Category:Metachromatic leukodystrophy

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metachromatic leukodystrophy 
sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system
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Instance ofdisease
Subclass ofsphingolipidosis,
rare hereditary metabolic disease with peripheral neuropathy,
rare genetic epilepsy,
unclassified primitive or secondary maculopathy,
metabolic disease with dementia,
hereditary retinal dystrophy,
rare dyslipidemia,
neurometabolic disease,
sphingolipidosis with epilepsy
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This category has only the following subcategory.