sclerosis of skull base Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased bone density of the skull base without significant changes in bony contour. (Human Phenotype Ontology, HP_0002694)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002694
Similar Terms
Downloads & Tools

Genes

6 genes associated with the sclerosis of skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANKH ANKH inorganic pyrophosphate transport regulator
FLNA filamin A, alpha
LBR lamin B receptor
PTDSS1 phosphatidylserine synthase 1
SETBP1 SET binding protein 1
TGFB1 transforming growth factor, beta 1