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M11.119

Billable

Familial chondrocalcinosis, unspecified shoulder

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 the shoulder joint, causing inflammation and joint damage.

Coding Tips

  • •This code is used when the specific shoulder (right or left) is not documented; query the provider if laterality is known
  • •Familial chondrocalcinosis is a genetic form of pseudogout; ensure you're not confusing it with secondary chondrocalcinosis

Code Hierarchy

└M11Other crystal arthropathies└M11.1Familial chondrocalcinosis└M11.11Familial chondrocalcinosis, shoulder└M11.119Familial chondrocalcinosis, unspecified shoulder
└M11.119Familial chondrocalcinosis, unspecified shoulder

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