All diseases

OMIM ID
612356
OMIM term:
HEPARIN COFACTOR II DEFICIENCY
Alternative terms:
THROMBOPHILIA DUE TO HEPARIN COFACTOR II DEFICIENCY; THPH10
HCF II DEFICIENCY
HCF2 DEFICIENCY
(∗) Location:
22q11.21  
(†) Associated OMIM genes:
HCF2  
(‡) Associated MGI genes:

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