ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Cardiomyopathy - hypotonia - lactic acidosis

Autosomal dominant optic atrophy and peripheral neuropathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SLC25A3	(0.49)	SPG7

Citations in the biomedical literature:

Cardiomyopathy - hypotonia - lactic acidosis		Autosomal dominant optic atrophy and peripheral neuropathy

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: - Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.