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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 phosphoglycerate kinase 1 deficiency
Muscular dystrophy, Selcen type

PGK1 BAG3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PGK1
(0.63)
BAG3



Citations in the biomedical literature:


Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
PGK1
Muscular dystrophy, Selcen type
BAG3



Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
Muscular dystrophy, Selcen type

Synonym(s):
- GSD due to phosphoglycerate kinase 1 deficiency
- Glycogenosis due to phosphoglycerate kinase 1 deficiency

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: x-linked recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
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.