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bn:00144880n
Noun Concept
Categories: Inborn errors of carbohydrate metabolism, Rare diseases, Red blood cell disorders, Autosomal recessive disorders
EN
aldolase A deficiency  Aldoa Deficiency  Aldolase Deficiency, Red Cell  Fructose-1,6-bisphosphate aldolase A deficiency  Glycogen Storage Disease type 12
EN
Aldolase A deficiency is an autosomal recessive metabolic disorder resulting in a deficiency of the enzyme aldolase A; the enzyme is found predominantly in red blood cells and muscle tissue. Wikipedia
Definitions
Relations
Sources
EN
Aldolase A deficiency is an autosomal recessive metabolic disorder resulting in a deficiency of the enzyme aldolase A; the enzyme is found predominantly in red blood cells and muscle tissue. Wikipedia
medical condition Wikidata
IS A
disease
rare disease
hemolytic anemia
glycogen storage disease
GENETIC ASSOCIATION
ALDOA
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
aldolase A deficiency
Wikidata
EN
Aldolase A deficiency
Wikipedia Redirections
EN
ALDOA deficiency, Aldolase a deficiency, Fructose-1,6-bisphosphate aldolase A deficiency, Glycogen storage disease type XII, Red cell aldolase deficiency
Wikidata Alias
EN
Aldoa Deficiency, Aldolase a Deficiency, Aldolase Deficiency, Red Cell, Glycogen Storage Disease type 12, Glycogen storage disease type XII, GLYCOGEN STORAGE DISEASE XII, GLYCOGEN STORAGE DISEASE XII; GSD12, Glycogenosis due to aldolase A deficiency, Glycogenosis type 12, Glycogenosis type XII, GSD12, Gsd 12, GSD due to aldolase A deficiency, GSD type 12, GSD type XII, Red Cell Aldolase Deficiency

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