ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

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

Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1

Charcot-Marie-Tooth disease type 2B1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GFM1	(0.72)	LMNA

Citations in the biomedical literature:

Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1		Charcot-Marie-Tooth disease type 2B1
	Synonym(s): - Hepatoencephalopathy due to COXPD1		Synonym(s): - AR-CMT2B1 - Autosomal recessive Charcot-Marie-Tooth disease type 2B1 - Autosomal recessive axonal CMT4C1

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hepatic 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: - 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 - 1 MeSH reference: C537990

No signs/symptoms info available.