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Details
Link-It Detail - Disease - von Willebrand Disease, Type 3
Debug Stats
  • ### Total Build Time: 95 ms 13.548 KB
  • CONCEPT_NAME gt=26 ms Completed: 26 ms rowSize= 358 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 266 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=58 ms Completed: 58 ms rowSize= 559 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.126 KB
  • CONCEPT_RELATIONSHIPS gt=5 ms Completed: 5 ms rowSize= 4.406 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 2.478 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
von Willebrand Disease, Type 3 C1264041
Definition (1)
A subtype of von Willebrand disease that results from a total or near total deficiency of VON WILLEBRAND FACTOR.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img von Willebrand Diseases C0042974
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img von Willebrand Diseases C0042974
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189396img von Willebrand Diseases C0042974
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501235img von Willebrand Diseases C0042974
Relationships (6)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 1
diso_​to_​diso : 1
diso_​to_​phen : 1


Relationships:
none : 2
alias_​of : 1
is_​associated_​anatomic_​site_​of : 1
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM7img von Willebrand Factor C0042971
DISO_to_PHEN7img genetic aspects C0017399
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg HEMOLYMPHORETICULAR TISSUE C1512398
DISO_to_ANATis_associated_anatomic_site_ofimg Hematopoietic and Lymphatic System C1512394
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Hematopoietic and Lymphoid Cell C1512385
DISO_to_DISOalias_ofimg 3 VWD, Type C1264041
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanANO257101anoctamin 2
img GENERIF, Score=947, Pubmed Id: 17371490, UMLKSK CUI: C1264041
HumanVWF7450von Willebrand factor
img GENERIF, Score=947, Pubmed Id: 17371490, UMLKSK CUI: C1264041
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1264041von Willebrand Disease, Type 30self