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Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.
Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"
Familial calcium pyrophosphate deposition
Calcium pyrophosphate dihydrate crystal deposition disease · Familial CC
OBSOLETE: Familial articular chondrocalcinosis type 1
OBSOLETE: CCAL1
OBSOLETE: Familial articular chondrocalcinosis type 2
OBSOLETE: CCAL2
Familial articular hypermobility syndrome
Familial joint instability syndrome · Familial joint laxity
Familial tumoral calcinosis