ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure

Turcot syndrome with polyposis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MT-ND4	(0.63)	APC

Citations in the biomedical literature:

Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure		Turcot syndrome with polyposis
	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): (no synonyms)

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: mitochondrial inheritance		Epidemiological data: (no data available)

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

No signs/symptoms info available.