ODCs

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

PROTEIN INTERACTIONS: 1

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

Mitochondrial neurogastrointestinal encephalomyopathy

Hyper-IgM syndrome type 2


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RRM2B	(0.63)	AICDA

Citations in the biomedical literature:

Mitochondrial neurogastrointestinal encephalomyopathy		Hyper-IgM syndrome type 2
	Synonym(s): - MNGIE		Synonym(s): - AID deficiency - Activation-induced cytidine deaminase deficiency - HIGM2

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	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: (no data available)

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

No signs/symptoms info available.