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Details
Link-It Detail - Disease - Anemia
Debug Stats
  • ### Total Build Time: 1,157 ms 44.257 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 310 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 423 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 556 bytes
  • CONCEPT_CHILDREN gt=8 ms Completed: 8 ms rowSize= 3.959 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.516 KB
  • CONCEPT_RELATIONSHIPS gt=819 ms Completed: 819 ms rowSize= 16.020 KB
  • CONCEPT_GENES gt=319 ms Completed: 319 ms rowSize= 20.152 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.141 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Anemia C0002871
Definition (1)
A disorder characterized by an reduction in the amount of hemoglobin in 100 ml of blood. Signs and symptoms of anemia may include pallor of the skin and mucous membranes, shortness of breath, palpitations of the heart, soft systolic murmurs, lethargy, and fatigability.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Hematologic Diseases C0018939
Children (9)
img Anemia, Neonatal C0002891
img Anemia, Macrocytic C0002886
img Anemia, Hypochromic C0002884
img Anemia, Hemolytic C0002878
img Anemia, Aplastic C0002874
img Red-Cell Aplasia, Pure C0034902
img Anemia, Refractory C0002893
img Anemia, Sideroblastic C0002896
img Anemia, Myelophthisic C0002890
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189393img Hematologic Diseases C0018939
Relationships (279)

Relation Types:
diso_​to_​anat : 10
diso_​to_​chem : 72
diso_​to_​diso : 187
diso_​to_​gene : 2
diso_​to_​phen : 2
diso_​to_​phys : 6


Relationships:
none : 142
classifies : 1
disease_​has_​associated_​disease : 15
gene_​associated_​with_​disease : 2
gene_​product_​malfunction_​associated_​with_​disease : 1
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 50
mapped_​to : 22
may_​treat : 35
parent_​is_​cdrh : 1
related_​to : 6
use : 1
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM879img Erythropoietin C0014822
DISO_to_ANAT849img In Blood C0005768
DISO_to_CHEM773img Erythropoietin C0014822
DISO_to_CHEM607img Hematinics C0018928
DISO_to_ANAT567img In Blood C0005768
DISO_to_DISO558img Complication Aspects C1171258
DISO_to_DISO408img Complication Aspects C1171258
DISO_to_DISO384img Kidney Failure, Chronic C0022661
DISO_to_DISO371img Kidney Failure, Chronic C0022661
DISO_to_CHEM334img Hemoglobin C0019046
DISO_to_DISO321img chemically induced C0007994
DISO_to_DISO284img chemically induced C0007994
DISO_to_DISO241img Neoplasms C0027651
DISO_to_DISO231img Neoplasms C0027651
DISO_to_DISO214img Kidney Diseases C0022658
DISO_to_CHEM200img Hematinics C0018928
DISO_to_CHEM198img Hemoglobin C0019046
DISO_to_CHEM187img Iron C0302583
DISO_to_DISO186img Heart Failure C0018801
DISO_to_CHEM138img Iron C0302583
DISO_to_DISO136img Heart Failure C0018801
DISO_to_DISO101img COMPL HEMATOL PREGN C0032964
DISO_to_PHEN101img genetic aspects C0017399
DISO_to_CHEM100img Antineoplastic Agents C0003392
DISO_to_DISO100img Malaria C0024530
Genes (295)

Species:
human : 295
Page Size
Current 25
  Page 1 of 12
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
img OMIM, Score=1000, UMLKSK CUI: C0002871
HumanNPHP4261734nephronophthisis 4
img OMIM, Score=1000, UMLKSK CUI: C0002871
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanFHQTL171515Fetal hemoglobin QTL on chromosome 8
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanSLEH1170682systemic lupus erythematosus with hemolytic anemia 1
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanMMAA166785methylmalonic aciduria (cobalamin deficiency) cblA type
img OMIM, Score=1000, UMLKSK CUI: C0002871
HumanTMPRSS6164656transmembrane protease, serine 6
img OMIM, Score=1000, UMLKSK CUI: C0002871
img OMIM, Score=1000, UMLKSK CUI: C0002871
HumanZFPM1161882zinc finger protein, FOG family member 1
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanCDAN1146059codanin 1
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanDBA2114086Diamond-Blackfan anemia 2
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanC19orf4091442chromosome 19 open reading frame 40
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanBRIP183990BRCA1 interacting protein C-terminal helicase 1
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanHBA@83587
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanAMN81693amnion associated transmembrane protein
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanCFHR581494complement factor H-related 5
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanPUS180324pseudouridylate synthase 1
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanPALB279728partner and localizer of BRCA2
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanSLEB364695systemic lupus erythematosus susceptibility 3
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanDCLRE1C64421DNA cross-link repair 1C
img OMIM, Score=1000, UMLKSK CUI: C0002871
HumanHBB@64162
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanHAMP57817hepcidin antimicrobial peptide
Click here to display 7 evidence detail records.
HumanALG156052ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase
INFERRED, Score=800, UMLKSK CUI: C0002871
HumanNHP255651NHP2 ribonucleoprotein
INFERRED, Score=800, UMLKSK CUI: C0002871
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0002871Anemia0self