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Nume Portal Vein Thrombosis
Pagina Web www.malacards.org
Clasificari ICD10 Portal vein thrombosis
Clasificare anatomică Malacards Blood diseases; Cardiovascular diseases

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Boli A-Z Abdominal Tuberculosis Acanthamoeba Keratitis Actinomycosis Acute Cholangitis Acute Liver Failure Acute Myocardial Infarction Acute Pancreatitis Adenocarcinoma Adenoma Afibrinogenemia, Congenital Aging Alpha-2-Plasmin Inhibitor Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Al-Raqad Syndrome Alveolar Echinococcosis Alzheimer Disease 3 Amaurosis Fugax Anaplastic Large Cell Lymphoma Anauxetic Dysplasia 1 Aneurysm Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Antithrombin Iii Deficiency Appendicitis Argentine Hemorrhagic Fever Arteriovenous Fistula Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Banti's Syndrome Beta-Thalassemia Bile Duct Carcinoma Biliary Atresia 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 Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Branch Retinal Artery Occlusion Budd-Chiari Syndrome Buerger Disease Carotid Artery Occlusion Carotid Artery Thrombosis Carotid Stenosis Catastrophic Antiphospholipid Syndrome Central Retinal Vein Occlusion Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebritis Cerebrovascular Disease Cholangiocarcinoma Cholangitis Cholecystitis Cholelithiasis Chorioangioma Chronic Cholangitis Chronic Venous Insufficiency Colitis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Coronary Thrombosis Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Crohn's Colitis Crohn's Disease Cryptogenic Cirrhosis Cytomegalovirus Infection Disseminated Intravascular Coagulation Dubin-Johnson Syndrome Duodenitis Dysfibrinogenemia Echinococcosis Eclampsia Encephalopathy Endocarditis Endometrial Small Cell Carcinoma Endometrial Stromal Sarcoma Endometriosis Esophageal Varix Essential Thrombocythemia Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Familial Adenomatous Polyposis Fibrinolytic Defect Fournier Gangrene Gastric Cancer Giant Hemangioma Hellp Syndrome Hemoglobin E Disease Hemoglobinuria Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatic Infarction Hepatic Tuberculosis Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis D Hepatocellular Adenoma Hepatocellular Carcinoma Hereditary Spherocytosis Homocysteinemia Homocystinuria Human Coronavirus Sensitivity Hypereosinophilic Syndrome Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Immune System Disease Infective Endocarditis Inferior Vena Cava Interruption Inflammatory Bowel Disease Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Intrahepatic Cholangiocarcinoma Ischemia Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Leech Infestation Legg-Calve-Perthes Disease Lemierre's Syndrome Leukemia Livedoid Vasculopathy Liver Cirrhosis Liver Disease Lupus Erythematosus Lymphadenitis Lymphoma Macrophage Activation Syndrome Marantic Endocarditis May-Thurner Syndrome Melioidosis Meningococcemia Mesenteric Lymphadenitis Mesenteric Vascular Occlusion Mitral Valve Stenosis Morbid Obesity Myelofibrosis Myeloid Leukemia Myeloproliferative Neoplasm Myocardial Infarction Myopathy Neonatal Stroke Nephrotic Syndrome Nodular Regenerative Hyperplasia Nonarteritic Anterior Ischemic Optic Neuropathy Obstructive Jaundice Osteonecrosis Pancreatic Cancer Pancreatitis Pancytopenia Papilledema Paracetamol Poisoning Parametritis Paroxysmal Nocturnal Hemoglobinuria Patent Foramen Ovale Pelvic Inflammatory Disease Peripheral Vertigo Peritonitis Persistent Idiopathic Facial Pain Placenta Disease Placental Abruption Platelet Aggregation, Spontaneous Polycythemia Polycythemia Vera Porencephaly Portal Hypertension Post-Thrombotic Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Primitive Portal Vein Thrombosis Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Psoriasis Psoriasis 13 Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Quebec Platelet Disorder Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Pigmentosa and Erythrocytic Microcytosis Sagittal Sinus Thrombosis Sarcoma Schistosomiasis Schizencephaly Scott Syndrome Severe Pre-Eclampsia Sickle Cell Disease Sneddon Syndrome Spinal Cord Infarction Splenic Infarction Splenomegaly Spondyloocular Syndrome Sticky Platelet Syndrome Stormorken Syndrome Stroke, Ischemic Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Systemic Lupus Erythematosus Systemic Mastocytosis Testicular Infarct Tetralogy of Fallot Thalassemia Thrombasthenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Tuberous Sclerosis Turner Syndrome Ulcerative Colitis Varicose Veins Vascular Disease Vein Disease Venous Insufficiency Visceral Myopathy Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Wandering Spleen X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome