midline facial cleft Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congenital malformation with a cleft (gap or opening) in the midline of the face. (Human Phenotype Ontology, HP_0100629)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100629
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5 genes associated with the midline facial cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
IFT80 intraflagellar transport 80
WDR34 WD repeat domain 34
WDR35 WD repeat domain 35
WDR60 WD repeat domain 60