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Details
Link-It Detail - Disease - Leukemia, Myelomonocytic, Juvenile
Debug Stats
  • ### Total Build Time: 175 ms 58.469 KB
  • CONCEPT_NAME gt=13 ms Completed: 13 ms rowSize= 366 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 397 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=20 ms Completed: 20 ms rowSize= 187 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 1,014 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.806 KB
  • CONCEPT_RELATIONSHIPS gt=77 ms Completed: 77 ms rowSize= 17.057 KB
  • CONCEPT_GENES gt=48 ms Completed: 48 ms rowSize= 35.485 KB
  • CONCEPT_XREFS gt=12 ms Completed: 12 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Leukemia, Myelomonocytic, Juvenile C0349639
Definition (1)
A leukemia affecting young children characterized by SPLENOMEGALY, enlarged lymph nodes, rashes, and hemorrhages. Traditionally classed as a myeloproliferative disease, it is now considered a mixed myeloproliferative-mylelodysplastic disorder.
Semantic Types (1)
Neoplastic Process (T191)
Parents (2)
img Leukemia, Myeloid C0023470
img Myelodysplastic-Myeloproliferative Diseases C1301355
Ancestral Roots
RootRoot Plus OneDepthParent
img Neoplasms C0027651img Neoplasms by Histologic Type C00276525img Leukemia, Myeloid C0023470
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Myelodysplastic-Myeloproliferative Diseases C1301355
Relationships (58)

Relation Types:
diso_​to_​anat : 10
diso_​to_​chem : 4
diso_​to_​diso : 31
diso_​to_​gene : 6
diso_​to_​phen : 5
diso_​to_​phys : 2


Relationships:
none : 11
gene_​associated_​with_​disease : 4
is_​abnormal_​cell_​of_​disease : 4
is_​associated_​anatomic_​site_​of : 1
is_​associated_​disease_​of : 1
is_​finding_​of_​disease : 6
is_​normal_​cell_​origin_​of_​disease : 2
is_​normal_​tissue_​origin_​of_​disease : 2
is_​not_​cytogenetic_​abnormality_​of_​disease : 2
is_​not_​finding_​of_​disease : 1
is_​not_​molecular_​abnormality_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
may_​be_​associated_​disease_​of_​disease : 3
may_​be_​cytogenetic_​abnormality_​of_​disease : 1
may_​be_​finding_​of_​disease : 13
may_​be_​molecular_​abnormality_​of_​disease : 2
permuted_​term_​of : 1
related_​to : 2
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN58img genetic aspects C0017399
DISO_to_DISO19img Complication Aspects C1171258
DISO_to_PHYS16img Mutation C0026882
DISO_to_DISO10img Dysmyelopoietic Syndromes C0026986
DISO_to_CHEM7img CBL E3 Ubiquitin Protein Ligase C0139026
DISO_to_CHEM7img Protein Tyrosine Phosphatase, Non-Receptor Type 11 C0656342
DISO_to_CHEM7img Proto-Oncogene Proteins c-cbl C0139026
DISO_to_CHEM5img Granulocyte-Macrophage Colony-Stimulating Factor C0079460
DISO_to_DISO5img Noonan Syndrome C0028326
DISO_to_GENE5img Genes, ras C0034677
DISO_to_PHYS5img Germ-Line Mutation C0206530
DISO_to_ANATis_associated_anatomic_site_ofimg 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 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_DISOis_associated_disease_ofimg Anemia C0002871
DISO_to_DISOis_not_finding_of_diseaseimg Auer Rods Present C1332354
DISO_to_DISOis_not_molecular_abnormality_of_diseaseimg BCR-ABL1 Fusion Protein Expression C1516132
DISO_to_DISOmay_be_associated_disease_of_diseaseimg Bronchitis C0006277
Genes (24)

