ODCs

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

PROTEIN INTERACTIONS: 1

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

Glycogen storage disease due to aldolase A deficiency

Hereditary fructose intolerance


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ALDOA	(0.72)	ALDOB

Citations in the biomedical literature:

Glycogen storage disease due to aldolase A deficiency		Hereditary fructose intolerance
	Synonym(s): - GSD due to aldolase A deficiency - GSD type 12 - Glycogen storage disease type 12 - Glycogenosis due to aldolase A deficiency - Glycogenosis type 12		Synonym(s): - Hereditary fructose-1-phosphate aldolase deficiency - Hereditary fructosemia

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hematologic disease		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 -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		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 - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D005633

No signs/symptoms info available.