Informaţii despre

Nume Hemorrhagic Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Haemorrhagic condition, unspecified; Haemorrhagic disorder due to circulating anticoagulants
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge
Boli din aceeaşi familie Hemorrhagic Disease Due to Alpha-1-Antitrypsin Pittsburgh Mutation

Vezi şi

Boli A-Z Acquired Hemophilia Acquired Hemophilia a Acquired Thrombocytopenia Acquired Von Willebrand Syndrome Acute Cor Pulmonale Acute Liver Failure Acute Myocardial Infarction Acute Pulmonary Heart Disease Afibrinogenemia Afibrinogenemia, Congenital Alcohol-Related Birth Defect Alpha-1-Antitrypsin Deficiency Alpha-2-Plasmin Inhibitor Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Amaurosis Fugax Amegakaryocytic Thrombocytopenia, Congenital Angel-Shaped Phalangoepiphyseal Dysplasia Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Antiphospholipid Syndrome Antithrombin Iii Deficiency Argentine Hemorrhagic Fever Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Aspirin Resistance Autoimmune Disease of Blood Autosomal Dominant Macrothrombocytopenia Basilar Artery Occlusion Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 11 Bleeding Disorder, Platelet-Type, 16 Blood Coagulation Disease Blood Group--Ahonen Blood Group, I System Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Bombay Phenotype Branch Retinal Artery Occlusion Brittle Bone Disorder Budd-Chiari Syndrome Cardiac Tamponade Carotid Artery Occlusion Carotid Artery Thrombosis Catastrophic Antiphospholipid Syndrome Central Retinal Vein Occlusion Central Serous Chorioretinopathy Cerebral Falx Meningioma Cerebral Sinovenous Thrombosis Chikungunya Cold Urticaria Congenital Cytomegalovirus Congenital Disorder of Glycosylation, Type Ia Coronary Thrombosis Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cryptogenic Cirrhosis Cytomegalovirus Infection Diarrhea Disseminated Intravascular Coagulation Dysfibrinogenemia Dyskeratosis Congenita, Autosomal Dominant 6 Eclampsia Eisenmenger Syndrome Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Endotheliitis Erythromelalgia Essential Thrombocythemia Exanthem Factor V and Factor Viii, Combined Deficiency of, 2 Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Fanconi Anemia, Complementation Group E Fetal and Neonatal Alloimmune Thrombocytopenia Fetal Hydantoin Syndrome Fibrinolytic Defect Fournier Gangrene Giant Hemangioma Glanzmann Thrombasthenia Hellp Syndrome Hemarthrosis Hemoglobin E Disease Hemolytic-Uremic Syndrome Hemophilia Hemophilia a Hemophilia B Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Homocysteinemia Hyperheparinemia Hypersplenism Immune System Disease Infective Endocarditis Inferior Vena Cava Interruption Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemic Colitis Ischemic Optic Neuropathy Kindler Syndrome Korean Hemorrhagic Fever Leech Infestation Legg-Calve-Perthes Disease Lemierre's Syndrome Livedoid Vasculopathy Liver Cirrhosis Liver Disease Lymphocytic Choriomeningitis Macular Dystrophy, Retinal, 1, North Carolina Type Malignant Dermis Tumor Malignant Skin Fibrous Histiocytoma Marantic Endocarditis Megakaryocytic Leukemia Meningococcemia Mercury Poisoning Mesenteric Vascular Occlusion Mild Hemophilia a Mucositis Multiple Mitochondrial Dysfunctions Syndrome 5 Myocardial Infarction Neuroblastoma Nonarteritic Anterior Ischemic Optic Neuropathy Noonan Syndrome 1 Noonan Syndrome 2 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy Osteonecrosis Papillomatosis, Confluent and Reticulated Paracetamol Poisoning Patent Foramen Ovale Peripheral Vertigo Placenta Disease Placental Abruption Plasminogen Activator Inhibitor-1 Deficiency Platelet Aggregation, Spontaneous Polycythemia Polycythemia Vera Porencephaly Portal Hypertension Portal Vein Thrombosis Postaxial Acrofacial Dysostosis Post-Thrombotic Syndrome Primary Thrombocytopenia Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pseudo-Von Willebrand Disease Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Quebec Platelet Disorder Renal Glucosuria Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Rett Syndrome Sagittal Sinus Thrombosis Sarcoma Scott Syndrome Severe Hemophilia a Severe Hemophilia B Shwartzman Phenomenon Sneddon Syndrome Spinal Cord Infarction Splenic Disease Splenomegaly Spotted Fever Sticky Platelet Syndrome Stroke, Ischemic Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Thrombasthenia Thrombocythemia 1 Thrombocytopenia Thrombocytopenia 3 Thrombocytopenia-Absent Radius Syndrome Thrombocytopenia Due to Platelet Alloimmunization Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Trichothiodystrophy 4, Nonphotosensitive Unilateral Absence of a Pulmonary Artery Uveitis Varicose Veins Vein Disease Venous Insufficiency Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Von Willebrand Disease, Type 3