D68.318 OTH HEMORRHAGIC DISORD D/T INTRNS CIRC ANTICOAG,ANTIB,INHIB

Code Information

  • Diagnosis Code: D68.318
  • Short Description: Oth hemorrhagic disord d/t intrns circ anticoag,antib,inhib
  • Long Description: Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
  • Code Version: 2025 ICD-10-CM

The code D68.318 is VALID for claim submission

Code Classification

Synonyms

  • Acquired coagulation factor inhibitor disorder
  • Drug-induced coagulation inhibitor disorder
  • Factor I inhibitor disorder
  • Hemorrhagic disorder due to antithrombinemia
  • Hemorrhagic disorder due to circulating anticoagulants
  • Hemorrhagic disorder due to increase in anti-11a
  • Hemorrhagic disorder due to increase in anti-9a
  • Hemorrhagic disorder due to increase in anti-VIIIa

References to Index of Diseases and Injuries

The code D68.318 has the following ICD-10-CM references to the Index of Diseases and Injuries

  • Inclusion Terms:
    • Antithromboplastinemia
    • Antithromboplastinogenemia
    • Hemorrhagic disorder due to intrinsic increase in antithrombin
    • Hemorrhagic disorder due to intrinsic increase in anti-VIIIa
    • Hemorrhagic disorder due to intrinsic increase in anti-IXa
    • Hemorrhagic disorder due to intrinsic increase in anti-XIa

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
D68.318 Right Arrow 286.59 Ot hem d/t circ anticoag
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
D68.32 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
D68.9 Coagulation defect, unspecified
This page was last updated on: 10/1/2024
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