|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||missing bony projection of the maxilla that normally fuses with palatine shelf to form secondary (hard) palate (Mammalian Phenotype Ontology, MP_0000430)|
|Downloads & Tools|
9 gene mutations causing the absent maxillary shelf phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.