cleft of chin Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Incomplete fusion of the chin, resulting from a developmental defect and manifesting as a midline cleft or fissure of the chin. (Human Phenotype Ontology, HP_0011323)
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2 genes associated with the cleft of chin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGFR2 fibroblast growth factor receptor 2
TWIST1 twist family bHLH transcription factor 1