cleft at the superior portion of the pinna Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description This term is used for Auriculocondylar syndrome (MIM:602483). Not clear if there is a clean delineation against cleft helix. (Human Phenotype Ontology, HP_0008537)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008537
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Genes

2 genes associated with the cleft at the superior portion of the pinna 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