MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expand
arthritis (MONDO:0005578)
Parent Node:
expand
metabolic disease (MONDO:0005066)
..Starting node
..expand
chondrocalcinosis ()

       Child Nodes:
........expandchondrocalcinosis due to apatite crystal deposition ()
........expandfamilial calcium pyrophosphate deposition ()



 Sister Nodes: 
..expandacquired metabolic disease ()
..expandbilirubin metabolism disease ()
..expandcarbohydrate metabolism disease ()
..expandcarotenemia ()
..expandchondrocalcinosis ()
..expandcomplement deficiency ()
..expanddevelopmental anomaly of metabolic origin ()
..expanddiabetic nephropathy ()
..expanddiabetic retinopathy ()
..expanddisorder of acid-base balance ()
..expanddisorder of glycosylation ()
..expanddisorder of organic acid metabolism ()
..expandDNA repair disease ()
..expandfamilial thyroid dyshormonogenesis ()
..expandglucose metabolism disease ()
..expandglutaric aciduria (disease) ()
..expandgout ()
..expandhemolytic anemia due to an erythrocyte nucleotide metabolism disorder ()
..expandhyperlipidemia (disease) ()
..expandhyperlipoproteinemia ()
..expandhypermanganesemia with dystonia ()
..expandhypertriglyceridemia (disease) ()
..expandhypoalphalipoproteinemia ()
..expandinborn errors of metabolism ()
..expandlactic acidosis ()
..expandlipodystrophy (disease) ()
..expandmetabolic disease with epilepsy ()
..expandmetabolic disease with intestinal involvement ()
..expandmetabolic disease with skin involvement ()
..expandmetabolic syndrome ()
..expandmineral metabolism disease ()
..expandporphyrin metabolism disease ()
..expandproteostasis deficiencies ()
..expandpurine metabolism disease ()
..expandpyrimidine metabolism disease ()
..expandsteroid metabolism disease ()
..expandthiopurine metabolic disease ()
..expandvitamin B12 deficiency ()
..expandxanthinuria ()
..expandxanthoma (disease) ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:1314
Name:chondrocalcinosis
Definition:An acute episode of pain, swelling, and redness, sometimes associated with fever. It is caused by the deposition of calcium pyrophosphate crystals in the joints.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:calcium pyrophosphate deposition disease; pseudogout
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal