Alpha-N-acetylgalactosaminidase deficiency
What is Alpha-N-acetylgalactosaminidase deficiency?
A very rare lysosomal storage disease that is clinically and pathologically heterogeneous and is characterized by deficient NAGA activity.
Other condition names
- NAGA deficiency
- Schindler disease
Inheritance type
Autosomal recessive
Prevalence
- Worldwide: <1 in 1,000 000
Age of Onset
- Adult
- Childhood
- Infancy
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.