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Details
Link-It Detail - Disease - Phosphorus Metabolism Disorders
Debug Stats
  • ### Total Build Time: 57 ms 32.550 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 360 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 214 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=5 ms Completed: 5 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 554 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 989 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.518 KB
  • CONCEPT_RELATIONSHIPS gt=26 ms Completed: 26 ms rowSize= 13.473 KB
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 14.116 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Phosphorus Metabolism Disorders C0031707
Definition (1)
A metabolic disorder that affects the phosphate homeostasis.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Metabolic Diseases C0025517
Children (2)
img Hyperphosphatemia C0085681
img Hypophosphatemia C0085682
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255173img Metabolic Diseases C0025517
Relationships (53)

Relation Types:
diso_​to_​anat : 1
diso_​to_​chem : 12
diso_​to_​diso : 39
diso_​to_​phys : 1


Relationships:
none : 9
associated_​with : 3
classifies : 2
isa : 1
mapped_​to : 31
may_​treat : 6
use : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO37img Kidney Failure, Chronic C0022661
DISO_to_ANAT26img In Blood C0005768
DISO_to_CHEM20img Phosphates C0031603
DISO_to_DISO19img Kidney Failure, Chronic C0022661
DISO_to_CHEM15img Epoxy Compounds C0014630
DISO_to_CHEM15img Phosphates C0031603
DISO_to_CHEM15img Phosphorus C0031705
DISO_to_CHEM15img Polyethylenes C0032487
DISO_to_DISO15img Complication Aspects C1171258
DISO_to_CHEMassociated_withimg Phosphorus C0031705
DISO_to_CHEMmay_treatimg SEVELAMER C0718050
DISO_to_CHEMmay_treatimg SEVELAMER CARBONATE C1721288
DISO_to_CHEMmay_treatimg SEVELAMER CARBONATE 0.8 gram ORAL POWDER IN PACKET C2719951
DISO_to_CHEMmay_treatimg SEVELAMER CARBONATE 2.4 gram ORAL POWDER IN PACKET C2719946
DISO_to_CHEMmay_treatimg SEVELAMER CARBONATE 800MG TAB C1968326
DISO_to_CHEMmay_treatimg SEVELAMER HCL C0772463
DISO_to_DISOclassifiesimg 6-30 DISORDERS OF MINERAL METABOLISM: GENERAL TERMS C0154260
DISO_to_DISOmapped_toimg Acquired hypophosphataemia C0342653
DISO_to_DISOmapped_toimg Adult hypophosphatasia (disorder) C0268413
DISO_to_DISOmapped_toimg Autosomal dominant hypophosphatemic rickets C0342642
DISO_to_DISOmapped_toimg Autosomal recessive hypophosphatemic vitamin D refractory rickets C0342643
DISO_to_DISOmapped_toimg Calcipenic type rickets C0271871
DISO_to_DISOmapped_toimg Childhood hypophosphatasia (disorder) C0220743
DISO_to_DISOmapped_toimg Dis phosphorus metabol C0031707
DISO_to_DISOassociated_withimg Disease C0012634
Genes (23)

Species:
human : 23
SpeciesGeneGeneIdGene NameEvidence
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanCYP2R1120227cytochrome P450, family 2, subfamily R, polypeptide 1
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanSLC9A3R19368solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanKL9365klotho
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanGCM29247glial cells missing homolog 2 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanSUCLG18802succinate-CoA ligase, alpha subunit
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanFGF238074fibroblast growth factor 23
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanTBCE6905tubulin folding cofactor E
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanSPP16696secreted phosphoprotein 1
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanSLC2A26514solute carrier family 2 (facilitated glucose transporter), member 2
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanRYR16261ryanodine receptor 1 (skeletal)
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanPTH1R5745parathyroid hormone 1 receptor
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanPTH5741parathyroid hormone
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanPHEX5251phosphate regulating endopeptidase homolog, X-linked
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanTNFRSF11B4982tumor necrosis factor receptor superfamily, member 11b
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanOCRL4952oculocerebrorenal syndrome of Lowe
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanGNAS2778GNAS complex locus
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanGALNT32591UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 3 (GalNAc-T3)
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanCYP27B11594cytochrome P450, family 27, subfamily B, polypeptide 1
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanCTNS1497cystinosin, lysosomal cystine transporter
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanCLCN51184chloride channel, voltage-sensitive 5
INFERRED, Score=800, UMLKSK CUI: C0031707
HumanCASR846calcium-sensing receptor
INFERRED, Score=800, UMLKSK CUI: C0031707
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0031707Phosphorus Metabolism Disorders0self