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Nume Protein C Deficiency
Pagina Web
Clasificare globală Malacards Boli rare
Clasificare anatomică Malacards Boli de sânge

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Boli A-Z Acquired Hemophilia Acquired Hemophilia a Acute Leukemia Acute Liver Failure Acute Myocardial Infarction Afibrinogenemia Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 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 Amaurosis Fugax Androgen Insensitivity Syndrome, Mild Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Antithrombin Iii Deficiency Arteries, Anomalies of Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Banti's Syndrome Beta-Thalassemia Bilateral Massive Adrenal Hemorrhage Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Protein Disease Blue Toe Syndrome Brain Injury Branch Retinal Artery Occlusion Breast Cancer Budd-Chiari Syndrome Buerger Disease Calciphylaxis Cardiac Tamponade Carotid Artery Occlusion Catastrophic Antiphospholipid Syndrome Central Retinal Vein Occlusion Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebritis Chickenpox Ciliary Dyskinesia, Primary, 1 Colitis Colorectal Cancer Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Ia Connective Tissue Disease Coronary Thrombosis Cryptogenic Cirrhosis Diffuse Lymphatic Malformation Disseminated Intravascular Coagulation Down Syndrome Dysfibrinogenemia Eclampsia Esophageal Varix Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Fournier Gangrene Giant Hemangioma Haemophilus Influenzae Hellp Syndrome Hemangioma Hematopoietic Stem Cell Transplantation Hemoglobin E Disease Hemolytic Anemia Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatitis C Hereditary Spherocytosis Homocysteinemia Homocystinuria Hydrocephalus Hydronephrosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Inferior Vena Cava Interruption Influenza Inherited Blood Coagulation Disease Interstitial Lung Disease Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Jacobsen Syndrome Kidney Papillary Necrosis Kindler Syndrome Leech Infestation Legg-Calve-Perthes Disease Leukemia Leukemia, Acute Myeloid Leukocoria Livedoid Vasculopathy Liver Disease Lung Disease Lymphoma Marantic Endocarditis Meningitis Meningococcemia Mesenteric Vascular Occlusion Mixed Connective Tissue Disease Monocytic Leukemia Moyamoya Disease 1 Muscular Dystrophy Myeloid Leukemia Myocardial Infarction Myotonic Dystrophy Nasopharyngitis Neonatal Stroke Neurodegeneration with Brain Iron Accumulation 2a Nonarteritic Anterior Ischemic Optic Neuropathy Osteonecrosis Pancreatitis Paracetamol Poisoning Patent Foramen Ovale Peripheral Artery Disease Peripheral Vertigo Persistent Hyperplastic Primary Vitreous Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Placenta Disease Placental Abruption Plasminogen Deficiency, Type I Porencephaly Portal Hypertension Portal Hypertension, Noncirrhotic Portal Vein Thrombosis Post-Thrombotic Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Premature Chromatid Separation Trait Priapism Protein-Losing Enteropathy Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Pulmonary Hypertension Purpura Purpura Fulminans Pyruvate Carboxylase Deficiency Renal Glucosuria Respiratory Syncytial Virus Infectious Disease Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Sagittal Sinus Thrombosis Schistosomiasis Schizencephaly Scott Syndrome Septic Arthritis Sneddon Syndrome Spinal Cord Infarction Splenic Infarction Sticky Platelet Syndrome Stroke, Ischemic Stuttering Sudden Sensorineural Hearing Loss Surfactant Metabolism Dysfunction, Pulmonary, 2 Tetraamelia Syndrome, Autosomal Recessive Thalassemia Thoracoabdominal Syndrome Thrombasthenia Thrombocytopenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Protein C Deficiency, Autosomal Recessive Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Tuberous Sclerosis Ulcerative Colitis Valproate Embryopathy Varicose Veins Vein Disease Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease