ODCs

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Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure

1 OMIM reference -
5 associated genes
No signs/symptoms info

COMMON GENES: 1

Mitochondrial myopathy with reversible cytochrome C oxidase deficiency

1 OMIM reference -
2 associated genes
No signs/symptoms info

Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure

Mitochondrial myopathy with reversible cytochrome C oxidase deficiency

MT-CO1	(UniProt - OMIM)	MT-TE	(OMIM)
MT-ND4	(UniProt - OMIM)	TRMU	(UniProt - OMIM)
MT-RNR1	(OMIM)
MT-TS1	(OMIM)
TRMU	(UniProt - OMIM)


COMMON GENES	TRMU

Citations in the biomedical literature:

Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure		Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
	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 nonsyndromic neurosensory deafness with susceptibility to aminoglycoside exposure - Mitochondrial nonsyndromic neurosensory hearing loss with susceptibility to aminoglycoside exposure - Mitochondrial nonsyndromic sensorineural hearing loss with susceptibility to aminoglycoside exposure		Synonym(s): - Benign COX deficiency - Infantile reversible cytochrome c oxidase deficiency myopathy - Mitochondrial myopathy with reversible COX deficiency - Mitochondrial myopathy with reversible complex IV deficiency - Reversible infantile cytochrome c oxidase deficiency - Reversible infantile respiratory chain deficiency

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare otorhinolaryngologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: mitochondrial inheritance		Epidemiological data: Class of prevalence: - Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: mitochondrial inheritance

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.