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Details
Link-It Detail - Disease - Atypical meningioma
Debug Stats
  • ### Total Build Time: 25 ms 31.006 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 336 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 395 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=5 ms Completed: 5 ms rowSize= 14.285 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 14.783 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Atypical meningioma C0431122
Definition (1)
A WHO grade II meningioma characterized by the presence of an increased mitotic activity or at least three of the following morphologic features: small cells, high cellularity, prominent nucleoli, lack of architectural pattern, and necrosis.
Relationships (26)

Relation Types:
diso_​to_​anat : 7
diso_​to_​diso : 19


Relationships:
clinically_​similar : 1
is_​abnormal_​cell_​of_​disease : 2
is_​associated_​anatomic_​site_​of : 3
is_​normal_​cell_​origin_​of_​disease : 1
isa : 1
may_​be_​abnormal_​cell_​of_​disease : 1
may_​be_​cytogenetic_​abnormality_​of_​disease : 10
may_​be_​finding_​of_​disease : 6
may_​be_​molecular_​abnormality_​of_​disease : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Arachnoidal Cell C1513123
DISO_to_ANATis_associated_anatomic_site_ofimg Central Nervous System C0927232
DISO_to_ANATis_associated_anatomic_site_ofimg Meninges C0025285
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Arachnoidal Cell C1514023
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Cell C0597032
DISO_to_ANATis_associated_anatomic_site_ofimg Nervous System C0027763
DISO_to_ANATmay_be_abnormal_cell_of_diseaseimg Small Meningothelial Cell C1519378
DISO_to_DISOisaimg Adult Atypical Meningioma C1332184
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Gain of Chromosome 12q C1517384
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Gain of Chromosome 15q C1517390
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Gain of Chromosome 17q C1517394
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Gain of Chromosome 1q C1517401
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Gain of Chromosome 20q C1517404
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Gain of Chromosome 9q C1517426
DISO_to_DISOmay_be_finding_of_diseaseimg Geographic Necrosis C1517527
DISO_to_DISOmay_be_finding_of_diseaseimg High Mitotic Activity C1334022
DISO_to_DISOmay_be_finding_of_diseaseimg Increased Cellularity Present C1512694
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Loss of Chromosome 14 C1517959
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Loss of Chromosome 1p C1517972
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Loss of Chromosome 22 C1517976
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Loss of Chromosome 3p C1517981
DISO_to_DISOclinically_similarimg Meningioma C0025286
DISO_to_DISOmay_be_molecular_abnormality_of_diseaseimg NF-2 Tumor-Suppressor Gene Inactivation C1513834
DISO_to_DISOmay_be_finding_of_diseaseimg Sheet-Like Growth Pattern C1710071
DISO_to_DISOmay_be_finding_of_diseaseimg Unfavorable Clinical Outcome C1519790
Genes (9)

Species:
human : 9
SpeciesGeneGeneIdGene NameEvidence
HumanNDRG257447NDRG family member 2
img NCI, Score=801, Pubmed Id: 16103061, UMLKSK CUI: C0431122
HumanCADM123705cell adhesion molecule 1
img NCI, Score=801, Pubmed Id: 15535129, UMLKSK CUI: C0431122
HumanWRN7486Werner syndrome, RecQ helicase-like
img NCI, Score=801, Pubmed Id: 16598422, UMLKSK CUI: C0431122
HumanTP537157tumor protein p53
img GENERIF, Score=1000, Pubmed Id: 15719270, UMLKSK CUI: C0431122
HumanTERC7012telomerase RNA component
img NCI, Score=801, Pubmed Id: 10845390, UMLKSK CUI: C0431122
img NCI, Score=801, Pubmed Id: 10845390, UMLKSK CUI: C0431122
img NCI, Score=801, Pubmed Id: 10845390, UMLKSK CUI: C0431122
HumanCD464179CD46 molecule, complement regulatory protein
img NCI, Score=801, Pubmed Id: 7526972, UMLKSK CUI: C0431122
HumanCENPF1063centromere protein F, 350/400kDa
img NCI, Score=801, Pubmed Id: 12507285, UMLKSK CUI: C0431122
img NCI, Score=801, Pubmed Id: 12507285, UMLKSK CUI: C0431122
HumanCDKN2C1031cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
img NCI, Score=801, Pubmed Id: 11485924, UMLKSK CUI: C0431122
img NCI, Score=801, Pubmed Id: 11485924, UMLKSK CUI: C0431122
HumanCDKN2B1030cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)
img NCI, Score=801, Pubmed Id: 11485924, UMLKSK CUI: C0431122
img NCI, Score=801, Pubmed Id: 11485924, UMLKSK CUI: C0431122
img NCI, Score=801, Pubmed Id: 11485924, UMLKSK CUI: C0431122
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0431122Atypical meningioma0self