bifid nose Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Visually assessable vertical indentation, cleft, or depression of the nasal bridge, ridge and tip. (Human Phenotype Ontology, HP_0011803)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011803
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Genes

3 genes associated with the bifid nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FREM1 FRAS1 related extracellular matrix 1
HYLS1 hydrolethalus syndrome 1
ZSWIM6 zinc finger, SWIM-type containing 6