D68.52ICD-10-CM 2027 · Billable
Prothrombin gene mutation
Sibling codes
Inherited from D68.5: Primary thrombophilia
Excludes1
- 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)
Inclusion terms
- Primary hypercoagulable states
Inherited from D68: Other coagulation defects
Excludes1
- abnormal coagulation profile NOS (
R79.1)
Excludes2
Part of: D68.5: Primary thrombophilia › D68: Other coagulation defects