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Details
Link-It Detail - Disease - Hyperphosphatemia
Debug Stats
  • ### Total Build Time: 19 ms 23.189 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 301 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=0 Completed: 0 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 567 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.530 KB
  • CONCEPT_RELATIONSHIPS gt=6 ms Completed: 6 ms rowSize= 7.829 KB
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 11.288 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 (1)
Hyperphosphatemia C0085681
Definition (1)
A condition of abnormally high level of PHOSPHATES in the blood, usually significantly above the normal range of 0.84-1.58 mmol per liter of serum.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Phosphorus Metabolism Disorders C0031707
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255174img Phosphorus Metabolism Disorders C0031707
Relationships (18)

Relation Types:
diso_​to_​anat : 1
diso_​to_​chem : 6
diso_​to_​diso : 10
diso_​to_​phen : 1


Relationships:
none : 14
isa : 2
mapped_​to : 2
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO102img Kidney Failure, Chronic C0022661
DISO_to_CHEM75img Phosphates C0031603
DISO_to_ANAT63img In Blood C0005768
DISO_to_CHEM54img Chelating Agents C0007974
DISO_to_CHEM46img Polyamine C0032433
DISO_to_DISO45img Complication Aspects C1171258
DISO_to_CHEM38img Lanthanum C0023031
DISO_to_DISO38img Kidney Diseases C0022658
DISO_to_CHEM35img Phosphorus C0031705
DISO_to_DISO32img Calcinosis C0006663
DISO_to_PHEN24img genetic aspects C0017399
DISO_to_DISO18img Cardiovascular Diseases C0007222
DISO_to_DISO18img chemically induced C0007994
DISO_to_CHEM13img Fibroblast Growth Factor C0016026
DISO_to_DISOmapped_toimg HYPERPHOSPHATAEMIA C0085681
DISO_to_DISOmapped_toimg Hyperostosis-hyperphosphatemia syndrome C1853256
DISO_to_DISOisaimg Iatrogenic hyperphosphataemia C0342657
DISO_to_DISOisaimg Raised calcium phosphate product C0342656
Genes (11)

Species:
human : 11
SpeciesGeneGeneIdGene NameEvidence
HumanKL9365klotho
img OMIM, Score=1000, UMLKSK CUI: C0085681
img GENERIF, Score=1000, Pubmed Id: 18308935, UMLKSK CUI: C0085681
HumanGCM29247glial cells missing homolog 2 (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0085681
HumanFGF238074fibroblast growth factor 23
img OMIM, Score=1000, UMLKSK CUI: C0085681
img GENERIF, Score=1000, Pubmed Id: 15590700, UMLKSK CUI: C0085681
HumanTBCE6905tubulin folding cofactor E
img OMIM, Score=1000, UMLKSK CUI: C0085681
HumanSPP16696secreted phosphoprotein 1
img GENERIF, Score=1000, Pubmed Id: 16817793, UMLKSK CUI: C0085681
HumanRYR16261ryanodine receptor 1 (skeletal)
img OMIM, Score=1000, UMLKSK CUI: C0085681
HumanPTH5741parathyroid hormone
img OMIM, Score=1000, UMLKSK CUI: C0085681
HumanTNFRSF11B4982tumor necrosis factor receptor superfamily, member 11b
img OMIM, Score=1000, UMLKSK CUI: C0085681
HumanGNAS2778GNAS complex locus
img OMIM, Score=1000, UMLKSK CUI: C0085681
HumanGALNT32591UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 3 (GalNAc-T3)
img OMIM, Score=1000, UMLKSK CUI: C0085681
HumanCASR846calcium-sensing receptor
img OMIM, Score=1000, UMLKSK CUI: C0085681
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0085681Hyperphosphatemia0self