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E72.539

Billable

Primary hyperoxaluria, unspecified

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

What This Code Means

A genetic disorder causing excessive oxalate production in the body, but the specific type has not been determined or specified.

Coding Tips

  • •Use this code only when primary hyperoxaluria is confirmed but the type cannot be determined
  • •Query the provider to determine if genetic testing has been performed to identify the specific type

Code Hierarchy

└E72Other disorders of amino-acid metabolism└E72.5Disorders of glycine metabolism└E72.53Primary hyperoxaluria└E72.539Primary hyperoxaluria, unspecified
└E72.539Primary hyperoxaluria, unspecified

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