What is another word for Hexosaminidase A Deficiency Disease?
Pronunciation: [hˈɛksəsˌamɪnˌɪde͡ɪs ɐ dɪfˈɪʃənsi dɪzˈiːz] (IPA) 
Hexosaminidase A deficiency disease is a genetic disorder that affects the enzyme hexosaminidase A, resulting in the accumulation of certain substances in the body. This condition is also known as Tay-Sachs disease, which is a more commonly used term to describe this illness. Tay-Sachs disease primarily affects the nervous system and can lead to severe developmental delays, muscle weakness, and vision and hearing problems.
The synonyms for Hexosaminidase A deficiency disease are:
1. Tay-Sachs disease
2. GM2 gangliosidosis
3. Hex A deficiency disease
4. Hexosaminidase A deficiency syndrome
5. Hexosaminidase A deficiency disorder
6. Tay-Sachs syndrome
7. GM2 gangliosideosis
8. Sandhoff disease (a variant of Tay-Sachs)
These terms are often used interchangeably to refer to the same disorder, and their use depends
