sclerosis of foot bone Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An elevation in bone density in one or more foot bones. Sclerosis is normally detected on a radiograph as an area of increased opacity. (Human Phenotype Ontology, HP_0100925)
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2 genes associated with the sclerosis of foot bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EBP emopamil binding protein (sterol isomerase)
LRP5 low density lipoprotein receptor-related protein 5