F3

coagulation factor III, tissue factor
OMIM: 134390, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber F3 in Thrombophilia with a likely monogenic cause


Version 2.5
Latest signed off version: v2.2 (22 Mar 2023)

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Wessex and West Midlands GLH
  • Expert Review Amber
  • NHS GMS
  • London South GLH
Phenotypes
  • Tissue factor deficiency (Factor III)