recurrent pharyngitis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased susceptibility to pharyngitis as manifested by a history of recurrent pharyngitis. (Human Phenotype Ontology, HP_0100776)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100776
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Genes

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

Symbol Name
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SH2D1A SH2 domain containing 1A
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A