vitamin b12 deficiency Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A vitamin metabolic disorder that results from low blood levels of vitamin B12. (Human Disease Ontology, DOID_0050731)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100502
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
GUCY2C guanylate cyclase 2C