|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||failure to produce and/or release a physiologically active substance (usually but not exclusively in liquid form) from a cell or a gland of the digestive system (Mammalian Phenotype Ontology, MP_0000507)|
|Downloads & Tools|
1 gene mutations causing the absent digestive secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|SLC26A9||solute carrier family 26 (anion exchanger), member 9|