ODCs

Click node...

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

COMMON GENES: 1

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

Autosomal recessive progressive external ophthalmoplegia

Mitochondrial DNA depletion syndrome, myopathic form

POLG	(UniProt - OMIM)		TK2	(UniProt - OMIM)
TK2	(UniProt - OMIM)

Citations in the biomedical literature:

Autosomal recessive progressive external ophthalmoplegia		Mitochondrial DNA depletion syndrome, myopathic form
	Synonym(s): - arPEO		Synonym(s): - mtDNA depletion syndrome, myopathic form

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

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

	Epidemiological data: Class of prevalence: - Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: - Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.