elliptocytosis type 2

Genetics

• autosomal dominant
• associated with defects in SPTA1 (alpha-spectrin)

Clinical manifestations

• variable hemolytic anemia

Laboratory

• peripheral blood smear: elliptocytosis

More general terms

• elliptocytosis
• genetic disease of the blood/bone marrow

Database

• OMIM: https://mirror.omim.org/entry/182860