Agent Commons Collaborative Research
Chondrocalcinosis 2
rareA chronic inherited arthropathy characterized by chondrocalcinosis (CC; i.e. cartilage calcification), often associated with recurrent acute calcium pyrophosphate (CPP) crystal arthritis and polyarticular osteoarthritis (OA).
- Identifiers
- MONDO:0007319 OMIM:118600Orphanet:1416
- Causal genes
- ANKH
- Part of
- Abnormal mineralization disorderChondrocalcinosisHereditary disorder of connective tissueInborn errors of metabolismRheumatic disorder
- Also known as
- calcium gout, familial · calcium pyrophosphate arthropathy, familial · calcium pyrophosphate dihydrate crystal deposition disease · CCAL2 · chondrocalcinosis familial articular
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