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Tay-Sachs disease

MONDO:0010100

GM2 gangliosidosis, variant B or Tay-Sachs disease is marked by accumulation of G2 gangliosides due to hexosaminidase A deficiency.

Also known as: GM2 gangliosidosis, B, B1 variant, GM2-gangliosidosis, several forms, Hex A pseudodeficiency, Tay Sachs Disease, Tay-Sachs disease, disease, Tay-Sachs, hexosaminidase A deficiency, B variant GM2 gangliosidosis

20 clinical trials for this condition and its sub-types.

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Sub-types

Tay-Sachs disease, B variant, adult form (3) Tay-Sachs disease, b variant, juvenile form (1) Tay-Sachs disease, B1 variant (0) Tay-Sachs disease, b variant, infantile form (0)

Broader categories

Disease (680) Metabolic disease (233) Nervous system disorder (231) Inherited lipid metabolism disorder (189) Hereditary disease (176) Neurodegenerative disease (171) Brain disorder (125) Peripheral nervous system disorder (114) Central nervous system disorder (107) Neuromuscular disease (106)
Trials to join now! 9 Not yet recruiting 1 Not yet finished but already full! 2 Completed 4 Terminated 4
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