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 of disease
Subclass of sphingolipidosis,
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
Authority control
Wikidata
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leucodistrofia metacromatica (it); Leucodystrophie métachromatique (fr); leucodistròfia metacromàtica (ca); Metachromatische Leukodystrophie (de); leucodistrofia metacromática (pt); لکودیستروفی متاکروماتیک (fa); 異染性腦白質退化症 (zh); Metakromatik lökodistrofi (tr); metakromatisk leukodystrofi (sv); Leukodystrofia metachromatyczna (pl); Metakromatisk leukodystrofi (nb); Metachromatische leukodystrofie (nl); Metakromaattinen leukodystrofia (fi); metachromatic leukodystrophy (en); Leucodistrofia metacromática (gl); Leucodistrofia metacromática (es); Метахроматическая лейкодистрофия (ru) sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system (en); Лизосомные болезни накопления (ru); Krankheit (de); vrozená vada nervové soustavy (cs) MLD, Scholz cerebral sclerosis, arylsulfatase A deficiency, deficiency of cerebroside-sulfatase, sulfatide lipoidosis (en); Leucodistrofia metacromatica (es)

Subcategories

This category has only the following subcategory.