| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_14737) |
| External Link | http://www.omim.org/entry/304110 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the craniofrontonasal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| EFNB1 | ephrin-B1 |
