|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
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.
|GIF||gastric intrinsic factor (vitamin B synthesis)|