MeSH Browser

MeSH Supplementary: Chondrocalcinosis 2
Unique ID: C563162
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563162
Entry Term(s): CCAL2; CPPDD; CPPDD Calcium Pyrophosphate Dihydrate Deposition Disease; Calcium Gout; Calcium Pyrophosphate Arthropathy; Calcium Pyrophosphate Dihydrate Deposition Disease; Chondrocalcinosis, Familial Articular
Registry Numbers: 0
Heading Mapped to: *Chondrocalcinosis
Frequency: 56
Note: A hereditary autosomal dominant form of chondrocalcinosis that is caused by mutations in the ANKH gene. OMIM: 118600
Date of Entry: 2012/11/05
Revision Date: 2019/06/20

Concept UI: M0563462
Registry Numbers: 0
Terms: Chondrocalcinosis 2 Preferred Term
Term UI T802322
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Calcium Gout
Term UI T802323
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Calcium Pyrophosphate Dihydrate Deposition Disease
Term UI T802325
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Calcium Pyrophosphate Arthropathy
Term UI T802326
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Chondrocalcinosis, Familial Articular
Term UI T802328
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); CCAL2
Term UI T825123
Date06/27/2012
LexicalTag NON
ThesaurusID OMIM (2013); CPPDD Calcium Pyrophosphate Dihydrate Deposition Disease
Term UI T000961657
Date06/20/2019
LexicalTag NON
ThesaurusID NLM (2019); CPPDD
Term UI T000961658
Date06/20/2019
LexicalTag NON
ThesaurusID NLM (2019)

Chondrocalcinosis 2 MeSH Supplementary Concept Data 2025