Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib

Get in touch with RARE Concierge.

Contact RARE Concierge

Synonyms: G6P deficiency type Ib | G6P translocase deficiency | G6PT deficiency | GSD due to G6P deficiency type 1b | GSD due to G6P deficiency type Ib | GSD due to G6PT deficiency | GSD type 1 non a | GSD type 1b | GSD type Ib | GSDIb | Glycogen storage disease due to G6P deficiency type Ib | Glycogen storage disease type 1b | Glycogen storage disease type Ib | Glycogenosis due to glucose-6-phosphatase deficiency type 1b | Glycogenosis due to glucose-6-phosphatase transport defect type Ib | Glycogenosis type 1b | Glycogenosis type Ib

Glycogenosis due to glucose-6-phosphatase deficiency (G6P) type b or glycogen storage disease (GSD) type 1b is a type of glycogenosis due to G6P deficiency (see this term).

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 June 2024

Newly diagnosed with
Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Advocacy Organizations

Accessia Health Foundation

Accessia Health pioneered the patient assistance model for people living with chronic medical conditions. We provide financial assistance to pay for prescriptions, medical treatments and expenses, travel and insurance premiums. Our program services include healthcare education, specialized legal services, and case management. We’re leveraging our three decades of our entrepreneurial spirit to expand patient assistance support to serve today’s healthcare consumers. Serving diverse populations is our #1 goal and we seek partners who share our belief that all people deserve to have access to healthcare. Over $1.1 billion has been distributed to patients throughout the country, helping them navigate their way through the complexities of the healthcare system. You can help us do even more.

Mississippi Metabolics Foundation

Our mission at Mississippi Metabolics Foundation (MMF) is to advocate, educate, and support families in MS affected by genetic metabolic disorders/inborn errors of metabolism (IEM's). MMF promotes initiatives and further advancements in legislation, education, research, clinical trials, studies, therapies, targeted treatments, and eventual cures for IEM’s and all rare diseases.

Ukrainian Association of Pediatric Immunology

Development of pediatric and clinical immunology in Ukraine. Raising awareness of inborn errors of immunity in Ukraine and rare immune diseases; Advocacy campaigns supporting patients with rare immune diseases and their treatment plans; Scientific research; Sharing knowledge about immunoprophylaxis; Advocacy campaigns supporting immunoprophylaxis.

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.

Don't see your organization here. Let us know here.

Clinical Trials

For a list of clinical trials in this disease area, please click here.