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Mitochondrial nonsyndromic sensorineural deafness
2 OMIM references -
6 associated genes
15 connected diseases
No signs/symptoms info
Disease Type of connection
Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure
MELAS syndrome
Isolated cytochrome C oxidase deficiency
Maternally-inherited Leigh syndrome
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Genetic recurrent myoglobinuria
Leber hereditary optic neuropathy
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
LIG4 syndrome
Omenn syndrome
Isolated NADH-CoQ reductase deficiency
Autosomal dominant spastic paraplegia type 13
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Parkinsonian-pyramidal syndrome
Young adult-onset Parkinsonism
Synonym(s):
- Isolated mitochondrial neurosensory deafness
- Isolated mitochondrial sensorineural deafness
- Mitochondrial nonsyndromic neurosensory deafness
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare otorhinolaryngologic disease
Classification (ICD10):
- Diseases of the ear and mastoid process -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: mitochondrial inheritance
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.