Glycogen Storage Disease Type VI

A hepatic GLYCOGEN STORAGE DISEASE in which there is an apparent deficiency of hepatic phosphorylase (GLYCOGEN PHOSPHORYLASE, LIVER FORM) activity.

Also Known As:

Glycogenosis Type VI; Hers' Disease; Glycogenosis VI; Hepatic Glycogen Phosphorylase Deficiency; Liver Phosphorylase Deficiency Syndrome; Disease, Hers; Disease, Hers'; Her Disease; Type VI, Glycogenosis; Glycogenosis 6; Hers Disease

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Carbohydrate Metabolism
      - Glycogen Storage Disease: 1461
        Glycogen Storage Disease Type VI: 586
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Carbohydrate Metabolism
      - Glycogen Storage Disease: 1461
        Glycogen Storage Disease Type VI: 586

Andre' Gatt Selected Research

Andre' Gatt Research Topics

Disease

Therapy/Procedure