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Lysosomal Alpha-N-Acetylgalactosaminidase Deficiency

Networked: 1 relevant articles (1 outcomes, 0 trials/studies)

Relationship Network

Disease Context: Research Results

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Lysosomal Storage Diseases: 2132
      - Lysosomal Alpha-N-Acetylgalactosaminidase Deficiency: 1
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Lysosomal Storage Diseases: 2132
      - Lysosomal Alpha-N-Acetylgalactosaminidase Deficiency: 1
Enzymes and Coenzymes: 1
- Enzymes: 152586
  - Hydrolases: 2166
    - Glycoside Hydrolases: 871
      - Hexosaminidases: 1037
        alpha-N-Acetylgalactosaminidase: 43
        Lysosomal Alpha-N-Acetylgalactosaminidase Deficiency: 1

Related Diseases

1.	Neuroaxonal Dystrophies (Neuroaxonal Dystrophy, Late Infantile)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Lysosomal Alpha-N-Acetylgalactosaminidase Deficiency:

1.	EnzymesIBA 08/01/1991 - "Known causes of the cutaneous manifestation were eliminated by enzyme analyses, and further characterization of the accumulated urinary O-linked sialopeptides revealed identity to those excreted by patients with an infantile neuroaxonal dystrophy due to lysosomal alpha-N-acetylgalactosaminidase deficiency. "