malabsorption of vitamin b12 Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0200118
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Genes

3 genes associated with the malabsorption of vitamin b12 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMN amnion associated transmembrane protein
CUBN cubilin (intrinsic factor-cobalamin receptor)
GIF gastric intrinsic factor (vitamin B synthesis)
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