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Details
Link-It Detail - Human Phenotype - Abnormality of von Willebrand factor
Debug Stats
  • ### Total Build Time: 5 ms 6.003 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 212 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= 459 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 805 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.113 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 1.272 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.031 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of von Willebrand factor HP:0012146
Parents (1)
img Abnormality of the coagulation cascade HP:0003256
Children (2)
img Reduced von Willebrand factor activity HP:0008330
img Reduced quantity of Von Willebrand factor HP:0012147
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the coagulation cascade HP:0003256
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the coagulation cascade HP:0003256
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanNBEAL223218neurobeachin-like 2
img HP RolledUp, OMIM ID: 139090
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0012146Abnormality of von Willebrand factor0self