ODCs

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1 associated gene
No signs/symptoms info

COMMON GENES: 1

3 OMIM references -
3 associated genes
No signs/symptoms info

Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy

Mitochondrial neurogastrointestinal encephalomyopathy

Citations in the biomedical literature:

Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		Mitochondrial neurogastrointestinal encephalomyopathy
	Synonym(s): - Adult-onset CPEO with mitochondrial myopathy		Synonym(s): - MNGIE

	Classification (Orphanet): - Inborn errors of metabolism - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease - Rare otorhinolaryngologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare eye disease - Rare gastroenterologic disease - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adolescence / young Average age of death: adult Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.