Ailesel kondrokalsinoz (CCAL2)
Otozomal dominant
ANKH varyantlarından kaynaklanan, eklem kıkırdağında erken yaşta başlayan kalsiyum pirofosfat kristal birikintilerinin pseudogut atakları ve artrite yol açmasıdır.
Analiz edilen genler
Diğer adları
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
