abnormality of the epiglottis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the epiglottis. (Human Phenotype Ontology, HP_0005483)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005483
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Genes

6 genes associated with the abnormality 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
FOXE1 forkhead box E1
GLI3 GLI family zinc finger 3
NEK1 NIMA-related kinase 1
PRRX1 paired related homeobox 1
SF3B4 splicing factor 3b, subunit 4, 49kDa