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Details
Link-It Detail - Human Phenotype - Abnormality of the epiglottis
Debug Stats
  • ### Total Build Time: 22 ms 13.148 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 204 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=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=4 ms Completed: 4 ms rowSize= 791 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.093 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 3.976 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 5.940 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.023 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the epiglottis HP:0005483
Parents (2)
img Abnormality of the upper respiratory tract HP:0002087
img Abnormality of the larynx HP:0001600
Children (3)
img Aplasia/Hypoplasia of the Epiglottis HP:0010565
img Abnormality of the aryepiglottic fold HP:0008744
img Bifid epiglottis HP:0010564
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the upper respiratory tract HP:0002087
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the upper respiratory tract HP:0002087
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the larynx HP:0001600
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the larynx HP:0001600
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanDYNC2H179659dynein, cytoplasmic 2, heavy chain 1
img HP RolledUp, OMIM ID: 263520
HumanSF3B410262splicing factor 3b, subunit 4, 49kDa
img HP RolledUp, OMIM ID: 154400
HumanPRRX15396paired related homeobox 1
img HP RolledUp, OMIM ID: 202650
HumanNEK14750NIMA-related kinase 1
img HP RolledUp, OMIM ID: 263520
HumanGLI32737GLI family zinc finger 3
img HP RolledUp, OMIM ID: 146510
HumanFOXE12304forkhead box E1 (thyroid transcription factor 2)
img HP RolledUp, OMIM ID: 241850
HumanAFD1171acrofacial dysostosis 1, Nager type
img HP RolledUp, OMIM ID: 154400
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0005483Abnormality of the epiglottis0self