|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 plate of the palatine bone that normally fuses with maxillary shelf to form secondary (hard) palate (Mammalian Phenotype Ontology, MP_0009896)|
|Downloads & Tools|
1 gene mutations causing the palatine bone horizontal plate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|MN1||meningioma (disrupted in balanced translocation) 1|