Anemia, Hemolytic, Congenital

Hemolytic anemia due to various intrinsic defects of the erythrocyte.

Year introduced: 1968

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Tree Number(s): C15.378.050.141.150, C16.320.070

MeSH Unique ID: D000745

Entry Terms:

• Congenital Hemolytic Anemia
• Anemia, Congenital Hemolytic
• Anemias, Congenital Hemolytic
• Congenital Hemolytic Anemias
• Hemolytic Anemias, Congenital
• Hemolytic Anemia, Congenital
• Hemolytic Anemia, Hereditary
• Anemia, Hereditary Hemolytic
• Anemias, Hereditary Hemolytic
• Hemolytic Anemias, Hereditary
• Hereditary Hemolytic Anemias
• Hereditary Hemolytic Anemia
• Anemia, Hemolytic, Hereditary

All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Dyserythropoietic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Sickle Cell
Acute Chest Syndrome
Hemoglobin SC Disease
Sickle Cell Trait
Elliptocytosis, Hereditary
Glucosephosphate Dehydrogenase Deficiency
Favism
Hemoglobin C Disease
Spherocytosis, Hereditary
Thalassemia
alpha-Thalassemia
beta-Thalassemia
delta-Thalassemia

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Dyserythropoietic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Sickle Cell
Acute Chest Syndrome
Hemoglobin SC Disease
Sickle Cell Trait
Elliptocytosis, Hereditary
Glucosephosphate Dehydrogenase Deficiency
Favism
Hemoglobin C Disease
Spherocytosis, Hereditary
Thalassemia
alpha-Thalassemia
beta-Thalassemia
delta-Thalassemia