midface prominence Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Anterior positioning of the infraorbital and perialar regions, or increased convexity of the face, or increased nasolabial angle. (Human Phenotype Ontology, HP_0012371)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012371
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Genes

2 genes associated with the midface prominence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
SPG20 spastic paraplegia 20 (Troyer syndrome)
STRADA STE20-related kinase adaptor alpha