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Details
Link-It Detail - Human Phenotype - Abnormality of the auditory canal
Debug Stats
  • ### Total Build Time: 25 ms 27.594 KB
  • CONCEPT_NAME gt=2 ms Completed: 1 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 248 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=2 ms Completed: 2 ms rowSize= 449 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.448 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.094 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 21.996 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the auditory canal HP:0000372
Definition (1)
An abnormality of the `External acoustic tube` (FMA:61734) (also known as the auditory canal).
Parents (1)
img Abnormality of the outer ear HP:0000356
Children (4)
img Stenosis of the external auditory canal HP:0000402
img Exostosis of the external auditory canal HP:0004459
img Atresia of the external auditory canal HP:0000413
img Dilatated internal auditory canal HP:0004458
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
Genes (42)

Species:
human : 42
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanARCODS100381211Ariculocondylar syndrome
img HP RolledUp, OMIM ID: 602483
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img HP RolledUp, OMIM ID: 219000
HumanHFM170474Hemifacial microsomia
img HP RolledUp, OMIM ID: 164210
HumanB3GALTL145173beta 1,3-galactosyltransferase-like
img HP RolledUp, OMIM ID: 261540
HumanFRAS180144Fraser syndrome 1
img HP RolledUp, OMIM ID: 219000
HumanFKRP79147fukutin related protein
img HP RolledUp, OMIM ID: 236670
HumanPORCN64840porcupine homolog (Drosophila)
img HP RolledUp, OMIM ID: 305600
HumanSALL457167sal-like 4 (Drosophila)
img HP RolledUp, OMIM ID: 607323
HumanPOMT229954protein-O-mannosyltransferase 2
img HP RolledUp, OMIM ID: 236670
HumanGRIP123426glutamate receptor interacting protein 1
img HP RolledUp, OMIM ID: 219000
HumanGJB610804gap junction protein, beta 6, 30kDa
img HP RolledUp, OMIM ID: 304400
HumanPOMT110585protein-O-mannosyltransferase 1
img HP RolledUp, OMIM ID: 236670
HumanSF3B410262splicing factor 3b, subunit 4, 49kDa
img HP RolledUp, OMIM ID: 154400
HumanTSHZ110194teashirt zinc finger homeobox 1
img HP RolledUp, OMIM ID: 607842
HumanEFTUD29343elongation factor Tu GTP binding domain containing 2
img HP RolledUp, OMIM ID: 610536
HumanLARGE9215like-glycosyltransferase
img HP RolledUp, OMIM ID: 236670
HumanTP638626tumor protein p63
img HP RolledUp, OMIM ID: 106260
HumanGHS7971Goldenhar syndrome
img HP RolledUp, OMIM ID: 141400
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
img HP RolledUp, OMIM ID: 194190
HumanWHCR7467Wolf-Hirschhorn syndrome chromosome region
img HP RolledUp, OMIM ID: 194190
HumanTCOF16949Treacher Collins-Franceschetti syndrome 1
img HP IEA, OMIM ID: 154500
HumanRPL266154ribosomal protein L26
img HP RolledUp, OMIM ID: 614900
HumanPTEN5728phosphatase and tensin homolog
img HP RolledUp, OMIM ID: 176920
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000372Abnormality of the auditory canal0self