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Paroxysmal Nocturnal Hemoglobinuria
Paroxysmal nocturnal hemoglobinuria
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Related in the Kosmos
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Hematology
(17)
Paroxysmal cold hemoglobinuria
Hemolysis
Myelodysplastic syndromes
Hemolytic anemia
Pancytopenia
Pancytopenia
RBCs
Myeloproliferative disorders
Hematopoiesis
Polycythemia
Hematopoietic stem cell transplantation
Leukemia
Pure red cell aplasia
Intrinsic factor
Decay accelerating factor
Thrombotic thrombocytopenic purpura
Thrombophilia
Iron deficiency anemia
more...
Genetic disorders
(9)
Beta thalassemia
Refractory anemia with ringed sideroblasts
Fanconi anemia
Thalassemia
Sly syndrome
Sly syndrome
Hurler-Scheie Syndrome
Sickle cell anemia
Von willebrand disease
Hereditary elliptocytosis
more...
Rare diseases
Sly syndrome
Thrombotic thrombocytopenic purpura
Diseases and disorders
(51)
Paraquat lung
Blood disorders
Hemoglobinuria
Myelofibrosis
Acute biphenotypic leukemia
Acute biphenotypic leukemia
Anemias
Aplastic
Reticular dysgenesis
Lymphohistiocytosis
Polyglucosan body disease adult
Purpura, schoenlein-henoch
Acute myelogenous leukemia
Acquired aplastic anemia
Cold agglutinin disease
Hemoglobin sc disease
Bjornstad syndrome
Polycythemia vera
Thrombocytopenia
Hypoplastic
Hyperbilirubinemia
Splenomegaly
Antithrombin
Thrombocytic
Megaloblastic anemia
Chronic myelogenous leukemia
Schizophrenia
Progressive osseous heteroplasia
Hemophilia b
Hypoplastic anemia
Portal hypertension
Pneumothorax
Spherocytes
Hairy cell leukemia
Hereditary spherocytosis
Paroxysmal cold hemoglobinuria
Myelodysplastic syndromes
Hemolytic anemia
Beta thalassemia
Myeloproliferative disorders
Refractory anemia with ringed sideroblasts
Fanconi anemia
Thalassemia
Sly syndrome
Leukemia
Pure red cell aplasia
Hurler-Scheie Syndrome
Sickle cell anemia
Von willebrand disease
Rare diseases
Iron deficiency anemia
Hereditary elliptocytosis
more...
Blood
Blood cells
Blood disorder
Decay accelerating factor
Medical specialties
Rehabiliation medicine
Immunology
Blood disorder
Immunosuppressants
Eculizumab
Lenalidomide
Antithymocyte globulin
Leukemia
(30)
Juvenile Myelomonocytic Leukemia (JMML)
Accelerated phase chronic myelogenous leukemia
Acute basophilic leukemia
Acute eosinophilic leukemia
Acute erythroid leukemia
Acute erythroid leukemia
Acute lymphoblastic leukemia
Acute monocytic leukemia
Acute myeloblastic leukemia with maturation
Acute myelogenous leukemia
Acute myeloid dendritic cell leukemia
Antileukemic drug
B-cell chronic lymphocytic leukemia
B-cell leukemia
B-cell prolymphocytic leukemia
Chronic myelogenous leukemia
Chronic myelomonocytic leukemia
Chronic neutrophilic leukemia
Hairy cell leukemia
Large granular lymphocytic leukemia
Lymphoid leukemia
Minimal residual disease
Minimally differentiated acute myeloblastic leukemia
Monocytic leukemia
Myeloid leukemia
Myelomonocyte
Plasma cell leukemia
Precursor B acute lymphoblastic leukemia/lymphoma
Prolymphocytic leukemia
T-cell leukemia
T-cell prolymphocytic leukemia
more...
Immune system
Immunosuppressive therapy
Complement protein
CD59
Decay accelerating factor
Antithymocyte globulin
Blood disorders
(128)
Thrombocytosis
Acquired hemolytic anemia
Acute eosinophilic leukemia
Acute lymphoblastic leukemia
Acute monocytic leukemia
Acute monocytic leukemia
Acute myeloblastic leukemia with maturation
Acute myelogenous leukemia
Acute myeloid dendritic cell leukemia
Acute promyelocytic leukemia
Adult T-cell leukemia/lymphoma
Aggressive NK-cell leukemia
Agranulocytosis
Alpha-thalassemia
Amyloid purpura
Analbuminaemia
Anaplastic large cell lymphoma
Anemia of chronic disease
Anemia of prematurity
Anemias
Angioimmunoblastic T-cell lymphoma
Antiphospholipid syndrome
Aplastic anemia
Atransferrinemia
Autoimmune hemolytic anemia
Autoimmune neutropenia
B symptoms
Bernard-Soulier syndrome
Beta thalassemia
Bisalbuminemia
Blood disorder
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
Congenital hemolytic anemia
Contaminated haemophilia blood products
Cyclic neutropenia
Deaths from blood disease
Delta-thalassemia
Diamond-Blackfan anemia
Drug-induced autoimmune hemolytic anemia
Drug-induced nonautoimmune hemolytic anemia
Enteropath- y-associated T-cell lymphoma
Eosinopenia
Essential thrombocytosis
Evans syndrome
Familial dysfibrinogenemia
Glanzmann's thrombasthenia
Haemophilia
Haemophilia A
Haemophilia C
Haemorrhagic and haematological disorders of fetus and newborn
Hairy cell leukemia
Harris platelet syndrome
Hematological malignancy
Hemoglobin variants
Hemoglobinemia
Hemolytic anemia
Hemolytic disease of the newborn
Hemolytic disease of the newborn (ABO)
Hemolytic disease of the newborn (anti-Kell)
Hemolytic disease of the newborn (anti-RhE)
Hemolytic disease of the newborn (anti-Rhc)
Hemophagocytic lymphohistiocytosis
Hemophilia b
Hepatosplenic T-cell lymphoma
Hereditary elliptocytosis
Hereditary pyropoikilocytosis
Hereditary spherocytosis
Hodgkin's lymphoma
Hypersegmented neutrophil
Hypochromic anemia
Hypoprothrombinemia
Idiopathic thrombocytopenic purpura
Laminopathy
Large granular lymphocytic leukemia
Leukemia
Leukopenia
Lindsay Tribunal
List of hemophilia organizations
Loxoscelism
Lymphocytopenia
Lymphoma
Macrocytic anemia
Mantle cell lymphoma
Mast cell leukemia
May-Hegglin anomaly
Megaloblastic anemia
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
Paroxysmal cold hemoglobinuria
Pel-Ebstein fever
Plummer-Vinson syndrome
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 anemia
Sickle cell trait
Spherocytes
Splenic marginal zone lymphoma
T-cell prolymphocytic leukemia
Thalassemia
Thrombocytopenia
Triosephosphate isomerase deficiency
Vaso-occlusive crisis
Von willebrand disease
Waldenström's macroglobulinemia
Warm autoimmune hemolytic anemia
Wiskott-Aldrich syndrome
Working Formulation
more...
See also
(20)
Secondary Parkinsons
Alexion
Orphan drugs
Aplastic anemia
Paroxysmal
Paroxysmal
Penis pain
Br. J. Haematol.
Refractory anemia with excess blasts in transformation
Mucolipidosis II
Erythropoietin
Intravascular
Bone marrow
Bone marrow diseases
Fanconi
Budd-Chiari syndrome
Refractory cytopenia with multilineage dysplasia
Hemolysin
PIGA
Orphan drug
G6PD
more...
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