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Details
Link-It Detail - Disease - Chondrocalcinosis
Debug Stats
  • ### Total Build Time: 38 ms 29.354 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 402 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 363 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 545 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.495 KB
  • CONCEPT_RELATIONSHIPS gt=21 ms Completed: 21 ms rowSize= 13.788 KB
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 11.421 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Chondrocalcinosis C0553730
Calcium pyrophosphate deposition disease
Definition (1)
Presence of calcium salts, especially calcium pyrophosphate, in the cartilaginous structures of one or more joints. When accompanied by attacks of goutlike symptoms, it is called pseudogout. (Dorland, 27th ed)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Arthritis C0003864
Ancestral Roots
RootRoot Plus OneDepthParent
img Musculoskeletal Diseases C0026857img Joint Diseases C00224084img Arthritis C0003864
Relationships (51)

Relation Types:
diso_​to_​anat : 7
diso_​to_​chem : 3
diso_​to_​diso : 39
diso_​to_​phen : 2


Relationships:
none : 20
associated_​with : 1
classifies : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 22
location_​of : 1
mapped_​to : 3
used_​for : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO43img Complication Aspects C1171258
DISO_to_DISO35img Complication Aspects C1171258
DISO_to_CHEM28img CALCIUM PYROPHOSPHATE C0006716
DISO_to_DISO23img Gout C0018099
DISO_to_ANAT16img Knee Joint C0022745
DISO_to_PHEN16img genetic aspects C0017399
DISO_to_ANAT15img Knee Joint C0022745
DISO_to_CHEM15img CALCIUM PYROPHOSPHATE C0006716
DISO_to_PHEN15img genetic aspects C0017399
DISO_to_ANAT13img Cartilage, Articular C0007303
DISO_to_DISO13img Calcinosis C0006663
DISO_to_DISO12img Neck Pain C0007859
DISO_to_DISO10img Temporomandibular Joint Disorders C0039494
DISO_to_DISO9img Degenerative polyarthritis C0029408
DISO_to_ANAT8img Odontoid Process C0028881
DISO_to_CHEM8img Membrane Associated Proteins C0025252
DISO_to_DISO8img ARTHRITIS GOUTY C0003868
DISO_to_DISO8img Arthritis, Rheumatoid C0003873
DISO_to_DISO8img Gout C0018099
DISO_to_DISO8img chemically induced C0007994
DISO_to_ANATlocation_ofimg Articular system C0392905
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg Connective and Soft Tissue C1516798
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Skeletal bone C0262950
DISO_to_DISOmapped_toimg CHONDROCALCINOSIS WITH EARLY-ONSET OSTEOARTHRITIS (disorder) C1833499
DISO_to_DISOassociated_withimg Calcification C1533591
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
img GENERIF, Score=937, Pubmed Id: 12707589, UMLKSK CUI: C0553730
img GENERIF, Score=901, Pubmed Id: 13130483, UMLKSK CUI: C0553730
img GENERIF, Score=1000, Pubmed Id: 15461680, UMLKSK CUI: C0553730
img OMIM, Score=833, UMLKSK CUI: C0553730
img GENERIF, Score=827, Pubmed Id: 15818664, UMLKSK CUI: C0553730
img GAD, Score=1000, Pubmed Id: 15818664, UMLKSK CUI: C0553730
img GENERIF, Score=827, Pubmed Id: 12297987, UMLKSK CUI: C0553730
HumanSLC12A36559solute carrier family 12 (sodium/chloride transporter), member 3
img OMIM, Score=1000, UMLKSK CUI: C0553730
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
img OMIM, Score=1000, UMLKSK CUI: C0553730
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
img OMIM, Score=1000, UMLKSK CUI: C0553730
HumanHFE3077hemochromatosis
img GENERIF, Score=1000, Pubmed Id: 17284543, UMLKSK CUI: C0553730
HumanATP7B540ATPase, Cu++ transporting, beta polypeptide
img OMIM, Score=1000, UMLKSK CUI: C0553730
HumanALPL249alkaline phosphatase, liver/bone/kidney
img OMIM, Score=1000, UMLKSK CUI: C0553730
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0553730Chondrocalcinosis0self