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Anemia, Hemolytic
Anemia, hemolytic
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Blood disorders
(126)
ABO incompatibility
Acquired hemolytic anemia
Agranulocytosis
Alpha Thalassemia
Anemia of chronic disease
Anemia of chronic disease
Anemia, aplastic
Anemia, sickle cell
Anemias
Antiphospholipid syndrome
Autoimmune hemolytic anemia
Congenital hemolytic anemia
Drug-induced autoimmune hemolytic anemia
Drug-induced nonautoimmune hemolytic anemia
Hematology
Hemolytic disease of the newborn
Hereditary spherocytosis
Idiopathic myelofibrosis
Immune thrombocytopenic purpura
Macrocytic anemia
Megaloblastic anemia
Paroxysmal cold hemoglobinuria
Spherocytosis
Thalassemia
Thrombocytopenia
Warm autoimmune hemolytic anemia
Acute eosinophilic leukemia
Acute lymphoblastic leukemia
Acute monocytic leukemia
Acute myeloblastic leukemia with maturation
Acute myeloid dendritic cell leukemia
Acute myeloid leukemia
Acute promyelocytic leukemia
Adult T-cell leukemia/lymphoma
Aggressive NK-cell leukemia
Amyloid purpura
Analbuminaemia
Anaplastic large cell lymphoma
Anemia of prematurity
Angioimmunoblastic T-cell lymphoma
Atransferrinemia
Autoimmune neutropenia
B symptoms
Bernard-Soulier syndrome
Beta-thalassemia
Bisalbuminemia
Blood hammer
Cavernous sinus thrombosis
Chemothera- py-induced neutropenia
Chromosome 5q deletion syndrome
Chronic myelogenous leukemia
Chronic neutrophilic leukemia
Congenital amegakaryocytic thrombocytopenia
Congenital dyserythropoietic anemia
Contaminated haemophilia blood products
Cyclic neutropenia
Deaths from blood disease
Delta-thalassemia
Diamond-Blackfan anemia
Enteropath- y-associated T-cell lymphoma
Eosinopenia
Essential thrombocytosis
Evans syndrome
Familial dysfibrinogenemia
Glanzmann's thrombasthenia
Haemophilia
Haemophilia A
Haemophilia B
Haemophilia C
Hairy cell leukemia
Harris platelet syndrome
Hematological malignancy
Hemoglobinemia
Hemolytic disease of the newborn (anti-Kell)
Hemolytic disease of the newborn (anti-RhE)
Hemolytic disease of the newborn (anti-Rhc)
Hemophagocytic lymphohistiocytosis
Hepatosplenic T-cell lymphoma
Hereditary elliptocytosis
Hereditary pyropoikilocytosis
Hodgkin's lymphoma
Hypersegmented neutrophil
Hypochromic anemia
Hypoprothrombinemia
Laminopathy
Large granular lymphocytic leukemia
Leukemia
Leukopenia
Lindsay Tribunal
List of hemophilia organizations
Loxoscelism
Lymphocytopenia
Lymphoma
Mantle cell lymphoma
Mast cell leukemia
Methemoglobinemia
Minimally differentiated acute myeloblastic leukemia
Monoclonal B-cell lymphocytosis
Monoclonal gammopathy of undetermined significance
Myeloid sarcoma
Myelophthisic anemia
Neonatal alloimmune thrombocytopenia
Neutropenia
Nodular lymphocyte predominant Hodgkin's lymphoma
Non-Hodgkin lymphoma
Pel-Ebstein fever
Plummer-Vinson syndrome
Polycythemia
Polycythemia vera
Primary effusion lymphoma
Protein S deficiency
Pseudo gray platelet syndrome
Quebec Platelet Disorder
Refractory anemia
Rh disease
Richter's transformation
Scott syndrome
Sickle cell trait
Splenic marginal zone lymphoma
T-cell prolymphocytic leukemia
Thrombocytosis
Triosephosphate isomerase deficiency
Vaso-occlusive crisis
Von Willebrand disease
Waldenström's macroglobulinemia
Wiskott-Aldrich syndrome
Working Formulation
more...
Hematology
(26)
Microangiopathic hemolytic anemia
Hemolysis
Hematologic disease
Activated protein c resistance
Iron deficiency anemia
Iron deficiency anemia
Microcytic anemia
Pernicious anemia
Pyruvate kinase deficiency
Red blood cells
G6pd deficiency
Coombs test
Hemoglobinopathies
Hemolytic uremic syndrome
Thrombotic thrombocytopenic purpura
Intrinsic factor
Macrocytosis
Autoimmune hemolytic anemia
Acquired hemolytic anemia
Congenital hemolytic anemia
Paroxysmal cold hemoglobinuria
Drug-induced nonautoimmune hemolytic anemia
Drug-induced autoimmune hemolytic anemia
Antiphospholipid syndrome
Hemolytic disease of the newborn
Idiopathic myelofibrosis
ABO incompatibility
more...
