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What is another word for Complete Argininosuccinic Acid Synthetase Deficiency Disease?

Pronunciation: [kəmplˈiːt ˌɑːd͡ʒɪnˌɪnəsəksˈɪnɪk ˈasɪd sˈɪnθɪtˌe͡ɪs dɪfˈɪʃənsi dɪzˈiːz] (IPA)

Complete Argininosuccinic Acid Synthetase Deficiency Disease, also known as Argininosuccinic aciduria, is a rare inherited metabolic disorder. This condition is characterized by a deficiency of the enzyme argininosuccinate synthetase, which leads to the accumulation of toxic levels of argininosuccinic acid in the blood. Symptoms can include developmental delays, intellectual disability, liver dysfunction, and neurological problems. While the term "Complete Argininosuccinic Acid Synthetase Deficiency Disease" accurately describes this condition, it can be helpful to use synonyms such as Argininosuccinic aciduria or ASL deficiency to simplify discussion and understanding. These synonyms facilitate communication among healthcare professionals, patients, and their families, aiding in better comprehension and management of this complex disorder.
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What are the opposite words for Complete Argininosuccinic Acid Synthetase Deficiency Disease?

The antonyms for the term "Complete Argininosuccinic Acid Synthetase Deficiency Disease" could include words such as "healthy," "well," "normal," and "functional." These terms describe a state in which an individual does not suffer from the genetic condition that affects the urea cycle, leading to a buildup of toxic ammonia in the bloodstream. While the rare disease can cause serious health complications, including intellectual disability and liver damage, the antonyms for Complete Argininosuccinic Acid Synthetase Deficiency Disease represent the opposite end of the spectrum - a healthy individual with a properly functioning urea cycle. Early diagnosis and treatment can help manage the symptoms of the condition and prevent long-term complications.

What are the antonyms for Complete argininosuccinic acid synthetase deficiency disease?

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