|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||absence of the anterior portion of the primitive digestive tube of the embryo that lies cephalic to the junction of the yolk stalk, consists of endodermal tissue, and gives rise to the pharynx, lower respiratory system, esophagus, stomach, duodenum proximal to the biliary tract, liver, pancreas, biliary tract, and gall bladder (Mammalian Phenotype Ontology, MP_0012083)|
|Downloads & Tools|
5 gene mutations causing the absent foregut phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.