broad chin Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased width of the midpoint of the mandible (mental protuberance) and overlying soft tissue. (Human Phenotype Ontology, HP_0011822)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011822
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Genes

1 genes associated with the broad chin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
KANSL1 KAT8 regulatory NSL complex subunit 1