complement deficiency Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation. (Human Disease Ontology, DOID_626)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0004431
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Genes

15 genes associated with the complement deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
C1QA	complement component 1, q subcomponent, A chain
C1QB	complement component 1, q subcomponent, B chain
C1QC	complement component 1, q subcomponent, C chain
C1R	complement component 1, r subcomponent
C3	complement component 3
C4A	complement component 4A (Rodgers blood group)
C5	complement component 5
C6	complement component 6
C7	complement component 7
C8A	complement component 8, alpha polypeptide
C8B	complement component 8, beta polypeptide
C9	complement component 9
CFD	complement factor D (adipsin)
CFH	complement factor H
CFI	complement factor I