ODCs

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2 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Fatal infantile cytochrome C oxidase deficiency

Adrenocortical carcinoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SCO2	(0.63)	TP53

Citations in the biomedical literature:

Fatal infantile cytochrome C oxidase deficiency		Adrenocortical carcinoma
	Synonym(s): - Fatal infantile COX deficiency - Fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic 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: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: sporadic

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D018268

No signs/symptoms info available.