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#613679 - PROTHROMBIN DEFICIENCY, CONGENITAL

DYSPROTHROMBINEMIA, INCLUDED

Cytogenetic locations: 11p11.2

8.

#613554 - VON WILLEBRAND DISEASE, TYPE 2; VWD2

VON WILLEBRAND DISEASE, TYPE 2A, INCLUDED; VWD2A, INCLUDED

Cytogenetic locations: 12p13.31

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%612348 - THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR; THPH9

HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR, INCLUDED

Cytogenetic locations: 1pter-p36.13, 8p11.21

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*612309 - COAGULATION FACTOR V; F5

FACTOR V LEIDEN, INCLUDED

Cytogenetic locations: 1q24.2

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#608446 - MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO

MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO, 1, INCLUDED; MCI1, INCLUDED

Cytogenetic locations: 6p21.33, 1pter-p36.13, 6p25.1, 1pter-p36.13, 1p32.3, 1pter-p36.13, 22q13.1, 1pter-p36.13, 22q12.1, 1pter-p36.13, 17q21.32, 1pter-p36.13, 1q25.1

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