ODCs

Click node...

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

Sensory ataxic neuropathy - dysarthria - ophthalmoparesis

Citations in the biomedical literature:

Mitochondrial neurogastrointestinal encephalomyopathy		Sensory ataxic neuropathy - dysarthria - ophthalmoparesis
	Synonym(s): - MNGIE		Synonym(s): - SANDO

	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 - Rare neurologic disease

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

	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: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal recessive

	External references: 3 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537583

No signs/symptoms info available.