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 4

Charcot-Marie-Tooth disease type 4G


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TUFM	(0.63)	HK1

Citations in the biomedical literature:

Combined oxidative phosphorylation defect type 4		Charcot-Marie-Tooth disease type 4G
	Synonym(s): - COXPD4		Synonym(s): - CMT4G - HMSNR - Hereditary motor and sensory neuropathy, Russe Type

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

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

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