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Details
Link-It Detail - Disease - Encounter due to other behavioral problems
Debug Stats
  • ### Total Build Time: 13 ms 14.431 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 382 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=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=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 12.708 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.176 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Encounter due to other behavioral problems C0260657
Genes (12)

Species:
human : 12
SpeciesGeneGeneIdGene NameEvidence
HumanHGSNAT138050heparan-alpha-glucosaminide N-acetyltransferase
img OMIM, Score=882, UMLKSK CUI: C0260657
HumanPANK280025pantothenate kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0260657
HumanEHMT179813euchromatic histone-lysine N-methyltransferase 1
img OMIM, Score=1000, UMLKSK CUI: C0260657
HumanNSD164324nuclear receptor binding SET domain protein 1
img OMIM, Score=1000, UMLKSK CUI: C0260657
HumanRAI110743retinoic acid induced 1
img OMIM, Score=1000, UMLKSK CUI: C0260657
HumanNPC210577Niemann-Pick disease, type C2
img OMIM, Score=1000, UMLKSK CUI: C0260657
HumanSNRPN6638small nuclear ribonucleoprotein polypeptide N
img OMIM, Score=1000, UMLKSK CUI: C0260657
img OMIM, Score=1000, UMLKSK CUI: C0260657
img OMIM, Score=1000, UMLKSK CUI: C0260657
HumanSGSH6448N-sulfoglucosamine sulfohydrolase
img OMIM, Score=882, UMLKSK CUI: C0260657
HumanNPC14864Niemann-Pick disease, type C1
img OMIM, Score=1000, UMLKSK CUI: C0260657
HumanNDN4692necdin, melanoma antigen (MAGE) family member
img OMIM, Score=1000, UMLKSK CUI: C0260657
img OMIM, Score=1000, UMLKSK CUI: C0260657
img OMIM, Score=1000, UMLKSK CUI: C0260657
HumanNAGLU4669N-acetylglucosaminidase, alpha
img OMIM, Score=882, UMLKSK CUI: C0260657
HumanGNS2799glucosamine (N-acetyl)-6-sulfatase
img OMIM, Score=882, UMLKSK CUI: C0260657
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0260657Encounter due to other behavioral problems0self