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... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > sphingolipidosis > metachromatic leukodystrophy
disease > metabolic diseases > lipoidosis > sphingolipidosis > metachromatic leukodystrophy
disease > enzymopathy > sphingolipidosis > metachromatic leukodystrophy
... > disease > genetic disease > hereditary disease > lysosomal storage disease > sphingolipidosis > metachromatic leukodystrophy
disease > metabolic diseases > lysosomal storage disease > sphingolipidosis > metachromatic leukodystrophy
disease > enzymopathy > lysosomal storage disease > sphingolipidosis > metachromatic leukodystrophy
disease > degenerative disease > metachromatic leukodystrophy
disease > genetic disease > hereditary disease > lysosomal storage disease > metachromatic leukodystrophy
disease > metabolic diseases > lysosomal storage disease > metachromatic leukodystrophy
disease > enzymopathy > lysosomal storage disease > metachromatic leukodystrophy
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > leukodystrophy > metachromatic leukodystrophy
disease > degenerative disease > leukodystrophy > metachromatic leukodystrophy

Terme préférentiel

metachromatic leukodystrophy  

Définition(s)

  • Metachromatic leukodystrophy (MLD) is a lysosomal storage disease which is commonly listed in the family of leukodystrophies as well as among the sphingolipidoses as it affects the metabolism of sphingolipids. (Wikipedia)

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http://data.loterre.fr/ark:/67375/VH8-NWHZ184V-G

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