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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.