diaphyseal cortical sclerosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An elevation in bone density of the cortex of one or more diaphyses. Sclerosis is normally detected on a radiograph as an area of increased opacity. (Human Phenotype Ontology, HP_0005045)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005045
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Genes

2 genes associated with the diaphyseal cortical sclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANO5 anoctamin 5
MTAP methylthioadenosine phosphorylase