ODCs

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

PROTEIN INTERACTIONS: 1

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

Combined oxidative phosphorylation defect type 2

Navajo neurohepatopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MRPS16	(0.49)	MPV17

Citations in the biomedical literature:

Combined oxidative phosphorylation defect type 2		Navajo neurohepatopathy
	Synonym(s): - COXPD2		Synonym(s): - Navajo neuropathy

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): (no data available)

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