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

Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency

Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LDHA	(0.83)	LDHB

Citations in the biomedical literature:

Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency
	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		Synonym(s): - GSD due to lactate dehydrogenase H-subunit deficiency - Glycogenosis due to lactate dehydrogenase H-subunit deficiency - LDH-H subunit deficiency - Lactate dehydrogenase B deficiency

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.