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Orphanet | References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 31/05/2006 |
Symbol | C2 |
Location | 6p21.3 |
Name | complement component 2 deficiency |
Other name(s) |
|
Corresponding gene | C2 |
related resource | C2base - Mutation registry for C2 deficiency |
Genetic determination | multigenic |
Function/system disorder | defense and immunity |
Type | susceptibility factor |