|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 large, irregular bone located at the base and side of the skull (Mammalian Phenotype Ontology, MP_0004424)|
|Downloads & Tools|
2 gene mutations causing the temporal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.