|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Developmental hypoplasia of the primary teeth. (Human Phenotype Ontology, HP_0006334)|
|Downloads & Tools|
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.
|UBR1||ubiquitin protein ligase E3 component n-recognin 1|