Glycogen storage disease due to liver glycogen phosphorylase deficiency
Synonyms: GSD due to liver glycogen phosphorylase deficiency | GSD type 6 | GSD type VI | Glycogen storage disease type 6 | Glycogen storage disease type VI | Glycogenosis due to liver glycogen phosphorylase deficiency | Glycogenosis type 6 | Glycogenosis type VI | Hepatic glycogen phosphorylase deficiency | Hepatic phosphorylase deficiency | Hers disease | Liver glycogen phosphorylase deficiency
Liver phosphorylase deficiency or glycogen storage disease type 6b (Hers’ disease GSD 6b) is a benign and rare form of glycogen storage disease.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version September 2023.
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Glycogen storage disease due to liver glycogen phosphorylase deficiency?
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Advocacy Organizations
association for glycogen storage disease
The Association for Glycogen Storage Disease (AGSD) is a patient advocacy organization dedicated to protecting and promoting the best interest of all persons affected by the glycogen storage disease. • AGSD is committed to the identification, treatment, and cure of glycogen storage disease through programs of education, advocacy, research, and patient services.
association for glycogen storage disease
The Association for Glycogen Storage Disease (AGSD) is a patient advocacy organization dedicated to protecting and promoting the best interest of all persons affected by the glycogen storage disease. • AGSD is committed to the identification, treatment, and cure of glycogen storage disease through programs of education, advocacy, research, and patient services.
Global Liver Institute
To improve the lives of individuals and families impacted by liver disease through promoting innovation, encouraging collaboration, and scaling optimal approaches to help eradicate liver diseases.
Mississippi Metabolics Foundation
Mississippi Metabolics Foundation (MMF) was founded to raise awareness, educate, and provide support to those living or caring for someone with genetic metabolic disorders/inborn errors of metabolism (IEM).
Louisiana Metabolic Disorders Coalition
We support, educate, and advocate for patients & families affected by metabolic disorders.
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.