Chondrocalcinosis 2
MESHC563162
A hereditary autosomal dominant form of chondrocalcinosis that is caused by mutations in the ANKH gene. OMIM: 118600
Synonyms
- Calcium Gout
- Calcium Pyrophosphate Dihydrate Deposition Disease
- Calcium Pyrophosphate Arthropathy
- Chondrocalcinosis, Familial Articular
- CCAL2
- CPPDD Calcium Pyrophosphate Dihydrate Deposition Disease
- CPPDD
Source last updated 2026-05-24T15:30:09.092Z