D68.5 Primary thrombophilia

Non-billable header with 3 child codes.

Applicable to

• Primary hypercoagulable states

Excludes1 (never code together)

• antiphospholipid syndrome (D68.61)
• lupus anticoagulant (D68.62)
• secondary activated protein C resistance (D68.69)
• secondary antiphospholipid antibody syndrome (D68.69)
• secondary lupus anticoagulant with hypercoagulable state (D68.69)
• secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
• systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
• systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
• thrombotic thrombocytopenic purpura (M31.19)

Applies from D68 Other coagulation defects

Excludes1 (never code together)

• abnormal coagulation profile NOS (R79.1)

Excludes2 (not included here)

• coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1)
• coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)

Codes under D68.5

• D68.51 Activated protein C resistance
• D68.52 Prothrombin gene mutation
• D68.59 Other primary thrombophilia

Code annotations containing back-references to D68.5

Back-references to D68

• Type 1 Excludes: R79.1 Abnormal coagulation profile ("coagulation defects (D68.-)")

Nearby codes

• 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 (this code)
• D68.51 Activated protein C resistance
• D68.52 Prothrombin gene mutation
• D68.59 Other primary thrombophilia
• D68.6 Other thrombophilia
• D68.61 Antiphospholipid syndrome