recurrent meningococcal disease Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Recurrent infections by Neisseria meningitidis (one of the most common causes of bacterial meningitis), which is also known as meningococcus. (Human Phenotype Ontology, HP_0005381)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005381
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Genes

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

Symbol Name
C6 complement component 6
C7 complement component 7
CFI complement factor I