congenital intrinsic factor deficiency Disease Ontology Browser

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congenital intrinsic factor deficiency (DOID:0050734)
Alliance: disease page
Synonyms: hereditary intrinsic factor deficiency
Alt IDs: OMIM:261000
Definition: A vitamin B12 deficiency that is characterized by megaloblastic anemia due to the absence of gastric intrinsic factor which results in abnormal vitamin B12 absorption.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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