Facial Palsy, Congenital, with Ptosis and Velopharyngeal Dysfunction (FPVEPD)

Facial Palsy, Congenital, with Ptosis and Velopharyngeal Dysfunction, is also known as fpvepd. An important gene associated with Facial Palsy, Congenital, with Ptosis and Velopharyngeal Dysfunction is TUBB6 (Tubulin Beta 6 Class V). Affiliated tissues include brain, and related phenotypes are hypernasal speech and facial palsy