Abnormal Pelvis Bone Ossification Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of the formation and mineralization of any bone of the bony pelvis. (Human Phenotype Ontology, HP_0009106)
External Link https://www.disgenet.org/browser/0/1/0/C4021525
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Genes

7 genes associated with the disease Abnormal Pelvis Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CTSK cathepsin K
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
IFT80 intraflagellar transport 80
LBR lamin B receptor
WDR34 WD repeat domain 34
WDR35 WD repeat domain 35
WDR60 WD repeat domain 60