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COMMON GENES: 2
PROTEIN INTERACTIONS: 1
2 OMIM references -
14 associated genes
No signs/symptoms info
Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure
Maternally-inherited Leigh syndrome

MT-CO1 MT-ATP6
MT-ND4 MT-CO1
MT-RNR1 MT-CO2
MT-TS1 MT-CO3
TRMU MT-ND1
MT-ND2
MT-ND3
MT-ND4
MT-ND5
MT-ND6
MT-TK
MT-TL1
MT-TV
MT-TW


COMMON
GENES
MT-CO1
MT-ND4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MT-CO1
(0.63)
MT-CO2



Citations in the biomedical literature:


Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure
MT-CO1 MT-ND4 MT-RNR1 MT-TS1 TRMU
Maternally-inherited Leigh syndrome
MT-ATP6 MT-CO2 MT-CO3 MT-ND1 MT-ND2
MT-ND3 MT-ND5 MT-ND6 MT-TK MT-TL1
MT-TV MT-TW



Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure
Maternally-inherited Leigh syndrome

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):
- MILS
- Maternally-inherited Leigh disease
- Maternally-inherited infantile subacute necrotizing encephalopathy

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare otorhinolaryngologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic 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: -
Type of inheritance: mitochondrial inheritance

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

No signs/symptoms info available.