D68.2Hereditary deficiency of other clotting factors
Code usage status
Primary diagnosis
May be used as the primary diagnosis
Apply only when it matches the confirmed diagnosis and the documented clinical record.
Specificity
Complete code in the classification
Use when the diagnosis matches and no exclusion applies.
- Chapter III
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
- Official Vietnamese name
- Thiếu hụt yếu tố đông máu khác do di truyền
- Additional WHO coding guidance
- a O Congenital afibrinogenaemia Deficiency: AC globulin proaccelerin Deficiency of factor: I [fibrinogen] II [prothrombin] V [labile] VII [stable] X [Stuart-Prower] XII [Hageman] XIII [fibrin-stabilizing] Dysfibrinogenaemia (congenital) Hypoproconvertinaemi wren disease
Related D68 codes
D68
Other coagulation defects
D68.0
Primary diagnosis candidate
Von Willebrand disease
D68.1
Primary diagnosis candidate
Hereditary factor XI deficiency
D68.3
Primary diagnosis candidate
Haemorrhagic disorder due to circulating anticoagulants
D68.4
Primary diagnosis candidate
Acquired coagulation factor deficiency
D68.5
Primary diagnosis candidate
Primary thrombophilia
D68.6
Primary diagnosis candidate
Other thrombophilia
D68.8
Primary diagnosis candidate
Other specified coagulation defects
D68.9
Primary diagnosis candidate
Coagulation defect, unspecified
Clinical record checklist
View coding guide →- Confirm that the code matches the final documented diagnosis.
- Use one primary-diagnosis code and record only relevant additional conditions.
- Review Ministry indicators, inclusions, exclusions and notes.
- Do not infer a diagnosis beyond the clinical record.
2026 regulatory basis
Indicators are taken from columns 24–29 of the classification accompanying Circular 06/2026/TT-BYT, cross-referenced with Decision 1849/QĐ-BYT and Official Dispatch 4059/BYT-BH.
