infantile 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 infantile onset. (Human Phenotype Ontology, HP_0008610)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008610
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Genes

1 genes associated with the infantile sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

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