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 and heart glycogen synthase deficiency

Glycogen storage disease due to glycogenin deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GYS1	(0.91)	GYG1

Citations in the biomedical literature:

Glycogen storage disease due to muscle and heart glycogen synthase deficiency		Glycogen storage disease due to glycogenin deficiency
	Synonym(s): - GSD due to muscle and heart glycogen synthase deficiency - GSD type 0b - Glycogen storage disease type 0b - Glycogenosis due to muscle and heart glycogen synthase deficiency - Glycogenosis type 0b		Synonym(s): - GSD due to glycogenin deficiency - GSD type 15 - GSD type XV - Glycogen storage disease type 15 - Glycogen storage disease type XV - Glycogenosis due to glycogenin deficiency - Glycogenosis type 15 - Glycogenosis type XV

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: child / adolescent Type of inheritance: sporadic		Epidemiological data: Class of prevalence: <1 / 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.