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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

Preferred term

GM1 gangliosidosis  

Definition(s)

  • 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)

Broader concept(s)

Narrower concept(s)

Synonym(s)

  • Landing disease

In other languages

  • gangliosidose à GM1

    French

  • 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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RDF/XML TURTLE JSON-LD Last modified 5/14/20