progressive sensorineural hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A progressive form of sensorineural hearing impairment. (Human Phenotype Ontology, HP_0000408)
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12 genes associated with the progressive sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTG1 actin gamma 1
ALMS1 Alstrom syndrome protein 1
DFNA5 deafness, autosomal dominant 5
MPZ myelin protein zero
MYH14 myosin, heavy chain 14, non-muscle
MYH9 myosin, heavy chain 9, non-muscle
NLRP3 NLR family, pyrin domain containing 3
OPA1 optic atrophy 1 (autosomal dominant)
POU3F4 POU class 3 homeobox 4
SYNE4 spectrin repeat containing, nuclear envelope family member 4
TIMM8A translocase of inner mitochondrial membrane 8 homolog A (yeast)
WFS1 Wolfram syndrome 1 (wolframin)