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elliptocytosis type 1
Genetics:
- associated with defects in EPB41
- Rhesus-linked form of hereditary elliptocytosis
- genetically heterogeneous
- autosomal dominant
Clinical manifestations:
- variable hemolytic anemia
Laboratory:
- peripheral blood smear: elliptocytosis
General
elliptocytosis
genetic disease of the blood/bone marrow
Database Correlations
OMIM 611804
References
OMIM :accession 611804