grayish enamel Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A grey discoloration of the dental enamel. (Human Phenotype Ontology, HP_0000683)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000683
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Genes

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

Symbol Name
GALNS galactosamine (N-acetyl)-6-sulfatase
GLB1 galactosidase, beta 1