Aldolase A deficiency, also called ALDOA deficiency and red cell aldolase deficiency,^[1] is an autosomal recessive^[2] metabolic disorder resulting in a deficiency of the enzyme aldolase A, which is found predominantly in muscle and red blood cells. It may lead to myopathy, exercise intolerance and rhabdomyolysis associated with hemolytic anaemia.

Aldolase A deficiency has an autosomal recessive pattern of inheritance.

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