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Phosphoenolpyruvate carboxykinase 1 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C
1 OMIM reference -
1 associated gene
No signs/symptoms info
Phosphoenolpyruvate carboxykinase 1 deficiency
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C

PCK1
(UniProt - OMIM)
 GPHN
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PCK1
(0.63)
GPHN


Citations in the biomedical literature:


Phosphoenolpyruvate carboxykinase 1 deficiency
PCK1
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C
GPHN



Phosphoenolpyruvate carboxykinase 1 deficiency
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C

Synonym(s):
- PEPCK1 deficiency
Synonym(s):
- Combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C
- MOCOD type C
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.