|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any anomaly in the ability of the body to take up calcium into the blood by absorption from the small intestine (Mammalian Phenotype Ontology, MP_0011219)|
|Downloads & Tools|
2 gene mutations causing the abnormal intestinal calcium absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.