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Details
Link-It Detail - Disease - Anemia, Hypochromic
Debug Stats
  • ### Total Build Time: 37 ms 26.233 KB
  • CONCEPT_NAME gt=11 ms Completed: 10 ms rowSize= 336 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 358 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=4 ms Completed: 4 ms rowSize= 542 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 561 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.502 KB
  • CONCEPT_RELATIONSHIPS gt=8 ms Completed: 8 ms rowSize= 10.954 KB
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 10.658 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Anemia, Hypochromic C0002884
Definition (1)
Anemia caused by the reduction of hemoglobin in relation to the red cell volume. As a result, the red cells have an area of central pallor which is increased in size. The leading cause is iron deficiency.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Anemia C0002871
Children (1)
img Anemia, Iron-Deficiency C0162316
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Anemia C0002871
Relationships (24)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 8
diso_​to_​diso : 10
diso_​to_​phen : 1


Relationships:
none : 13
is_​associated_​anatomic_​site_​of : 1
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
isa : 1
mapped_​to : 4
may_​treat : 3
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM38img Erythropoietin C0014822
DISO_to_ANAT32img In Blood C0005768
DISO_to_ANAT20img In Blood C0005768
DISO_to_CHEM19img Iron C0302583
DISO_to_DISO19img Neoplasms C0027651
DISO_to_DISO17img Complication Aspects C1171258
DISO_to_DISO17img chemically induced C0007994
DISO_to_PHEN16img genetic aspects C0017399
DISO_to_CHEM13img Hematinics C0018928
DISO_to_DISO11img Kidney Failure, Chronic C0022661
DISO_to_CHEM10img Hemoglobin C0019046
DISO_to_CHEM10img Hemoglobins C0019046
DISO_to_DISO10img chemically induced C0007994
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg HEMOLYMPHORETICULAR TISSUE C1512398
DISO_to_ANATis_associated_anatomic_site_ofimg Hematopoietic and Lymphatic System C1512394
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Hematopoietic and Lymphoid Cell C1512385
DISO_to_CHEMmay_treatimg FERRIC AMMONIUM CITRATE C0060228
DISO_to_CHEMmay_treatimg FERRIC AMMONIUM CITRATE 150MG/ML INJ C0976883
DISO_to_CHEMmay_treatimg FERRIC AMMONIUM CITRATE, GREEN C0982154
DISO_to_DISOmapped_toimg Anemia, Hypochromic C0002884
DISO_to_DISOisaimg Anemia, Iron-Deficiency C0162316
DISO_to_DISOmapped_toimg Decreased haemoglobin C0162119
DISO_to_DISOmapped_toimg Microcytic hypochromic anemia (disorder) C0271901
DISO_to_DISOmapped_toimg Serum iron low (finding) C0235988
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanPUS180324pseudouridylate synthase 1
img OMIM, Score=1000, UMLKSK CUI: C0002884
HumanGHRL51738ghrelin/obestatin prepropeptide
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanWAS7454Wiskott-Aldrich syndrome
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanTNF7124tumor necrosis factor
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanTFRC7037transferrin receptor (p90, CD71)
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanTF7018transferrin
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanSTK116794serine/threonine kinase 11
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanSLC11A16556solute carrier family 11 (proton-coupled divalent metal ion transporter), member 1
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanSLC11A24891solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanMC1R4157melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanHLA-DQB13119
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanHLA-DQA13117
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanHFE3077hemochromatosis
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanCYP1A11543cytochrome P450, family 1, subfamily A, polypeptide 1
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanCASP10843caspase 10, apoptosis-related cysteine peptidase
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanFAS355Fas cell surface death receptor
INFERRED, Score=800, UMLKSK CUI: C0002884
HumanACO148aconitase 1, soluble
INFERRED, Score=800, UMLKSK CUI: C0002884
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0002884Anemia, Hypochromic0self