KnowraLysosomal storage diseaseLinked fromLinked fromThe 11 pages that link to Lysosomal storage disease, each with the reason it gives.All 11Related 4Narrower topic 7LysosomeRelated: Impaired lysosomal digestion produces these diseases and their characteristic cellular deposits.Enzyme replacement therapyNarrower topic: These disorders account for many established enzyme replacement treatments.SphingolipidNarrower topic: Several sphingolipid disorders belong to this broader disease family.LeukodystrophyNarrower topic: Metabolic storage disorders account for several leukodystrophies, including metachromatic leukodystrophy and Krabbe disease.Endomembrane systemRelated: These diseases reveal the consequences of failed endomembrane degradation and transport.Protein targetingRelated: Some cases arise when lysosomal enzymes are not properly sorted to their destination.Christian de DuveRelated: Recognizing lysosomes made their enzyme deficiencies intelligible as causes of disease.Tay–Sachs diseaseNarrower topic: Tay–Sachs belongs to this group because undegraded material builds up inside cells.Farber diseaseNarrower topic: Farber disease belongs to this group because a lysosomal enzyme defect causes substrate accumulation.Glycogen storage disease type IINarrower topic: Pompe disease belongs to this family because lysosomal enzyme activity is deficient.Sanfilippo syndromeNarrower topic: Sanfilippo syndrome belongs to this broader group of disorders.