|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||inability to degrade the organic and inorganic phases of bone by absorption, usually by the abnormal function or by absence of osteoclasts (Mammalian Phenotype Ontology, MP_0000064)|
|Downloads & Tools|
5 gene mutations causing the failure of secondary bone resorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.