|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||The presence of a single, median maxillary incisor, affecting both the primary maxillary incisor and the permanent maxillary incisor. (Human Phenotype Ontology, HP_0006315)|
|Downloads & Tools|
7 genes associated with the single median maxillary incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.