| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A syndrome characterized by the combination of lower lip pits, cleft lip with or without cleft palate and cleft palate alone. (Human Disease Ontology, DOID_0060239) |
| External Link | http://www.omim.org/entry/119300 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the van der woude syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| IRF6 | interferon regulatory factor 6 |
