| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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://ctdbase.org/detail.go?type=disease&acc=MESH:C536534 |
| Similar Terms | |
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2 genes/proteins associated with the disease VATER association from the curated CTD Gene-Disease Associations dataset.
