|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||underdevelopment, usually due to a deficiency in the number of cells, of the bony projection of the maxilla that normally fuses with palatine shelf to form secondary (hard) palate (Mammalian Phenotype Ontology, MP_0009898)|
|Downloads & Tools|
4 gene mutations causing the maxillary shelf hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.