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Alpha-N-acetylgalactosaminidase deficiency

MONDO:0017779

Alpha-N-acetylgalactosaminidase (NAGA) deficiency is a very rare lysosomal storage disease that is clinically and pathologically heterogeneous and is characterized by deficient NAGA activity.

Also known as: NAGA deficiency, Schindler disease, alpha-N-acetylgalactosaminidase activity disease, disorder of alpha-N-acetylgalactosaminidase activity

0 clinical trials for this condition and its sub-types.

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Sub-types

Alpha-N-acetylgalactosaminidase deficiency type 1 (0) Alpha-N-acetylgalactosaminidase deficiency type 2 (0) Alpha-N-acetylgalactosaminidase deficiency type 3 (0)

Broader categories

Disease (717) Metabolic disease (241) Hereditary disease (188) Inborn errors of metabolism (47) Lysosomal storage disease (36) Human disease (15) Developmental defect during embryogenesis (8) Carbohydrate metabolism disease (4) Disease of genetic or genomic mechanism (2) Inborn carbohydrate metabolic disorder (2)

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