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GM2 gangliosidosis
ORPHA:309152
Classification level: Group of disorders- Synonym(s): -
- Prevalence: 1-9 / 100 000
- Inheritance: -
- Age of onset: -
- ICD-10: E75.0
- ICD-11: 5C56.00
- OMIM: -
- UMLS: C0268274
- MeSH: D020143
- GARD: -
- MedDRA: 10083933
Summary
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
Detailed information
General public
- Article for general public
- English (2010) - Socialstyrelsen
- Svenska (2016) - Socialstyrelsen
Guidelines
- Emergency guidelines
- Français (2013, pdf) - Orphanet Urgences
- Clinical practice guidelines
- Français (2021) - PNDS


Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
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