chondrocalcinosis 2

Preferred Label : chondrocalcinosis 2;

MeSH note : PROM mutation in ANKH gene;

MeSH synonym : CCAL2; calcium pyrophosphate dihydrate deposition disease; chondrocalcinosis, familial articular; calcium gout; calcium pyrophosphate arthropathy; CPPDD Calcium Pyrophosphate Dihydrate Deposition Disease; CPPDD;

Details

Origin ID

C563162;

UMLS CUI

C0856830;

Currated CISMeF NLP mapping
- Chondrocalcinosis 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- chondrocalcinosis [MeSH Descriptor]
Record concept(s)
- chondrocalcinosis 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Calcium pyrophosphate arthropathy [MedDRA LLT]
- Calcium pyrophosphate dihydrate deposition disease [MedDRA LLT]
- Chondrocalcinosis 2 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

Main resources

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