Diagnosis Code: D68.8

Short Description: Other specified coagulation defects

Long Description: Other specified coagulation defects

The code D68.8 is VALID for claim submission

Code Classification:

• Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50–D89)
  • Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
    • Other coagulation defects (D68)
      • D68.8 Other specified coagulation defects

Code Version: 2022 ICD-10-CM

Synonyms

• A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency
• Abnormal fibrinolysis
• Acquired coagulation disorder
• Acquired coagulation factor inhibitor disorder
• Acquired coagulation factor inhibitor disorder
• Acquired coagulation factor inhibitor disorder
• Acquired fibrinogen abnormality
• Acquired hypofibrinogenemia
• Acquired hypoplasminogenemia
• Acquired inhibitor of coagulation
• Afibrinogenemia
• Alpha-2-antiplasmin deficiency
• Alpha-2-antiplasmin deficiency
• Anticoagulant excess without bleeding
• Anti-factor II disorder
• Antiprothrombin disorder
• Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• Blood coagulation disorder with impaired clot retraction time
• Blood coagulation disorder with prolonged bleeding time
• Blood coagulation disorder with prolonged coagulation time
• Blood coagulation disorder with shortened bleeding time
• Blood coagulation disorder with shortened coagulation time
• Blood coagulation disorder, categorized by value of screening test
• Blood coagulation disorder, categorized by value of screening test
• Blood coagulation disorder, categorized by value of screening test
• Blood coagulation disorder, categorized by value of screening test
• Blood coagulation disorder, categorized by value of screening test
• Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency
• Combined coagulation factor deficiency
• Congenital alpha-2-antiplasmin deficiency
• Congenital fibrinogen abnormality
• Congenital hypofibrinogenemia
• Decreased fibrinolysis
• Defect of purinergic receptor p2y G protein-coupled 12
• Deficiency of naturally occurring coagulation factor inhibitor
• Disorder involving the fibrinolytic system
• Drug-induced coagulation inhibitor disorder
• Drug-induced coagulation inhibitor disorder
• East Texas bleeding disorder
• Factor IX inhibitor disorder
• Factor XI inhibitor disorder
• Familial multiple factor deficiency syndrome
• Familial multiple factor deficiency syndrome, type I
• Familial multiple factor deficiency syndrome, type II
• Familial multiple factor deficiency syndrome, type III
• Familial multiple factor deficiency syndrome, type IV
• Familial multiple factor deficiency syndrome, type V
• Familial multiple factor deficiency syndrome, type VI
• Familial thrombomodulin anomalies
• Fibrinolytic bleeding syndrome
• Fibrinolytic bleeding syndrome
• Fibrinolytic bleeding syndrome
• Fibrinolytic bleeding syndrome
• Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
• Hereditary combined coagulation factor deficiency
• Hereditary factor I deficiency disease
• Hereditary hypoplasminogenemia
• Hypofibrinogenemia
• Hypoplasminogenemia
• Hypoplasminogenemia
• Pseudo von Willebrand disease
• Thrombomodulin-related bleeding disorder

References to Index of Diseases and Injuries

The code D68.8 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • COVID-19 associated coagulopathy
• Type 1 Excludes Notes:
  • hemorrhagic disease of newborn (@P53*)
• Code Also:
  • , if applicable, associated condition

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

« Previous Code