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Details
Link-It Detail - Disease - Neurofibrosarcoma
Debug Stats
  • ### Total Build Time: 143 ms 26.365 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 768 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= 187 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=13 ms Completed: 13 ms rowSize= 1.386 KB
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=84 ms Completed: 84 ms rowSize= 14.205 KB
  • CONCEPT_RELATIONSHIPS gt=27 ms Completed: 27 ms rowSize= 6.970 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 1.361 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Neurofibrosarcoma C0206729
Definition (1)
A malignant tumor that arises from small cutaneous nerves, is locally aggressive, and has a potential for metastasis. Characteristic histopathologic features include proliferating atypical spindle cells with slender wavy and pointed nuclei, hypocellular areas, and areas featuring organized whorls of fibroblastic proliferation. The most common primary sites are the extremities, retroperitoneum, and trunk. These tumors tend to present in childhood, often in association with NEUROFIBROMATOSIS 1. (From DeVita et al., Cancer: Principles & Practice of Oncology, 5th ed, p1662; Mayo Clin Proc 1990 Feb;65(2):164-72)
Semantic Types (1)
Neoplastic Process (T191)
Parents (3)
img Neurofibroma C0027830
img Fibrosarcoma C0016057
img Nerve Sheath Neoplasms C0206727
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Neuromuscular Diseases C00278687img Neurofibroma C0027830
img Neoplasms C0027651img Neoplasms by Site C00276537img Neurofibroma C0027830
img Nervous System Diseases C0027765img Nervous System Neoplasms C00277666img Neurofibroma C0027830
img Neoplasms C0027651img Neoplasms by Histologic Type C00276526img Neurofibroma C0027830
img Neoplasms C0027651img Neoplasms by Histologic Type C00276527img Fibrosarcoma C0016057
img Skin and Connective Tissue Diseases C0175166img Connective Tissue Diseases C00097826img Fibrosarcoma C0016057
img Neoplasms C0027651img Neoplasms by Histologic Type C00276526img Fibrosarcoma C0016057
img Nervous System Diseases C0027765img Neuromuscular Diseases C00278686img Nerve Sheath Neoplasms C0206727
img Neoplasms C0027651img Neoplasms by Site C00276536img Nerve Sheath Neoplasms C0206727
img Nervous System Diseases C0027765img Nervous System Neoplasms C00277665img Nerve Sheath Neoplasms C0206727
img Neoplasms C0027651img Neoplasms by Histologic Type C00276525img Nerve Sheath Neoplasms C0206727
Relationships (16)

Relation Types:
diso_​to_​diso : 14
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 13
permuted_​term_​of : 1
used_​for : 2
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO3img Lung Neoplasms C0024121
DISO_to_DISO3img Neurofibromatosis 1 C0027831
DISO_to_DISO2img Bone Neoplasms C0005967
DISO_to_DISO2img Complication Aspects C1171258
DISO_to_DISO2img Cutaneous tumor C0037286
DISO_to_DISO2img Lung Neoplasms C0024121
DISO_to_DISO2img Neoplasms, Multiple Primary C0027663
DISO_to_DISO2img Neurofibroma C0027830
DISO_to_DISO2img Neurofibromatosis 1 C0027831
DISO_to_DISO2img Soft Tissue Neoplasms C0037579
DISO_to_DISO2img Spinal Neoplasms C0037939
DISO_to_PHEN2img genetic aspects C0017399
DISO_to_PHYS2img GENET PREDISPOSITION C0314657
DISO_to_DISOused_forimg Fibrosarcoma C0016057
DISO_to_DISOused_forimg Nerve Sheath Neoplasms C0206727
DISO_to_DISOpermuted_term_ofimg Neurofibrosarcoma C0206729
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanMSH24436mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli)
img OMIM, Score=1000, UMLKSK CUI: C0206729
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0206729Neurofibrosarcoma0self