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Details
Link-It Detail - Disease - Congenital Fibrosarcoma
Debug Stats
  • ### Total Build Time: 24 ms 23.787 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 344 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 506 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= 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=18 ms Completed: 18 ms rowSize= 12.303 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 9.427 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Congenital Fibrosarcoma C0334459
Definition (1)
A fibrosarcoma that is histologically identical to classical fibrosarcoma of adults, but has a much more favorable prognosis. It occurs in infants and young children, metastasizes rarely and is morphologically and genetically related to congenital mesoblastic nephroma. Most infantile fibrosarcomas have the chromosomal translocation t(12;15)(p13;q26).
Relationships (24)

Relation Types:
diso_​to_​anat : 12
diso_​to_​diso : 12


Relationships:
is_​abnormal_​cell_​of_​disease : 6
is_​finding_​of_​disease : 2
is_​normal_​cell_​origin_​of_​disease : 2
is_​normal_​tissue_​origin_​of_​disease : 1
is_​not_​finding_​of_​disease : 3
is_​not_​normal_​cell_​origin_​of_​disease : 2
is_​not_​normal_​tissue_​origin_​of_​disease : 1
may_​be_​cytogenetic_​abnormality_​of_​disease : 5
may_​be_​finding_​of_​disease : 1
may_​be_​molecular_​abnormality_​of_​disease : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATis_abnormal_cell_of_diseaseimg Cancer Cell C0334227
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Cell of connective tissue C0009781
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg Connective and Soft Tissue C1516798
DISO_to_ANATis_not_normal_cell_origin_of_diseaseimg Epithelial Cells C0014597
DISO_to_ANATis_not_normal_tissue_origin_of_diseaseimg Epithelial Tissue C0014609
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Fibroblasts C0016030
DISO_to_ANATis_abnormal_cell_of_diseaseimg Malignant Fibroblast C1708876
DISO_to_ANATis_abnormal_cell_of_diseaseimg Malignant Spindle-Shaped Fibroblast C1708911
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Cell C0597032
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Connective and Soft Tissue Cell C1513942
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Fibroblast C1709175
DISO_to_ANATis_not_normal_cell_origin_of_diseaseimg Nerve Cell, Neuroepithelial Cell, and Supporting Cell of the Nervous System C1518293
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg 8 trisomy C0432412
DISO_to_DISOis_finding_of_diseaseimg Childhood Lesion C1880068
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Chromosome 17 duplication C1096168
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Chromosome 20 duplication C0265479
DISO_to_DISOmay_be_molecular_abnormality_of_diseaseimg ETV6-NTRK3 Fusion Protein Expression C1512143
DISO_to_DISOmay_be_finding_of_diseaseimg Favorable Clinical Outcome C1333602
DISO_to_DISOis_finding_of_diseaseimg Herringbone Growth Pattern C1333997
DISO_to_DISOis_not_finding_of_diseaseimg Indolent Clinical Course C1334168
DISO_to_DISOis_not_finding_of_diseaseimg Intermediate Filaments Present C1708535
DISO_to_DISOis_not_finding_of_diseaseimg Intracytoplasmic Eosinophilic Inclusion C1711292
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg Trisomy 11 C0432409
DISO_to_DISOmay_be_cytogenetic_abnormality_of_diseaseimg t(12;15)(p13;q26) C1515715
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanNTRK34916neurotrophic tyrosine kinase, receptor, type 3
img NCI, Score=801, Pubmed Id: 12210087, UMLKSK CUI: C0334459
img NCI, Score=801, Pubmed Id: 11169520, UMLKSK CUI: C0334459
img NCI, Score=801, Pubmed Id: 12650516, UMLKSK CUI: C0334459
img NCI, Score=801, Pubmed Id: 9778053, UMLKSK CUI: C0334459
img NCI, Score=801, Pubmed Id: 11169520, UMLKSK CUI: C0334459
img NCI, Score=801, Pubmed Id: 11169520, UMLKSK CUI: C0334459
img NCI, Score=801, Pubmed Id: 12606136, UMLKSK CUI: C0334459
img NCI, Score=801, Pubmed Id: 11169520, UMLKSK CUI: C0334459
img NCI, Score=801, Pubmed Id: 10702799, UMLKSK CUI: C0334459
img NCI, Score=801, Pubmed Id: 11751416, UMLKSK CUI: C0334459
HumanSERPINA312serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 3
img NCI, Score=801, Pubmed Id: 3035524, UMLKSK CUI: C0334459
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0334459Congenital Fibrosarcoma0self