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Hereditary fructose intolerance
1 OMIM reference -
1 associated gene
11 connected diseases
No signs/symptoms info
Disease Type of connection
Bardet-Biedl syndrome
Glycogen storage disease due to aldolase A deficiency
Infantile cerebellar-retinal degeneration
Spondylometaphyseal dysplasia - cone-rod dystrophy
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Synonym(s):
- Hereditary fructose-1-phosphate aldolase deficiency
- Hereditary fructosemia
Classification (Orphanet):
- Inborn errors of metabolism
- Rare gastroenterologic disease
- Rare genetic disease
- Rare hepatic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
1 MeSH reference: D005633
Gene symbol UniProt reference OMIM reference
ALDOB P05062612724
No signs/symptoms info available.