| 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 |
| Similar Terms | |
| 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.
| Symbol | Name |
|---|---|
| UBR1 | ubiquitin protein ligase E3 component n-recognin 1 |
