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Succinyl-CoA:3-ketoacid CoA transferase deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Succinyl-CoA:3-ketoacid CoA transferase deficiency
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency

OXCT1
(UniProt - OMIM)
 PGK1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
OXCT1
(0.49)
PGK1


Citations in the biomedical literature:


Succinyl-CoA:3-ketoacid CoA transferase deficiency
OXCT1
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
PGK1



Succinyl-CoA:3-ketoacid CoA transferase deficiency
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency

Synonym(s):
- OXCT1 deficiency
- SCOT deficiency
- Succinyl-CoA acetoacetate transferase deficiency
- Succinyl-CoA:3-oxoacid CoA transferase deficiency
Synonym(s):
- GSD due to phosphoglycerate kinase 1 deficiency
- Glycogenosis due to phosphoglycerate kinase 1 deficiency
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hematologic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.