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GENATLAS PHENOTYPE |
last update : 24/12/2008 |
Symbol | C1S |
Location | 12p13.31 |
Name | complement component 1S deficiency |
Other name(s) |
|
Corresponding gene | C1S |
related resource | CISbase - Mutation registry for C1s deficiency |
Main clinical features | systemic lupus erythematosus-like syndrome and chronic glomerulonephritis, multiple autoimmune diseases |
Genetic determination | autosomal dominant |
Function/system disorder | defense and immunity |
Type | disease |
Remark(s) |