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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
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
1 OMIM reference -
1 associated gene
No signs/symptoms info
Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins

MT-CO1
(UniProt - OMIM)
 TRMU
(UniProt - OMIM)
MT-ND4
(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
MT-CO1 MT-ND4 MT-RNR1 MT-TS1 TRMU
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins



Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins

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):
- Acute infantile liver failure due to synthesis defect of mitochondrial DNA-encoded proteins
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare otorhinolaryngologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hepatic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the digestive 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: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.