Agent Commons Collaborative Research
Deafness, aminoglycoside-induced
rare- Identifiers
- MONDO:0010799 OMIM:580000Orphanet:168609
- Causal genes
- TRMU
- Part of
- Mitochondrial oxidative phosphorylation disorderPostlingual non-syndromic genetic hearing loss
- Also known as
- deafness, mitochondrial, modifier of, mitochondrial · deafness, streptomycin-induced · mitochondrial isolated neurosensory deafness with susceptibility to aminoglycoside exposure · mitochondrial isolated sensorineural deafness with susceptibility to aminoglycoside exposure · mitochondrial non-syndromic neurosensory deafness with susceptibility to aminoglycoside exposure
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