progressive hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A progressive form of hearing impairment. (Human Phenotype Ontology, HP_0001730)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001730
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Genes

19 genes associated with the progressive 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
C10ORF2 chromosome 10 open reading frame 2
DFNA5 deafness, autosomal dominant 5
DIAPH1 diaphanous-related formin 1
LARS2 leucyl-tRNA synthetase 2, mitochondrial
MIR96 microRNA 96
MPZ myelin protein zero
MYH14 myosin, heavy chain 14, non-muscle
MYH9 myosin, heavy chain 9, non-muscle
MYO3A myosin IIIA
NLRP3 NLR family, pyrin domain containing 3
OPA1 optic atrophy 1 (autosomal dominant)
PEX11B peroxisomal biogenesis factor 11 beta
POU3F4 POU class 3 homeobox 4
SERPINB6 serpin peptidase inhibitor, clade B (ovalbumin), member 6
SYNE4 spectrin repeat containing, nuclear envelope family member 4
TIMM8A translocase of inner mitochondrial membrane 8 homolog A (yeast)
WFS1 Wolfram syndrome 1 (wolframin)