flat forehead Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A forehead with abnormal flatness. (Human Phenotype Ontology, HP_0004425)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004425
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Genes

5 genes associated with the flat forehead phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHST14 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
FGFR2 fibroblast growth factor receptor 2
LRP5 low density lipoprotein receptor-related protein 5
RECQL4 RecQ protein-like 4
TWIST1 twist family bHLH transcription factor 1