ODCs

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

COMMON GENES: 1

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

Mitochondrial neurogastrointestinal encephalomyopathy

Autosomal recessive progressive external ophthalmoplegia

Citations in the biomedical literature:

Mitochondrial neurogastrointestinal encephalomyopathy		Autosomal recessive progressive external ophthalmoplegia
	Synonym(s): - MNGIE		Synonym(s): - arPEO

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the eye and adnexa -

	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		Epidemiological data: Class of prevalence: - Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive

	External references: 3 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.