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

Pathology

• hereditary megaloblastic anemia 1
  • defect in absorption of vitamin B12

Genetics

• hereditary megaloblastic anemia 1 (MGA1 Norwegian type, Imerslund-Grasbeck syndrome)
  • autosomal recessive
  • associated defects in CUBN gene
  • associated with defects in AMN gene (amnionless)

More general terms

• megaloblastic anemia
• genetic disease of the blood/bone marrow

Database

• OMIM: https://mirror.omim.org/entry/261100