esophageal ulcer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A gastrointestinal system disease that is located_in the esophagus. (Human Disease Ontology, DOID_6050)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004547
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Genes

1 gene mutations causing the esophageal ulcer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
PLG plasminogen