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E88.02

Billable

Plasminogen deficiency

This code does not map to an HCC category in any model (V28, V24, ESRD, RxHCC).

What This Code Means

A rare blood disorder where the body lacks sufficient plasminogen, a protein needed for breaking down blood clots.

Coding Tips

  • •Confirm whether this is congenital or acquired; acquired cases may relate to liver disease or other conditions
  • •Document any thrombotic complications or treatment with plasminogen replacement therapy

Use Additional Code

  • code for associated findings, such as:
  • hydrocephalus (G91.4)
  • otitis media (H67.-)
  • respiratory disorder related to plasminogen deficiency (J99)

Code Also

  • , if applicable, ligneous conjunctivitis (H10.51-)

Code Hierarchy

└E88Other and unspecified metabolic disorders└E88.0Disorders of plasma-protein metabolism, not elsewhere classified└E88.02Plasminogen deficiency
└E88.02Plasminogen deficiency

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