prelingual sensorineural hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of sensorineural deafness with either congenital onset or infantile onset, i.e., before the acquisition of speech. (Human Phenotype Ontology, HP_0000399)
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4 genes associated with the prelingual sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADCY1 adenylate cyclase 1 (brain)
CDH23 cadherin-related 23
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
MARVELD2 MARVEL domain containing 2