velopharyngeal insufficiency Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Inability of velopharyngeal sphincter to sufficiently separate the nasal cavity from the oral cavity during speech. (Human Phenotype Ontology, HP_0000220)
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4 genes associated with the velopharyngeal insufficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
RAI1 retinoic acid induced 1
SF3B4 splicing factor 3b, subunit 4, 49kDa
TBX1 T-box 1
TP63 tumor protein p63