Category:Lysosomal storage diseases

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See main article: Lysosomal storage disease.

Pages in category "Lysosomal storage diseases"

The following 26 pages are in this category, out of 26 total. Updates to this list can occasionally be delayed for a few days.

*

  • Lysosomal storage disease

A

  • Alpha-mannosidosis
  • Aspartylglucosaminuria

B

  • Batten disease

C

  • Canavan disease
  • Cystinosis

F

  • Fabry's disease
  • Farber disease

G

  • Gaucher's disease
  • Glycogen storage disease type II
  • Glycoproteinosis

H

  • Hunter syndrome
  • Hurler syndrome

I

  • I-cell disease

K

  • Krabbe disease

M

  • Morquio syndrome
  • Mucolipidosis

M cont.

  • Mucolipidosis type IV
  • Mucopolysaccharidosis

N

  • Neuronal ceroid lipofuscinosis
  • Niemann-Pick disease

P

  • Pseudo-Hurler polydystrophy

S

  • Salla disease
  • Sanfilippo syndrome
  • Sialidosis
  • Sly syndrome
Categories: Inborn errors of metabolism
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  • This page was last modified 08:36, 18 March 2006 by Wikipedia user Deborah-jl.
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