ankyloblepharon Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Partial fusion of the upper and lower eyelid margins by single or multiple bands of tissue. (Human Phenotype Ontology, HP_0009755)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009755
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
IRF6 interferon regulatory factor 6
RAX retina and anterior neural fold homeobox
RIPK4 receptor-interacting serine-threonine kinase 4
TP63 tumor protein p63