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elliptocytosis type 4
Genetics:
- associated with defects in SLC4A1
- Rhesus-unlinked form of hereditary
- 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 109270
MORBIDMAP 109270
References
OMIM :accession 109270