RxDB
ICD-10-CM Codes Browse (Tabular) Diagnostic External Drug Neoplasm

D68.52 – Prothrombin gene mutation

Overview

Coding Notes

Active
Billable, valid for HIPAA-covered transactions

GEM Conversion to ICD-9 CM

Fs: 10000 – Primary hypercoagulable state

MDC / MS-DRG Reference

RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH MCC
RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH CC
RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITHOUT CC/MCC

Back Reference of Diagnostic Codes


Sibling Codes

Activated protein C resistance
Other primary thrombophilia

Parent Sibling Codes

Von Willebrand's disease
Hereditary factor XI deficiency
Hereditary deficiency of other clotting factors
Hemorrhagic disorder due to circulating anticoagulants
Acquired coagulation factor deficiency
Primary thrombophilia
Other thrombophilia
Other specified coagulation defects
Coagulation defect, unspecified

View in Tabular

Code Title
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
D65-D69 Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
D68 Other coagulation defects
D68.5 Primary thrombophilia
D68.52 Prothrombin gene mutation