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Details
Link-It Detail - Disease - 21-hydroxylase deficiency
Debug Stats
  • ### Total Build Time: 19 ms 8.055 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 348 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=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 6.382 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
21-hydroxylase deficiency C0852654
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
img GENERIF, Score=845, Pubmed Id: 18777204, UMLKSK CUI: C0852654
HumanPOR5447P450 (cytochrome) oxidoreductase
img GENERIF, Score=1000, Pubmed Id: 18397975, UMLKSK CUI: C0852654
HumanHLA-B3106
img GENERIF, Score=845, Pubmed Id: 18777204, UMLKSK CUI: C0852654
HumanCYP21A1P1590cytochrome P450, family 21, subfamily A, polypeptide 1 pseudogene
img GENERIF, Score=1000, Pubmed Id: 17666484, UMLKSK CUI: C0852654
img GAD, Score=1000, Pubmed Id: 15793784, UMLKSK CUI: C0852654
HumanCYP21A21589cytochrome P450, family 21, subfamily A, polypeptide 2
Click here to display 21 evidence detail records.
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C085265421-hydroxylase deficiency0self