|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any anomaly in the ability to take in any of a group of organic substances, present in food, that are essential to normal metabolism (Mammalian Phenotype Ontology, MP_0001671)|
|Downloads & Tools|
4 gene mutations causing the abnormal vitamin absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.