aplasia of the nose Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Complete absence of all nasal structures. (Human Phenotype Ontology, HP_0009927)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009927
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1 genes associated with the aplasia of the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
SIX3 SIX homeobox 3