small forehead Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of a forehead that is abnormally small. (Human Phenotype Ontology, HP_0000350)
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2 genes associated with the small forehead phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
KDM5C lysine (K)-specific demethylase 5C
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)