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... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > sphingolipidosis > gangliosidosis > Sandhoff disease
... > disease > metabolic diseases > lipoidosis > sphingolipidosis > gangliosidosis > Sandhoff disease
disease > enzymopathy > sphingolipidosis > gangliosidosis > Sandhoff disease
... > disease > genetic disease > hereditary disease > lysosomal storage disease > sphingolipidosis > gangliosidosis > Sandhoff disease
... > disease > metabolic diseases > lysosomal storage disease > sphingolipidosis > gangliosidosis > Sandhoff disease
... > disease > enzymopathy > lysosomal storage disease > sphingolipidosis > gangliosidosis > Sandhoff disease

Terme préférentiel

Sandhoff disease  

Définition

  • Sandhoff disease, is a lysosomal genetic, lipid storage disorder caused by the inherited deficiency to create functional beta-hexosaminidases A and B. (Wikipedia)

Concept générique

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-N9BQ3S0B-5

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