deafness, aminoglycoside-induced

Findings

No curated finding names deafness, aminoglycoside-induced yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Inheritance

Mitochondrial inheritance

HPO, annotations 2026-09-02

What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.

Where it sits

A kind of

• mitochondrial oxidative phosphorylation disorder
• postlingual non-syndromic genetic hearing loss

Resolves to: deafness, aminoglycoside-induced

Also called

deafness, mitochondrial, modifier of, mitochondrialdeafness, streptomycin-inducedmitochondrial isolated neurosensory deafness with susceptibility to aminoglycoside exposuremitochondrial isolated sensorineural deafness with susceptibility to aminoglycoside exposuremitochondrial non-syndromic neurosensory deafness with susceptibility to aminoglycoside exposuremitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposurestreptomycin ototoxicity