Glycogen storage disease

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Glycogen storage disease due to glycogen debranching enzyme deficiency

ORPHA:366Disease

Also called Amylo-1,6-glucosidase deficiency · Cori disease · Cori-Forbes disease · Forbes disease · GDE deficiency · GSD due to glycogen debranching enzyme deficiency · GSD type 3 · GSDIII · Glycogen storage disease type 3 · Glycogen storage disease type III · Glycogenosis due to glycogen debranching enzyme deficiency · Glycogenosis type 3 · Glycogenosis type III · Limit dextrinosis

What it is

A rare inborn error of metabolism disease characterized by variable liver, skeletal muscle and cardiac involvement, usually presenting in early childhood.

Key facts

Prevalence
1-9 / 100 000 (at birth, United States)
Age of onset
Childhood, Infancy
Inheritance
Autosomal recessive
Classified as
Disease

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Signs and symptoms

These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.

Gene

AGLDisease-causing germline mutation(s)

ICD-10 codes

E74.0filed under a broader ICD-10 category — shared with 36 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

GARD 9442MEDDRA 10053250MESH D006010MONDO 0009291OMIM 232400UMLS C0017922

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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