About The Medical Condition Deficiency Disease, GM2 Protein Activator

ClusterMed

Find the definition of the medical term Deficiency Disease, GM2 Protein Activator. Deficiency Disease, GM2 Protein Activator defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.

Deficiency Disease, GM2 Protein Activator

Deficiency Disease, GM2 Protein Activator Medical Condition Defined & Explained
Deficiency Disease, GM2 Protein Activator Medical Condition

What's The Definition Of The Medical Condition Deficiency Disease, GM2 Protein Activator?

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.

More Medical Conditions

A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z

Medical Conditions Definitions Of The Day