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glycogen storage disease IXb

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

A disorder of glycogen metabolism caused by a deficiency in liver and muscle phosphorylase kinase subunit b, is autosomal recessive and can lead to hepatomegaly, hypoglycemia after prolonged fasting, and growth retardation.

Synonyms

  • GSD IXb
  • GSD due to liver and muscle phosphorylase kinase deficiency
  • GSD type 9B
  • GSD type IXb
  • GSD9B
  • PHKB glycogen storage disease
  • PHKB-related glycogen storage disease type IX
  • glycogen storage disease 9B
  • glycogen storage disease IXb
  • glycogen storage disease caused by mutation in PHKB
  • glycogen storage disease due to liver and muscle phosphorylase kinase deficiency
  • glycogen storage disease type 9B
  • glycogen storage disease type IXb
  • glycogenosis due to liver and muscle phosphorylase kinase deficiency
  • glycogenosis of liver and muscle, autosomal recessive
  • glycogenosis type 9B
  • glycogenosis type IXb
  • phosphorylase kinase deficiency of liver and muscle, autosomal recessive
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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