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Details
Link-It Detail - Disease - Fibrous Hamartoma of Infancy
Debug Stats
  • ### Total Build Time: 11 ms 13.904 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 354 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 447 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=3 ms Completed: 3 ms rowSize= 7.581 KB
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 4.309 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Fibrous Hamartoma of Infancy C0265979
Definition (1)
A poorly circumscribed neoplasm arising from the soft tissues in infants. It is characterized by the presence of bland fibroblastic spindle cells, collagenous stroma formation, primitive mesenchymal round cells, and mature fat cells. These components combined form a distinct organoid pattern.
Relationships (13)

Relation Types:
diso_​to_​anat : 9
diso_​to_​diso : 4


Relationships:
is_​abnormal_​cell_​of_​disease : 4
is_​associated_​anatomic_​site_​of : 1
is_​finding_​of_​disease : 2
is_​normal_​cell_​origin_​of_​disease : 2
is_​normal_​tissue_​origin_​of_​disease : 1
is_​not_​finding_​of_​disease : 1
is_​not_​normal_​cell_​origin_​of_​disease : 1
may_​be_​finding_​of_​disease : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Cell of connective tissue C0009781
DISO_to_ANATis_associated_anatomic_site_ofimg Connective and Soft Tissue C1516798
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Fibroblasts C0016030
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_ANATis_abnormal_cell_of_diseaseimg Primitive Mesenchymal Round Cell C1514437
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg soft tissue C0225317
DISO_to_DISOis_finding_of_diseaseimg Indolent Clinical Course C1334168
DISO_to_DISOis_finding_of_diseaseimg Myxoid Stroma Formation C1334857
DISO_to_DISOmay_be_finding_of_diseaseimg Rapidly Enlarging Mass C1335663
DISO_to_DISOis_not_finding_of_diseaseimg Well-Circumscribed Lesion C1707398
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanNTRK34916neurotrophic tyrosine kinase, receptor, type 3
img NCI, Score=801, Pubmed Id: 11169520, UMLKSK CUI: C0265979
HumanCYP11B11584cytochrome P450, family 11, subfamily B, polypeptide 1
img NCI, Score=801, Pubmed Id: 7817466, UMLKSK CUI: C0265979
img NCI, Score=801, Pubmed Id: 9553195, UMLKSK CUI: C0265979
img NCI, Score=801, Pubmed Id: 10191347, UMLKSK CUI: C0265979
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0265979Fibrous Hamartoma of Infancy0self