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Glutathione synthetase deficiency without 5-oxoprolinuria
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Glutathione synthetase deficiency with 5-oxoprolinuria
1 OMIM reference -
1 associated gene
No signs/symptoms info
Glutathione synthetase deficiency without 5-oxoprolinuria
Glutathione synthetase deficiency with 5-oxoprolinuria

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

COMMON
GENES 		GSS


Citations in the biomedical literature:


Glutathione synthetase deficiency without 5-oxoprolinuria
GSS
Glutathione synthetase deficiency with 5-oxoprolinuria



Glutathione synthetase deficiency without 5-oxoprolinuria
Glutathione synthetase deficiency with 5-oxoprolinuria

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
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.