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Details
Link-It Detail - Disease - Anemia, Iron-Deficiency
Debug Stats
  • ### Total Build Time: 71 ms 39.854 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 269 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 998 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 2.805 KB
  • CONCEPT_RELATIONSHIPS gt=51 ms Completed: 51 ms rowSize= 15.077 KB
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 18.972 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Anemia, Iron-Deficiency C0162316
Iron deficiency anemia
Definition (1)
Anemia caused by low iron intake, inefficient iron absorption in the gastrointestinal tract, or chronic blood loss.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Anemia, Hypochromic C0002884
img Iron Metabolism Disorders C0012715
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Anemia, Hypochromic C0002884
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255174img Iron Metabolism Disorders C0012715
Relationships (152)

Relation Types:
diso_​to_​anat : 6
diso_​to_​chem : 99
diso_​to_​diso : 42
diso_​to_​phen : 2
diso_​to_​phys : 3


Relationships:
none : 61
classified_​as : 1
classifies : 1
clinically_​similar : 3
induces : 3
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 4
mapped_​to : 11
may_​prevent : 27
may_​treat : 38
Page Size
Current 25
  Page 1 of 7
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT496img In Blood C0005768
DISO_to_CHEM417img Iron C0302583
DISO_to_ANAT340img In Blood C0005768
DISO_to_CHEM332img Iron C0302583
DISO_to_DISO235img Complication Aspects C1171258
DISO_to_CHEM169img Iron, Dietary C0376520
DISO_to_DISO167img Complication Aspects C1171258
DISO_to_CHEM128img Dietary Iron C0376520
DISO_to_CHEM118img Hematinics C0018928
DISO_to_CHEM109img Compounds, Ferric C0015860
DISO_to_CHEM105img Hemoglobin C0019046
DISO_to_CHEM105img Hemoglobins C0019046
DISO_to_CHEM89img Ferritin C0015879
DISO_to_DISO78img COMPL HEMATOL PREGN C0032964
DISO_to_CHEM76img Hemoglobin C0019046
DISO_to_DISO72img Kidney Failure, Chronic C0022661
DISO_to_CHEM70img Ferritin C0015879
DISO_to_DISO69img COMPL HEMATOL PREGN C0032964
DISO_to_CHEM68img Compounds, Ferrous C0015889
DISO_to_PHYS66img Nutritional Status C0392209
DISO_to_PHEN63img genetic aspects C0017399
DISO_to_CHEM62img Compounds, Ferric C0015860
DISO_to_CHEM58img Receptors, Transferrin C0034845
DISO_to_DISO55img Kidney Failure, Chronic C0022661
DISO_to_DISO54img Helicobacter Infections C0079487
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanGHRL51738ghrelin/obestatin prepropeptide
img GENERIF, Score=1000, Pubmed Id: 17551399, UMLKSK CUI: C0162316
HumanWAS7454Wiskott-Aldrich syndrome
img OMIM, Score=1000, UMLKSK CUI: C0162316
HumanTNF7124tumor necrosis factor
img GENERIF, Score=1000, Pubmed Id: 18716131, UMLKSK CUI: C0162316
HumanTFRC7037transferrin receptor (p90, CD71)
img GENERIF, Score=901, Pubmed Id: 18665828, UMLKSK CUI: C0162316
img GENERIF, Score=1000, Pubmed Id: 16271988, UMLKSK CUI: C0162316
img GENERIF, Score=1000, Pubmed Id: 15623846, UMLKSK CUI: C0162316
HumanTF7018transferrin
img GAD, Score=1000, Pubmed Id: 11703331, UMLKSK CUI: C0162316
HumanSTK116794serine/threonine kinase 11
img OMIM, Score=1000, UMLKSK CUI: C0162316
HumanSLC11A16556solute carrier family 11 (proton-coupled divalent metal ion transporter), member 1
img GENERIF, Score=1000, Pubmed Id: 17466092, UMLKSK CUI: C0162316
HumanSLC11A24891solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
img GENERIF, Score=861, Pubmed Id: 12949888, UMLKSK CUI: C0162316
HumanMC1R4157melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
img OMIM, Score=1000, UMLKSK CUI: C0162316
HumanHLA-DQB13119
img OMIM, Score=1000, UMLKSK CUI: C0162316
img OMIM, Score=1000, UMLKSK CUI: C0162316
HumanHLA-DQA13117
img OMIM, Score=1000, UMLKSK CUI: C0162316
img OMIM, Score=1000, UMLKSK CUI: C0162316
HumanHFE3077hemochromatosis
img GENERIF, Score=1000, Pubmed Id: 14642607, UMLKSK CUI: C0162316
HumanCYP1A11543cytochrome P450, family 1, subfamily A, polypeptide 1
img GAD, Score=1000, Pubmed Id: 12934333, UMLKSK CUI: C0162316
HumanCASP10843caspase 10, apoptosis-related cysteine peptidase
img OMIM, Score=1000, UMLKSK CUI: C0162316
HumanFAS355Fas cell surface death receptor
img OMIM, Score=1000, UMLKSK CUI: C0162316
HumanACO148aconitase 1, soluble
img GENERIF, Score=1000, Pubmed Id: 16503547, UMLKSK CUI: C0162316
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0162316Anemia, Iron-Deficiency0self