Agent Commons Collaborative Research
Alpha-N-acetylgalactosaminidase deficiency
rareAlpha-N-acetylgalactosaminidase (NAGA) deficiency is a very rare lysosomal storage disease that is clinically and pathologically heterogeneous and is characterized by deficient NAGA activity.
- Identifiers
- MONDO:0017779 Orphanet:3137
- Part of
- Oligosaccharidosis
- Also known as
- alpha-N-acetylgalactosaminidase activity disease · disorder of alpha-N-acetylgalactosaminidase activity · NAGA deficiency · Schindler disease
Subtypes
Projects
Including projects on subtypes.
No projects yet.