosylation, Type Ia Coronary Thrombosis Cryptogenic Cirrhosis Diffuse Lymphatic Malformation Disseminated Intravascular Coagulation Dysfibrinogenemia Encephalopathy Esophageal Varix Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Femoral Neuropathy Fournier Gangrene Fragile X Syndrome Giant Hemangioma Glanzmann Thrombasthenia Glomerulonephritis Goblet Cell Carcinoid Hantavirus Pulmonary Syndrome Hellp Syndrome Hemarthrosis Hemoglobin E Disease 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 Hepatitis a Homocysteinemia Homocystinuria Hypercholesterolemia, Autosomal Dominant, 3 Hypertrophic Cardiomyopathy Immune System Disease Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemic Colitis Ischemic Optic Neuropathy Keratomalacia Kindler Syndrome Korean Hemorrhagic Fever Leech Infestation Legg-Calve-Perthes Disease Leukemia Livedoid Vasculopathy Liver Disease Lymphoma Marantic Endocarditis Membranoproliferative Glomerulonephritis Mesenteric Vascular Occlusion Mild Hemophilia a Mucositis Nephrotic Syndrome Nonarteritic Anterior Ischemic Optic Neuropathy Osteomyelitis Paracetamol Poisoning Patent Foramen Ovale Peripheral Vertigo Peritonitis Placenta Disease Placental Abruption Platelet Aggregation, Spontaneous Pneumonia Porencephaly Portal Vein Thrombosis Post-Thrombotic Syndrome Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Quebec Platelet Disorder Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Sagittal Sinus Thrombosis Scott Syndrome Severe Hemophilia a Sneddon Syndrome Spinal Cord Infarction Spindle Cell Thymoma Spondylocarpotarsal Synostosis Syndrome Sticky Platelet Syndrome Stroke, Ischemic Sudden Sensorineural Hearing Loss Thrombasthenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thymoma Transitional Cell Carcinoma Varicose Veins Vein Disease Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2