Familiær kondrokalcinose (CCAL2)
Autosomal dominant
Tidligt debuterende aflejringer af calciumpyrophosphatkrystaller i ledbrusk, som forårsager pseudogigtanfald og artrit. Tilstanden skyldes varianter i ANKH.
Analyserede gener
Også kendt som
calcium gout, familial; calcium pyrophosphate arthropathy, familial; calcium pyrophosphate dihydrate crystal deposition disease; CCAL2; chondrocalcinosis familial articular; chondrocalcinosis type 2; CPPDD; familial calcium pyrophosphate deposition; Familial Calcium Pyrophosphate Deposition Disease; familial calcium pyrophosphate dihydrate deposition disease; familial CC; familial CPPD; hereditary articular chondrocalcinosis; hereditary calcium pyrophosphate deposition; hereditary CC; Pseudogout, familial
