| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A syndrome that is acterized by a pattern of congenital anomalies including choanal atresia and malformations of the heart, inner ear, and retina. (Human Disease Ontology, DOID_0050834) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D058747 |
| Similar Terms | |
| Downloads & Tools |
2 genes/proteins associated with the disease CHARGE Syndrome from the curated CTD Gene-Disease Associations dataset.