Medical condition
(44)
Hereditary spherocytic hemolytic anemia
Angiofibroma
Sideroblastic anemia
Autistic psychopathy
Drug abuse
Drug abuse
Antithrombin iii deficiency
Hand-Schul- ler-Christian disease
Intraparenchymal hemorrhage
Hansens Disease
Hemoglobin c disease
Hemoglobinuria
Hereditary amyloidosis
Hypersplenism
Bergers disease
Hageman factor
Intestinal pseudo-obstruction
Mesangial proliferative glomerulonephritis
Ichthyosis vulgaris
Iga deficiency
Enzymopathy
Cold agglutinin disease
Autoimmune hemolytic anemia
Congenital hemolytic anemia
Paroxysmal cold hemoglobinuria
Hematologic disease
Iron deficiency anemia
Alpha Thalassemia
Hereditary spherocytosis
Anemias
Pernicious anemia
Pyruvate kinase deficiency
Spherocytosis
Megaloblastic anemia
Anemia, sickle cell
G6pd deficiency
Thalassemia
Agranulocytosis
Hemoglobinopathies
Antiphospholipid syndrome
Hemolytic uremic syndrome
Hemolytic disease of the newborn
Thrombocytopenia
Idiopathic myelofibrosis
Immune thrombocytopenic purpura
more...
Immunology
Immune-mediated
Autoimmune
Autoimmune hemolytic anemia
Coombs test
Immune system
Immune disorders
Autoimmune hemolytic anemia
Immune-mediated
Autoimmune
Autoimmune diseases
Warm autoimmune hemolytic anemia
Anemia, aplastic
Antiphospholipid syndrome
Thrombotic thrombocytopenic purpura
Autoimmune
Cold agglutinin disease
Metabolism
Enzyme
Direct bilirubin
Enzymopathy
Blood
Blood cells
Reticulocytosis
Blood loss
Hematology
Pathology
Thrombotic microangiopathy
Peripheral blood smear
Microcytic anemia
Macrocytosis
Blood proteins
Hemoglobin
Haptoglobin
Hemoglobin c disease
Diseases and disorders
(12)
Australian Antigen
Normocytic
Hyperproth- rombinemia
Basopenia
Gianotti–Crosti syndrome
Gianotti–Crosti syndrome
Paroxysmal cold hemoglobinuria
Activated protein c resistance
Sideroblastic anemia
Pyruvate kinase deficiency
Hand-Schul- ler-Christian disease
Hemoglobinuria
Mesangial proliferative glomerulonephritis
more...
Symptoms
(10)
Dark urine
Dyspnea
Fatigue
Pale
Tachycardia
Tachycardia
Yellow skin color
Anemia
Hypersplenism
Reticulocytosis
Blood loss
more...
Causes, incidence, and risk factors
(11)
Immune hemolytic anemia
Idiopathic autoimmune hemolytic anemia
Hemolytic anemia due to G6PD deficiency
Autoimmune disease
Hereditary ovalocytosis
Hereditary ovalocytosis
Paroxysmal nocturnal hemoglobinuria
Hereditary spherocytosis
Sickle-cell disease
Thalassemia
Intrinsic factor
Hereditary elliptocytosis
more...
Signs and tests
(20)
Reticulocyte
AST
Alkaline phosphatase
Blood differential
CBC
CBC
Coombs' test, direct
Donath-Landsteiner test
Febrile or cold agglutinins
Ferritin
Hematocrit
Indirect bilirubin
Platelet count
Potassium test
Red blood cell count
Serum haptoglobin
Serum iron
Total iron-binding capacity
Uric acid
Urine protein
Hemoglobin
more...
See also
(20)
Diseases and disorders
Cytosis
Asian Flu
ApoCII
Penia
Penia
Folic-Acid- -Deficiency Anemia
Aortic aneurysm
Hemoglobin electrophoresis
Elemental Iron
Ferrous gluconate
Splenectomy
G6PD
Amateur Ice Hockey Association of Singapore
Harrington rod
Hypochromic
Transfusion reaction
Arthroscopic
Alpha globin
Ferrous fumarate
Red blood count
more...
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