| Dataset | ClinVar Gene-Phenotype 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.ncbi.nlm.nih.gov/medgen/?term=C1735591 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the VACTERL association phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| HOXD13 | homeobox D13 |
