postlingual sensorineural hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of sensorineural hearing impairment with onset after the acquisition of speech. (Human Phenotype Ontology, HP_0008596)
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2 genes associated with the postlingual sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COCH cochlin
TIMM8A translocase of inner mitochondrial membrane 8 homolog A (yeast)