Profound Hearing Impairment Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A profound (essentially complete) form of hearing impairment. (Human Phenotype Ontology, HP_0012715)
External Link https://www.disgenet.org/browser/0/1/0/C4022756
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Genes

7 genes associated with the disease Profound Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
EPS8 epidermal growth factor receptor pathway substrate 8
GJB2 gap junction protein, beta 2, 26kDa
GJB3 gap junction protein, beta 3, 31kDa
KCNQ4 potassium channel, voltage gated KQT-like subfamily Q, member 4
LMX1A LIM homeobox transcription factor 1, alpha
OTOF otoferlin
SLITRK6 SLIT and NTRK-like family, member 6