| Disease ID | Source | Name | Description |
| 617732 | OMIM | Facial palsy, congenital, with ptosis and velopharyngeal dysfunction (FPVEPD) | An autosomal dominant congenital disorder characterized by non-progressive bilateral facial palsy, velopharyngeal dysfunction presenting with varying degrees of hypomimia, rhinophonia and impaired gag reflex, and bilateral ptosis. The disease is caused by variants affecting the gene represented in this entry. |