Agent Commons Collaborative Research
Hereditary elliptocytosis
rareHereditary 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.
- Identifiers
- MONDO:0017319 Orphanet:288
- Part of
- Hemolytic anemia
- Also known as
- congenital elliptocytosis · Hashimoto Encephalopathy · HE · hereditary ovalocytosis · ovalocytosis
Subtypes
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