All diseases

OMIM ID
118600
OMIM term:
CHONDROCALCINOSIS 2; CCAL2
Alternative terms:
CHONDROCALCINOSIS, FAMILIAL ARTICULAR
CALCIUM GOUT
CALCIUM PYROPHOSPHATE ARTHROPATHY
CALCIUM PYROPHOSPHATE DIHYDRATE DEPOSITION DISEASE; CPPDD
(∗) Location:
5p15.2  
(†) Associated OMIM genes:
ANKH  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/vp5xuxw9