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Mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure
ORPHA:168609
Classification level: Subtype of disorder
- Synonym(s):
- Mitochondrial isolated neurosensory deafness with susceptibility to aminoglycoside exposure
- Mitochondrial isolated neurosensory hearing loss with susceptibility to aminoglycoside exposure
- Mitochondrial isolated sensorineural deafness with susceptibility to aminoglycoside exposure
- Mitochondrial isolated sensorineural hearing loss with susceptibility to aminoglycoside exposure
- Mitochondrial non-syndromic neurosensory deafness with susceptibility to aminoglycoside exposure
- Mitochondrial non-syndromic neurosensory hearing loss with susceptibility to aminoglycoside exposure
- Mitochondrial non-syndromic sensorineural hearing loss with susceptibility to aminoglycoside exposure
- Prevalence: -
- Inheritance: -
- Age of onset: -
- ICD-10: -
- OMIM: -
- UMLS: -
- MeSH: -
- GARD: -
- MedDRA: -
Summary
An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page.
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