Informaţii despre

Nume Hemoglobin E Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Other haemoglobinopathies
Clasificare anatomică Malacards Boli de sânge; Boli endocrine
Boli din aceeaşi familie Hemoglobin C Disease; Hemoglobin D Disease; Hemoglobin Se Disease

Vezi şi

Boli A-Z Acute Liver Failure Afibrinogenemia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Autosomal Genetic Disease Beta-Thalassemia Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Budd-Chiari Syndrome Central Retinal Vein Occlusion Cerebral Sinovenous Thrombosis Cerebritis Choroiditis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Hemolytic Anemia Cryptogenic Cirrhosis Disseminated Intravascular Coagulation Dysfibrinogenemia Factor V Deficiency Factor Viii Deficiency Factor X Deficiency Fetal Hemoglobin Quantitative Trait Locus 1 Hellp Syndrome Hemoglobin C Disease Hemoglobin D Disease Hemoglobin H Disease Hemoglobin Lepore-Beta-Thalassemia Syndrome Hemoglobinopathy Hemoglobin Se Disease Hemorrhagic Disease Homocysteinemia Hyper Ige Syndrome Hypophosphatemic Bone Disease Intracranial Hypertension Ischemic Colitis Ischemic Optic Neuropathy Kluver-Bucy Syndrome Livedoid Vasculopathy Malignant Essential Hypertension Malignant Secondary Hypertension Nonarteritic Anterior Ischemic Optic Neuropathy Osgood-Schlatter's Disease Paracetamol Poisoning Patent Foramen Ovale Peripheral Vertigo Placental Abruption Pleuropneumonia Polycythemia Porencephaly Portal Vein Thrombosis Post-Thrombotic Syndrome Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Purpura Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Sagittal Sinus Thrombosis Scott Syndrome Sickle Cell Anemia Sickle Cell Disease Sneddon Syndrome Spherocytosis, Type 2 Spinal Cord Infarction Splenic Disease Splenic Infarction Stroke, Ischemic Sudden Sensorineural Hearing Loss Thalassemia Thrombasthenia Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Vein Disease Von Willebrand's Disease