|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A bony defect in the skull base. (Human Phenotype Ontology, HP_0009752)|
|Downloads & Tools|
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.
|HYLS1||hydrolethalus syndrome 1|