hypomineralization of enamel Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A decreased amount of enamel mineralization. (Human Phenotype Ontology, HP_0006285)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006285
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Genes

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

Symbol Name
C4ORF26 chromosome 4 open reading frame 26
ENAM enamelin
PHEX phosphate regulating endopeptidase homolog, X-linked
WDR72 WD repeat domain 72