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Hereditary elliptocytosis

MONDO:0017319

Hereditary elliptocytosis (HE) is a rare clinically and genetically heterogeneous disorder of the red cell membrane characterized by manifestations ranging from mild to severe transfusion-dependent hemolytic anemia but with the majority of patients being asymptomatic.

Also known as: HE, Hashimoto Encephalopathy, congenital elliptocytosis, hereditary ovalocytosis, ovalocytosis

11 clinical trials for this condition and its sub-types, 0 tagged with Hereditary elliptocytosis itself.

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