generalized osteosclerosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal increase of bone mineral density with generalized involvement of the skeleton. (Human Phenotype Ontology, HP_0005789)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005789
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Genes

4 genes associated with the generalized osteosclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CLCN7 chloride channel, voltage-sensitive 7
DHCR24 24-dehydrocholesterol reductase
LRP5 low density lipoprotein receptor-related protein 5
PTH1R parathyroid hormone 1 receptor