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GENATLAS PHENOTYPE
last update : 3/07/2006
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
    Gene product
    Name gamma-glutamyl carboxylase
    Remark(s)