Category:Metachromatic leukodystrophy

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<nowiki>Leucodistrofia metacromática; leucodystrophie métachromatique; leucodistròfia metacromàtica; Metachromatische Leukodystrophie; leucodistrofia metacromática; لکودیستروفی متاکروماتیک; 異染性腦白質退化症; Metachromatinė leukodistorfija; Metakromatik lökodistrofi; metakromatska levkodistrofija; Metakromatisk leukodystrofi; Метахроматска леукодистрофија; metakromatisk leukodystrofi; Leukodystrofia metachromatyczna; Metachromatic leukodystrophy; metachromatische leukodystrofie; metachromatic leukodystrophy; Метахроматическая лейкодистрофия; leucodistrofia metacromatica; Metakromaattinen leukodystrofia; Leucodistrofia metacromática; حثل المادة البيضاء متبدل اللون; metachromatická leukodystrofie; Metahromatska leukodistrofija; malattia da accumulo lisosomiale di tipo autosomico recessivo, ed è comunemente classificata nel gruppo delle malattie leucodistrofiche; plus fréquente des leucodystrophies causée par la mutation du gène codant l'arylsulfatase A entraînant une incapacité à cataboliser le cérébroside sulfate; хвороба людини; Лизосомные болезни накопления; մարդու հիվանդություն; Krankheit; useita neurologisia oireita aiheuttava, geenivirheestä johtuva aivojen surkastumishäiriö; human disease; وضعیت پزشکی; vrozená vada nervové soustavy; najpogostejša levkodistrofija, ki jo povzroča mutacija gena, ki kodira arilsulfatazo A, zaradi česar telo ne more katabolizirati cerebrozidnega sulfata; MLD; MLD; Scholz cerebral sclerosis; arylsulfatase A deficiency; deficiency of cerebroside-sulfatase; sulfatide lipoidosis; Leucodistrofia metacromatica</nowiki>
metachromatic leukodystrophy 
human disease
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  • 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
  • sulfatidosis
  • disease
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