Informaţii despre

Nume Hemolytic Anemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Haemolytic anaemias
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge
Boli din aceeaşi familie Anemia, Autoimmune Hemolytic; Congenital Hemolytic Anemia; Hemolytic Anemia Due to Erythrocyte Adenosine Deaminase Overproduction

Vezi şi

Boli A-Z 6-Phosphogluconate Dehydrogenase Deficiency Abdominal Tuberculosis Acalculous Cholecystitis Achalasia Acquired Angioedema Acquired Hemophilia Acquired Von Willebrand Syndrome Acute Disseminated Encephalomyelitis Acute Generalized Exanthematous Pustulosis Acute Leukemia Acute Lymphocytic Leukemia Acute Pancreatitis Acute Respiratory Distress Syndrome Adenocarcinoma Adie Pupil Aging Aland Island Eye Disease Albinism Alcoholic Hepatitis Alopecia Alopecia Areata Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Thalassemia Alport Syndrome, X-Linked Al-Raqad Syndrome Anaplastic Large Cell Lymphoma Anemia, Autoimmune Hemolytic Anemia, Congenital Dyserythropoietic, Type Ia Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency Angel-Shaped Phalangoepiphyseal Dysplasia Angioedema Angioimmunoblastic T-Cell Lymphoma Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Aplastic Anemia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Aseptic Meningitis Aspergillosis Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Atrioventricular Septal Defect Atrophic Gastritis Autoimmune Disease Autoimmune Hemolytic Anemia, Warm Type Autoimmune Hepatitis Autoimmune Lymphoproliferative Syndrome, Type V Autoimmune Pancreatitis Babesiosis B-Cell Expansion with Nfkb and T-Cell Anergy B-Cell Lymphomas B Cell Prolymphocytic Leukemia Beta-Thalassemia Blastic Plasmacytoid Dendritic Cell Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, Gerbich System Blood Group Incompatibility Blood Group, I System Breast Cancer Bronchopneumonia Brucellosis Burkitt Lymphoma Burns Candidiasis Capillary Leak Syndrome Cartilage-Hair Hypoplasia Castleman Disease Catastrophic Antiphospholipid Syndrome Cavernous Hemangioma Chickenpox Cholangitis Cholecystitis Cholelithiasis Cholestasis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chorioangioma Chronic Eosinophilic Leukemia Chronic Graft Versus Host Disease Chronic Mucocutaneous Candidiasis Chronic Pyelonephritis Churg-Strauss Syndrome Cleft Mitral Valve Clostridium Perfringens Infection Cold Agglutinin Disease Colitis Colon Adenocarcinoma Common Variable Immunodeficiency Complement Factor H Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Congenital Dyserythropoietic Anemia Congenital Hemolytic Anemia Congenital Nonspherocytic Hemolytic Anemia Congenital Rubella Connective Tissue Disease Cor Triatriatum Crescentic Glomerulonephritis Crohn's Colitis Crohn's Disease Cutaneous Anthrax Cystic Fibrosis Cytomegalic Inclusion Disease Cytomegalovirus Infection Dementia De Novo Thrombotic Microangiopathy After Kidney Transplantation Dermatomyositis Dermoid Cyst Diabetes Mellitus Diffuse Alveolar Hemorrhage Diffuse Large B-Cell Lymphoma Digeorge Syndrome Diphtheria Disseminated Intravascular Coagulation Down Syndrome Drug-Induced Autoimmune Hemolytic Anemia Dysgammaglobulinemia Dyskeratosis Congenita Echo Virus 11 Sensitivity Eclampsia Encephalopathy Endocarditis Endotheliitis Enteropathy-Associated T-Cell Lymphoma Eosinophilic Fasciitis Erythema Infectiosum Evans' Syndrome Extrinsic Allergic Alveolitis Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Familial Drusen Fasciitis Fascioliasis Fetal Erythroblastosis Fibrillary Glomerulonephritis Gallbladder Disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to Gardner-Diamond Syndrome Gastric Adenocarcinoma Gastric Cancer Gastritis Germ Cells Tumors Gerstmann-Straussler Disease Giant Hemangioma Gilbert Syndrome Gingival Overgrowth Gingivitis Glioma Glomerulonephritis Glucosephosphate Dehydrogenase Deficiency Glucosephosphate Isomerase Deficiency Glucose Phosphate Isomerase Deficiency Glutathione Peroxidase Deficiency Glutathione Synthetase Deficiency Glycogen Storage Disease Xii Graft-Versus-Host Disease Granulocytopenia Graves' Disease Hairy Cell Leukemia Hansen's Disease Heinz Body Anemias Hellp Syndrome Hemangioma Hemangioma-Thrombocytopenia Syndrome Hematopoietic Stem Cell Transplantation Hemoglobin C Disease Hemoglobinemia Hemoglobin H Disease Hemoglobinopathy Hemoglobinuria Hemolytic Anemia, Nonspherocytic, Due to Hexokinase Deficiency Hemolytic-Uremic Syndrome Hemophagocytic Lymphohistiocytosis Hemophilia Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hepatitis a Hepatitis C Hepatitis C Virus Hepatitis E Hepatocellular Carcinoma Hepatosplenic T-Cell Lymphoma Hereditary Elliptocytosis Hereditary Spherocytosis Herpetiform Pemphigus Histiocytic Sarcoma Histiocytosis Histoplasmosis Human Coronavirus Sensitivity