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Disease Lysosomal Alpha-N-Acetylgalactosaminidase Deficiency

Name Lysosomal Alpha-N-Acetylgalactosaminidase Deficiency
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C538648

Top ↑ Ancestors

1. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Lysosomal Storage Diseases Has associated chemicals Has associated genes Lysosomal Alpha-N-Acetylgalactosaminidase Deficiency
2. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Lysosomal Storage Diseases Has associated chemicals Has associated genes Lysosomal Alpha-N-Acetylgalactosaminidase Deficiency

Top ↑ Descendants

None.