childhood onset sensorineural hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Sensorineural hearing impairment with childhood onset. (Human Phenotype Ontology, HP_0011474)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011474
Similar Terms
Downloads & Tools

Genes

6 genes associated with the childhood onset 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
COCH cochlin
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
MARVELD2 MARVEL domain containing 2
TIMM8A translocase of inner mitochondrial membrane 8 homolog A (yeast)