hypoplasia of the primary teeth Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Developmental hypoplasia of the primary teeth. (Human Phenotype Ontology, HP_0006334)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006334
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1 genes associated with the hypoplasia of the primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
UBR1 ubiquitin protein ligase E3 component n-recognin 1