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Details
Link-It Detail - Human Phenotype - Abnormality of lower-limb metaphyses
Debug Stats
  • ### Total Build Time: 9 ms 18.087 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 211 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= 1.108 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 799 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 9.623 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 5.194 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.030 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of lower-limb metaphyses HP:0006490
Parents (3)
img Abnormality of the metaphyses HP:0000944
img Abnormality involving the metaphyses of the limbs HP:0006506
img Abnormality of the lower limb HP:0002814
Children (2)
img Abnormality of the femoral metaphysis HP:0006489
img Abnormality of the tibial metaphysis HP:0006491
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the metaphyses HP:0000944
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the metaphyses HP:0000944
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the metaphyses HP:0000944
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the metaphyses HP:0000944
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality involving the metaphyses of the limbs HP:0006506
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality involving the metaphyses of the limbs HP:0006506
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality involving the metaphyses of the limbs HP:0006506
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality involving the metaphyses of the limbs HP:0006506
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the lower limb HP:0002814
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the lower limb HP:0002814
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
img HP RolledUp, OMIM ID: 156530
HumanBFHD50947Beukes familial hip dysplasia
img HP RolledUp, OMIM ID: 142669
HumanSETBP126040SET binding protein 1
img HP RolledUp, OMIM ID: 269150
HumanTRIP119321thyroid hormone receptor interactor 11
img HP RolledUp, OMIM ID: 200600
HumanFGFR32261fibroblast growth factor receptor 3
img HP RolledUp, OMIM ID: 610474
HumanCOL10A11300collagen, type X, alpha 1
img HP RolledUp, OMIM ID: 156500
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0006490Abnormality of lower-limb metaphyses0self