Informaţii despre

Nume Factor Xii Deficiency
Pagina Web www.malacards.org
Clasificare globală Malacards Genetic diseases; Rare diseases
Clasificari ICD10 Hereditary deficiency of other clotting factors
Clasificare anatomică Malacards Blood diseases

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Boli A-Z Abducens Nerve Disease Acanthamoeba Keratitis Acquired Hemophilia Acquired Hemophilia a Afibrinogenemia, Congenital Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Arthrochalasia Ehlers-Danlos Syndrome Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, I System Blue Toe Syndrome Branch Retinal Artery Occlusion Budd-Chiari Syndrome Carotid Artery Occlusion Catastrophic Antiphospholipid Syndrome Central Retinal Vein Occlusion Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 Cerebral Sinovenous Thrombosis Cerebritis Chediak-Higashi Syndrome Cluster Headache Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Ia Coronary Thrombosis Disseminated Intravascular Coagulation Dysfibrinogenemia Factor V Deficiency Factor Vii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xiii Deficiency Fournier Gangrene Giant Hemangioma Glanzmann Thrombasthenia Gout Headache Hellp Syndrome Hemolytic-Uremic Syndrome Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatic Infarction Hepatic Veno-Occlusive Disease Hereditary Spastic Paraplegia Homocystinuria Immune System Disease Inherited Blood Coagulation Disease Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemic Colitis Ischemic Optic Neuropathy Korean Hemorrhagic Fever Leech Infestation Legg-Calve-Perthes Disease Livedoid Vasculopathy Lupus Erythematosus Marantic Endocarditis May-Thurner Syndrome Meningococcemia Myocardial Infarction Nephrotic Syndrome Neuritis Nonarteritic Anterior Ischemic Optic Neuropathy Paraplegia Patent Foramen Ovale Peripheral Vertigo Pharyngitis Placenta Disease Placental Abruption Portal Vein Thrombosis Post-Thrombotic Syndrome Pregnancy Loss, Recurrent 1 Prekallikrein Deficiency Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Purpura Purpura Fulminans Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Rosai-Dorfman Disease Sagittal Sinus Thrombosis Severe Pre-Eclampsia Sneddon Syndrome Spasticity Spinal Cord Infarction Sticky Platelet Syndrome Stroke, Ischemic Sudden Sensorineural Hearing Loss Systemic Lupus Erythematosus Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Vein Disease Von Willebrand's Disease