Chondrocalcinosis 2

MONDO:0007319

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).

Also known as: Familial Calcium Pyrophosphate Deposition Disease, calcium pyrophosphate dihydrate crystal deposition disease, chondrocalcinosis 2, chondrocalcinosis type 2, familial CC, familial CPPD, familial articular chondrocalcinosis, familial calcium pyrophosphate deposition

24 clinical trials for this condition and its sub-types, 0 tagged with Chondrocalcinosis 2 itself.

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Part of

↑ Inborn errors of metabolism (2228) ↑ Rheumatic disorder (1792) ↑ Hereditary disorder of connective tissue (1311) ↑ Abnormal mineralization disorder (22) ↑ Chondrocalcinosis (7)

Including sub-types (24) Tagged with Chondrocalcinosis 2 (0)

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