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GENATLAS PHENOTYPE |
last update : 11-05-2011 |
Symbol | FMFD2 |
Location | 18q21.3-q22 |
Name | factor V and factor VIII combined deficiency 2 |
Other name(s) | multiple coagulation deficiency |
Corresponding gene | LMAN1 |
Other symbol(s) | F5F8D, MCFD1 |
Main clinical features | bleeding diathesis, mild to moderate |
Genetic determination | autosomal recessive |
Function/system disorder | hematology |
Type | disease |
Gene product |
Name | lectin mannose-binding 1 |
Remark(s) |