severe hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A severe form of hearing impairment. (Human Phenotype Ontology, HP_0012714)
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2 genes associated with the severe hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GPSM2 G-protein signaling modulator 2
TRIOBP TRIO and F-actin binding protein