ICD 10 CM Codes

D68.52 Prothrombin gene mutation
Billable Code  is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
GEMS
ICD-10-CM D68.52 converts approximately to:ICD-9-CM
2015 ICD-9-CM 289.81 Primary hypercoagulable state
ICD-10-CM D68.52is grouped within Diagnostic Related Group(s) (MS-DRG v30.0)
814 RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH MCC
815 RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH CC
816 RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITHOUT CC/MCC
Alternate Description
Factor V Leiden mutation
ICD-10-CM Index Entry
ICD-10-CM Index entries containing back-references to ICD-10-CM '.D68.52.'
Hypercoagulable (state); prothrombin gene mutation
Mutation (s); prothrombin gene
Prothrombin gene mutation