has material basis in germline mutation in ANKH chondrocalcinosis rheumatic disorder chondrocalcinosis 2 https://github.com/monarch-initiative/mondo/issues/4948 https://www.malacards.org/card/chondrocalcinosis_2 chondrocalcinosis familial articular Pseudogout, familial OMIM:118600 calcium pyrophosphate dihydrate crystal deposition disease MESH:C563162 hereditary articular chondrocalcinosis familial CC GARD:0001292 MONDO:0007319 familial calcium pyrophosphate deposition 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). Familial Calcium Pyrophosphate Deposition Disease hereditary CC MEDGEN:163633 UMLS:C0856830 chondrocalcinosis 2 CPPDD Orphanet:1416 calcium gout, familial familial CPPD NORD:930 familial calcium pyrophosphate dihydrate deposition disease familial articular chondrocalcinosis CCAL2 hereditary calcium pyrophosphate deposition chondrocalcinosis type 2 calcium pyrophosphate arthropathy, familial inborn errors of metabolism hereditary disorder of connective tissue abnormal mineralization disorder