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GENATLAS PHENOTYPE

last update : 6/07/2006

Symbol	HCF2
Location	22q11.21
Name	thrombosis, recurrent
Corresponding gene	SERPIND1
Main clinical features	congenital deficiency of HCF II classified into type I (quantitative) and type II (qualitative) deficiency, thrombophilia
Genetic determination	autosomal dominant
Function/system disorder	hematology
Type	disease

Gene product

Name	heparin cofactor II (SERPIND1)

Remark(s)