alveolar ridge cleft Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A gap (cleft) affecting one of the alveolar ridges. (Human Phenotype Ontology, HP_0010289)
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1 genes associated with the alveolar ridge cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EIF4A3 eukaryotic translation initiation factor 4A3