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What is another word for Glycogen Debranching Enzyme Deficiency?

Pronunciation: [ɡlˈa͡ɪkəd͡ʒən dˈɛbɹant͡ʃɪŋ ˈɛnza͡ɪm dɪfˈɪʃənsi] (IPA)

Glycogen Debranching Enzyme Deficiency refers to a rare genetic disorder that affects the metabolism of glycogen in the body. This condition, also known as Glycogen Storage Disease Type III, leads to the impaired breakdown of a complex sugar called glycogen, resulting in its abnormal accumulation in various organs. As an autosomal recessive disorder, it is caused by mutations in the AGL gene. This hereditary condition can cause a wide range of symptoms, including muscle weakness, low blood sugar, enlarged liver, growth delay, and various liver problems. Although it is commonly referred to as Glycogen Debranching Enzyme Deficiency, it can also be described as Cori Disease, Forbes Disease, Brancher Deficiency, or GDE-D.
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What are the opposite words for Glycogen Debranching Enzyme Deficiency?

The antonyms for the word "Glycogen Debranching Enzyme Deficiency" are healthy, normal, functioning, and adequate. Glycogen Debranching Enzyme Deficiency is a rare genetic disorder that affects the breakdown of glycogen, the stored form of glucose. This condition results in an abnormal accumulation of glycogen in the liver and muscles, leading to a range of symptoms including fatigue, muscle weakness, and liver enlargement. However, individuals without this disorder have well-functioning glycogen debranching enzymes that efficiently break down glycogen for energy. Therefore, the antonyms of this condition refer to individuals who do not have defective glycogen debranching enzymes and have a normal and healthy metabolism of glycogen.

What are the antonyms for Glycogen debranching enzyme deficiency?

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