diaphyseal sclerosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An elevation in bone density in one or more diaphyses. Sclerosis is normally detected on a radiograph as an area of increased opacity. (Human Phenotype Ontology, HP_0003034)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003034
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Genes

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

Symbol Name
ANO5 anoctamin 5
CA2 carbonic anhydrase II
MTAP methylthioadenosine phosphorylase
SOST sclerostin
TGFB1 transforming growth factor, beta 1
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11