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Details
Link-It Detail - Disease - CGL, Philadelphia chromosome negative
Debug Stats
  • ### Total Build Time: 15 ms 18.719 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 372 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 490 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=9 ms Completed: 9 ms rowSize= 15.066 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 1.569 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
CGL, Philadelphia chromosome negative C0279549
Definition (1)
A chronic myelogenous leukemia which does not have the characteristic t(9;22)(q34;q11.2) translocation but it has either a variant translocation or a cryptic translocation that can not be detected by conventional cytogenetic analysis. In such cases the BCR-ABL1 fusion gene is always detected by RT-PCR, FISH, or Southern blot analysis.
Relationships (29)

Relation Types:
diso_​to_​anat : 13
diso_​to_​diso : 16


Relationships:
clinically_​similar : 1
is_​abnormal_​cell_​of_​disease : 5
is_​finding_​of_​disease : 2
is_​normal_​cell_​origin_​of_​disease : 3
is_​normal_​tissue_​origin_​of_​disease : 2
is_​not_​cytogenetic_​abnormality_​of_​disease : 2
is_​not_​finding_​of_​disease : 2
is_​not_​molecular_​abnormality_​of_​disease : 3
is_​not_​normal_​cell_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 2
may_​be_​associated_​disease_​of_​disease : 1
may_​be_​finding_​of_​disease : 5
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
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_normal_tissue_origin_of_diseaseimg HEMOLYMPHORETICULAR TISSUE C1512398
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg Haematopoietic tissue C0229619
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Hematopoietic and Lymphatic System C1512394
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Hematopoietic and Lymphoid Cell C1512385
DISO_to_ANATis_abnormal_cell_of_diseaseimg Leukemic Cell C1517806
DISO_to_ANATis_not_normal_cell_origin_of_diseaseimg Lymphocyte C0024264
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Cell C0597032
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Hematopoietic and Lymphoid Cell C1513983
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Myeloid Cell C1514039
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Pluripotent Bone Marrow Stem Cell C1514186
DISO_to_DISOmay_be_associated_disease_of_diseaseimg Anemia C0002871
DISO_to_DISOmay_be_finding_of_diseaseimg Body Weight decreased C0043096
DISO_to_DISOmay_be_finding_of_diseaseimg Chronic Clinical Course C1333035
DISO_to_DISOmay_be_finding_of_diseaseimg Enlarged Liver C0019209
DISO_to_DISOis_finding_of_diseaseimg Enlarged Spleen C0038002
DISO_to_DISOis_not_molecular_abnormality_of_diseaseimg FGFR1 Gene Rearrangement C2827358
DISO_to_DISOmay_be_finding_of_diseaseimg Fatigue C0015672
DISO_to_DISOis_finding_of_diseaseimg Hypercellular bone marrow C1334068
DISO_to_DISOis_not_finding_of_diseaseimg Ineffective Hematopoiesis C1334171
DISO_to_DISOclinically_similarimg Leukemia, Myelogenous, Chronic, BCR-ABL Positive C0023473
DISO_to_DISOis_not_molecular_abnormality_of_diseaseimg PDGFRA Gene Rearrangement C2707644
DISO_to_DISOis_not_molecular_abnormality_of_diseaseimg PDGFRB Gene Rearrangement C2827357
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanBCR613breakpoint cluster region
img GENERIF, Score=756, Pubmed Id: 16631477, UMLKSK CUI: C0279549
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0279549CGL, Philadelphia chromosome negative0self