Please sign in to follow a disease.

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.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Inborn errors of metabolism (2229) ↑ Rheumatic disorder (1792) ↑ Hereditary disorder of connective tissue (1312) ↑ Abnormal mineralization disorder (22) ↑ Chondrocalcinosis (7)

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

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.