patchy changes of bone mineral density Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Patchy (irregular) changes in bone mineral density. These changes can either be patchy reduction or increase of mineral density as seen on x-rays. Depending on the pathomechanism and the underlying disease, these changes can either appear solely as reduction or increase or as a combination of both (patches of bone showing an increased density while others are affected by reduction of mineral density). (Human Phenotype Ontology, HP_0010658)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010658
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Genes

4 genes associated with the patchy changes of bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GJA1 gap junction protein, alpha 1, 43kDa
LBR lamin B receptor
MTAP methylthioadenosine phosphorylase
TBCE tubulin folding cofactor E