|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any anomaly in the ability of the body to take up inorganic substances that have importance in body functions into the blood by absorption from the small intestine (Mammalian Phenotype Ontology, MP_0001670)|
|Downloads & Tools|
6 gene mutations causing the abnormal intestinal mineral absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.