absent toenail Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Congenital absence of the toenail. (Human Phenotype Ontology, HP_0001802)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001802
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Genes

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

Symbol Name
ARID1A AT rich interactive domain 1A (SWI-like)
LBR lamin B receptor
PORCN porcupine homolog (Drosophila)
WNT7A wingless-type MMTV integration site family, member 7A