cleft helix Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A notched form of the helix of the ear. That is, a defect in the continuity of the helix, which may occur at any point along its length. (Human Phenotype Ontology, HP_0009902)
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2 genes associated with the cleft helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GNAI3 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 3
PLCB4 phospholipase C, beta 4