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Details
Link-It Detail - Disease - Anemia, Refractory, with Excess of Blasts
Debug Stats
  • ### Total Build Time: 44 ms 28.073 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 422 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=5 ms Completed: 5 ms rowSize= 554 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=10 ms Completed: 10 ms rowSize= 2.793 KB
  • CONCEPT_RELATIONSHIPS gt=12 ms Completed: 12 ms rowSize= 15.302 KB
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 7.261 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Anemia, Refractory, with Excess of Blasts C0002894
Definition (1)
A myelodysplastic syndrome characterized by the presence of 5-19% myeloblasts in the bone marrow or 2-19% blasts in the peripheral blood. It includes two categories: RAEB-1and RAEB-2. Cases with significant bone marrow reticulin fibrosis are called RAEB with fibrosis.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Anemia, Refractory C0002893
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Anemia, Refractory C0002893
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189396img Anemia, Refractory C0002893
Relationships (54)

Relation Types:
diso_​to_​anat : 23
diso_​to_​chem : 3
diso_​to_​diso : 23
diso_​to_​phen : 5


Relationships:
none : 14
is_​abnormal_​cell_​of_​disease : 6
is_​associated_​anatomic_​site_​of : 1
is_​associated_​disease_​of : 1
is_​finding_​of_​disease : 4
is_​normal_​cell_​origin_​of_​disease : 3
is_​normal_​tissue_​origin_​of_​disease : 2
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 3
may_​be_​abnormal_​cell_​of_​disease : 9
may_​be_​cytogenetic_​abnormality_​of_​disease : 4
may_​be_​finding_​of_​disease : 5
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN19img genetic aspects C0017399
DISO_to_DISO12img Complication Aspects C1171258
DISO_to_DISO11img Dysmyelopoietic Syndromes C0026986
DISO_to_PHEN11img genetic aspects C0017399
DISO_to_DISO10img Complication Aspects C1171258
DISO_to_DISO8img Leukemia, Myelocytic, Acute C0023467
DISO_to_ANAT7img In Blood C0005768
DISO_to_DISO7img Leukemia, Myeloid C0023470
DISO_to_CHEM5img Azacitidine C0004475
DISO_to_DISO5img Leukemia, Myelocytic, Acute C0023467
DISO_to_ANAT4img In Blood C0005768
DISO_to_CHEM4img .beta.-Cytosine arabinoside C0010711
DISO_to_CHEM4img Granulocyte Colony-Stimulating Factor C0079459
DISO_to_DISO4img Dysmyelopoietic Syndromes C0026986
DISO_to_ANATis_abnormal_cell_of_diseaseimg Abnormal Hematopoietic and Lymphoid Cell C1510725
DISO_to_ANATmay_be_abnormal_cell_of_diseaseimg Atypically Small Megakaryocyte C0333861
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_ANATmay_be_abnormal_cell_of_diseaseimg Dysplastic Erythroid Precursor C1512102
DISO_to_ANATmay_be_abnormal_cell_of_diseaseimg Dysplastic Granulocyte C1512105
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg HEMOLYMPHORETICULAR TISSUE C1512398
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg Haematopoietic tissue C0229619
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
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanDLK18788delta-like 1 homolog (Drosophila)
img GENERIF, Score=1000, Pubmed Id: 15959531, UMLKSK CUI: C0002894
HumanPCNA5111proliferating cell nuclear antigen
img GENERIF, Score=1000, Pubmed Id: 18604718, UMLKSK CUI: C0002894
HumanNME44833NME/NM23 nucleoside diphosphate kinase 4
img GENERIF, Score=1000, Pubmed Id: 18604718, UMLKSK CUI: C0002894
HumanJAK23717Janus kinase 2
img GENERIF, Score=1000, Pubmed Id: 17344916, UMLKSK CUI: C0002894
HumanFLT12321fms-related tyrosine kinase 1
img GENERIF, Score=1000, Pubmed Id: 18604718, UMLKSK CUI: C0002894
HumanERCC12067excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence)
img GENERIF, Score=1000, Pubmed Id: 18604718, UMLKSK CUI: C0002894
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0002894Anemia, Refractory, with Excess of Blasts0self