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Template
:
Diseases of RBCs
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Diseases
of
red blood cells
↑
Polycythemia
Polycythemia vera
↓
Anemia
Nutritional
Micro-
:
Iron-deficiency anemia
Plummer–Vinson syndrome
Macro-
:
Megaloblastic anemia
Pernicious anemia
Hemolytic
(mostly
normo-
)
Hereditary
enzymopathy
:
Glucose-6-phosphate dehydrogenase deficiency
glycolysis
pyruvate kinase deficiency
triosephosphate isomerase deficiency
hexokinase deficiency
hemoglobinopathy
:
Thalassemia
alpha
beta
delta
Sickle cell disease
/
trait
Hemoglobin C disease
membrane
:
Hereditary spherocytosis
Minkowski–Chauffard syndrome
Hereditary elliptocytosis
Southeast Asian ovalocytosis
Hereditary stomatocytosis
Acquired
AIHA
Warm antibody autoimmune hemolytic anemia
Cold agglutinin disease
Donath–Landsteiner hemolytic anemia
Paroxysmal cold hemoglobinuria
Mixed autoimmune hemolytic anemia
membrane
paroxysmal nocturnal hemoglobinuria
Microangiopathic hemolytic anemia
Thrombotic microangiopathy
Hemolytic–uremic syndrome
Drug-induced autoimmune
Drug-induced nonautoimmune
Hemolytic disease of the newborn
Aplastic
(mostly
normo-
)
Hereditary
:
Fanconi anemia
Diamond–Blackfan anemia
Acquired:
Pure red cell aplasia
Sideroblastic anemia
Myelophthisic
Blood tests
Mean corpuscular volume
normocytic
microcytic
macrocytic
Mean corpuscular hemoglobin concentration
normochromic
hypochromic
Other
Methemoglobinemia
Sulfhemoglobinemia
Reticulocytopenia
Hereditary persistence of fetal hemoglobin
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