About The Medical Condition Hexosaminidase Activator Protein Deficiency Disease

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Find the definition of the medical term Hexosaminidase Activator Protein Deficiency Disease. Hexosaminidase Activator Protein Deficiency Disease defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.

Hexosaminidase Activator Protein Deficiency Disease

Hexosaminidase Activator Protein Deficiency Disease Medical Condition Defined & Explained
Hexosaminidase Activator Protein Deficiency Disease Medical Condition

What's The Definition Of The Medical Condition Hexosaminidase Activator Protein Deficiency Disease?

Inherited diseases characterized by the accumulation of G(M2) GANGLIOSIDE in central nervous system lysosomes and variably in other tissues. Subtypes include TAY-SACHS DISEASE and SANDHOFF DISEASE, as well as an AB variant of BETA-N-ACETYLHEXOSAMINIDASE deficiency and an adult onset form of GM2 Gangliosidosis.

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