|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Pierre Robin malformation is a sequence of developmental malformations characterized by micrognathia (mandibular hypoplasia), glossoptosis and cleft palate. (Human Phenotype Ontology, HP_0000201)|
|Downloads & Tools|
7 genes associated with the pierre-robin sequence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.