: MeSH: Elliptocytosis, Hereditary

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Anemia, Hemolytic, Congenital > Elliptocytosis, Hereditary

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Elliptocytosis, Hereditary

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An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.

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