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GM2 gangliosidosis
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ORPHA:309152
Classification level: Group of disorders
Prevalence: 1-9 / 100 000
Inheritance: -
Age of onset:
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
: produced/endorsed by ERN(s)
: produced/endorsed by FSMR(s)
General public
Article for general public
Guidelines
Emergency guidelines
Clinical practice guidelines
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
- Research project(s) (56)
- Clinical trial(s) (5)
- Biobank(s) (11)
- Registry(ies) (25)
- Network of experts (9)
Newborn screening
The documents contained in this website are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.