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Glycogen storage disease due to GLUT2 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Glycogen storage disease due to GLUT2 deficiency
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

SLC2A2
(UniProt - OMIM)
 APP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SLC2A2
(0.56)
APP


Citations in the biomedical literature:


Glycogen storage disease due to GLUT2 deficiency
SLC2A2
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Glycogen storage disease due to GLUT2 deficiency
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- Bickel-Fanconi glycogenosis
- Fanconi-Bickel disease
- GSD due to GLUT2 deficiency
- Glycogenosis due to GLUT2 deficiency
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hepatic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
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.