ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Glycogen storage disease due to muscle phosphorylase kinase deficiency

Progressive supranuclear palsy - parkinsonism

PHKA1	(UniProt - OMIM)		MAPT	(UniProt - OMIM)
PHKG1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PHKG1	(0.63)	MAPT

Citations in the biomedical literature:

Glycogen storage disease due to muscle phosphorylase kinase deficiency		Progressive supranuclear palsy - parkinsonism
	Synonym(s): - GSD due to muscle phosphorylase kinase deficiency - GSD type 9D - GSD type 9E - GSD type IXd - GSD type IXe - Glycogen storage disease type 9D - Glycogen storage disease type 9E - Glycogen storage disease type IXd - Glycogen storage disease type IXe - Glycogenosis due to muscle phosphorylase kinase deficiency - Glycogenosis type 9D - Glycogenosis type 9E - Glycogenosis type IXd - Glycogenosis type IXe		Synonym(s): - PSP-p - PSP-parkinsonism

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare eye 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: adolescence / young Average age of death: normal Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: elderly Type of inheritance: sporadic

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

No signs/symptoms info available.