Home Page |
Orphanet | References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 29/11/2005 |
Symbol | F13A1 | |||
Location | 6p25.1 | |||
Name | fibrin-stabilizing factor deficiency, type II | |||
Corresponding gene | F13A1 | |||
Main clinical features | bleeding tendency, defective wound healing, habitual abortion | |||
Genetic determination
Function/system disorder
| hematology | Type
| disease
| |
Gene product |
Name | coagulation factor XIII, A1 polypeptide (F13A1) |
Remark(s) |