Hydrocephalus Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hypercoagulability Syndrome Due to Glycosylphosphatidylinositol Deficiency Hypersensitivity Reaction Type Iii Disease Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperuricemia Hypogonadotropic Hypogonadism 1 with or Without Anosmia Hypokalemia Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatemia Hypotonia Igg4-Related Sclerosing Cholangitis Immunodeficiency 20 Immunoglobulin a Deficiency 1 Immunoglobulin Alpha Deficiency Immunoglobulin E Concentration, Serum Inflammatory Bowel Disease Inflammatory Bowel Disease 1 Influenza Interstitial Nephritis Intestinal Tuberculosis Intracranial Hypertension Intracranial Hypotension Intravascular Large B-Cell Lymphoma Invasive Aspergillosis Ischemia Kawasaki Disease Kernicterus Large Granular Lymphocyte Leukemia Larsen Syndrome Leiomyosarcoma Leishmaniasis Leukemia Liver Cirrhosis Liver Disease Lung Cancer Lung Disease Lung Papillary Adenocarcinoma Lupus Erythematosus Lyme Disease Lymphadenitis Lymphoblastic Leukemia Lymphocytic Choriomeningitis Lymphoma Lymphosarcoma Macroglobulinemia Malaria Malignant Hypertension Malignant Spiradenoma Marden-Walker Syndrome Meckel Syndrome, Type 1 Megaloblastic Anemia Meningitis Menkes Disease Metabolic Acidosis Methemoglobinemia Methemoglobinemia, Beta-Globin Type Microcephaly, Epilepsy, and Diabetes Syndrome Mitochondrial Dna Depletion Syndrome 4a Mitral Valve Insufficiency Mixed Connective Tissue Disease Mixed-Type Autoimmune Hemolytic Anemia Monocytic Leukemia Mowat-Wilson Syndrome Mucopolysaccharidosis, Type Vii Mucositis Multicentric Castleman Disease Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Multiple Sclerosis Myasthenia Gravis Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloma, Multiple Myocardial Infarction Myoglobinuria Myoglobinuria, Acute Recurrent, Autosomal Recessive Myopathy Myositis Neonatal Anemia Neonatal Autoimmune Hemolytic Anemia Neonatal Jaundice Nephrosclerosis Neuromyelitis Optica Neuromyelitis Optica Spectrum Disorder Neuropathy Neutropenia Nicolaides-Baraitser Syndrome Nocardiosis Nodular Lymphocyte Predominant Hodgkin Lymphoma Nonseminomatous Germ Cell Tumor Obstructive Jaundice Optic Pathway Glioma Ovarian Cancer Ovarian Cyst Ovarian Lymphoma Pancreatic Cancer Pancreatitis Pancytopenia Panniculitis Papillary Adenocarcinoma Paroxysmal Cold Hemoglobinuria Paroxysmal Exertion-Induced Dyskinesia Paroxysmal Nocturnal Hemoglobinuria Pediatric Systemic Lupus Erythematosus Pemphigus Peritonitis Pernicious Anemia Pertussis Pfeiffer Syndrome Phosphoglycerate Kinase Deficiency Plasmodium Vivax Malaria Pneumonia Polymorphic Reticulosis Polyneuropathy Porphyria Porphyria Cutanea Tarda Pre-Eclampsia Prieto X-Linked Mental Retardation Syndrome Primary Biliary Cirrhosis Primary Cerebellar Degeneration Primary Effusion Lymphoma Proctitis Proliferative Glomerulonephritis Prolymphocytic Leukemia Protein C Deficiency Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Embolism Pulmonary Emphysema Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hemosiderosis Pulmonary Hypertension Pulmonary Sarcoidosis Pure Red-Cell Aplasia Purine Nucleoside Phosphorylase Deficiency Purpura Purpura Fulminans Pyelonephritis Pyropoikilocytosis, Hereditary Pyruvate Kinase Deficiency of Red Cells Q Fever Rapp-Hodgkin Syndrome Reactive Arthritis Refractory Anemia Relapsing Polychondritis Renal Glucosuria Renal Tubular Acidosis Retinitis Retinitis Pigmentosa and Erythrocytic Microcytosis Rheumatoid Arthritis Rosai-Dorfman Disease Rubella Sacrococcygeal Teratoma Salmonellosis Salt and Pepper Developmental Regression Syndrome Sarcoidosis 2 Sarcoma Sclerosing Cholangitis Severe Combined Immunodeficiency Severe Pre-Eclampsia Sickle Cell Disease Sideroblastic Anemia Sitosterolemia Spinocerebellar Degeneration Splenic Abscess Splenic Disease Splenic Infarction Splenic Marginal Zone Lymphoma Splenic Sequestration Splenomegaly Spondylocarpotarsal Synostosis Syndrome Spondyloocular Syndrome Subacute Bacterial Endocarditis Sulfhemoglobinemia Systemic Capillary Leak Syndrome Systemic Lupus Erythematosus Systemic Lupus Erythematosus with Hemolytic Anemia 1 T Cell Deficiency T-Cell/histiocyte Rich Large B Cell Lymphoma T-Cell Large Granular Lymphocyte Leukemia Teratoma Tetanus Thalassemia Thrombocytopenia Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombosis Thrombotic Thrombocytopenic Purpura Thrombotic Thrombocytopenic Purpura, Congenital Thymoma Thyroiditis Tolosa-Hunt Syndrome Transient Erythroblastopenia of Childhood Trichuriasis Triosephosphate Isomerase Deficiency Ulcerative Colitis Ulcerative Proctitis Uncombable Hair Syndrome 1 Uremia Vascular Hemostatic Disease Ventricular Septal Defect Viral Hepatitis Viral Pneumonia Visceral Leishmaniasis Vitamin B12 Deficiency Warm Antibody Hemolytic Anemia Wilson Disease Wolff-Parkinson-White Syndrome