289.81 PRIM HYPERCOAGULABLE ST

Code Information

  • Diagnosis Code: 289.81
  • Short Description: Prim hypercoagulable st
  • Long Description: Primary hypercoagulable state
  • Code Version: 2015 ICD-9-CM

Code Classification

  • Diseases of the blood and blood-forming organs (280–289)
    • Diseases of the blood and blood-forming organs (280-289)
      • 289 Other diseases of blood and blood-forming organs
        • 289.81 Prim hypercoagulable st

Synonyms

  • Antiphospholipid syndrome in pregnancy
  • Catastrophic antiphospholipid syndrome
  • Factor V Leiden mutation
  • Hereditary antithrombin III deficiency
  • Hereditary heparin cofactor II deficiency
  • Hereditary protein C deficiency
  • Hereditary protein S deficiency
  • Hereditary thrombophilia
  • Heterozygous protein C deficiency
  • Heterozygous protein S deficiency
  • Heterozygous prothrombin G20210A mutation
  • Homozygous protein C deficiency
  • Homozygous protein S deficiency
  • Homozygous prothrombin G20210A mutation
  • Protein S deficiency disease
  • Prothrombin G20210A mutation
  • Resistance to activated protein C due to Factor V Leiden
  • Thrombophilia due to acquired antithrombin III deficiency
  • Thrombophilia due to acquired protein C deficiency
  • Thrombophilia due to acquired protein S deficiency
  • Thrombophilia due to antiphospholipid antibody
  • Upper gastrointestinal hemorrhage associated with hypercoagulability state

References to Index of Diseases and Injuries

The code 289.81 has the following ICD-9-CM references to the Index of Diseases and Injuries

  • Antibody
    • anticardiolipin 795.79
      • with
        • hypercoagulable state 289.81
    • antiphosphatidylglycerol 795.79
      • with
        • hypercoagulable state 289.81
    • antiphosphatidylinositol 795.79
      • with
        • hypercoagulable state 289.81
    • antiphosphatidylserine 795.79
      • with
        • hypercoagulable state 289.81
    • antiphospholipid 795.79
      • with
        • hypercoagulable state 289.81
  • Anticoagulant
    • lupus (LAC) 795.79
      • with
        • hypercoagulable state 289.81
  • Deficiency, deficient
    • antithrombin III 289.81
    • protein 260
      • C 289.81
      • S 289.81
  • Factor
    • V Leiden mutation 289.81
  • Hypercoagulation syndrome (primary) 289.81
    • secondary 289.82
  • Inhibitor
    • systemic lupus erythematosus (presence of) 795.79
      • with
        • hypercoagulable state 289.81
  • Lupus 710.0
    • anticoagulant 795.79
      • with
        • hypercoagulable state 289.81
    • erythematosus (discoid) (local) 695.4
      • systemic 710.0
        • inhibitor (presence of) 795.79
          • with hypercoagulable state 289.81
  • Mutation(s)
    • factor V Leiden 289.81
    • prothrombin gene 289.81
  • Resistance, resistant (to)
    • activated protein C 289.81
  • State
    • hypercoagulable (primary) 289.81
      • secondary 289.82
  • Syndrome - see also Disease
    • Albright-McCune-Sternberg (osteitis fibrosa disseminata) 756.59
    • anticardiolipin antibody 289.81
    • antiphospholipid antibody 289.81
    • anxiety (see also Anxiety) 300.00
    • Beals 759.82
    • Caplan (-Colinet) syndrome 714.81

Crosswalk Information

The code 289.81 converts into the following ICD-10 code(s):

ICD-9 Code ICD-10 Code ICD-10 Description
289.81 Right Arrow D68.51 Activated protein C resistance
D68.52 Prothrombin gene mutation
D68.59 Other primary thrombophilia
D68.61 Antiphospholipid syndrome
D68.62 Lupus anticoagulant syndrome
This ICD-9 to ICD-10 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-9 Code ICD-9 Description
289.0 Polycythemia, secondary
289.1 Chronic lymphadenitis
289.2 Nonspecific mesenteric lymphadenitis
289.3 Lymphadenitis, unspecified, except mesenteric
289.4 Hypersplenism
289.50 Disease of spleen, unspecified
289.51 Chronic congestive splenomegaly
289.52 Splenic sequestration
289.53 Neutropenic splenomegaly
289.59 Other diseases of spleen
289.6 Familial polycythemia
289.7 Methemoglobinemia
289.82 Secondary hypercoagulable state
289.83 Myelofibrosis
289.84 Heparin-induced thrombocytopenia (HIT)
289.89 Other specified diseases of blood and blood-forming organs
289.9 Unspecified diseases of blood and blood-forming organs
This page was last updated on: 10/1/2014
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