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Summary Literature (0)
MIM:617732 - FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD

Xenbase Genes: tubb6

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0060589 - facial palsy, congenital, with ptosis and velopharyngeal dysfunction