Informaţii despre

Nume Budd-Chiari Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Budd-Chiari syndrome
Clasificare anatomică Malacards Boli cardiovasculare; Boli de sânge; Boli hepatice

Vezi şi

Boli A-Z Acanthamoeba Keratitis Acquired Hemophilia Acquired Hemophilia a Acute Leukemia Acute Liver Failure Acute Promyelocytic Leukemia Adrenal Neuroblastoma Afibrinogenemia Afibrinogenemia, Congenital Aging Al Amyloidosis Alcoholic Liver Cirrhosis 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 Al-Raqad Syndrome Alveolar Echinococcosis Amaurosis Fugax Amyloidosis Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Antiphospholipid Syndrome Antithrombin Iii Deficiency Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Atypical Chronic Myeloid Leukemia Autoimmune Hepatitis Autosomal Dominant Polycystic Kidney Disease Blood Coagulation Disease Blood Group--Ahonen Blood Group, I System Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Bone Marrow Cancer Branch Retinal Artery Occlusion Buerger Disease Castleman Disease Catastrophic Antiphospholipid Syndrome Cavernous Hemangioma Celiac Disease 1 Central Retinal Vein Occlusion Cerebral Falx Meningioma Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebritis Cholangiocarcinoma Churg-Strauss Syndrome Cirrhotic Cardiomyopathy Cogan Syndrome Colitis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Conjunctivitis Coronary Thrombosis Cor Triatriatum Cryptogenic Cirrhosis Disseminated Intravascular Coagulation Dysfibrinogenemia Echinococcosis Eclampsia Encephalopathy Endocarditis Endomyocardial Fibrosis Endotheliitis Epithelioid Hemangioendothelioma 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 Mediterranean Fever Fournier Gangrene Giant Hemangioma Hantavirus Pulmonary Syndrome Hellp Syndrome Hemangioendothelioma Hemangioma Hemoglobin E Disease Hemoglobinuria Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Encephalopathy Hepatic Infarction Hepatic Tuberculosis Hepatic Vascular Disease Hepatitis Hepatitis a Hepatitis C Hepatocellular Carcinoma Hepatopulmonary Syndrome Hereditary Antithrombin Deficiency Heterotaxy Heterotaxy, Visceral, 1, X-Linked Homocysteinemia Homocystinuria Hypereosinophilic Syndrome Hypereosinophilic Syndrome, Idiopathic Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Immune System Disease Inferior Vena Cava Interruption Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Intrahepatic Cholangiocarcinoma Intravenous Leiomyomatosis Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Korean Hemorrhagic Fever Leech Infestation Legg-Calve-Perthes Disease Leiomyomatosis Leiomyosarcoma Leishmaniasis Leukemia Livedoid Vasculopathy Liver Cirrhosis Liver Disease Loeffler Endocarditis Lupus Erythematosus Marantic Endocarditis May-Thurner Syndrome Melanoma Mesenteric Vascular Occlusion Multicentric Castleman Disease Myelofibrosis Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 Myeloproliferative Neoplasm Neuroblastoma Neuroendocrine Tumor Nodular Regenerative Hyperplasia Nonarteritic Anterior Ischemic Optic Neuropathy Obstructive Jaundice Ocular Melanoma Omphalocele Osteonecrosis Papilledema Paracetamol Poisoning Parametritis Paroxysmal Nocturnal Hemoglobinuria Patent Ductus Venosus Patent Foramen Ovale Pdgfra-Associated Chronic Eosinophilic Leukemia Peripheral Vertigo Placenta Disease Placental Abruption Plasmacytoma Polyarteritis Nodosa Polycystic Kidney Disease Polycystic Liver Disease Polycythemia Polycythemia Vera Porencephaly Portal Hypertension Portal Vein Thrombosis Post-Thrombotic Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Primary Hypereosinophilic Syndrome Primitive Portal Vein Thrombosis Protein C Deficiency Protein-Losing Enteropathy Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Refractory Anemia Relapsing Polychondritis Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Sagittal Sinus Thrombosis Sarcoidosis 2 Severe Hemophilia a Severe Pre-Eclampsia Sm-Ahnmd Sneddon Syndrome Spinal Cord Infarction Splenic Infarction Splenomegaly Sticky Platelet Syndrome Stroke, Ischemic Sudden Sensorineural Hearing Loss Systemic Lupus Erythematosus Systemic Mastocytosis Thalassemia Thrombasthenia Thrombocythemia 1 Thrombocytopenia Thrombocytopenia-Absent Radius Syndrome Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombophlebitis Migrans Thrombosis Trichohepatoenteric Syndrome 1 Ulcerative Colitis Undifferentiated Pleomorphic Sarcoma Varicose Veins Vein Disease Visceral Leishmaniasis Von Willebrand's Disease Von Willebrand Disease, Type 1 Xanthomatosis