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elliptocytosis type 2
Genetics:
- autosomal dominant
- associated with defects in SPTA1 (alpha-spectrin)
Clinical manifestations:
- variable hemolytic anemia
Laboratory:
- peripheral blood smear: elliptocytosis
General
elliptocytosis
genetic disease of the blood/bone marrow
Database Correlations
OMIM 182860
MORBIDMAP 182860
References
OMIM :accession 182860