Cytoscape Web
Click node...

Hemolytic anemia due to glutathione reductase deficiency
1 associated gene
12 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal dominant spastic paraplegia type 13
Charcot-Marie-Tooth disease type 4D
Encephalopathy due to hydroxykynureninuria
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Prolidase deficiency
Spinocerebellar ataxia type 26
Familial retinoblastoma
Monosomy 13q14
Neurodegenerative syndrome due to cerebral folate transport deficiency
Unilateral retinoblastoma
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
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: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
GSR P00390138300
No signs/symptoms info available.