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M11.10

Billable

Familial chondrocalcinosis, unspecified site

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

What This Code Means

An inherited genetic condition where calcium pyrophosphate crystals deposit in joints, but the specific joint location is not documented.

Coding Tips

  • •This is a familial form, so document family history when available
  • •Use only when site is unspecified; assign more specific codes if location is documented

Code Hierarchy

└M11Other crystal arthropathies└M11.1Familial chondrocalcinosis└M11.10Familial chondrocalcinosis, unspecified site
└M11.10Familial chondrocalcinosis, unspecified site

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