GenTIGSA Gene Database on Rare Genetic Disorders
Imerslund-Grasbeck Syndrome Type 1  
Disease Aliases (16)

Enterocyte cobalamin malabsorption

Enterocyte intrinsic factor receptor, defect of

Familial megaloblastic anaemia

Familial megaloblastic anemia

Imerslund disease

Imerslund's syndrome

Imerslund-grasbeck anemia

Imerslund-grasbeck disease

Imerslund-gräsbeck syndrome

Imerslund-najman-grasbeck syndrome

Juvenile megaloblastic anaemia

Juvenile megaloblastic anemia

Megaloblastic anemia due to inborn errors of metabolism

Pernicious anemia, juvenile, due to selective intestinal malabsorption of vitamin b12, with proteinuria

Selective cobalamin malabsorption with proteinuria

Selective malabsorption of cyanocobalamin

Associated Genes (1)