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Details
Link-It Detail - Disease - Hypophosphatemia
Debug Stats
  • ### Total Build Time: 251 ms 37.189 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 377 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 218 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=7 ms Completed: 7 ms rowSize= 567 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 564 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 1.530 KB
  • CONCEPT_RELATIONSHIPS gt=188 ms Completed: 188 ms rowSize= 13.406 KB
  • CONCEPT_GENES gt=29 ms Completed: 29 ms rowSize= 19.206 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Hypophosphatemia C0085682
HYPOPHOSPHATAEMIA
Definition (1)
Lower than normal levels of phosphates in the circulating blood.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Phosphorus Metabolism Disorders C0031707
Children (1)
img Hypophosphatemia, Familial C0020631
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255174img Phosphorus Metabolism Disorders C0031707
Relationships (59)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 35
diso_​to_​diso : 17
diso_​to_​gene : 2
diso_​to_​phen : 2


Relationships:
none : 23
disease_​has_​finding : 1
gene_​associated_​with_​disease : 2
isa : 4
mapped_​to : 2
may_​prevent : 9
may_​treat : 18
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO50img Complication Aspects C1171258
DISO_to_CHEM39img Fibroblast Growth Factor C0016026
DISO_to_CHEM39img Fibroblast Growth Factors C0016026
DISO_to_ANAT37img In Blood C0005768
DISO_to_DISO35img Osteomalacia C0029442
DISO_to_CHEM33img Phosphates C0031603
DISO_to_DISO32img Complication Aspects C1171258
DISO_to_ANAT31img In Blood C0005768
DISO_to_PHEN30img genetic aspects C0017399
DISO_to_DISO28img chemically induced C0007994
DISO_to_CHEM26img Phosphates C0031603
DISO_to_PHEN23img genetic aspects C0017399
DISO_to_DISO18img Osteomalacia C0029442
DISO_to_CHEM14img Fibroblast Growth Factor C0016026
DISO_to_CHEM14img Phosphorus C0031705
DISO_to_DISO12img chemically induced C0007994
DISO_to_DISO11img Hypercalcemia C0020437
DISO_to_DISO11img Rickets C0035579
DISO_to_CHEM10img Adenine C0001407
DISO_to_DISO10img Malnutrition C0162429
DISO_to_ANAT9img Kidney C0022646
DISO_to_CHEM9img Calcium C0006675
DISO_to_DISO9img Paraneoplastic Syndromes C0030472
DISO_to_CHEMmay_treatimg Calciferol 1.25mg tablet C0976697
DISO_to_CHEMmay_treatimg Calciferol, 500000 iu/ml injectable solution C0976696
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
img OMIM, Score=1000, UMLKSK CUI: C0085682
HumanCYP2R1120227cytochrome P450, family 2, subfamily R, polypeptide 1
img OMIM, Score=1000, UMLKSK CUI: C0085682
HumanSLC9A3R19368solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1
img OMIM, Score=1000, UMLKSK CUI: C0085682
HumanSUCLG18802succinate-CoA ligase, alpha subunit
img OMIM, Score=1000, UMLKSK CUI: C0085682
HumanFGF238074fibroblast growth factor 23
img GENERIF, Score=1000, Pubmed Id: 16337659, UMLKSK CUI: C0085682
img GENERIF, Score=827, Pubmed Id: 16941023, UMLKSK CUI: C0085682
img GENERIF, Score=1000, Pubmed Id: 12032180, UMLKSK CUI: C0085682
img GENERIF, Score=1000, Pubmed Id: 17359508, UMLKSK CUI: C0085682
img GENERIF, Score=660, Pubmed Id: 17129170, UMLKSK CUI: C0085682
img OMIM, Score=1000, UMLKSK CUI: C0085682
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
img OMIM, Score=1000, UMLKSK CUI: C0085682
HumanSLC2A26514solute carrier family 2 (facilitated glucose transporter), member 2
img OMIM, Score=1000, UMLKSK CUI: C0085682
HumanPTH1R5745parathyroid hormone 1 receptor
img OMIM, Score=1000, UMLKSK CUI: C0085682
HumanPHEX5251phosphate regulating endopeptidase homolog, X-linked
img OMIM, Score=1000, UMLKSK CUI: C0085682
img GENERIF, Score=694, Pubmed Id: 15940367, UMLKSK CUI: C0085682
img OMIM, Score=1000, UMLKSK CUI: C0085682
HumanOCRL4952oculocerebrorenal syndrome of Lowe
img OMIM, Score=1000, UMLKSK CUI: C0085682
img OMIM, Score=833, UMLKSK CUI: C0085682
HumanCYP27B11594cytochrome P450, family 27, subfamily B, polypeptide 1
img OMIM, Score=1000, UMLKSK CUI: C0085682
HumanCTNS1497cystinosin, lysosomal cystine transporter
img OMIM, Score=1000, UMLKSK CUI: C0085682
HumanCLCN51184chloride channel, voltage-sensitive 5
img OMIM, Score=1000, UMLKSK CUI: C0085682
img OMIM, Score=833, UMLKSK CUI: C0085682
img OMIM, Score=833, UMLKSK CUI: C0085682
img OMIM, Score=1000, UMLKSK CUI: C0085682
HumanCASR846calcium-sensing receptor
img OMIM, Score=1000, UMLKSK CUI: C0085682
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0085682Hypophosphatemia0self