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

Glycogen storage disease due to muscle beta-enolase deficiency

Autosomal recessive limb-girdle muscular dystrophy type 2C


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ENO3	(0.63)	SGCG

Citations in the biomedical literature:

Glycogen storage disease due to muscle beta-enolase deficiency		Autosomal recessive limb-girdle muscular dystrophy type 2C
	Synonym(s): - GSD due to muscle beta-enolase deficiency - GSDXIII - Glycogenosis due to muscle beta-enolase deficiency - Glycogenosis type 13 - Muscle enolase deficiency - Muscular enolase deficiency		Synonym(s): - Gamma-sarcoglycanopathy - LGMD2C - Limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare cardiac disease - 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: <1 / 1 000 000 Average age onset: adulthood Average age of death: normal Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 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.