Familial chondrocalcinosis
Familial chondrocalcinosis
M11.1 is a header (parent) code in the ICD-10-CM hierarchy. It is not billable for claim submission. Use one of the billable child codes listed below.
Billable codes in this category
Each of the codes below is billable. Choose the one that most accurately describes the patient's diagnosis.
Familial chondrocalcinosis with no specific joint site documented — a hereditary crystal arthropathy characterized by calcium pyrophosphate dihydrate (CPPD) deposits in cartilage, assigned when the affected joint is not identified in the record.
Calcium pyrophosphate crystal deposition in the fibrocartilaginous structures of the vertebral column, occurring as a heritable (familial) form of chondrocalcinosis.
Familial chondrocalcinosis affecting multiple joint sites simultaneously, caused by an inherited predisposition to calcium pyrophosphate dihydrate (CPPD) crystal deposition in articular cartilage.