Aplasia Of The Epiglottis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Absence of the epiglottis. (Human Phenotype Ontology, HP_0008753)
External Link https://www.disgenet.org/browser/0/1/0/C4024628
Similar Terms
Downloads & Tools

Genes

2 genes associated with the disease Aplasia Of The Epiglottis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
C2CD3 C2 calcium-dependent domain containing 3
EIF4A3 eukaryotic translation initiation factor 4A3