decreased calvarial ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal reduction in ossification of the calvaria (roof of the skull consisting of the frontal bone, parietal bones, temporal bones, and occipital bone). (Human Phenotype Ontology, HP_0005474)
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7 genes associated with the decreased calvarial ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALPL alkaline phosphatase, liver/bone/kidney
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
CRTAP cartilage associated protein
LMNA lamin A/C
WNT7A wingless-type MMTV integration site family, member 7A
ZMPSTE24 zinc metallopeptidase STE24