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
Similar Terms
Downloads & Tools


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