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Thrombophilia due to thrombin defect

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Description

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

239

SEE THE VARIANTS →

Genes

  • F13A1
  • F2
  • HABP2
  • MTHFR
  • F5
  • PROC
  • PROS1
  • SERPINC1

External Links

  • OMIM

    188050

  • Orphanet
  • HPO
  • Medgen

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