Informaţii despre

Nume Hemoglobinuria
Pagina Web www.malacards.org
Clasificari ICD10 Haemoglobinuria; Haemoglobinuria due to haemolysis from other external causes
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge; Boli nefrologice (ale rinichilor)

Vezi şi

Boli A-Z Aarskog-Scott Syndrome Ablepharon-Macrostomia Syndrome Acquired Angioedema Acute Hemorrhagic Conjunctivitis Acute Kidney Tubular Necrosis Acute Leukemia Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Acute Myocardial Infarction Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Anemia, Autoimmune Hemolytic Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Aplastic Anemia Arthrochalasia Ehlers-Danlos Syndrome Blackwater Fever Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bornholm Eye Disease Brain Small Vessel Disease with or Without Ocular Anomalies Budd-Chiari Syndrome Burkitt Lymphoma Cardiomyopathy, Familial Hypertrophic, 1 Central Retinal Artery Occlusion Central Retinal Vein Occlusion Cerebellar Degeneration-Related Autoantigen 3 Cerebritis Cholangitis Chronic Graft Versus Host Disease Complement Deficiency Complement Factor I Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Congenital Syphilis Dense Deposit Disease Disseminated Intravascular Coagulation Duodenal Obstruction Duodenitis Dystonia Encephalopathy Endotheliitis End Stage Renal Failure Eosinophilic Fasciitis Evans' Syndrome Extrinsic Allergic Alveolitis Fanconi Syndrome Fasciitis Glucose Phosphate Isomerase Deficiency Glycosylphosphatidylinositol Deficiency Graft-Versus-Host Disease Hematopoietic Stem Cell Transplantation Hemoglobinemia Hemolytic Anemia Hemolytic Anemia, Cd59-Mediated, with or Without Immune-Mediated Polyneuropathy Hemolytic-Uremic Syndrome Hemosiderosis Heparin-Induced Thrombocytopenia Hepatic Encephalopathy Hepatitis Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hereditary Spherocytosis Hereditary Wilms' Tumor Hypercoagulability Syndrome Due to Glycosylphosphatidylinositol Deficiency Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Inherited Bone Marrow Failure Syndromes Interstitial Nephritis Intestinal Perforation Intracranial Embolism Ischemia Lactic Acidosis Large Granular Lymphocyte Leukemia Latent Syphilis Leukemia Localized Scleroderma Lupus Erythematosus Lymphoblastic Leukemia Lymphocytes Absent Lymphoma Lymphoplasmacytic Lymphoma Malaria Mirage Syndrome Monocytic Leukemia Moyamoya Disease 1 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloma, Multiple Myeloproliferative Neoplasm Myocardial Infarction Myoglobinuria Myoglobinuria, Acute Recurrent, Autosomal Recessive Necrobiotic Xanthogranuloma Necrotizing Fasciitis Neutropenia Non-a-E Hepatitis Non-Involuting Congenital Hemangioma Obstructive Jaundice Osteomyelitis Pancreatitis, Hereditary Pancytopenia Papilledema Papillon-Lefevre Syndrome Paroxysmal Cold Hemoglobinuria Paroxysmal Nocturnal Hemoglobinuria Paroxysmal Nocturnal Hemoglobinuria 1 Patent Foramen Ovale Plasminogen Deficiency, Type I Plasmodium Falciparum Malaria Pneumonia Portal Hypertension Portal Vein Thrombosis Potocki-Lupski Syndrome Primary Lateral Sclerosis, Adult, 1 Properdin Deficiency Properdin Deficiency, X-Linked Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Purpura Rapp-Hodgkin Syndrome Refractory Anemia Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Sagittal Sinus Thrombosis Sickle Cell Disease Siderosis Spasticity Spastic Paraparesis Splenic Infarction Sveinsson Chorioretinal Atrophy Syphilis Systemic Lupus Erythematosus Temporal Arteritis Thalassemia Thrombocytopenia Thrombocytosis Thrombosis Thrombotic Thrombocytopenic Purpura Thymoma Treacher Collins Syndrome 1 Tropical Spastic Paraparesis