aplasia of the epiglottis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the epiglottis. (Human Phenotype Ontology, HP_0008753)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008753
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Genes

1 genes associated with the aplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EIF4A3 eukaryotic translation initiation factor 4A3