Schindler Disease, Type I [Supplementary Concept]
Date introduced: August 25, 2010
MeSH Unique ID: C536631
Heading Mapped to:
Entry Terms:
- Alpha-N-acetylgalactosaminidase deficiency, type 1
- Angiokeratoma Corporis Diffusum-Glycopeptiduria
- Galb Deficiency
- Lysosomal Glycoaminoacid Storage Disease-Angiokeratoma Corporis Diffusum
- Naga Deficiency
- Naga Deficiency, Type I
- Neuroaxonal dystrophy, Schindler type
- Neuronal Axonal Dystrophy, Schindler Type
- Schindler Disease
- Schindler disease, type 1
- Alpha-Galactosidase B Deficiency
- Alpha-Galnac Deficiency, Schindler Type
- Alpha-N-Acetylgalactosaminidase Deficiency
- Alpha-N-Acetylgalactosaminidase Deficiency, Type I
- Alpha-Naga Deficiency
- Schindler Disease, Type III
- NAGA Deficiency, Type III
- Alpha-N-Acetylgalactosaminidase Deficiency, Type III
- Schindler Disease, Type II
- Alpha-N-acetylgalactosaminidase deficiency adult onset
- Alpha-N-acetylgalactosaminidase deficiency type 2
- Schindler disease, type 2
- alpha-N-Acetylgalactosaminidase Deficiency, Type II
- NAGA deficiency type 2
- NAGA Deficiency, Type II
- Kanzaki disease
- Alpha-N-Acetylgalactosaminidase Deficiency, Adult-Onset