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Details
Link-It Detail - Anatomy - Cochlear Nerve
Debug Stats
  • ### Total Build Time: 71 ms 28.941 KB
  • CONCEPT_NAME gt=16 ms Completed: 16 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 422 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
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  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.115 KB
  • CONCEPT_RELATIONSHIPS gt=30 ms Completed: 30 ms rowSize= 13.276 KB
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 11.890 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Anatomy (1)
Cochlear Nerve C0009201
Definition (1)
cochlear part of the 8th cranial nerve (vestibulocochlear nerve); cochlear nerve fibers originate from neurons of the spiral ganglion and project peripherally to cochlear hair cells and centrally to the cochlear nuclei of the brain stem; mediates the sense of hearing.
Semantic Types (1)
Body Part, Organ, or Organ Component (T023)
Parents (1)
img Vestibulocochlear Nerve C0001162
Ancestral Roots
RootRoot Plus OneDepthParent
img Vestibulocochlear Nerve C00011622img Vestibulocochlear Nerve C0001162
Relationships (42)

Relation Types:
anat_​to_​anat : 21
anat_​to_​diso : 7
anat_​to_​phen : 1
anat_​to_​phys : 13


Relationships:
none : 32
anatomic_​structure_​is_​physical_​part_​of : 1
has_​physical_​part_​of_​anatomic_​structure : 2
is_​location_​of_​anatomic_​structure : 1
isa : 3
permuted_​term_​of : 1
sib_​in_​isa : 2
Page Size
Current 25
  Page 1 of 2
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
ANAT_to_PHYS180img physiological aspects C0031843
ANAT_to_PHYS177img physiological aspects C0031843
ANAT_to_DISO48img Hearing Loss, Sensorineural C0018784
ANAT_to_ANAT42img Cochlea C0009195
ANAT_to_PHYS38img Action Potentials C0001272
ANAT_to_DISO35img Hearing Loss, Sensorineural C0018784
ANAT_to_DISO33img Deafness C0581883
ANAT_to_ANAT32img Cochlea C0009195
ANAT_to_ANAT31img Auditory Pathways C0004308
ANAT_to_DISO31img Complete Hearing Loss C0581883
ANAT_to_ANAT29img Cochlear Nucleus C0152411
ANAT_to_DISO29img Vestibulocochlear Nerve Diseases C0001163
ANAT_to_PHYS28img Acoustic Evoked Brain Stem Potentials C0079319
ANAT_to_PHYS26img Action Potential C0001272
ANAT_to_DISO25img Vestibulocochlear Nerve Diseases C0001163
ANAT_to_PHYS25img Auditory Evoked Potentials C0015215
ANAT_to_PHYS23img Auditory Evoked Potentials C0015215
ANAT_to_PHYS22img Acoustic Evoked Brain Stem Potentials C0079319
ANAT_to_ANAT19img Cochlear Nucleus C0152411
ANAT_to_ANAT17img Nerve Fiber C0027749
ANAT_to_ANAT17img Neurons C0027882
ANAT_to_PHYS17img Auditory Perception C0004309
ANAT_to_PHYS17img Speech Perception C0037826
ANAT_to_ANAT16img Neurons C0027882
ANAT_to_DISO16img trauma qualifier C1510467
Genes (359)

Species:
human : 359
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanDFNB72791116
HumanDFNB59494513deafness, autosomal recessive 59
HumanDFNB55494148deafness, autosomal recessive 55
HumanDFNB45449483deafness, autosomal recessive 45
HumanDFNA54448962deafness, autosomal dominant 54
HumanGDF6392255growth differentiation factor 6
HumanDFNB40379003deafness, autosomal recessive 40
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
HumanDFNA53353347deafness, autosomal dominant 53
HumanFREM2341640FRAS1 related extracellular matrix protein 2
HumanDPH3285381diphthamide biosynthesis 3
HumanSUMF1285362sulfatase modifying factor 1
HumanRSPO1284654R-spondin 1
HumanTMIE259236transmembrane inner ear
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
HumanDFNB33170508deafness, autosomal recessive 33
HumanMARVELD2153562MARVEL domain containing 2
HumanPTPRVP148713protein tyrosine phosphatase, receptor type, V, pseudogene
HumanHGSNAT138050heparan-alpha-glucosaminide N-acetyltransferase
HumanGJB4127534gap junction protein, beta 4, 30.3kDa
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
HumanTMC2117532transmembrane channel-like 2
HumanTMC1117531transmembrane channel-like 1
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0009201Cochlear Nerve0self