Hereditary intrinsic factor deficiency

Congenital intrinsic factor deficiency (IFD) is a rare disorder of vitamin B12 (cobalamin) absorption that is characterized by megaloblastic anemia and neurological abnormalities.

Also known as: intrinsic factor deficiency, IFD, congenital intrinsic factor deficiency, congenital pernicious anaemia, congenital pernicious anemia, gastric intrinsic factor deficiency, hereditary juvenile megaloblastic anaemia due to intrinsic factor deficiency, hereditary juvenile megaloblastic anemia due to intrinsic factor deficiency

72 clinical trials for this condition and its sub-types.