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Details
Link-It Detail - Human Phenotype - Abnormality of the clivus
Debug Stats
  • ### Total Build Time: 27 ms 5.926 KB
  • CONCEPT_NAME gt=14 ms Completed: 14 ms rowSize= 200 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 306 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=2 ms Completed: 2 ms rowSize= 463 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 438 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.121 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 1.267 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the clivus HP:0010558
Definition (1)
An abnormality of the clivus, which is the inclined bony region of the posterior cranial fossa located between the sella turcica and the foramen magnum.
Parents (1)
img Abnormality of the posterior cranial fossa HP:0000932
Children (1)
img Vertical clivus HP:0010559
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the posterior cranial fossa HP:0000932
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the posterior cranial fossa HP:0000932
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanFLNA2316filamin A, alpha
img HP RolledUp, OMIM ID: 304120
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010558Abnormality of the clivus0self