abnormal pelvis bone ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the formation and mineralization of any bone of the bony pelvis. (Human Phenotype Ontology, HP_0009106)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009106
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4 genes associated with the abnormal pelvis bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL2A1 collagen, type II, alpha 1
GSC goosecoid homeobox
LBR lamin B receptor
RUNX2 runt-related transcription factor 2