absent nares Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The nostrils (the paired channels of the nose) are not present. (Human Phenotype Ontology, HP_0100596)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100596
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3 genes associated with the absent nares phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGFR1 fibroblast growth factor receptor 1
OTX2 orthodenticle homeobox 2
PRRX1 paired related homeobox 1