Diagnosis Code: D68.2

Short Description: Hereditary deficiency of other clotting factors

Long Description: Hereditary deficiency of other clotting factors

The code D68.2 is VALID for claim submission

Code Classification:

• Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50–D89)
  • Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
    • Other coagulation defects (D68)
      • D68.2 Hereditary deficiency of other clotting factors

Code Version: 2022 ICD-10-CM

Synonyms

• Acquired coagulation factor inhibitor disorder
• Alpha chain defect dysfibrinogenemia
• Autosomal dominant deficiency of plasminogen
• Beta chain defect dysfibrinogenemia
• Combined deficiency of factor V and factor VIII
• Congenital afibrinogenemia
• Congenital fibrinogen abnormality
• Congenital plasminogen activator inhibitor deficiency type 1
• Contact factor deficiency
• Drug-induced coagulation inhibitor disorder
• Dysfibrinogenemia
• Dysplasminogenemia
• Factor I deficiency
• Factor I deficiency
• Factor I deficiency disease
• Factor II deficiency
• Factor V deficiency
• Factor V deficiency
• Factor VII deficiency
• Factor X deficiency
• Factor XII deficiency disease
• Factor XIII deficiency disease
• Factor XIII inhibitor disorder
• Fibrinogen abnormality
• Fibrinogen deficiency
• Fibrinogen in blood above reference range
• Fibrinolytic bleeding syndrome
• Gamma chain defect dysfibrinogenemia
• Hemorrhagic disease of the newborn due to factor II deficiency
• Heparin cofactor II deficiency
• Hereditary combined coagulation factor deficiency
• Hereditary combined coagulation factor deficiency
• Hereditary combined deficiency of vitamin K-dependent clotting factors
• Hereditary congenital prekallikrein deficiency
• Hereditary dysfibrinogenemia
• Hereditary dysplasminogenemia
• Hereditary factor I deficiency disease
• Hereditary factor II deficiency disease
• Hereditary factor V deficiency disease
• Hereditary factor VII deficiency disease
• Hereditary factor X deficiency disease
• Hereditary factor XII deficiency disease
• Hereditary factor XIII A subunit and B subunit deficiency
• Hereditary factor XIII A subunit deficiency
• Hereditary factor XIII B subunit deficiency
• Hereditary factor XIII deficiency disease
• Hereditary hypoplasminogenemia
• Hereditary thrombophilic dysfibrinogenemia
• High molecular weight kininogen deficiency
• Hyperfibrinogenemia
• Hypodysfibrinogenemia
• Hypoplasminogenemia
• Immunodeficiency with factor I anomaly
• Neonatal coagulation disorder
• Passovoy factor deficiency
• Platelet factor V deficiency
• Platelet procoagulant activity deficiency
• Prekallikrein deficiency
• Prothrombin complex deficiency

References to Index of Diseases and Injuries

The code D68.2 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • AC globulin deficiency
  • Congenital afibrinogenemia
  • Deficiency of factor I [fibrinogen]
  • Deficiency of factor II [prothrombin]
  • Deficiency of factor V [labile]
  • Deficiency of factor VII [stable]
  • Deficiency of factor X [Stuart-Prower]
  • Deficiency of factor XII [Hageman]
  • Deficiency of factor XIII [fibrin stabilizing]
  • Dysfibrinogenemia (congenital)
  • Hypoproconvertinemia
  • Owren's disease
  • Proaccelerin deficiency

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

« Previous Code