recurrent meningitis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased susceptibility to meningitis as manifested by a medical history of recurrent episodes of meningitis. (Human Phenotype Ontology, HP_0006946)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006946
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Genes

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

Symbol Name
C5 complement component 5
CFI complement factor I
IL2RG interleukin 2 receptor, gamma