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Details
Link-It Detail - Disease - Microcytic hypochromic anemia (disorder)
Debug Stats
  • ### Total Build Time: 10 ms 5.088 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 293 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=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 3.085 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Microcytic hypochromic anemia (disorder) C0271901
Definition (1)
anemia featuring pale erythrocytes smaller than 6 microns in diameter; typically due to iron deficiency or abnormalities in hememetabolism.
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanSLC11A24891solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
img GENERIF, Score=923, Pubmed Id: 16439678, UMLKSK CUI: C0271901
img GENERIF, Score=923, Pubmed Id: 15459009, UMLKSK CUI: C0271901
HumanABCB722ATP-binding cassette, sub-family B (MDR/TAP), member 7
img OMIM, Score=1000, UMLKSK CUI: C0271901
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0271901Microcytic hypochromic anemia (disorder)0self