|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||underdevelopment or reduced size, usually due to a reduced number of cells, in the bone of the cranium that lies above and anterior to the occipital bone in some mammals (Mammalian Phenotype Ontology, MP_0004385)|
|Downloads & Tools|
4 gene mutations causing the interparietal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.