| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | absence of the portion of the embryonic gut between the foregut and the hindgut (Mammalian Phenotype Ontology, MP_0009706) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009706 |
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3 gene mutations causing the absent midgut phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.