ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

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

Leigh syndrome with nephrotic syndrome

Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DLD	(0.63)	LDHA

Citations in the biomedical literature:

Leigh syndrome with nephrotic syndrome		Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
	Synonym(s): - Infantile subacute necrotizing encephalopathy with nephrotic syndrome - Leigh disease with nephrotic syndrome		Synonym(s): - GSD due to lactate dehydrogenase M-subunit deficiency - GSD type 11 - Glycogen storage disease type 11 - Glycogenosis due to lactate dehydrogenase M-subunit deficiency - Glycogenosis type 11 - LDH-M subunit deficiency - Lactate dehydrogenase A deficiency

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

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

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

No signs/symptoms info available.