calcific stippling Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal punctate (speckled, dot-like) pattern of calcifications in soft tissues within or surrounding bones (as observed on radiographs). (Human Phenotype Ontology, HP_0002832)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002832
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Genes

4 genes associated with the calcific stippling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCD3 ATP-binding cassette, sub-family D (ALD), member 3
GNPAT glyceronephosphate O-acyltransferase
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
PEX5 peroxisomal biogenesis factor 5