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What is another word for Non Neuronopathic Gaucher Disease?

Pronunciation: [nˈɒn njˌuːɹənəpˈaθɪk ɡˈɔːt͡ʃə dɪzˈiːz] (IPA)

Non Neuronopathic Gaucher Disease is a rare genetic disorder characterized by the accumulation of a fatty substance in cells and certain organs. Also known as Type 1 Gaucher Disease, it involves the malfunctioning of an enzyme responsible for breaking down the fatty substance. Synonyms for Non Neuronopathic Gaucher Disease include Type 1 Gaucher Disease, Non-Neuropathic Gaucher Disease, and Glucocerebrosidase Deficiency. This condition primarily affects the liver, spleen, and bone marrow, leading to a range of symptoms such as anemia, bone pain, fatigue, enlarged spleen, and liver dysfunction. Treatment options for Non Neuronopathic Gaucher Disease include enzyme replacement therapy and supportive care to manage symptoms and improve overall quality of life.
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What are the opposite words for Non Neuronopathic Gaucher Disease?

Non Neuronopathic Gaucher Disease (NN-GD) is a hereditary disorder that causes a deficiency of the enzyme glucocerebrosidase, which leads to an abnormal accumulation of fatty substances in organs such as the liver, spleen, and bone marrow. The antonym for this term would be Neuronopathic Gaucher Disease (N-GD) which causes similar symptoms, but also affects the brain and nervous system. The symptoms of N-GD include seizures, muscle weakness, and an enlarged spleen and liver. Unlike NN-GD, N-GD can be life-threatening and requires prompt medical attention. There is currently no cure for N-GD, but early intervention with enzyme replacement therapy can significantly improve outcomes.

What are the antonyms for Non neuronopathic gaucher disease?

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