sagittal craniosynostosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A kind of craniosynostosis affecting the sagittal suture. (Human Phenotype Ontology, HP_0004442)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004442
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Genes

6 genes associated with the sagittal craniosynostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGFR2 fibroblast growth factor receptor 2
IFT122 intraflagellar transport 122
KRAS Kirsten rat sarcoma viral oncogene homolog
RAB23 RAB23, member RAS oncogene family
RECQL4 RecQ protein-like 4
WDR19 WD repeat domain 19