subcutaneous calcification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Deposition of calcium salts in subcutaneous tissue (i.e., the the lowermost layer of the integument). (Human Phenotype Ontology, HP_0007618)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007618
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Genes

1 genes associated with the subcutaneous calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
WRN Werner syndrome, RecQ helicase-like