single naris Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of only a single nostril. (Human Phenotype Ontology, HP_0009932)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009932
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Genes

3 genes associated with the single naris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CSPP1 centrosome and spindle pole associated protein 1
GLI2 GLI family zinc finger 2
WNT3 wingless-type MMTV integration site family, member 3