All diseases

OMIM ID
188050
OMIM term:
THROMBOPHILIA DUE TO THROMBIN DEFECT; THPH1
Alternative terms:
THROMBOPHILIA DUE TO FACTOR 2 DEFECT
VENOUS THROMBOSIS
VENOUS THROMBOEMBOLISM THROMBOSIS, PROTECTION AGAINST, INCLUDED
(∗) Location:
10q25.3   11p11.2   1p36.22   6p25.1  
(†) Associated OMIM genes:
F13A1   F2   HABP2   MTHFR  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/32iscgj3