Category:Lysosomal storage diseases
From WikiMD's Wellness Encyclopedia
Pages in category "Lysosomal storage diseases"
The following 91 pages are in this category, out of 91 total.
A
C
- Cathepsin A
- Ceroid lipofuscinois, neuronal 2, late infantile
- Ceroid lipofuscinois, neuronal 3, juvenile
- Ceroid lipofuscinois, neuronal 4, adult type
- Ceroid lipofuscinois, neuronal 5, late infantile
- Ceroid lipofuscinois, neuronal 6, late infantile
- CLN3
- CLN5
- CTSD
- Cystin transport, protein defect of
- Cystinosis
G
- Galactosamine-6-sulfatase deficiency
- Galactosyl ceramide lipidosis
- Gangliosidosis type1
- Gaucher's
- Glucosylceramidase
- Generalized gangliosidoses
- Glycogen storage disease type 2
- Glycogen storage disease type II
- GM2
- GM2 gangliosidosis, 0 variant
- 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 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
N
- N-acetyl-glucosamine-6-sulfate sulfatase deficiency
- N-acetylgalactosamine-4-sulfatase
- N-acetylgalactosamine-6-sulfatase
- N-acetylglucosamine-6-sulfatase
- Neuraminidase beta-galactosidase deficiency
- Neuronal ceroid lipofuscinosis
- Niemann-Pick disease type D
- Niemann–Pick disease
- Niemann–Pick disease type C
