ICD-10 Code: D68.52 – Prothrombin gene mutation

ICD-10 code D68.52 corresponds to Prothrombin gene mutation. This code is classified under the chapter D68 Other coagulation defects, which is part of the D65-D69: Coagulation defects, purpura and other hemorrhagic conditions category.

The parent chapter is Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.