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What is another word for Inclusion Diseases?

Pronunciation: [ɪnklˈuːʒən dɪzˈiːzɪz] (IPA)

Inclusion diseases, also known as storage diseases or lysosomal storage disorders, encompass a group of rare genetic disorders characterized by the accumulation or inclusion of abnormal substances within cells. These disorders are caused by deficiencies or abnormalities in certain enzymes that are responsible for breaking down waste materials within the body. As a result, these substances accumulate within the lysosomes, leading to various symptoms and organ damage. Some common inclusion diseases include Gaucher disease, Fabry disease, Tay-Sachs disease, and Niemann-Pick disease. Though these disorders have distinct clinical features, they share the common feature of improper waste material processing, highlighting the importance of early diagnosis and comprehensive treatment approaches.
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What are the opposite words for Inclusion Diseases?

The term "Inclusion Diseases" refers to a range of medical conditions characterized by the presence of abnormal substances or structures within cells. Antonyms, or words that mean the opposite of inclusion diseases, include exclusion diseases, which refer to medical conditions caused by the absence or lack of a particular substance or structure within cells. Other antonyms may include normal cell function or normal cellular composition, which refer to the absence of any abnormal substances or structures within cells. Effective treatments for inclusion diseases typically need to target the underlying cause of the abnormal cellular inclusion, such as genetic mutations, infections, or toxic exposures.

What are the antonyms for Inclusion diseases?

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