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Hereditary factor I deficiency disease

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Description

An inherited blood coagulation disorder characterized by the partial or complete absence of fibrinogen in the blood, resulting in bleeding.

NCI

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

0

Genes

External Links

  • OMIM
  • Orphanet
  • HPO
  • Medgen

    C0019250

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