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Concept information

... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > sphingolipidosis > gangliosidosis > GM1 gangliosidosis
... > disease > metabolic diseases > lipoidosis > sphingolipidosis > gangliosidosis > GM1 gangliosidosis
disease > enzymopathy > sphingolipidosis > gangliosidosis > GM1 gangliosidosis
... > disease > genetic disease > hereditary disease > lysosomal storage disease > sphingolipidosis > gangliosidosis > GM1 gangliosidosis
... > disease > metabolic diseases > lysosomal storage disease > sphingolipidosis > gangliosidosis > GM1 gangliosidosis
... > disease > enzymopathy > lysosomal storage disease > sphingolipidosis > gangliosidosis > GM1 gangliosidosis

Término preferido

GM1 gangliosidosis  

Definición

  • The GM1 gangliosidoses are caused by a deficiency of beta-galactosidase, with resulting abnormal storage of acidic lipid materials in cells of the central and peripheral nervous systems, but particularly in the nerve cells. (Wikipedia)

Concepto genérico

Conceptos específicos

etiqueta alternativa (skos)

  • Landing disease

En otras lenguas

  • gangliosidose à GM1

    francés

  • gangliosidose à GM1 infantile
  • gangliosidose de Landing type 2
  • maladie de Landing

URI

http://data.loterre.fr/ark:/67375/VH8-MXRHG0SC-N

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