ivory epiphyses Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Sclerosis of the epiphyses, leading to an increased degree of radiopacity (white or ivory appearance) in X-rays. (Human Phenotype Ontology, HP_0010583)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010583
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Genes

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

Symbol Name
ATR ATR serine/threonine kinase
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
PCNT pericentrin
TRPS1 trichorhinophalangeal syndrome I