| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A syndrome that is characterized by the presence of at least three of the following: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities. (Human Disease Ontology, DOID_14679) |
| External Link | http://www.omim.org/entry/192350 |
| Similar Terms | |
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1 genes associated with the ?vacterl association phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| HOXD13 | homeobox D13 |
