| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/214800 |
| Similar Terms | |
| Downloads & Tools |
2 genes associated with the charge syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
