2009 ICD-9-CM Diagnosis Code 289.81
Primary hypercoagulable state
- Short description: PRIM HYPERCOAGULABLE ST.
- ICD-9-CM 289.81 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 289.81 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
- You are viewing the 2009 version of ICD-9-CM 289.81.
- More recent version(s) of ICD-9-CM 289.81: 2010 2011 2012 2013 2014 2015.
Convert to ICD-10-CM:
289.81 converts approximately to:
- 2015/16 ICD-10-CM D68.51 Activated protein C resistance
Or:
- 2015/16 ICD-10-CM D68.52 Prothrombin gene mutation
Or:
- 2015/16 ICD-10-CM D68.59 Other primary thrombophilia
Or:
- 2015/16 ICD-10-CM D68.61 Antiphospholipid syndrome
Or:
- 2015/16 ICD-10-CM D68.62 Lupus anticoagulant syndrome
Approximate Synonyms
- Activated Protein C resistance
- Anticardiolipin syndrome
- Antiphospholipid syndrome
- Antiphospholipid syndrome complication in pregnancy
- Antiphospholipid syndrome in pregnancy
- Antiphospholipid syndrome postpartum
- Antithrombin 3 deficiency
- Antithrombin III deficiency
- Factor 5 Leiden mutation
- Factor 5 Leiden mutation, heterozygous
- Factor 5 Leiden mutation, homozygous
- Factor V Leiden mutation
- Factor V Leiden mutation, heterozygous
- Factor V Leiden mutation, homozygous
- Hereditary antithrombin III deficiency
- Hereditary heparin cofactor II deficiency
- Hereditary protein C deficiency
- Hereditary protein S deficiency
- Hereditary thrombophilia
- Heterozygous Factor V Leiden mutation
- Heterozygous protein C deficiency
- Heterozygous protein S deficiency
- Heterozygous prothrombin G20210A mutation
- Homozygous Factor V Leiden mutation
- Homozygous protein C deficiency
- Homozygous protein S deficiency
- Homozygous prothrombin G20210A mutation
- Hypercoagulability state
- Hypercoagulable state
- Hypercoagulable state (tendency to form clots)
- Hypercoagulable state, primary
- Lupus anticoagulant
- Lupus anticoagulant disorder
- Postpartum (after childbirth) antiphospholipid syndrome
- Postpartum antiphospholipid syndrome
- Protein C deficiency disease
- Protein C deficiency disorder
- Protein C resistance
- Protein S deficiency disease
- Protein S deficiency disorder
- Prothrombin G20210A mutation
- Prothrombin gene 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
Applies To
- Activated protein C resistance
- Antithrombin III deficiency
- Factor V Leiden mutation
- Lupus anticoagulant
- Protein C deficiency
- Protein S deficiency
- Prothrombin gene mutation
antithrombin III 289.81
secondary 289.82
