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Details
Link-It Detail - Human Phenotype - Abnormality of cochlea
Debug Stats
  • ### Total Build Time: 22 ms 20.030 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 197 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 198 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= 794 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.722 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 7.729 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 8.257 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.017 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of cochlea HP:0000375
Definition (1)
An abnormality of the `cochlea` (FMA:60201).
Parents (2)
img Abnormality of the inner ear HP:0000359
img Morphological abnormality of the inner ear HP:0011390
Children (5)
img Enlarged cochlear aqueduct HP:0011388
img Hypoplasia of the cochlea HP:0008586
img Aplasia/Hypoplasia of the cochlea HP:0011395
img Cochlear malformation HP:0008554
img Cochlear degeneration HP:0005102
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the inner ear HP:0000359
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the inner ear HP:0000359
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the inner ear HP:0000359
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the inner ear HP:0000359
img All HP:0000001img Phenotypic abnormality HP:00001186img Morphological abnormality of the inner ear HP:0011390
img All HP:0000001img Phenotypic abnormality HP:00001188img Morphological abnormality of the inner ear HP:0011390
img All HP:0000001img Phenotypic abnormality HP:00001187img Morphological abnormality of the inner ear HP:0011390
img All HP:0000001img Phenotypic abnormality HP:00001189img Morphological abnormality of the inner ear HP:0011390
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanSCAR385502spinocerebellar ataxia, autosomal recessive 3
img HP RolledUp, OMIM ID: 271250
HumanSLC26A45172solute carrier family 26 (anion exchanger), member 4
img HP RolledUp, OMIM ID: 600791
img HP RolledUp, OMIM ID: 274600
HumanORC14998origin recognition complex, subunit 1
img HP RolledUp, OMIM ID: 224690
HumanKCNJ103766potassium inwardly-rectifying channel, subfamily J, member 10
img HP RolledUp, OMIM ID: 274600
img HP RolledUp, OMIM ID: 600791
HumanFOXI12299forkhead box I1
img HP RolledUp, OMIM ID: 600791
img HP RolledUp, OMIM ID: 274600
HumanEYA12138eyes absent homolog 1 (Drosophila)
img HP RolledUp, OMIM ID: 602588
img HP RolledUp, OMIM ID: 113650
HumanCOCH1690cochlin
img HP RolledUp, OMIM ID: 601369
HumanDDX111663DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11
img HP RolledUp, OMIM ID: 613398
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000375Abnormality of cochlea0self