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Differential Diagnosis For Family history/Anemia

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Family history/Anemia
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Allergic, Collagen, Auto-Immune Disorders: Hemoglobin Bart hydrops fetalis syndr.
Metabolic, Storage Disorders: Erythrocyte glycolytic enzyme defect; Glucose 6 PD deficiency; Anemia due to glutathione metab def; RBC membrane enzyme defects
Congenital, Developmental Disorders: Congenital dyserythropoetic anemia
Hereditary, Familial, Genetic Disorders: Erythrocyte membrane disorders; Hemoglobin E thalassemia; Hemoglobinopathy; Sickle cell/thalassemia disease; Thalassemia major; Thalassemia minor; Spherocytosis, crisis phase; Hereditary hemolytic anemia syndromes; Hereditary sideroblastic anemia; Pyruvate kinase deficiency RBC's; Sickle cell anemia; Sickle cell-hemoglobin D disease; Spherocytosis, hereditary; Hemoglobin C disease; Hemoglobin C/E disease; Hemoglobin S/C disease; Anemia, hereditary hemolytic,nonspher'c; Hereditary fetal hemoglobinemia; Shwachman (Shwachman-Diamond) syndrome; Thalassemia-hemoglobin C disease
Reference to Organ System: Paroxysmal Nocturnal Hemoglobinuria; Pernicious anemia; Sideroblastic Anemia Siderochrestic
Synonyms: Anaemia, Anaemia (disorder), Anaemia unspecified, Anemia, Anemia (disorder), Anemia (dup) (disorder), anemia essential, Anemia unspecified, Anemia unspecified (disorder), Anemias, Family history, Unspecified anaemia, Unspecified anemia
External Links Related to Family history/Anemia: Google; Wikipedia; Merck; Images; PubMed (National Library of Medicine); NGC (National Guideline Clearinghouse); Medscape (eMedicine); Harrison's Online (accessmedicine); NEJM (The New England Journal of Medicine)

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