Hereditary elliptocytosis
MONDO:0017319Hereditary 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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Sub-types of Hereditary elliptocytosis
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Southeast Asian ovalocytosis 2 trials
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Elliptocytosis 1 0 trials
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Elliptocytosis 2 0 trials
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Elliptocytosis 3 0 trials
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