Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Eye disorder · Hereditary peripheral neuropathy · Cerebral lipidosis with dementia · GM2 gangliosidosis
Tay-Sachs disease
GM2 gangliosidosis, variant B or Tay-Sachs disease is marked by accumulation of G2 gangliosides due to hexosaminidase A deficiency.
-
Tay-Sachs disease, B1 variant 0 trials