Bifid Epiglottis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A midline anterior-posterior cleft of the epiglottis that involves at least two-thirds of the epiglottic leaf. It is a useful feature for clinical diagnosis because it appears to be very rare in syndromes other than Pallister-Hall-Syndrome and is also rare as an isolated malformation. (Human Phenotype Ontology, HP_0010564)
External Link https://www.disgenet.org/browser/0/1/0/C0339864
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Genes

8 genes associated with the disease Bifid Epiglottis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
FOXE1 forkhead box E1
GLI3 GLI family zinc finger 3
IFT80 intraflagellar transport 80
TTF2 transcription termination factor, RNA polymerase II
WDR34 WD repeat domain 34
WDR35 WD repeat domain 35
WDR60 WD repeat domain 60