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Details
Link-It Detail - Human Phenotype - Abnormal auditory evoked potentials
Debug Stats
  • ### Total Build Time: 37 ms 16.734 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 210 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 10.037 KB
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Human Phenotype (1)
Abnormal auditory evoked potentials HP:0006958
Definition (1)
An abnormality of the auditory evoked potentials, which are used to trace the signal generated by a sound, from the cochlear nerve, through the lateral lemniscus, to the medial geniculate nucleus, and to the cortex.
Parents (2)
img Neurophysiological abnormality HP:0001311
img Abnormal neurological laboratory findings HP:0003129
Children (3)
img abnormal or absent auditory nerve and brainstem responses HP:0004462
img Prolonged brainstem auditory evoked potentials HP:0004466
img Absent brainstem auditory responses HP:0004463
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Neurophysiological abnormality HP:0001311
img All HP:0000001img Phenotypic abnormality HP:00001185img Neurophysiological abnormality HP:0001311
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormal neurological laboratory findings HP:0003129
Genes (12)

Species:
human : 12
SpeciesGeneGeneIdGene NameEvidence
HumanDIAPH381624diaphanous-related formin 3
img HP IEA, OMIM ID: 609129
HumanSH3TC279628SH3 domain and tetratricopeptide repeats 2
img HP RolledUp, OMIM ID: 601596
HumanNDRG110397N-myc downstream regulated 1
img HP TAS, OMIM ID: 601455
HumanOTOF9381otoferlin
img HP RolledUp, OMIM ID: 601071
HumanMTMR28898myotubularin related protein 2
img HP IEA, OMIM ID: 601382
HumanTGFBR17046transforming growth factor, beta receptor 1
img HP IEA, OMIM ID: 609129
HumanSOX106663SRY (sex determining region Y)-box 10
img HP RolledUp, OMIM ID: 609136
HumanOPA14976optic atrophy 1 (autosomal dominant)
img HP IEA, OMIM ID: 125250
HumanMYH34621myosin, heavy chain 3, skeletal muscle, embryonic
img HP IEA, OMIM ID: 193700
HumanERCC62074excision repair cross-complementing rodent repair deficiency, complementation group 6
img HP IEA, OMIM ID: 133540
HumanEDNRB1910endothelin receptor type B
img HP IEA, OMIM ID: 600501
HumanERCC81161excision repair cross-complementing rodent repair deficiency, complementation group 8
img HP PCS, OMIM ID: 216400
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0006958Abnormal auditory evoked potentials0self