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

Autosomal recessive ataxia due to ubiquinone deficiency

Adult-onset distal myopathy due to VCP mutation


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ADCK3	(0.63)	VCP

Citations in the biomedical literature:

Autosomal recessive ataxia due to ubiquinone deficiency		Adult-onset distal myopathy due to VCP mutation
	Synonym(s): - ARCA2 - Autosomal recessive ataxia due to coenzyme Q10 deficiency - Autosomal recessive cerebellar ataxia type 2 - Autosomal recessive spinocerebellar ataxia type 9 - SCAR9		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - 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: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood 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.