| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Reduction in size of the Premaxilla, which is the embryonic structure that forms the anterior part of the maxilla. (Human Phenotype Ontology, HP_0010650) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0010650 |
| Similar Terms | |
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2 genes associated with the premaxillary underdevelopment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
