absence of intrinsic factor Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of gastric intrinsic factor, which is normally produced by the parietal cells of the stomach, and is required for the absorption of vitamin B12. (Human Phenotype Ontology, HP_0005219)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005219
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Genes

1 genes associated with the absence of intrinsic factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GIF gastric intrinsic factor (vitamin B synthesis)