2022 ICD-10-CM Code D68.59

Tabular List of Diseases and Injuries

The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code D68.59:

Inclusion Terms

• Antithrombin III deficiency
• Hypercoagulable state NOS
• Primary hypercoagulable state NEC
• Primary thrombophilia NEC
• Protein C deficiency
• Protein S deficiency
• Thrombophilia NOS

Index to Diseases and Injuries

The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code D68.59 are found in the index:

• - Deficiency, deficient
  • - antithrombin (antithrombin III) - D68.59
  • - protein - See Also: Malnutrition; - E46
    • - C - D68.59
    • - S - D68.59

• - Hypercoagulable (state) - D68.59
  • - antithrombin (III) deficiency - D68.59
  • - primary NEC - D68.59
  • - protein C deficiency - D68.59
  • - protein S deficiency - D68.59

• - Hypercoagulation (state) - D68.59

• - Thrombophilia - D68.59
  • - primary NEC - D68.59

Approximate Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

• Antithrombin III deficiency
• Cerebral ischemic stroke due to hypercoagulable state
• Fibrinogen in blood above reference range
• Heparin cofactor II deficiency
• Hereditary antithrombin III deficiency
• Hereditary elevated factor VIII
• Hereditary elevated factor XI
• Hereditary heparin cofactor II deficiency
• Hereditary hyperfibrinogenemia
• Hereditary protein C deficiency
• Hereditary protein S deficiency
• Hereditary thrombophilia
• Hereditary thrombophilia due to congenital histidine-rich glycoprotein deficiency
• Heterozygous protein C deficiency
• Heterozygous protein S deficiency
• Homozygous protein C deficiency
• Homozygous protein S deficiency
• Hypercoagulability state
• Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
• Hyperfibrinogenemia
• Protein C deficiency disease
• Protein S deficiency disease
• Thrombophilia
• Thrombophilia due to acquired antithrombin III deficiency
• Thrombophilia due to acquired protein S deficiency
• Thrombotic tendency observations
• Upper gastrointestinal hemorrhage associated with hypercoagulability state