Informaţii despre

Nume Factor Vii 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 Afibrinogenemia Afibrinogenemia, Congenital Aging Alcohol-Related Birth Defect Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aneurysm Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Antiphospholipid Syndrome Antithrombin Iii Deficiency Aortic Aneurysm Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Atrial Fibrillation Beckwith-Wiedemann Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Blue Toe Syndrome Budd-Chiari Syndrome Cardiac Tamponade Carotid Artery Thrombosis Cerebral Aneurysms Cerebral Falx Meningioma Cerebral Sinovenous Thrombosis Cerebritis Chiari Malformation Chromosomal Triplication Colorectal Cancer Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Conjunctivitis Craniosynostosis Disseminated Intravascular Coagulation Dubin-Johnson Syndrome Dysfibrinogenemia Epilepsy Factor V Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Familial Mediterranean Fever Femoral Neuropathy Fournier Gangrene Giant Hemangioma Gilbert Syndrome Glanzmann Thrombasthenia Hantavirus Pulmonary Syndrome Hemarthrosis Hematopoietic Stem Cell Transplantation Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hereditary Spastic Paraplegia Homocystinuria Hypertrophic Cardiomyopathy Inherited Blood Coagulation Disease Intestinal Impaction Intracranial Embolism Intracranial Thrombosis Leech Infestation Leukemia Liposarcoma Malaria Marfan Syndrome Mesenteric Vascular Occlusion Mild Hemophilia a Mucopolysaccharidosis-Plus Syndrome Mucositis Myeloid Leukemia Nephrotic Syndrome Paracetamol Poisoning Paraplegia 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 Red Cell Phospholipid Defect with Hemolysis Retinal Artery Occlusion Retinitis Retroperitoneal Fibrosis Sagittal Sinus Thrombosis Scoliosis Scott Syndrome Severe Hemophilia a Severe Hemophilia B Spasticity Sveinsson Chorioretinal Atrophy Thrombasthenia Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Undifferentiated Pleomorphic Sarcoma Vaginitis Vasculitis Vein Disease Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Wilms Tumor 6 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome