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Orphanet | References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 30/06/2006 |
Symbol | F12 | |||
Location | 5q35.3 | |||
Name | Hageman factor deficiency | |||
Other name(s) | HAF deficiency | |||
Corresponding gene | F12 | |||
Main clinical features | without bleeding diathesis | |||
Genetic determination
Function/system disorder
| hematology | Type
| disease
| |
Gene product |
Name | coagulation factor XII, Hageman (F12) |
Remark(s) |