ODCs

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1 associated gene
No signs/symptoms info

COMMON GENES: 1

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

Mitochondrial DNA depletion syndrome, hepatocerebrorenal form

Sensory ataxic neuropathy - dysarthria - ophthalmoparesis

C10ORF2	(UniProt - OMIM)		C10ORF2	(UniProt - OMIM)
			POLG	(UniProt - OMIM)

Citations in the biomedical literature:

Mitochondrial DNA depletion syndrome, hepatocerebrorenal form		Sensory ataxic neuropathy - dysarthria - ophthalmoparesis
	Synonym(s): - mtDNA depletion syndrome, hepatocerebrorenal form		Synonym(s): - SANDO

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hepatic disease - Rare neurologic disease - Rare renal disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - 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: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537583

No signs/symptoms info available.