Disorders

Factor V and Factor VIII, Combined Deficiency of

Gene	Locus	Protein
MCFD2	2p21	Protein ERGIC-53

Laboratory	Test Method	Prenatal	Carrier *
GSTS Pathology - Guy's and St. Thomas' NHS Foundation Trust, Molecular Haemostasis and Thrombosis - London, Great Britain

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.