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)
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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