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Details
Link-It Detail - Disease - ESOPHAGEAL VARICES
Debug Stats
  • ### Total Build Time: 12 ms 14.466 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 198 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 12.620 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
ESOPHAGEAL VARICES C0014867
Definition (1)
Abnormally dilated vein(s) of the esophagus.
Genes (11)

Species:
human : 11
SpeciesGeneGeneIdGene NameEvidence
HumanVEGFA7422vascular endothelial growth factor A
img GENERIF, Score=1000, Pubmed Id: 15754412, UMLKSK CUI: C0014867
HumanPKHD15314polycystic kidney and hepatic disease 1 (autosomal recessive)
img OMIM, Score=1000, UMLKSK CUI: C0014867
HumanSERPINA15265serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1
img GENERIF, Score=1000, Pubmed Id: 18089349, UMLKSK CUI: C0014867
HumanNOS34846nitric oxide synthase 3 (endothelial cell)
img GAD, Score=1000, Pubmed Id: 11707686, UMLKSK CUI: C0014867
HumanKRT183875keratin 18
img OMIM, Score=1000, UMLKSK CUI: C0014867
HumanKRT83856keratin 8
img OMIM, Score=1000, UMLKSK CUI: C0014867
HumanGBE12632glucan (1,4-alpha-), branching enzyme 1
img OMIM, Score=1000, UMLKSK CUI: C0014867
HumanACE1636angiotensin I converting enzyme
img GAD, Score=1000, Pubmed Id: 11707686, UMLKSK CUI: C0014867
HumanATP7B540ATPase, Cu++ transporting, beta polypeptide
img OMIM, Score=1000, UMLKSK CUI: C0014867
HumanAGTR1185angiotensin II receptor, type 1
img GAD, Score=1000, Pubmed Id: 11707686, UMLKSK CUI: C0014867
HumanAGT183angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
img GAD, Score=1000, Pubmed Id: 11707686, UMLKSK CUI: C0014867
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0014867ESOPHAGEAL VARICES0self