Cytoscape Web
Click node...

Glutathione synthetase deficiency without 5-oxoprolinuria
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Acute neonatal citrullinemia type I
1 associated gene
No signs/symptoms info
Glutathione synthetase deficiency without 5-oxoprolinuria
Acute neonatal citrullinemia type I

GSS
(UniProt - OMIM)
 ASS1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
GSS
(0.63)
ASS1


Citations in the biomedical literature:


Glutathione synthetase deficiency without 5-oxoprolinuria
GSS
Acute neonatal citrullinemia type I
ASS1



Glutathione synthetase deficiency without 5-oxoprolinuria
Acute neonatal citrullinemia type I

Synonym(s):
(no synonyms)

Synonym(s):
- Acute neonatal citrullinemia type 1
- Classic citrullinemia type 1
- Classic citrullinemia type I
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.