pilonidal sinus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A sinus in the coccygeal region (the region of the intergluteal cleft). A pilonidal sinus often contains hair and skin debris. (Human Phenotype Ontology, HP_0010769)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010769
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Genes

1 genes associated with the pilonidal sinus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
WNT7A wingless-type MMTV integration site family, member 7A