|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||greater than the expected number of benign focal malformations in the colon in a specific population in a given time period; results from faulty colonic development, and is composed of an abnormal mixture of tissue elements, or an abnormal proportion of a single element normally present at that site (Mammalian Phenotype Ontology, MP_0002043)|
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1 gene mutations causing the increased colon hamartoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|CDX2||caudal type homeobox 2|