1. ICD-10-CM Codes
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2. D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
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3. D65-D69 Coagulation defects, purpura and other hemorrhagic conditions
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4. D68- Other coagulation defects
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5. 2020 ICD-10-CM Diagnosis Code D68.2

2020 ICD-10-CM Diagnosis Code D68.2

Hereditary deficiency of other clotting factors

2016 2017 2018 2019 2020 Billable/Specific Code

• D68.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
• The 2020 edition of ICD-10-CM D68.2 became effective on October 1, 2019.
• This is the American ICD-10-CM version of D68.2 - other international versions of ICD-10 D68.2 may differ.

• Clotting factor deficiency, congenital
• Congenital coagulation factor deficiency
• Dysfibrinogenemia
• Dysfibrinogenemia, congenital
• Factor 10 deficiency
• Factor 12 deficiency
• Factor 2 mutation
• Factor 5 deficiency
• Factor 7 deficiency
• Factor ii deficiency
• Factor v deficiency
• Factor v quebec
• Factor vii deficiency
• Factor x deficiency
• Factor xii deficiency disease
• Hereditary dysfibrinogenemia
• Platelet factor v deficiency (factor v quebec)

• A blood coagulation disorder characterized by the complete absence of fibrinogen in the blood, resulting in bleeding.
• A deficiency of blood coagulation factor v (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as owren's disease or parahemophilia. It varies greatly in severity. Factor v deficiency is an autosomal recessive trait. (Dorland, 27th ed)
• A deficiency or absence of fibrinogen in the blood.
• A usually inherited blood coagulation disorder characterized by the partial or complete absence of fibrinogen in the blood, resulting in bleeding.
• A very rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of factor v, resulting in bleeding.
• An autosomal recessive characteristic or a coagulation disorder acquired in association with vitamin k deficiency. Factor vii is a vitamin k dependent glycoprotein essential to the extrinsic pathway of coagulation.
• Deficiency or absence of fibrinogen (coagulation factor i) in the blood.

• 813 Coagulation disorders

Convert D68.2 to ICD-9-CM

• 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
• 2017 (effective 10/1/2016): No change
• 2018 (effective 10/1/2017): No change
• 2019 (effective 10/1/2018): No change
• 2020 (effective 10/1/2019): No change

• Absence (of) (organ or part) (complete or partial)
  • fibrinogen (congenital) D68.2
• Afibrinogenemia D68.8
  - see also Defect, coagulation
  ICD-10-CM Diagnosis Code D68.8

  Other specified coagulation defects

  2016 2017 2018 2019 2020 Billable/Specific Code

  Type 1 Excludes

  • hemorrhagic disease of newborn (P53)
  • congenital D68.2
• Defect, defective Q89.9
  ICD-10-CM Diagnosis Code Q89.9

  Congenital malformation, unspecified

  2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt

  Applicable To

  • Congenital anomaly NOS
  • Congenital deformity NOS
  • coagulation (factor) D68.9
    - see also Deficiency, factor
    ICD-10-CM Diagnosis Code D68.9

    Coagulation defect, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code
    • hereditary NEC D68.2
  • fibrin polymerization D68.2
  • Hageman D68.2 (factor)
• Deficiency, deficient
  • AC globulin (congenital) (hereditary) D68.2
  • autoprothrombin
    • I D68.2
    • C D68.2
  • coagulation NOS D68.9
    ICD-10-CM Diagnosis Code D68.9

    Coagulation defect, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code
    • clotting factor NEC D68.2 - see also Deficiency, factor
  • factor - see also Deficiency, coagulation
    • Hageman D68.2
    • I D68.2 (congenital) (hereditary)
    • II D68.2 (congenital) (hereditary)
    • V D68.2 (congenital) (hereditary)
    • VII D68.2 (congenital) (hereditary)
    • X D68.2 (congenital) (hereditary)
    • XII D68.2 (congenital) (hereditary)
    • XIII D68.2 (congenital) (hereditary)
  • fibrin-stabilizing factor (congenital) (hereditary) D68.2
  • fibrinogen (congenital) (hereditary) D68.2
  • labile factor (congenital) (hereditary) D68.2
  • proaccelerin (congenital) (hereditary) D68.2
  • proconvertin factor (congenital) (hereditary) D68.2
  • prothrombin (congenital) (heredItary) D68.2
  • stable factor (congenital) (hereditary) D68.2
  • thrombokinase D68.2
  • accelerator globulin D68.2 (Ac G) (blood)
  • activating factor D68.2 (blood)
  • clotting factor NEC D68.2 (hereditary) - see also Deficiency, factor
  • contact factor D68.2
  • fibrinase D68.2
  • glass factor D68.2
  • Hageman factor D68.2
  • Laki-Lorand factor D68.2
  • Prower factor D68.2
  • SPCA D68.2 (factor VII)
  • Stuart-Prower D68.2 (factor X)
• Disease, diseased - see also Syndrome
  • Hageman D68.2 (congenital factor XII deficiency)
  • Stuart-Prower D68.2 (congenital factor X deficiency)
  • Stuart's D68.2 (congenital factor X deficiency)
• Dysfibrinogenemia D68.2 (congenital)
• Fibrinogenopenia D68.8
  ICD-10-CM Diagnosis Code D68.8

  Other specified coagulation defects

  2016 2017 2018 2019 2020 Billable/Specific Code

  Type 1 Excludes

  • hemorrhagic disease of newborn (P53)
  • congenital D68.2
• Fibrinopenia (hereditary) D68.2
• Hageman's factor defect, deficiency or disease D68.2
• Hypofibrinogenemia D68.8
  ICD-10-CM Diagnosis Code D68.8

  Other specified coagulation defects

  2016 2017 2018 2019 2020 Billable/Specific Code

  Type 1 Excludes

  • hemorrhagic disease of newborn (P53)
  • congenital D68.2 (hereditary)
• Hypoproconvertinemia, congenital D68.2 (hereditary)
• Hypoprothrombinemia (congenital) (hereditary) (idiopathic) D68.2
• Owren's disease or syndrome D68.2 (parahemophilia)
• Parahemophilia D68.2 - see also Defect, coagulation
• Stuart deficiency disease D68.2 (factor X)
• Stuart-Prower factor deficiency D68.2 (factor X)
• Syndrome - see also Disease
  • Owren's D68.2

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.