| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | absence of the part of the digestive canal through which food passes from the pharynx to the stomach (Mammalian Phenotype Ontology, MP_0004544) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004544 |
| Similar Terms | |
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1 gene mutations causing the absent esophagus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| CHRD | chordin |
