Mucopolysaccharidoses

Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.

Also Known As:

Mucopolysaccharidosis

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Lysosomal Storage Diseases: 2132
      - Mucopolysaccharidoses: 1610
    - Inborn Errors Carbohydrate Metabolism
      - Mucopolysaccharidoses: 1610
Skin and Connective Tissue Diseases
- Connective Tissue Diseases: 3269
  - Mucinoses: 170
    - Mucopolysaccharidoses: 1610
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Lysosomal Storage Diseases: 2132
      - Mucopolysaccharidoses: 1610
    - Inborn Errors Carbohydrate Metabolism
      - Mucopolysaccharidoses: 1610

David S Karlin Selected Research

David S Karlin Research Topics

Disease

Drug/Important Bio-Agent (IBA)