hyperorality Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A tendency or compulsion to examine objects by mouth. (Human Phenotype Ontology, HP_0000710)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000710
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Genes

5 genes associated with the hyperorality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHMP2B charged multivesicular body protein 2B
GRN granulin
MAPT microtubule-associated protein tau
PSEN1 presenilin 1
SHANK3 SH3 and multiple ankyrin repeat domains 3