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hereditary megaloblastic anemia 1; MGA1 Norwegian type; Imerslund-Grasbeck syndrome

Genetics: - hereditary megaloblastic anemia 1 (MGA1 Norwegian type, Imerslund-Grasbeck syndrome) a) autosomal recessive b) associated defects in CUBN gene c) associated with defects in AMN gene (amnionless) Pathology: - hereditary megaloblastic anemia 1 - defect in absorption of vitamin B12

General

megaloblastic anemia genetic disease of the blood/bone marrow

Database Correlations

OMIM 261100

References

OMIM :accession 261100