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Details
Link-It Detail - Human Phenotype - Abnormality of superior crus of antihelix
Debug Stats
  • ### Total Build Time: 17 ms 8.967 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 216 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 386 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= 449 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 803 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 3.955 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 2.021 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.035 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of superior crus of antihelix HP:0011245
Definition (1)
An abnormality of the superior crus of the antihelix is the upper cartilaginous ridge arising at the bifurcation of the antihelix that ends beneath the fold of the ascending helix, and separates the concha from the triangular fossa.
Parents (1)
img Abnormality of the antihelix HP:0009738
Children (2)
img Prominent superior crus of antihelix HP:0011247
img Underdeveloped superior crus of antihelix HP:0011246
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the antihelix HP:0009738
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of the antihelix HP:0009738
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the antihelix HP:0009738
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the antihelix HP:0009738
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanFLNA2316filamin A, alpha
img HP RolledUp, OMIM ID: 300321
HumanFGS22270FG syndrome 2
img HP RolledUp, OMIM ID: 300321
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011245Abnormality of superior crus of antihelix0self