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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)