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Details
Link-It Detail - Human Phenotype - Abnormality of the crus of the helix
Debug Stats
  • ### Total Build Time: 21 ms 12.764 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 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=3 ms Completed: 3 ms rowSize= 776 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 3.020 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 3.946 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 3.659 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.030 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the crus of the helix HP:0009895
Parents (2)
img Abnormality of the outer ear HP:0000356
img Abnormality of the helix HP:0011039
Children (9)
img Horizontal crus of helix HP:0009897
img Prominent crus of helix HP:0009899
img Tragal bridge of crus of helix HP:0011258
img Expanded terminal portion of crus of helix HP:0011259
img Absent crus of helix HP:0011255
img Underdeveloped crus of the helix HP:0009898
img Crus of helix connected to antihelix HP:0011256
img Serpiginous crus of helix HP:0011257
img Stahl ear HP:0100015
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the outer ear HP:0000356
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the outer ear HP:0000356
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the helix HP:0011039
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the helix HP:0011039
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanTWIST17291twist basic helix-loop-helix transcription factor 1
img HP RolledUp, OMIM ID: 101400
HumanSLC16A26567solute carrier family 16, member 2 (thyroid hormone transporter)
img HP RolledUp, OMIM ID: 300523
HumanSALL16299sal-like 1 (Drosophila)
img HP RolledUp, OMIM ID: 107480
HumanFGFR22263fibroblast growth factor receptor 2
img HP RolledUp, OMIM ID: 101400
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0009895Abnormality of the crus of the helix0self