D68.52 - Prothrombin gene mutation
The ICD 10 Code for Prothrombin gene mutation is listed as D68.52.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.
| ICD 10 CM Field | Value |
|---|---|
| Diagnosis Code: | D68.52
|
| Description: | Prothrombin gene mutation |
| Diagnostic Related Groups
(MS-DRG v30.0) |
814 - Reticuloendothelial & Immunity Disorders W Mcc
815 - Reticuloendothelial & Immunity Disorders W Cc 816 - Reticuloendothelial & Immunity Disorders W/o Cc/mcc |
| Chapter | Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89) |
| Block | Coagulation defects, purpura and other hemorrhagic conditions (D65-D69) |
| Parent | D68.5 - Primary thrombophilia |
| ICD-9-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD 9 Dx Code: | 289.81 - Primary hypercoagulable state (approximate) |
| ICD-10-CM Siblings (same level / similar specificity) of D68.52: | |
| D68.51 - Activated protein C resistance | |
| D68.59 - Other primary thrombophilia | |