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Details
Link-It Detail - Disease - Oncholysis ICD10CM:L60.1
Debug Stats
  • ### Total Build Time: 17 ms 7.160 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 346 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=6 ms Completed: 6 ms rowSize= 5.490 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.158 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Oncholysis ICD10CM:L60.1 C1863011
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanGRDX117189Graves disease, susceptibility to, X-linked
img OMIM, Score=1000, UMLKSK CUI: C1863011
HumanIFIH164135interferon induced with helicase C domain 1
img OMIM, Score=1000, UMLKSK CUI: C1863011
HumanGRD250976Graves disease, susceptibility to, 2
img OMIM, Score=1000, UMLKSK CUI: C1863011
HumanTGM59333transglutaminase 5
img OMIM, Score=1000, UMLKSK CUI: C1863011
HumanGC2638group-specific component (vitamin D binding protein)
img OMIM, Score=1000, UMLKSK CUI: C1863011
HumanCTLA41493cytotoxic T-lymphocyte-associated protein 4
img OMIM, Score=1000, UMLKSK CUI: C1863011
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1863011Oncholysis ICD10CM:L60.10self