Informaţii despre

Nume Protein S Deficiency
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificare anatomică Malacards Boli de sânge

Vezi şi

Boli A-Z Acanthamoeba Keratitis Acquired Hemophilia Acquired Hemophilia a Acquired Immunodeficiency Syndrome Acute Liver Failure Acute Myocardial Infarction Acute Pancreatitis Afibrinogenemia Afibrinogenemia, Congenital Aging Agraphia Alcohol-Related Birth Defect Alexia 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 Anca-Associated Vasculitis Aneurysm Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Antithrombin Iii Deficiency Aphasia Arteriovenous Fistula Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthritis 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 Buerger Disease Calciphylaxis Carotid Artery Occlusion Carotid Stenosis Catastrophic Antiphospholipid Syndrome Cellulitis Central Retinal Artery Occlusion Central Retinal Vein Occlusion Cerebral Falx Meningioma Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebritis Chickenpox Colitis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congestive Heart Failure Connective Tissue Disease Coronary Thrombosis Cryptogenic Cirrhosis Cutaneous T Cell Lymphoma Cytomegalovirus Infection Dermatitis Diffuse Lymphatic Malformation Disseminated Intravascular Coagulation Dysfibrinogenemia Eclampsia Endocarditis Endotheliitis End Stage Renal Failure Epilepsy Esophageal Varix Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Femoral Neuropathy Fournier Gangrene Giant Hemangioma Graves' Disease Hantavirus Pulmonary Syndrome Headache Hellp Syndrome Hemiplegia Hemoglobin E Disease Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis a Hereditary Spherocytosis Homocysteinemia Homocystinuria Hyperparathyroidism Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Idiopathic Hemiconvulsion-Hemiplegia Syndrome Immune System Disease Infective Endocarditis Inferior Vena Cava Interruption Inflammatory Bowel Disease Inherited Blood Coagulation Disease Intermittent Claudication Interstitial Nephritis Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemia Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Korean Hemorrhagic Fever Lateral Sinus Thrombosis Leech Infestation Legg-Calve-Perthes Disease Leukemia Livedoid Vasculopathy Lupus Erythematosus Lymphoma Marantic Endocarditis May-Thurner Syndrome Mesenteric Vascular Occlusion Metal Allergy Mixed Connective Tissue Disease Moyamoya Disease 1 Myocardial Infarction Nephrotic Syndrome Neuropathy Nodular Regenerative Hyperplasia Nonarteritic Anterior Ischemic Optic Neuropathy Osteonecrosis Pancreatitis Papilledema Paracetamol Poisoning Patent Foramen Ovale Peripheral Vertigo Peritonitis Phaeochromocytoma Phelan-Mcdermid Syndrome Placenta Disease Placental Abruption Pneumonia Porencephaly Portal Hypertension Portal Vein Thrombosis Post-Thrombotic Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Priapism Protein C Deficiency Protein-Losing Enteropathy Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Pulmonary Hypertension Pulmonary Tuberculosis Purpura Purpura Fulminans Qualitative Platelet Defect Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vasculitis Retinal Vein Occlusion Retinitis Rheumatoid Arthritis Sagittal Sinus Thrombosis Schizencephaly Scott Syndrome Severe Hemophilia a Severe Pre-Eclampsia Sickle Cell Anemia Sickle Cell Disease Sneddon Syndrome Spasticity Spastic Paraparesis Spinal Cord Infarction Splenic Disease Splenic Infarction Sticky Platelet Syndrome Stroke, Ischemic Sudden Sensorineural Hearing Loss Systemic Lupus Erythematosus Testicular Infarct Thrombasthenia Thrombocytopenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Toxoplasmoză Tropical Spastic Paraparesis Ulcerative Colitis Varicose Veins Vasculitis Vein Disease Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1