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Orphanet | References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 22/06/2006 |
Symbol | C5 | |||
Location | 9q33.2 | |||
Name | complement component 5 deficiency | |||
Other name(s) |
| |||
Corresponding gene | C5 | |||
related resource | C5base - Mutation registry for C5 deficiency | |||
Main clinical features |
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Genetic determination
Function/system disorder
| defense and immunity | Type
| disease
| |
Gene product |
Name | complement component 5 |
Remark(s) |