hepatic calcification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of abnormal calcium deposition in the liver. (Human Phenotype Ontology, HP_0006559)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006559
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Genes

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

Symbol Name
CPT2 carnitine palmitoyltransferase 2
LBR lamin B receptor