broad jaw Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Bigonial distance (lower facial width) more than 2 SD above the mean (objective); or an apparently increased width of the lower jaw (mandible) when viewed from the front (subjective). (Human Phenotype Ontology, HP_0012802)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012802
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Genes

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

Symbol Name
SNIP1 Smad nuclear interacting protein 1