Category:Lysosomal storage diseases
From WikiMD's Wellness Encyclopedia
Pages in category "Lysosomal storage diseases"
The following 87 pages are in this category, out of 87 total.
A
C
G
- Galactocerebrosidase
- Galactosamine-6-sulfatase deficiency
- Gangliosidosis type1
- Glucosylceramidase
- Generalized gangliosidoses
- Glycogen storage disease type 2
- Glycogen storage disease type II
- GM2
- GM2 gangliosidosis, 0 variant
- GM2 gangliosidosis, type 2
- GM2-gangliosidosis, AB variant
- GM2-gangliosidosis, B, B1, AB variant
- GM2A
- GNAQ
I
M
- Mannosidosis
- Maroteaux–Le Merrer–Bensahel syndrome
- MCOLN1
- MCOLN3
- MPS
- Mucolipidosis
- Mucolipidosis type IV
- Mucolipidosis type 4
- Mucopolysaccharidosis Ih
- Mucopolysaccharidosis Is
- Mucopolysaccharidosis type I
- Mucopolysaccharidosis type I Hurler/Scheie syndrome
- Mucopolysaccharidosis type I Scheie syndrome
- Mucopolysaccharidosis type II Hunter syndrome- mild form
- Mucopolysaccharidosis type II Hunter syndrome- severe form
- Mucopolysaccharidosis type IV-A Morquio syndrome
- Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate
- Mucopolysaccharidosis type VII Sly syndrome
- Multiple sulfatase deficiency disease
