bifid nasal tip Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A splitting of the nasal tip. Visually assessable vertical indentation, cleft, or depression of the nasal tip. (Human Phenotype Ontology, HP_0000456)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000456
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Genes

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

Symbol Name
ALX3 ALX homeobox 3
ALX4 ALX homeobox 4
BCOR BCL6 corepressor
EFNB1 ephrin-B1