abnormal auditory evoked potentials Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description 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. (Human Phenotype Ontology, HP_0006958)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006958
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Genes

11 genes associated with the abnormal auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DIAPH3 diaphanous-related formin 3
EDNRB endothelin receptor type B
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
MTMR2 myotubularin related protein 2
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
NDRG1 N-myc downstream regulated 1
OPA1 optic atrophy 1 (autosomal dominant)
OTOF otoferlin
SH3TC2 SH3 domain and tetratricopeptide repeats 2
SOX10 SRY (sex determining region Y)-box 10