midline defect of mandible Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010753
Similar Terms
Downloads & Tools

Genes

3 genes associated with the midline defect of mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EIF4A3 eukaryotic translation initiation factor 4A3
FLNA filamin A, alpha
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2