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What is another word for Argininosuccinic Acid Synthase Deficiency Disease?

Pronunciation: [ˌɑːd͡ʒɪnˌɪnəsəksˈɪnɪk ˈasɪd sˈɪnθe͡ɪs dɪfˈɪʃənsi dɪzˈiːz] (IPA)

Argininosuccinic Acid Synthase Deficiency Disease, also known as citrullinemia type I, is a rare inherited metabolic disorder. This condition is caused by the deficiency of the enzyme argininosuccinic acid synthase, which is responsible for converting citrulline into argininosuccinic acid in the urea cycle. Due to this deficiency, toxic levels of ammonia can build up in the blood, leading to various health issues. Although commonly referred to as citrullinemia type I, some synonyms can be used interchangeably, such as argininosuccinate synthetase deficiency disease or ASSD, argininosuccinic acid synthetase deficiency disease, or even simply as urea cycle disorder type I. Early diagnosis and appropriate medical management are essential for individuals affected by this condition.
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What are the opposite words for Argininosuccinic Acid Synthase Deficiency Disease?

Antonyms are words with opposite meanings. However, for the term "Argininosuccinic Acid Synthase Deficiency Disease," finding an antonym may prove challenging. This is because it is a medical term used to describe a rare genetic disorder that affects the way the body processes proteins. Individuals with this condition lack the necessary enzymes needed to break down protein, leading to a buildup of toxic substances in the body. Given the importance of this condition, it is unlikely that there are any opposing terms or antonyms. Instead, efforts should be focused on developing effective treatments and raising awareness about the disease.

What are the antonyms for Argininosuccinic acid synthase deficiency disease?

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