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Details
Link-It Detail - Disease - Hyperostosis of skull
Debug Stats
  • ### Total Build Time: 13 ms 10.076 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 340 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=6 ms Completed: 6 ms rowSize= 4.522 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 3.996 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperostosis of skull C0020496
Relationships (8)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 6


Relationships:
classifies : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
mapped_​to : 5
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg Connective and Soft Tissue C1516798
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Skeletal bone C0262950
DISO_to_DISOmapped_toimg CRANIOTABES C0392452
DISO_to_DISOmapped_toimg HYPEROSTOSIS FRONTALIS INTERNA C0020494
DISO_to_DISOmapped_toimg Hyperostosis of skull C0020496
DISO_to_DISOmapped_toimg Large head (disorder) C2243051
DISO_to_DISOmapped_toimg Leonine bones C0086544
DISO_to_DISOclassifiesimg Other bone disease and musculoskeletal deformities C0810059
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanAURKC6795aurora kinase C
img GENERIF, Score=658, Pubmed Id: 17435757, UMLKSK CUI: C0020496
HumanLBR3930lamin B receptor
img OMIM, Score=1000, UMLKSK CUI: C0020496
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
img OMIM, Score=1000, UMLKSK CUI: C0020496
HumanGJA12697gap junction protein, alpha 1, 43kDa
img OMIM, Score=1000, UMLKSK CUI: C0020496
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020496Hyperostosis of skull0self