| Symbol
| GGCXD
|
| Location
| 2p12
|
| Name
|
combined deficiency of vitamin K-dependent clotting factors |
| Other name(s)
|
vitamin K-dependent coagulation defect
familial multiple coagulation factor deficiency III |
| Corresponding gene
|
GGCX
|
| Other symbol(s)
| VKCFD1, FMFD III, MCFD3
|
| Main clinical features
|
bleeding tendancy
episodes of intracranial hemorrhage in the first weeks of life, sometimes leading to a fatal outcome. |
| Genetic determination
| autosomal recessive |
| Function/system disorder
| metabolism/aminoacids |
|
| metabolism/vitamin |
| Type
| disease
|