broad skull Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased width of the skull. (Human Phenotype Ontology, HP_0002682)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002682
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Genes

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

Symbol Name
ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 motif, 10
FBN1 fibrillin 1