increased vertebral height Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased top to bottom height of vertebral bodies. (Human Phenotype Ontology, HP_0004570)
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5 genes associated with the increased vertebral height phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CCDC8 coiled-coil domain containing 8
CUL7 cullin 7
FGFR3 fibroblast growth factor receptor 3
MAN2B1 mannosidase, alpha, class 2B, member 1
NOTCH2 notch 2