ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy

Adrenocortical carcinoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RRM2B	(0.87)	TP53

Citations in the biomedical literature:

Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		Adrenocortical carcinoma
	Synonym(s): - Adult-onset CPEO with mitochondrial myopathy		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease - Rare otorhinolaryngologic disease		Classification (Orphanet): - Rare circulatory system disease - Rare endocrine disease - Rare infertility - Rare oncologic disease - Rare renal disease

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

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: sporadic

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D018268

No signs/symptoms info available.