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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.

This disease is not rare in Europe. It does not belong to the Orphanet nomenclature of rare diseases.

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.

This term designates an indication for a pharmacogenetic test.

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ORPHA:645

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Summary

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

Newborn screening