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chondrocalcinosis 2

Disease Summary
Associated Targets (1)
Tbio

1


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Mondo Description A 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).
Uniprot Description Chondrocalcinosis is a common cause of joint pain and arthritis caused by calcium deposition in articular cartilage and the presence of calcium hypophosphate crystals in synovial fluid, cartilage and periarticular soft tissue. CCAL2 inheritance is autosomal dominant.
Mondo Term and Equivalent IDs
MONDO:0007319:  chondrocalcinosis 2
GARD:0001292: 
MESH:C563162: 
Orphanet:1416: 
UMLS:CN199517: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found