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Diagnosis Code

D68.9 COAGULATION DEFECT, UNSPECIFIED


Code Information

Diagnosis Code: D68.9

Short Description: Coagulation defect, unspecified

Long Description: Coagulation defect, unspecified

The code D68.9 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)
        • D68.9 Coagulation defect, unspecified

Code Version: 2022 ICD-10-CM


Synonyms

  • Abnormal uterine bleeding due to coagulopathy
  • Bleeds easily
  • Blood coagulation disorder
  • Blood coagulation disorder complicating childbirth
  • Blood coagulation disorder complicating pregnancy
  • Blood coagulation disorder, categorized by value of screening test
  • Blood does not clot properly
  • Coagulation factor deficiency syndrome
  • Disorder of hemostatic system
  • Glomerular disease due to coagulation disorder
  • Hereditary coagulation factor deficiency
  • Menorrhagia
  • Menorrhagia due to bleeding disorder
  • Occlusion of microvasculature of skin caused by embolus
  • Occlusion of microvasculature of skin due to coagulopathy
  • Purpura of skin and/or skin-associated mucous membrane co-occurrent and due to coagulation disorder
  • Tendency to bleed - finding
  • Tendency to bleed - finding

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
D68.9 Right Arrow 286.9 Coagulat defect NEC/NOS

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
D68 Other coagulation defects
D68.0 Von Willebrand disease
D68.00 Von Willebrand disease, unspecified
D68.01 Von Willebrand disease, type 1
D68.02 Von Willebrand disease, type 2
D68.020 Von Willebrand disease, type 2A
D68.021 Von Willebrand disease, type 2B
D68.022 Von Willebrand disease, type 2M
D68.023 Von Willebrand disease, type 2N
D68.029 Von Willebrand disease, type 2, unspecified
D68.03 Von Willebrand disease, type 3
D68.04 Acquired von Willebrand disease
D68.09 Other von Willebrand disease
D68.1 Hereditary factor XI deficiency
D68.2 Hereditary deficiency of other clotting factors
D68.3 Hemorrhagic disorder due to circulating anticoagulants
D68.31 Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68.311 Acquired hemophilia
D68.312 Antiphospholipid antibody with hemorrhagic disorder
D68.318 Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68.32 Hemorrhagic disorder due to extrinsic circulating anticoagulants
D68.4 Acquired coagulation factor deficiency
D68.5 Primary thrombophilia
D68.51 Activated protein C resistance
D68.52 Prothrombin gene mutation
D68.59 Other primary thrombophilia
D68.6 Other thrombophilia
D68.61 Antiphospholipid syndrome
D68.62 Lupus anticoagulant syndrome
D68.69 Other thrombophilia
D68.8 Other specified coagulation defects

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

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