Species:
human : 24
SpeciesGeneGeneIdGene NameEvidence
HumanSPECC192521sperm antigen with calponin homology and coiled-coil domains 1
img NCI, Score=801, Pubmed Id: 15087372, UMLKSK CUI: C0349639
HumanARHGAP2623092Rho GTPase activating protein 26
img NCI, Score=801, Pubmed Id: 15382263, UMLKSK CUI: C0349639
HumanCD839308CD83 molecule
img NCI, Score=801, Pubmed Id: 12522453, UMLKSK CUI: C0349639
HumanCCL226367chemokine (C-C motif) ligand 22
img NCI, Score=801, Pubmed Id: 12522453, UMLKSK CUI: C0349639
HumanPTPN115781protein tyrosine phosphatase, non-receptor type 11
Click here to display 35 evidence detail records.
HumanPDGFRB5159platelet-derived growth factor receptor, beta polypeptide
img NCI, Score=801, Pubmed Id: 15087372, UMLKSK CUI: C0349639
HumanMX14599myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse)
img NCI, Score=801, Pubmed Id: 15454834, UMLKSK CUI: C0349639
HumanMPL4352myeloproliferative leukemia virus oncogene
img NCI, Score=801, Pubmed Id: 9596651, UMLKSK CUI: C0349639
HumanIRF23660interferon regulatory factor 2
img NCI, Score=801, Pubmed Id: 10609788, UMLKSK CUI: C0349639
img NCI, Score=801, Pubmed Id: 10609788, UMLKSK CUI: C0349639
HumanIL13RA23598interleukin 13 receptor, alpha 2
img NCI, Score=801, Pubmed Id: 9012477, UMLKSK CUI: C0349639
HumanIL133596interleukin 13
img NCI, Score=801, Pubmed Id: 9012477, UMLKSK CUI: C0349639
img NCI, Score=801, Pubmed Id: 9012477, UMLKSK CUI: C0349639
img NCI, Score=801, Pubmed Id: 9012477, UMLKSK CUI: C0349639
img NCI, Score=801, Pubmed Id: 9012477, UMLKSK CUI: C0349639
HumanIL33562interleukin 3 (colony-stimulating factor, multiple)
img NCI, Score=801, Pubmed Id: 8641332, UMLKSK CUI: C0349639
img NCI, Score=801, Pubmed Id: 1886426, UMLKSK CUI: C0349639
img NCI, Score=801, Pubmed Id: 1915702, UMLKSK CUI: C0349639
HumanIL1A3552interleukin 1, alpha
img NCI, Score=801, Pubmed Id: 1915702, UMLKSK CUI: C0349639
HumanHBA23040hemoglobin, alpha 2
img NCI, Score=801, Pubmed Id: 7795240, UMLKSK CUI: C0349639
img NCI, Score=801, Pubmed Id: 7795240, UMLKSK CUI: C0349639
HumanFANCG2189Fanconi anemia, complementation group G
img NCI, Score=801, Pubmed Id: 10994546, UMLKSK CUI: C0349639
HumanFANCA2175Fanconi anemia, complementation group A
img NCI, Score=801, Pubmed Id: 10994546, UMLKSK CUI: C0349639
HumanCSF1R1436colony stimulating factor 1 receptor
img NCI, Score=801, Pubmed Id: 2968914, UMLKSK CUI: C0349639
HumanCPOX1371coproporphyrinogen oxidase
img NCI, Score=801, Pubmed Id: 10609786, UMLKSK CUI: C0349639
HumanCD38952CD38 molecule
img NCI, Score=801, Pubmed Id: 8839860, UMLKSK CUI: C0349639
HumanCD80941CD80 molecule
img NCI, Score=801, Pubmed Id: 12522453, UMLKSK CUI: C0349639
HumanCD14929CD14 molecule
img NCI, Score=801, Pubmed Id: 9012477, UMLKSK CUI: C0349639
HumanCD1D912CD1d molecule
img NCI, Score=801, Pubmed Id: 12764370, UMLKSK CUI: C0349639
HumanCA1759carbonic anhydrase I
img NCI, Score=801, Pubmed Id: 807771, UMLKSK CUI: C0349639
img NCI, Score=801, Pubmed Id: 807771, UMLKSK CUI: C0349639
HumanANXA2302annexin A2
img NCI, Score=801, Pubmed Id: 12699894, UMLKSK CUI: C0349639
img NCI, Score=801, Pubmed Id: 12699894, UMLKSK CUI: C0349639
img NCI, Score=801, Pubmed Id: 12699894, UMLKSK CUI: C0349639
img NCI, Score=801, Pubmed Id: 12699894, UMLKSK CUI: C0349639
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0349639Leukemia, Myelomonocytic, Juvenile0self