|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||underdevelopment or reduced size, usually due to a reduced number of cells, in either of either of two irregularly L-shaped bones located posterior to the maxilla that in part forms the back of the hard palate, part of the nasal cavity and part of the floor of the orbits (Mammalian Phenotype Ontology, MP_0004475)|
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3 gene mutations causing the palatine bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.