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Details
Link-It Detail - Disease - Dominant sensorineural hearing loss
Debug Stats
  • ### Total Build Time: 7 ms 5.501 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 368 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 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=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 3.799 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Dominant sensorineural hearing loss C0395971
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanWFS17466Wolfram syndrome 1 (wolframin)
img GENERIF, Score=895, Pubmed Id: 17492394, UMLKSK CUI: C0395971
HumanGJB22706gap junction protein, beta 2, 26kDa
img GAD, Score=864, Pubmed Id: 11354642, UMLKSK CUI: C0395971
HumanCOCH1690cochlin
img GENERIF, Score=875, Pubmed Id: 18312449, UMLKSK CUI: C0395971
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0395971Dominant sensorineural hearing loss0self