increased skull ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increase in the magnitude or amount of ossification of the skull. (Human Phenotype Ontology, HP_0004330)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004330
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Genes

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

Symbol Name
HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
NAGLU N-acetylglucosaminidase, alpha
SGSH N-sulfoglucosamine sulfohydrolase