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

Mitochondrial DNA depletion syndrome, hepatocerebrorenal form

Adrenocortical carcinoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	C10ORF2	(0.63)	TP53

Citations in the biomedical literature:

Mitochondrial DNA depletion syndrome, hepatocerebrorenal form		Adrenocortical carcinoma
	Synonym(s): - mtDNA depletion syndrome, hepatocerebrorenal form		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hepatic disease - Rare neurologic disease - Rare renal disease		Classification (Orphanet): - Rare circulatory system disease - Rare endocrine disease - Rare infertility - Rare oncologic disease - Rare renal disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	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: 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.