congenital sensorineural hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of hearing impairment caused by an abnormal functionality of the cochlear nerve with congenital onset. (Human Phenotype Ontology, HP_0008527)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008527
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Genes

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

Symbol Name
ADGRV1 adhesion G protein-coupled receptor V1
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
MITF microphthalmia-associated transcription factor
PAX3 paired box 3
PCDH15 protocadherin-related 15
PDZD7 PDZ domain containing 7
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SNAI2 snail family zinc finger 2
USH1C Usher syndrome 1C (autosomal recessive, severe)
USH2A Usher syndrome 2A (autosomal recessive, mild)