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Lysosomal storage disease

Lysosomal storage disease

Metabolic disorders affecting a cell's lysosomes.

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  1. Tay–Sachs disease

    Rare, severe disease of lysosomal storage.

    9.4%

  2. Gaucher's disease

    Medical condition.

    8.7%

  3. Hunter syndrome

    X-linked recessive genetic condition.

    8.3%

  4. Niemann–Pick disease type C

    Medical condition.

    8.1%

  5. Fabry disease

    Rare human genetic lysosomal storage disorder.

    6.5%

  6. Niemann–Pick disease

    Medical condition.

    5.3%

  7. Lysosome

    Cell membrane organelle.

    4.5%

  8. Glycogen storage disease type II

    Medical condition.

    3.7%

  9. Lipid storage disorder

    Group of genetic diseases involving the harmful accumulation of lipids in cells.

    3.7%

  10. Mucopolysaccharidosis

    Medical condition.

    3.2%

Readers come from

Share of the 1,943 readers arriving from another article

  1. Tay–Sachs disease

    Rare, severe disease of lysosomal storage.

    25%

  2. Fabry disease

    Rare human genetic lysosomal storage disorder.

    8.6%

  3. Mucopolysaccharidosis

    Medical condition.

    7.6%

  4. Hepatosplenomegaly

    Enlargement of the liver and spleen.

    6.3%

  5. Gaucher's disease

    Medical condition.

    5.5%

  6. Krabbe disease

    Medical condition.

    4.5%

  7. Niemann–Pick disease

    Medical condition.

    3.9%

  8. Neuronal ceroid lipofuscinosis

    Medical condition.

    3.3%

  9. Metabolic disorder

    Any disease hindering the body's ability to process and distribute nutrients.

    2.5%

  10. Pycnodysostosis

    Metabolic disorder leading to high bone density and malformation.

    2.4%