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M11.19

Billable

Familial chondrocalcinosis, multiple sites

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

What This Code Means

A hereditary condition where calcium deposits form in the cartilage of multiple joints throughout the body, causing inflammation and joint pain.

Coding Tips

  • •This code indicates a familial/genetic form of chondrocalcinosis affecting multiple sites - do not use if only one joint is affected
  • •Verify documentation confirms family history or genetic predisposition; if etiology is unknown or secondary, use M11.20 series instead

Code Hierarchy

└M11Other crystal arthropathies└M11.1Familial chondrocalcinosis└M11.19Familial chondrocalcinosis, multiple sites
└M11.19Familial chondrocalcinosis, multiple sites

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