cleft in skull base Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A bony defect in the skull base. (Human Phenotype Ontology, HP_0009752)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009752
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Genes

1 genes associated with the cleft in skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HYLS1 hydrolethalus syndrome 1