| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch. (Human Disease Ontology, DOID_2907) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D006053 |
| Similar Terms | |
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2 genes/proteins associated with the disease Goldenhar Syndrome from the curated CTD Gene-Disease Associations dataset.
