|Dataset||OMIM 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|
1 genes associated with the single median maxillary central incisor phenotype from the curated OMIM Gene-Disease Associations dataset.