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What is another word for Hypoxanthine Phosphoribosyl Transferase Deficiency Disease?

Pronunciation: [hˌa͡ɪpə͡ʊzˈanθa͡ɪn fˈɒsfɔːɹˌɪbəsˌɪl tɹansfˈɜːɹe͡ɪz dɪfˈɪʃənsi dɪzˈiːz] (IPA)

Hypoxanthine Phosphoribosyl Transferase Deficiency Disease, also known as Lesch-Nyhan syndrome, is a rare genetic disorder that affects the metabolism of purine. This condition leads to the accumulation of uric acid in the body, causing severe health issues. Individuals with this disease experience a wide range of symptoms, such as joint stiffness, muscle weakness, intellectual disability, and self-injurious behavior. While there may not be absolute synonyms for this specific condition, it is often referred to as HPRT deficiency or HGprt deficiency. These alternative names help simplify and facilitate communication amongst medical professionals, researchers, and patients dealing with this challenging disorder.
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What are the opposite words for Hypoxanthine Phosphoribosyl Transferase Deficiency Disease?

Hypoxanthine Phosphoribosyl Transferase Deficiency Disease also known as Lesch-Nyhan syndrome is a rare inherited disorder that affects the nervous system and results in abnormal behavior, gout-like arthritis, and self-injurious tendencies. However, there are no antonyms for this disease as it is a medical condition with no opposite or contrasting term. Individuals with Hypoxanthine Phosphoribosyl Transferase Deficiency Disease require lifelong medical care and treatment to manage their symptoms. Although there are no antonyms for this disease, managing and treating its symptoms can improve the overall quality of life for those affected.

What are the antonyms for Hypoxanthine phosphoribosyl transferase deficiency disease?

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