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Details
Link-It Detail - Disease - Anemia, Refractory
Debug Stats
  • ### Total Build Time: 50 ms 35.514 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 270 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=6 ms Completed: 6 ms rowSize= 985 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 579 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.788 KB
  • CONCEPT_RELATIONSHIPS gt=13 ms Completed: 13 ms rowSize= 15.205 KB
  • CONCEPT_GENES gt=19 ms Completed: 19 ms rowSize= 13.993 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Anemia, Refractory C0002893
Refractory anemias
Definition (1)
A severe sometimes chronic anemia, usually macrocytic in type, that does not respond to ordinary antianemic therapy.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Myelodysplastic Syndromes C0026986
img Anemia C0002871
Children (1)
img Anemia, Refractory, with Excess of Blasts C0002894
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Myelodysplastic Syndromes C0026986
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Anemia C0002871
Relationships (51)

Relation Types:
diso_​to_​anat : 15
diso_​to_​chem : 4
diso_​to_​diso : 22
diso_​to_​phen : 9
diso_​to_​phys : 1


Relationships:
none : 18
is_​abnormal_​cell_​of_​disease : 6
is_​associated_​disease_​of : 1
is_​finding_​of_​disease : 7
is_​normal_​cell_​origin_​of_​disease : 2
is_​normal_​tissue_​origin_​of_​disease : 2
is_​not_​finding_​of_​disease : 2
is_​primary_​anatomic_​site_​of_​disease : 2
mapped_​to : 2
may_​be_​cytogenetic_​abnormality_​of_​disease : 2
may_​be_​finding_​of_​disease : 5
permuted_​term_​of : 1
replaces : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN38img genetic aspects C0017399
DISO_to_DISO28img Anemia, Sideroblastic C0002896
DISO_to_DISO28img Dysmyelopoietic Syndromes C0026986
DISO_to_PHEN22img genetic aspects C0017399
DISO_to_DISO21img Dysmyelopoietic Syndromes C0026986
DISO_to_DISO18img Complication Aspects C1171258
DISO_to_ANAT14img In Blood C0005768
DISO_to_DISO14img Anemia, Sideroblastic C0002896
DISO_to_DISO13img Complication Aspects C1171258
DISO_to_DISO11img Thrombocytosis C0836924
DISO_to_CHEM9img Immunosuppressive Agents C0021081
DISO_to_CHEM9img Janus Kinase 2 C0169661
DISO_to_PHYS9img Mutation C0026882
DISO_to_CHEM8img Cyclosporine C0010592
DISO_to_ANAT6img Bone Marrow Cell C0005955
DISO_to_ANAT6img In Blood C0005768
DISO_to_CHEM6img Erythropoietin C0014822
DISO_to_DISO6img Anemia, Aplastic C0002874
DISO_to_ANATis_abnormal_cell_of_diseaseimg Abnormal Hematopoietic and Lymphoid Cell C1510725
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Bone Marrow C0005953
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Bone Marrow Stem Cell C1511246
DISO_to_ANATis_abnormal_cell_of_diseaseimg Cancer Cell C0334227
DISO_to_ANATis_abnormal_cell_of_diseaseimg Dysplastic Erythroid Precursor C1512102
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg HEMOLYMPHORETICULAR TISSUE C1512398
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg Haematopoietic tissue C0229619
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanDLK18788delta-like 1 homolog (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0002893
HumanWT17490Wilms tumor 1
img GENERIF, Score=1000, Pubmed Id: 17803653, UMLKSK CUI: C0002893
HumanTNF7124tumor necrosis factor
img GENERIF, Score=1000, Pubmed Id: 15860935, UMLKSK CUI: C0002893
HumanTGFB17040transforming growth factor, beta 1
img GENERIF, Score=1000, Pubmed Id: 15860935, UMLKSK CUI: C0002893
HumanTBXAS16916thromboxane A synthase 1 (platelet)
img OMIM, Score=1000, UMLKSK CUI: C0002893
HumanRB15925retinoblastoma 1
img GENERIF, Score=861, Pubmed Id: 16682076, UMLKSK CUI: C0002893
HumanPCNA5111proliferating cell nuclear antigen
INFERRED, Score=800, UMLKSK CUI: C0002893
HumanNME44833NME/NM23 nucleoside diphosphate kinase 4
INFERRED, Score=800, UMLKSK CUI: C0002893
HumanMPL4352myeloproliferative leukemia virus oncogene
img GENERIF, Score=1000, Pubmed Id: 18040685, UMLKSK CUI: C0002893
HumanJAK23717Janus kinase 2
img GENERIF, Score=1000, Pubmed Id: 18166783, UMLKSK CUI: C0002893
img GENERIF, Score=1000, Pubmed Id: 18059483, UMLKSK CUI: C0002893
img GENERIF, Score=1000, Pubmed Id: 18040685, UMLKSK CUI: C0002893
HumanIRF13659interferon regulatory factor 1
img OMIM, Score=858, UMLKSK CUI: C0002893
HumanFLT12321fms-related tyrosine kinase 1
INFERRED, Score=800, UMLKSK CUI: C0002893
HumanERCC12067excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence)
INFERRED, Score=800, UMLKSK CUI: C0002893
HumanABCB722ATP-binding cassette, sub-family B (MDR/TAP), member 7
img GENERIF, Score=1000, Pubmed Id: 18398482, UMLKSK CUI: C0002893
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0002893Anemia, Refractory0self