ODCs

Click node...

1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Hereditary fructose intolerance

Infantile cerebellar-retinal degeneration


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ALDOB	(0.63)	ACO2

Citations in the biomedical literature:

Hereditary fructose intolerance		Infantile cerebellar-retinal degeneration
	Synonym(s): - Hereditary fructose-1-phosphate aldolase deficiency - Hereditary fructosemia		Synonym(s): - Mitochondrial aconitase deficiency

	Classification (Orphanet): - Inborn errors of metabolism - Rare gastroenterologic disease - Rare genetic disease - Rare hepatic disease - Rare renal disease		Classification (Orphanet): - Inborn errors of metabolism - Rare eye disease - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		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		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - 1 MeSH reference: D005633		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.