Glycogen storage disease

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Glycogen storage disease

ORPHA:79201Category

Also called GSD · Glycogenosis

What it is

Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.

Key facts

Prevalence
1-9 / 100 000 (China)
Classified as
Category

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.

Genes reported in subtypes

AGLALDOAENO3GYG1LAMP2PFKMPGAM2PGK1PGM1PRKAG2PYGLPYGMRBCK1SLC2A2

Orphanet records these genes on 15 more specific entries under this disorder, not on this entry itself:

A well-studied disease is usually split into subtypes, and the gene is curated on whichever one the evidence belongs to. Open a subtype to see which gene goes with it.

ICD-10 codes

E74.0ICD-10 names this disease exactly — 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

MEDDRA 10061990MESH D006008MONDO 0002412MONDO 2412UMLS C0017919

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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